CN113368248A - 包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物 - Google Patents
包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物 Download PDFInfo
- Publication number
- CN113368248A CN113368248A CN202110619829.XA CN202110619829A CN113368248A CN 113368248 A CN113368248 A CN 113368248A CN 202110619829 A CN202110619829 A CN 202110619829A CN 113368248 A CN113368248 A CN 113368248A
- Authority
- CN
- China
- Prior art keywords
- proline
- liver
- active ingredient
- cyclamic acid
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000004480 active ingredient Substances 0.000 title claims abstract description 28
- 239000000203 mixture Substances 0.000 title claims description 21
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 25
- 210000005229 liver cell Anatomy 0.000 claims abstract description 9
- 208000019423 liver disease Diseases 0.000 claims abstract description 6
- 229960004316 cisplatin Drugs 0.000 claims description 37
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims description 37
- 150000003839 salts Chemical class 0.000 claims description 29
- 230000006907 apoptotic process Effects 0.000 claims description 20
- 125000004122 cyclic group Chemical group 0.000 claims description 17
- 206010067125 Liver injury Diseases 0.000 claims description 16
- 239000002246 antineoplastic agent Substances 0.000 claims description 15
- 231100000753 hepatic injury Toxicity 0.000 claims description 13
- 230000002401 inhibitory effect Effects 0.000 claims description 13
- 230000036541 health Effects 0.000 claims description 12
- 208000006454 hepatitis Diseases 0.000 claims description 12
- 239000003242 anti bacterial agent Substances 0.000 claims description 7
- 208000022309 Alcoholic Liver disease Diseases 0.000 claims description 6
- 206010019663 Hepatic failure Diseases 0.000 claims description 6
- 231100000354 acute hepatitis Toxicity 0.000 claims description 6
- 230000001684 chronic effect Effects 0.000 claims description 6
- 208000007386 hepatic encephalopathy Diseases 0.000 claims description 6
- 231100000283 hepatitis Toxicity 0.000 claims description 6
- 208000007903 liver failure Diseases 0.000 claims description 6
- 231100000835 liver failure Toxicity 0.000 claims description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- KLNFSAOEKUDMFA-UHFFFAOYSA-N azanide;2-hydroxyacetic acid;platinum(2+) Chemical compound [NH2-].[NH2-].[Pt+2].OCC(O)=O KLNFSAOEKUDMFA-UHFFFAOYSA-N 0.000 claims description 5
- VSRXQHXAPYXROS-UHFFFAOYSA-N azanide;cyclobutane-1,1-dicarboxylic acid;platinum(2+) Chemical compound [NH2-].[NH2-].[Pt+2].OC(=O)C1(C(O)=O)CCC1 VSRXQHXAPYXROS-UHFFFAOYSA-N 0.000 claims description 5
- 229960004562 carboplatin Drugs 0.000 claims description 5
- 239000003814 drug Substances 0.000 claims description 5
- 229950007221 nedaplatin Drugs 0.000 claims description 5
- 229960001756 oxaliplatin Drugs 0.000 claims description 5
- DWAFYCQODLXJNR-BNTLRKBRSA-L oxaliplatin Chemical compound O1C(=O)C(=O)O[Pt]11N[C@@H]2CCCC[C@H]2N1 DWAFYCQODLXJNR-BNTLRKBRSA-L 0.000 claims description 5
- 230000003115 biocidal effect Effects 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 231100000234 hepatic damage Toxicity 0.000 claims description 3
- 230000008818 liver damage Effects 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 230000028974 hepatocyte apoptotic process Effects 0.000 claims 1
- 210000004027 cell Anatomy 0.000 abstract description 23
- 230000000694 effects Effects 0.000 abstract description 14
- 210000003292 kidney cell Anatomy 0.000 abstract description 10
- 230000004224 protection Effects 0.000 abstract description 6
- 208000017169 kidney disease Diseases 0.000 abstract description 3
- 231100000331 toxic Toxicity 0.000 abstract description 2
- 230000002588 toxic effect Effects 0.000 abstract description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 28
- 241000699670 Mus sp. Species 0.000 description 21
- -1 organic base salt Chemical class 0.000 description 16
- 206010061481 Renal injury Diseases 0.000 description 14
- 229960005489 paracetamol Drugs 0.000 description 13
- 230000001681 protective effect Effects 0.000 description 13
- 229930182566 Gentamicin Natural products 0.000 description 12
- CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 description 12
- DDRJAANPRJIHGJ-UHFFFAOYSA-N creatinine Chemical compound CN1CC(=O)NC1=N DDRJAANPRJIHGJ-UHFFFAOYSA-N 0.000 description 12
- 229960002518 gentamicin Drugs 0.000 description 12
- 208000037806 kidney injury Diseases 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 239000008280 blood Substances 0.000 description 11
- 210000004369 blood Anatomy 0.000 description 11
- 235000013305 food Nutrition 0.000 description 10
- 210000003494 hepatocyte Anatomy 0.000 description 10
- 201000010099 disease Diseases 0.000 description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 9
- 238000005259 measurement Methods 0.000 description 9
- 230000003907 kidney function Effects 0.000 description 8
- 231100000417 nephrotoxicity Toxicity 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 229940109239 creatinine Drugs 0.000 description 6
- 102100036475 Alanine aminotransferase 1 Human genes 0.000 description 5
- 108010082126 Alanine transaminase Proteins 0.000 description 5
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- 231100000304 hepatotoxicity Toxicity 0.000 description 5
- 230000002265 prevention Effects 0.000 description 5
- 206010019851 Hepatotoxicity Diseases 0.000 description 4
- 241000699666 Mus <mouse, genus> Species 0.000 description 4
- 206010029164 Nephrotic syndrome Diseases 0.000 description 4
- 108090000340 Transaminases Proteins 0.000 description 4
- 235000015872 dietary supplement Nutrition 0.000 description 4
- 239000003651 drinking water Substances 0.000 description 4
- 235000020188 drinking water Nutrition 0.000 description 4
- 230000007686 hepatotoxicity Effects 0.000 description 4
- 230000003908 liver function Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000013642 negative control Substances 0.000 description 4
- 210000002307 prostate Anatomy 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- 102000014898 transaminase activity proteins Human genes 0.000 description 4
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical class CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical class CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
- 206010029155 Nephropathy toxic Diseases 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical class CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 235000001014 amino acid Nutrition 0.000 description 3
- 229940024606 amino acid Drugs 0.000 description 3
- 230000001093 anti-cancer Effects 0.000 description 3
- 229940088710 antibiotic agent Drugs 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 239000008101 lactose Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000006654 negative regulation of apoptotic process Effects 0.000 description 3
- 230000007694 nephrotoxicity Effects 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000003826 tablet Substances 0.000 description 3
- 238000012795 verification Methods 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical class NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 208000009304 Acute Kidney Injury Diseases 0.000 description 2
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 2
- 108010003415 Aspartate Aminotransferases Proteins 0.000 description 2
- 102000004625 Aspartate Aminotransferases Human genes 0.000 description 2
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 description 2
- 208000011514 Familial renal glucosuria Diseases 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical class OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical class Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 201000001431 Hyperuricemia Diseases 0.000 description 2
- 206010021036 Hyponatraemia Diseases 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 206010037597 Pyelonephritis acute Diseases 0.000 description 2
- 206010037601 Pyelonephritis chronic Diseases 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 208000033626 Renal failure acute Diseases 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- NKANXQFJJICGDU-QPLCGJKRSA-N Tamoxifen Chemical compound C=1C=CC=CC=1C(/CC)=C(C=1C=CC(OCCN(C)C)=CC=1)/C1=CC=CC=C1 NKANXQFJJICGDU-QPLCGJKRSA-N 0.000 description 2
- 208000030886 Traumatic Brain injury Diseases 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical class OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 102100026383 Vasopressin-neurophysin 2-copeptin Human genes 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 201000011040 acute kidney failure Diseases 0.000 description 2
- 201000001555 acute pyelonephritis Diseases 0.000 description 2
- 208000012998 acute renal failure Diseases 0.000 description 2
- 238000000540 analysis of variance Methods 0.000 description 2
- 238000010171 animal model Methods 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 239000003125 aqueous solvent Substances 0.000 description 2
- LNHWXBUNXOXMRL-VWLOTQADSA-N belotecan Chemical compound C1=CC=C2C(CCNC(C)C)=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 LNHWXBUNXOXMRL-VWLOTQADSA-N 0.000 description 2
- 229950011276 belotecan Drugs 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 230000005779 cell damage Effects 0.000 description 2
- 208000037887 cell injury Diseases 0.000 description 2
- 230000003833 cell viability Effects 0.000 description 2
- 201000006368 chronic pyelonephritis Diseases 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical class NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 235000003599 food sweetener Nutrition 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 235000013376 functional food Nutrition 0.000 description 2
- 230000002440 hepatic effect Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 201000008383 nephritis Diseases 0.000 description 2
- 238000007911 parenteral administration Methods 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000006187 pill Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920000136 polysorbate Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 208000007278 renal glycosuria Diseases 0.000 description 2
- 239000008109 sodium starch glycolate Substances 0.000 description 2
- 229920003109 sodium starch glycolate Polymers 0.000 description 2
- 229940079832 sodium starch glycolate Drugs 0.000 description 2
- 208000020431 spinal cord injury Diseases 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 229940032147 starch Drugs 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000829 suppository Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000003765 sweetening agent Substances 0.000 description 2
- 239000006188 syrup Substances 0.000 description 2
- 235000020357 syrup Nutrition 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Chemical class OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 230000009529 traumatic brain injury Effects 0.000 description 2
- VMPHSYLJUKZBJJ-UHFFFAOYSA-N trilaurin Chemical compound CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC VMPHSYLJUKZBJJ-UHFFFAOYSA-N 0.000 description 2
- 208000037999 tubulointerstitial fibrosis Diseases 0.000 description 2
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 description 2
- 229960004528 vincristine Drugs 0.000 description 2
- OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 description 2
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- XWKFPIODWVPXLX-UHFFFAOYSA-N 2-methyl-5-methylpyridine Chemical class CC1=CC=C(C)N=C1 XWKFPIODWVPXLX-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical class CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical class NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical class COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 208000030090 Acute Disease Diseases 0.000 description 1
- 208000024827 Alzheimer disease Diseases 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- 208000023275 Autoimmune disease Diseases 0.000 description 1
- 201000006474 Brain Ischemia Diseases 0.000 description 1
- 206010068621 Cerebellar ischaemia Diseases 0.000 description 1
- 206010008120 Cerebral ischaemia Diseases 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 229920002785 Croscarmellose sodium Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical class C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- 108010016626 Dipeptides Proteins 0.000 description 1
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Chemical class OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical class NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical class NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical class OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical class OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical class NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- 239000005517 L01XE01 - Imatinib Substances 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Chemical class NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Chemical class 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical class O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- HVRLZEKDTUEKQH-NOILCQHBSA-N Olopatadine hydrochloride Chemical compound Cl.C1OC2=CC=C(CC(O)=O)C=C2C(=C/CCN(C)C)\C2=CC=CC=C21 HVRLZEKDTUEKQH-NOILCQHBSA-N 0.000 description 1
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Chemical class NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 1
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Chemical class OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229930012538 Paclitaxel Natural products 0.000 description 1
- 208000018737 Parkinson disease Diseases 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 101710098398 Probable alanine aminotransferase, mitochondrial Proteins 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 244000299461 Theobroma cacao Species 0.000 description 1
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 1
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 1
- 102000011923 Thyrotropin Human genes 0.000 description 1
- 108010061174 Thyrotropin Proteins 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 208000036142 Viral infection Diseases 0.000 description 1
- 230000003187 abdominal effect Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical class CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229940009456 adriamycin Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 208000011775 arteriosclerosis disease Diseases 0.000 description 1
- 210000001367 artery Anatomy 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 235000001046 cacaotero Nutrition 0.000 description 1
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 229920003123 carboxymethyl cellulose sodium Polymers 0.000 description 1
- 229940084030 carboxymethylcellulose calcium Drugs 0.000 description 1
- 229940063834 carboxymethylcellulose sodium Drugs 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000010609 cell counting kit-8 assay Methods 0.000 description 1
- 238000012200 cell viability kit Methods 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 206010008118 cerebral infarction Diseases 0.000 description 1
- 229940045110 chitosan Drugs 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 229960001681 croscarmellose sodium Drugs 0.000 description 1
- 229960000913 crospovidone Drugs 0.000 description 1
- 235000010947 crosslinked sodium carboxy methyl cellulose Nutrition 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 235000019700 dicalcium phosphate Nutrition 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
- 229940093471 ethyl oleate Drugs 0.000 description 1
- VJJPUSNTGOMMGY-MRVIYFEKSA-N etoposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@H](C)OC[C@H]4O3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 VJJPUSNTGOMMGY-MRVIYFEKSA-N 0.000 description 1
- 229960005420 etoposide Drugs 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 229960002949 fluorouracil Drugs 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001530 fumaric acid Chemical class 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 229940080856 gleevec Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Chemical class 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- YLMAHDNUQAMNNX-UHFFFAOYSA-N imatinib methanesulfonate Chemical compound CS(O)(=O)=O.C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 YLMAHDNUQAMNNX-UHFFFAOYSA-N 0.000 description 1
- 230000001976 improved effect Effects 0.000 description 1
- 208000027866 inflammatory disease Diseases 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000010255 intramuscular injection Methods 0.000 description 1
- 239000007927 intramuscular injection Substances 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 229960001375 lactose Drugs 0.000 description 1
- 229940040145 liniment Drugs 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 230000007056 liver toxicity Effects 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 229940031703 low substituted hydroxypropyl cellulose Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229940098895 maleic acid Drugs 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 208000030159 metabolic disease Diseases 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000004770 neurodegeneration Effects 0.000 description 1
- 208000015122 neurodegenerative disease Diseases 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 239000011022 opal Substances 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229960001592 paclitaxel Drugs 0.000 description 1
- 230000009457 physiological apoptosis Effects 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 description 1
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000010149 post-hoc-test Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 229940069328 povidone Drugs 0.000 description 1
- 229920003124 powdered cellulose Polymers 0.000 description 1
- 235000019814 powdered cellulose Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 230000009979 protective mechanism Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Chemical class COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 235000021067 refined food Nutrition 0.000 description 1
- 230000009711 regulatory function Effects 0.000 description 1
- 239000003488 releasing hormone Substances 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007901 soft capsule Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229960001603 tamoxifen Drugs 0.000 description 1
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
- 210000000115 thoracic cavity Anatomy 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/12—Cyclic peptides with only normal peptide bonds in the ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/18—Peptides; Protein hydrolysates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/555—Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/24—Heavy metals; Compounds thereof
- A61K33/243—Platinum; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/05—Dipeptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/12—Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues
- C12N5/0602—Vertebrate cells
- C12N5/067—Hepatocytes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues
- C12N5/0602—Vertebrate cells
- C12N5/0684—Cells of the urinary tract or kidneys
- C12N5/0686—Kidney cells
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/308—Foods, ingredients or supplements having a functional effect on health having an effect on cancer prevention
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2250/00—Food ingredients
- A23V2250/54—Proteins
- A23V2250/55—Peptide, protein hydrolysate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Gastroenterology & Hepatology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- Biomedical Technology (AREA)
- Biochemistry (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Mycology (AREA)
- Food Science & Technology (AREA)
- Biophysics (AREA)
- Urology & Nephrology (AREA)
- Cell Biology (AREA)
- Microbiology (AREA)
- General Engineering & Computer Science (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Inorganic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
本发明涉及包含环组氨酸‑脯氨酸作为有效成分的细胞保护用药学组合物,本发明的包含环组氨酸‑脯氨酸作为有效成分的细胞保护用药学组合物因保护肾细胞或肝细胞免受毒性侵害的效果显著,因此可有效地用于肾疾病或肝疾病的预防或治疗。
Description
本申请是申请日为2017年7月13日,申请号为201780042925.4,题为“包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物”的专利申请的分案申请。
技术领域
本发明涉及包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物。
背景技术
环组氨酸-脯氨酸(Cyclo His-Pro,CHP)是在结构上与促甲状腺激素释放激素(thyrotropin-releasing hormone,TRH)相关的自然产生的环二肽。组氨酸-脯氨酸(CHP)为分布在动物和人的组织和体液中的缩氨酸,可在血液、精液、胃肠道、小便等中找到,尤其,属于前列腺(prostate)的丰富的代谢产物。组氨酸-脯氨酸具有抗糖尿病、抗肥胖、抗炎症、抗氧化作用等多种生理活性功能。
细胞凋亡(apoptosis)对多细胞生命体的正常发育及功能来说是重要的过程。生理性的细胞凋亡虽然在正常过程中起重要的作用,但非正常的细胞凋亡会引起多种疾病。例如,若细胞凋亡受阻碍,就会导致癌、自身免疫性疾病、炎症性疾病、病毒感染等疾病。
并且,众所周知,细胞凋亡也与阿尔茨海默病、帕金森病、肌萎缩侧索硬化(amyotrophic lateral sclerosis)、卢伽雷病等的神经退行性疾病及大脑局部缺血(cerebral ischemia)、创伤性脑损伤(traumatic brain injury)、脊髓损伤(spinal cordinjury)、脑卒中等的急性疾病有着密切的关系。
但是,对组氨酸-脯氨酸的细胞的保护效果与机制的研究尚未报告。
发明内容
技术问题
因此,本发明人已通过实验确认了环组氨酸-脯氨酸抑制因高浓度的药物处理引起的肾细胞、肝细胞的细胞凋亡并且保护细胞的事实,从而完成了本发明。
本发明的目的为提供包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分的细胞保护用药学组合物。
本发明的另一目的为提供包含环组氨酸-脯氨酸或食品学上允许的环组氨酸-脯氨酸的盐作为有效成分且预防或改善肝损伤或肾损伤的保健品。
技术方案
为了实现上述目的,本发明提供包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分的细胞保护用药学组合物。
根据本发明的实施例,上述细胞可以为肾细胞或肝细胞。
根据本发明的实施例,上述组合物用于抑制细胞凋亡。
根据本发明的实施例,上述组合物用于抑制因药剂引起的细胞损伤。
根据本发明的实施例,上述药剂为抗癌剂或抗生素,抗癌剂可以为选自由顺铂(cisplatin)、卡铂(carboplatin)、奥沙利铂(oxaliplatin)以及奈达铂(nedaplatin)组成的组中的一种以上的铂类抗癌剂。
并且,本发明提供包含环组氨酸-脯氨酸或食品学上允许的环组氨酸-脯氨酸的盐作为有效成分且用于预防或改善肝损伤或肾损伤的保健品。
根据本发明的实施例,引起上述肝的毒性或肾的毒性的药剂可以为选自由顺铂、庆大霉素及醋氨酚组成的组中的一种以上的抗癌剂或抗生素。
根据本发明的实施例,上述药学组合物包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分。
根据本发明的实施例,上述药学组合物包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分,所述肝疾病选自由肝功能衰竭、急性肝炎、慢性肝炎、慢性间质性肝炎、肝性脑病以及酒精性肝病组成的组。
根据本发明的实施例,上述药学组合物环组氨酸-脯氨酸或食品学上允许的环组氨酸-脯氨酸的盐作为有效成分。
根据本发明的实施例,上述组合物包含环组氨酸-脯氨酸或食品学上允许的环组氨酸-脯氨酸的盐作为有效成分,所述肝疾病选自由肝功能衰竭、急性肝炎、慢性肝炎、慢性间质性肝炎、肝性脑病以及酒精性肝病组成的组。
有益效果
已确认了本发明的包含环组氨酸-脯氨酸作为有效成分的细胞保护用药学组合物抑制肾细胞或肝细胞因受到毒性影响而引起的细胞凋亡,因此可作为预防及治疗肾毒性或肝毒性的组合物来使用。
附图说明
图1示出环组氨酸-脯氨酸对因庆大霉素引起的肾细胞(LLC-PK1 cell)的细胞凋亡的抑制效果:**P<0.01,***P<0.001。CHP;环组氨酸-脯氨酸,GM;庆大霉素。
图2示出环组氨酸-脯氨酸对因醋氨酚引起的肝细胞(Chang liver cell)的细胞凋亡的抑制效果:*P<0.05,***P<0.001。CHP;环组氨酸-脯氨酸,APAP;醋氨酚。
图3为为了确认实验鼠摄取的环组氨酸-脯氨酸对因顺铂引起的肝毒性起到保护作用而测量谷丙转氨酶(ALT)的曲线图。
图4为为了确认实验鼠摄取的环组氨酸-脯氨酸对因顺铂引起的肝毒性起到保护作用而测量谷草转氨酶(AST)的曲线图。
图5为为了确认实验鼠摄取的环组氨酸-脯氨酸对因顺铂引起的肾毒性起到保护作用而测量肌氨酸酐(Creatinine)的曲线图。
图6为为了确认实验鼠摄取的环组氨酸-脯氨酸对因顺铂引起的肾毒性起到保护作用而测量血尿素氮(BUN)的曲线图。
具体实施方式
以下,对本发明进行详细的说明。
确认了本发明的包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物具有抑制肾细胞或肝细胞的细胞凋亡的效果。
本发明提供包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分的用于保护细胞的组合物。根据本发明的实施例,上述环组氨酸-脯氨酸可从前列腺提取物(Prostate extract)分离。
化学式1:
本发明的包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分的用于保护细胞的组合物可保护肾细胞或肝细胞。
本发明的包含环组氨酸-脯氨酸作为有效成分的组合物可抑制细胞凋亡。
本发明的组合物抑制因药剂引起的细胞损伤,上述药剂可以为抗癌剂或抗生素,具体地,可以为选自由顺铂、卡铂、奥沙利铂以及奈达铂组成的组中的一种以上的如铂类抗癌剂或庆大霉素或醋氨酚等的抗生素。
本发明的药学组合物可额外包含在药学组合物的制造过程中通常使用的适当的载体、赋形剂或稀释剂。在此情况下,上述组合物所包含的上述环组氨酸-脯氨酸、环组氨酸-脯氨酸的盐、提取物或分馏物的含量并不特别受此限制,但是,相对于组合物总重量,可制备成包含0.0001重量百分比至10重量百分比,优选地,包含0.001重量百分比至1重量百分比。
本发明的术语“药学上允许的盐”意味着阳离子与阴离子通过静电引力相结合而成的盐中的药剂学上可使用的形态的盐,通常为金属盐、有机碱盐、无机酸盐、有机酸盐、碱性及酸性氨基酸盐等。例如,金属盐可包括碱金属盐(钠盐、钾盐等)、碱土金属盐(钙盐、镁盐、钡盐等)、铝盐等;有机碱盐可包括三乙胺、吡啶、甲基吡啶、2,6-二甲基吡啶、乙醇胺、二乙醇胺、三乙醇胺、环己胺、二环己基胺、N,N-二苄乙烯二胺等的盐;无机酸盐可包括盐酸、氢溴酸、硝酸、硫酸、磷酸等的盐;有机酸盐包括甲酸、乙酸、三氟乙酸、邻苯二甲酸、反丁烯二酸、二乙酸、果酸、顺丁烯二酸、柠檬酸、琥珀酸、甲磺酸、苯磺酸、p-甲苯磺酸等的盐;碱性氨基酸盐可包括精氨酸、赖氨酸、鸟氨酸等的盐;酸性氨基酸盐可包括天冬氨酸、谷氨酸等的盐。
本发明的组合物优选为药学组合物,上述药学组合物可以口服或非经口给药,在非经口给药的情况下,优选地,选择皮肤外用或腹腔内注射、直肠内注射、皮下注射、静脉注射、肌肉注射或胸部注射等给药方式。
根据本发明的药学组合物还可包括通常使用的赋形剂、分裂剂、甜味剂、润滑剂、增香剂等。上述分裂剂包括淀粉乙醇酸钠、交联聚维酮、交联羧甲基纤维素钠、海藻酸、羧甲基纤维素钙、羟甲基纤维素钠、几丁聚糖、瓜尔胶、低取代羟基丙基纤维素、镁铝硅酸盐、聚克立林钾等。并且,本发明的药学组合物还可包含药学上允许的添加剂,在此情况下,药学上允许的添加剂可使用淀粉、凝胶淀粉、微晶纤维素、乳糖、聚维酮、二氧化硅、磷酸氢钙、乳糖(Lactose)、甘露醇、麦芽糖、阿拉伯树胶、预糊化淀粉、玉米淀粉、粉状纤维素、羟丙基纤维素、欧巴代、淀粉乙醇酸钠、巴西棕榈蜡、复合硅酸铝、硬脂酸、硬脂酸镁、硬脂酸铝、硬脂酸钙、白糖、葡萄糖、山梨醇、滑石等。优选地,根据本发明的药剂学上可接受的添加剂相对于上述药学组合物包含0.1~90重量份。
用于口服的固形制剂包括散剂、颗粒剂、片剂、胶囊、软胶囊剂、丸等。悬浮剂、口服溶液剂、乳剂、糖浆剂、喷雾剂等属于用于口服的液体药剂,可包括经常使用的作为单纯稀释剂的水、液体石蜡、此外还有各种赋形剂,例如润湿剂、甜味剂、芳香剂、保鲜剂等。用于非经口给药的制剂各自根据通常的方法通过以散剂、颗粒剂、片剂、胶囊、灭菌水溶液、液体制剂、非水溶剂、悬浮剂、乳液、糖浆、栓剂、喷雾剂等的外用剂及灭菌注射制剂的形态来进行成型化的方式使用,优选地,可制备乳霜、凝胶、补丁、喷雾剂、软膏、石膏、乳液、擦剂、贴剂或泥敷剂等皮肤外用药学组合物来使用,但不限于此。作为非水溶剂、悬浮剂可使用丙二醇(propylene glycol)、聚乙二醇、如橄榄油的植物油、如油酸乙酯的可注射的酯等。作为栓剂的基质可使用半合成脂肪酸酯(witepsol)、聚乙二醇、吐温(tween)61、可可油脂、甘油三月桂酸酯、甘油明胶等。
本发明的药学组合物的优选给药量可根据体内的活性成分的吸收度、杀菌率及排泄速度、患者的年龄、性别及状态、要治疗的疾病的重症程度而异,但是也可以被相关技术人员适当地选择。但是为了优选的效果,在口服剂的情况下,通常给成人按每1公斤体重每日给药0.0001mg/kg至100mg/kg的本发明的药学组合物为佳,优选地,给药0.001mg/kg至100mg/kg为佳。给药可以每日给药一次或者分多次来给药。上述给药量在任何方面都不限定本发明的范围。本发明的药学组合物基本上没有毒性或副作用,长时间服用时也可以放心使用。
本发明的药学组合物在保护肾细胞方面有明显的效果,选自由肾炎、急性肾盂肾炎、慢性肾盂肾炎、急性肾功能衰竭、肾小管间质纤维化障碍、肾病综合征(Nephroticsyndrome)、肾性尿崩症、电解质代谢异常高尿酸血症以及低钠血症组成的组中且对保护肝细胞有明显的效果,因此有效地利用于选自由肝功能衰竭、急性肝炎、慢性肝炎、慢性间质性肝炎、肝性脑病以及酒精性肝病组成的组中且很好地利用于预防及治疗疾病。
本发明的包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分的组合物可作为用于预防或治疗因抗癌剂引起的肝毒性或肾毒性的抗癌补助剂来使用。
上述抗癌补助剂可与顺铂、卡铂、奥沙利铂、奈达铂、阿霉素、紫杉酚、他莫昔芬、CKD602(CamTOBELL)、氟尿嘧啶、格列卫、依托泊苷、择泰、长春新碱(oncovin)等现有的抗癌剂并行给药,以减少肝毒性或肾毒性而增加抗癌效果。
并且,本发明提供包含环组氨酸-脯氨酸或食品学上允许的环组氨酸-脯氨酸的盐作为有效成分且用于预防或改善肝损伤或肾损伤的保健品。
上述可引起肝损伤或肾损伤的药剂可以为选自由顺铂、庆大霉素及醋氨酚组成的组中的一种以上的抗癌剂或抗生素。
本发明的术语“食品学上允许的盐”表示在阳离子与阴离子通过静电引力来结合而成的盐中的食品学上可使用的形态的盐,关于其种类的具体例包含上述的“药学上允许的盐”的例。
在本发明,术语“保健品(health food)”表示相比于普通食品,能够积极地维持健康或有提高效果的食品,保健补品(health supplement food)表示具有健康补助目的的食品。根据情况,功能食品、保健品、保健补品的术语可互用。上述食品为了得到好的效果,可以制备成片剂、胶囊、粉末、颗粒、液相、丸等多种形态。
在本发明,术语“功能食物(functional food)”与特殊保健品(food for specialhealth use,FoSHU)是相同的术语,表示以除供给营养之外能够有效地呈现人体调节功能的方式被加工的医学、医疗效果高的食品。
作为这种保健品的具体例,可制备通过利用上述组合物发挥农产物、畜产物或水产物等的特性来使得进行变形的同时,便于存储的加工食品。
本发明的保健品具有保护肾细胞的效果突出,因此可用于预防及治疗选自由肾炎、急性肾盂肾炎、慢性肾盂肾炎、急性肾功能衰竭、肾小管间质纤维化障碍、肾病综合征(Nephrotic syndrome)、肾性尿崩症、电解质代谢异常高尿酸血症以及低钠血症组成的组中的疾病;本发明的保健品具有保护肝细胞的效果突出,因此作为保健品可有效地利用于预防或改善选自由肝功能衰竭、急性肝炎、慢性肝炎、慢性间质性肝炎、肝性脑病以及酒精性肝病组成的组中的疾病。
<实施例1>对环组氨酸-脯氨酸抑制肾细胞凋亡的分析
确认了通过环组氨酸-脯氨酸对因庆大霉素引起的肾细胞的细胞凋亡的抑制效果。
具体地,邀请了缩氨酸专门制造企业(Bachem;布本多夫,瑞士)来只制备了目标规格为99%纯度的环组氨酸-脯氨酸。庆大霉素是从西格玛化工公司(Sigma Chemical Co.,美国密苏里州圣路易斯)购买的,肾细胞(LLC-PK1cell)是从美国模式培养物保藏所(American Type Culture Collection;ATCC;美国弗吉尼亚州马纳萨斯市)购买的。在肾细胞,使0.1mg/mL、1mg/mL、5mg/mL及10mg/mL的环组氨酸-脯氨酸分别与5mg/mL的庆大霉素同时进行处理并培养了6小时(图1的A部分)。
并且,在肾细胞,对0.1mg/mL、1mg/mL、5mg/mL及10mg/mL的环组氨酸-脯氨酸分别进行预处理并培养了2小时后,添加庆大霉素5mg/mL来进一步培养了4小时(图1的B部分)。使用细胞活性检测试剂盒(cell counting kit-8;日本同仁化学研究所;日本熊本)分析并使用酶标仪(分子器件;美国加州桑尼维尔)测量了细胞存活率。
结果,庆大霉素引起了肾细胞的细胞凋亡,环组氨酸-脯氨酸浓度依赖性地抑制了因庆大霉素引起的肾细胞的细胞凋亡。尤其,对环组氨酸-脯氨酸在肾细胞进行预处理时,大大地抑制了因庆大霉素引起的细胞凋亡。
<实施例2>对环组氨酸-脯氨酸抑制肝细胞凋亡的分析
确认了环组氨酸-脯氨酸对因醋氨酚(acetaminophen,APAP)引起的肝细胞的细胞凋亡的抑制效果。
具体地,醋氨酚是从西格玛化工公司(Sigma Chemical Co.;美国密苏里州圣路易斯)购买的,肝细胞(Chang liver cell)是从美国模式培养物保藏所(American TypeCulture Collection;ATCC;美国弗吉尼亚州马纳萨斯市)购买的。在肝细胞,对0.1mg/mL、1mg/mL、5mg/mL或10mg/mL的环组氨酸-脯氨酸分别与15mM的醋氨酚一起同时进行预处理并培养了24小时(图2的A部分)。
并且,在肝细胞,在对0.1mg/mL、1mg/mL、5mg/mL及10mg/mL的环组氨酸-脯氨酸分别进行预处理并培养24小时后,添加15mM的醋氨酚,进一步培养了24小时(图2的B部分)。使用细胞活性检测试剂盒来分析并使用酶标仪来测量了细胞存活率。
结果,醋氨酚引起了肝细胞的细胞凋亡,环组氨酸-脯氨酸浓度依赖性地抑制了因醋氨酚引起的肝细胞的细胞凋亡。尤其,在肝细胞对环组氨酸-脯氨酸与醋氨酚同时进行处理时,大大地抑制了因醋氨酚引起的细胞凋亡。
<实施例3>对摄取环组氨酸-脯氨酸的动物模型中因顺铂引起的肝损伤的抑制效果分析
<3-1>环组氨酸-脯氨酸的摄取及顺铂的给药
为了测量环组氨酸-脯氨酸对实验鼠的肝毒性的保护效果,从韩国科泰克(CoreTech Co.,Ltd.)购买了SD小鼠,并在规定条件下(温度:23±3℃、相对湿度:55±10%、一周期:12小时)进行了饲养。5只作为一组并在笼子里自由供给了水和食物,而且在实验前经过一个星期驯化后在实验中使用。顺应期间结束后,分为5个组来进行了如下表1的实验。
表1
第1组摄取水并设定为阴性对照组,第2组摄取水后设定为因给药顺铂导致的肝损伤的对照组,第3组以饮水方式摄取1mg/L的环组氨酸-脯氨酸,第4组以饮水方式摄取5mg/L的环组氨酸-脯氨酸,第5组以饮水方式摄取10mg/L的环组氨酸-脯氨酸并在一个星期后,设定为对因给药顺铂导致的肝损伤的保护效果组。以饮水方式每2日更换1次供给环组氨酸-脯氨酸。
<3-2>测量对小鼠的肝功能的保护效果
为了确认环组氨酸-脯氨酸对肝功能的保护效果,首先给小鼠分浓度给药了环组氨酸-脯氨酸一个星期后,给药顺铂,过24小时后确认了肝功能。为了测量谷丙转氨酶与谷草转氨酶,从小鼠的腹动脉采集了血液后,通过离心分离器只把血清分离后,利用自动分析器(automatic analyzer;Hitachi 7180;日本东京)来进行了测量。
结果,如图3及图4所示,阴性对照组与因顺铂引起的肝损伤组实施了验证t并验证了其显著性,统计学上呈现出显著的差异(#p<0.05,###p<0.0005)。
并且,因顺铂引起的肝损伤组与给药环组氨酸-脯氨酸组之间利用方差分析(ANOVA)的显著差来进行多重比较,并利用图基事后检验法来做了个别比较,在统计学上呈现出显著的差异(*p<0.05,**p<0.005)。
给小鼠给药顺铂就会引起肝损伤,可以确认谷丙转氨酶及谷草转氨酶增加。并且,确认了摄取环组氨酸-脯氨酸的小鼠因顺铂增加的谷丙转氨酶及谷草转氨酶明显减少。
因此,环组氨酸-脯氨酸有效减少能确认血中肝功能数据的谷丙转氨酶及谷草转氨酶浓度,包含环组氨酸-脯氨酸作为有效成分的药学组合物对保护肝细胞效果显著,所以更好地使用于由肝病组成的疾病的预防及治疗。
<实施例4>对摄取环组氨酸-脯氨酸的动物模型中因顺铂引起的肾损伤的抑制效果分析
<4-1>环组氨酸-脯氨酸的摄取及顺铂的给药
为了测量环组氨酸-脯氨酸对实验鼠的肾毒性的保护效果,从韩国科泰克购买了ICR小鼠,在规定条件下(温度:23±3℃、相对湿度:55±10%、一周期:12小时)进行了饲养。5只作为一组并在笼子里自由供给了水和食物,而且在实验前经过一个星期驯化后用于实验了。在顺应期间结束后,分为3个组来进行了如下表2的实验。
表2
第1组摄取水后设定为阴性对照组,第2组摄取水后设定为对因给药顺铂导致的肾损伤的对照组,第3组每日摄取1mg/L的环组氨酸-脯氨酸一个星期,并设定为对因给药顺铂导致的肾损伤的保护效果组。
<4-2>测量对小鼠的肾功能的保护效果
为了确认环组氨酸-脯氨酸对肾功能的保护效果,首先使用1ml注射器,在每天给小鼠口服浓度为1mg/kg的环组氨酸-脯氨酸后,给药顺铂,经过72小时后确认了肾功能。为了测量肌氨酸酐,从小鼠心脏采集了血液,通过离心分离器只把血清分离后,利用全自动生化分析仪(BS-390,中国迈瑞生物医学电子有限公司,Mindray Bio-Medical ElectronicsCo.,Ltd.,)来进行了测量。图5示出了其结果。上述实验结果通过与经过顺铂处理的肝损伤组不同的实验组之间实施验证t来验证其显著性,统计学上呈现出显著的差异(#p<0.05,##p<0.005)。
如图5所示,给小鼠给药顺铂就会导致肾损伤并可确认肌氨酸酐增加。并且,确认了摄取环组氨酸-脯氨酸的小鼠因顺铂而增加的肌氨酸酐明显减少。
因此,有效减少能确认环组氨酸-脯氨酸的血中肾功能数据的肌氨酸酐的浓度,包含环组氨酸-脯氨酸作为有效成分的药学组合物对保护肾细胞效果显著,所以更好地使用于由肾疾病组成的疾病的预防及治疗。
<实施例5>对摄取环组氨酸-脯氨酸的小鼠中因顺铂引起的肾损伤的抑制效果测量
<5-1>环组氨酸-脯氨酸的摄取及顺铂的给药
为了测量环组氨酸-脯氨酸对小鼠的肾毒性的保护效果,从韩国科泰克购买了ICR小鼠,在规定条件下(温度:23±3℃、相对湿度:55±10%、一周期:12小时)进行了饲养。5只作为一组并在笼子里自由供给了水和食物,而且在实验前经过一个星期驯化后在实验中使用。顺应期间结束后,分3个组来进行了如下表3的实验。
表3
1组取水后设定为摄阴性对照组,2组摄取水后设定为对因给药顺铂导致的肾损伤的对照组,3组每日口服1mg/kg的环组氨酸-脯氨酸一个星期后,设定为对因给药顺铂导致的肾损伤的保护效果组。
<5-2>测量对小鼠的肾功能的保护效果
为了确认环组氨酸-脯氨酸对肾功能的保护效果,首先每日口服浓度为1mg/kg的环组氨酸-脯氨酸一个星期,给药顺铂,经过24小时后确认了肾功能。为了测量血尿素氮,从小鼠心脏采集血液,通过离心分离器只把血清分离后,利用全自动生化分析仪来进行了测量。
最终,如图6所示,上述实验结果通过与因顺铂引起的肝损伤组不同的实验组之间实施验证t来验证了其显著性,统计学上呈现出显著的差异(#p<0.05)。
给小鼠给药顺铂就会导致肾损伤,因此可以确认血尿素氮增加。并且,确认了摄取环组氨酸-脯氨酸的小鼠因顺铂而增加的血尿素氮明显减少(图6)。
因此,有效减少可确认环组氨酸-脯氨酸的血中肾功能数据的血尿素氮的浓度,包含环组氨酸-脯氨酸作为有效成分的药学组合物对保护肾细胞效果显著,所以更好地使用于由肾疾病组成的疾病的预防及治疗。确认了根据本发明的环组氨酸-脯氨酸对作为抗癌剂的顺铂抑制及减少肝损伤或肾损伤具有优秀的效果,可作为用于预防及治疗由抗癌剂引起的肝损伤或肾损伤的药学组合物或保健品来有效使用。
以上,对本发明重点查看了其优选实施例。本发明所属技术领域的普通技术人员可在不脱离本发明的本质特性的范围内以变形的实施方式体现本发明。因此,所公开的实施例,应从说明的观点来进行理解,而不是限定的观点。本发明的范围由发明要求保护范围来体现,而不是上述说明,应理解的是,与发明要求保护范围等同的范围内的所有不同之处均属于本发明的范围。
Claims (5)
1.一种药学组合物在制备抑制因抗癌剂或抗生素引起的肝细胞凋亡的药物中的应用,其特征在于,所述药学组合物包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分。
2.根据权利要求1所述的应用,其特征在于,上述抗癌剂为选自由顺铂、卡铂、奥沙利铂及奈达铂组成的组中的一种以上的铂类抗癌剂。
3.一种药学组合物在制备抑制因肝疾病引起的肝细胞凋亡的药物中的应用,其特征在于,所述药学组合物包含环组氨酸-脯氨酸或药学上允许的环组氨酸-脯氨酸的盐作为有效成分,所述肝疾病选自由肝功能衰竭、急性肝炎、慢性肝炎、慢性间质性肝炎、肝性脑病以及酒精性肝病组成的组。
4.一种组合物在制备预防或改善因抗癌剂或抗生素引起的肝损伤的保健品中的应用,其特征在于,所述药学组合物环组氨酸-脯氨酸或食品学上允许的环组氨酸-脯氨酸的盐作为有效成分。
5.一种组合物在制备预防或改善因肝疾病引起的肝损伤的保健品中的应用,其特征在于,所述组合物包含环组氨酸-脯氨酸或食品学上允许的环组氨酸-脯氨酸的盐作为有效成分,所述肝疾病选自由肝功能衰竭、急性肝炎、慢性肝炎、慢性间质性肝炎、肝性脑病以及酒精性肝病组成的组。
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2016-0088751 | 2016-07-13 | ||
KR20160088751 | 2016-07-13 | ||
KR1020170088341A KR102012554B1 (ko) | 2016-07-13 | 2017-07-12 | 사이클로 히스티딘-프롤린을 유효성분으로 포함하는 세포 보호용 조성물 |
KR10-2017-0088341 | 2017-07-12 | ||
PCT/KR2017/007518 WO2018012901A1 (ko) | 2016-07-13 | 2017-07-13 | 사이클로 히스티딘-프롤린을 유효성분으로 포함하는 세포 보호용 조성물 |
CN201780042925.4A CN109476701B (zh) | 2016-07-13 | 2017-07-13 | 包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201780042925.4A Division CN109476701B (zh) | 2016-07-13 | 2017-07-13 | 包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113368248A true CN113368248A (zh) | 2021-09-10 |
CN113368248B CN113368248B (zh) | 2022-09-16 |
Family
ID=61029076
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201780042925.4A Active CN109476701B (zh) | 2016-07-13 | 2017-07-13 | 包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物 |
CN202110619829.XA Active CN113368248B (zh) | 2016-07-13 | 2017-07-13 | 包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201780042925.4A Active CN109476701B (zh) | 2016-07-13 | 2017-07-13 | 包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物 |
Country Status (5)
Country | Link |
---|---|
US (3) | US10918693B2 (zh) |
EP (2) | EP3797788A1 (zh) |
JP (3) | JP6750087B2 (zh) |
KR (2) | KR102012554B1 (zh) |
CN (2) | CN109476701B (zh) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102012554B1 (ko) * | 2016-07-13 | 2019-08-23 | 주식회사 노브메타파마 | 사이클로 히스티딘-프롤린을 유효성분으로 포함하는 세포 보호용 조성물 |
WO2019098811A2 (ko) | 2017-11-20 | 2019-05-23 | 주식회사 노브메타파마 | Chp(시클로-히스프로)를 포함하는 골 손실 질환의 예방, 개선 또는 치료용 조성물 |
KR102133151B1 (ko) * | 2019-03-28 | 2020-07-13 | 주식회사 노브메타파마 | Chp(사이클로-히스프로)를 포함하는 복막 섬유증의 예방, 개선 또는 치료용 조성물 |
KR102115353B1 (ko) * | 2019-05-17 | 2020-05-26 | 주식회사 노브메타파마 | Chp(사이클로-히스프로) 및 부갑상선 호르몬을 포함하는 골 손실 질환의 예방, 개선 또는 치료용 조성물 |
JP2023518955A (ja) * | 2020-03-20 | 2023-05-09 | ノブメタファーマ カンパニー リミテッド | 血圧降下のためのchp(シクロ-ヒスプロ)の用途 |
WO2021255691A1 (en) * | 2020-06-17 | 2021-12-23 | Novmetapharma Co., Ltd. | Compositions and methods for treating virus infection |
EP4199949A4 (en) * | 2020-08-20 | 2024-10-16 | Novmetapharma Co Ltd | METHOD OF TREATMENT OF INFLAMMATORY ABDOMINAL CONDITIONS |
US12053467B2 (en) * | 2020-12-18 | 2024-08-06 | NovMeta Pharma Co., Ltd. | Method of treating fibrosis |
WO2024069524A1 (en) * | 2022-09-29 | 2024-04-04 | Novmetapharma Co., Ltd. | Peg-modified cyclic dipeptides |
WO2024121811A1 (en) * | 2022-12-08 | 2024-06-13 | Novmetapharma Co., Ltd. | Composition and method for prolong survival of transplant and recipient |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6060446A (en) * | 1994-04-29 | 2000-05-09 | Wake Forest University | Method and composition for treating renal disease and failure |
CN1997365A (zh) * | 2004-06-14 | 2007-07-11 | 措泽·B.·扎拉马 | 含有脯氨酸或其衍生物以及抗肿瘤抗体的抗癌组合物 |
US20100048887A1 (en) * | 2008-04-18 | 2010-02-25 | Eric Anderson | Compounds including an anti-inflammatory pharmacore and methods of use |
CN101674842A (zh) * | 2007-03-02 | 2010-03-17 | 普瑞芬医药有限公司 | 治疗阿尔茨海默氏病和痴呆的组合物和方法 |
US20100183520A1 (en) * | 2009-01-20 | 2010-07-22 | The Penn State Research Foundation | Netrin-1 as a biomarker of injury and disease |
US20140113884A1 (en) * | 2011-04-06 | 2014-04-24 | John David Imig | Epoxyeicosatrienoic acid analogs and methods of making and using the same |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2774959C (en) * | 2000-08-04 | 2016-05-31 | Dmi Biosciences, Inc. | Method of using diketopiperazines and composition containing them |
KR100562385B1 (ko) * | 2004-06-10 | 2006-03-20 | 서형주 | 플라보자임에 의한 신경전달물질인 Cyclo-His-Pro 함유하는 효모 가수분해물 제조방법 |
US8507496B2 (en) * | 2010-09-07 | 2013-08-13 | Dmi Acquisition Corp. | Treatment of diseases |
KR101418968B1 (ko) * | 2011-07-08 | 2014-07-14 | 대구대학교 산학협력단 | CHP(cyclo(His-Pro))를 고농도로 함유한 대두 가수분해물을 포함하는 혈당 조절용 조성물 |
US10556964B2 (en) * | 2014-07-21 | 2020-02-11 | Wuhan Yzy Biopharma Co., Ltd. | Bispecific antibody-mediated cancer therapy with cytokine-induced killer cell |
EP3313435A1 (en) * | 2015-06-26 | 2018-05-02 | Institute for Research in Biomedicine | Novel vaccines in prevention and treatment of malaria |
WO2017002906A1 (ja) * | 2015-07-02 | 2017-01-05 | サントリーホールディングス株式会社 | アルコール吸収抑制用組成物 |
KR102012554B1 (ko) * | 2016-07-13 | 2019-08-23 | 주식회사 노브메타파마 | 사이클로 히스티딘-프롤린을 유효성분으로 포함하는 세포 보호용 조성물 |
WO2018030879A1 (ko) * | 2016-08-12 | 2018-02-15 | 주식회사 노브메타파마 | 아모디아퀸 및 항당뇨 약물을 유효성분으로 함유하는 당뇨병의 예방 또는 치료용 약학적 조성물 |
-
2017
- 2017-07-12 KR KR1020170088341A patent/KR102012554B1/ko active IP Right Grant
- 2017-07-13 CN CN201780042925.4A patent/CN109476701B/zh active Active
- 2017-07-13 US US16/316,595 patent/US10918693B2/en active Active
- 2017-07-13 CN CN202110619829.XA patent/CN113368248B/zh active Active
- 2017-07-13 JP JP2019501912A patent/JP6750087B2/ja active Active
- 2017-07-13 EP EP20206943.1A patent/EP3797788A1/en active Pending
- 2017-07-13 EP EP17827971.7A patent/EP3486252B1/en active Active
-
2019
- 2019-08-13 KR KR1020190098520A patent/KR102179736B1/ko active IP Right Grant
-
2020
- 2020-05-13 JP JP2020084215A patent/JP6929413B2/ja active Active
- 2020-12-07 JP JP2020202646A patent/JP7128880B2/ja active Active
-
2021
- 2021-02-10 US US17/172,879 patent/US11433114B2/en active Active
-
2022
- 2022-07-01 US US17/856,729 patent/US11890317B2/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6060446A (en) * | 1994-04-29 | 2000-05-09 | Wake Forest University | Method and composition for treating renal disease and failure |
CN1997365A (zh) * | 2004-06-14 | 2007-07-11 | 措泽·B.·扎拉马 | 含有脯氨酸或其衍生物以及抗肿瘤抗体的抗癌组合物 |
CN101674842A (zh) * | 2007-03-02 | 2010-03-17 | 普瑞芬医药有限公司 | 治疗阿尔茨海默氏病和痴呆的组合物和方法 |
US20100048887A1 (en) * | 2008-04-18 | 2010-02-25 | Eric Anderson | Compounds including an anti-inflammatory pharmacore and methods of use |
US20100183520A1 (en) * | 2009-01-20 | 2010-07-22 | The Penn State Research Foundation | Netrin-1 as a biomarker of injury and disease |
US20140113884A1 (en) * | 2011-04-06 | 2014-04-24 | John David Imig | Epoxyeicosatrienoic acid analogs and methods of making and using the same |
Non-Patent Citations (6)
Title |
---|
A. MINELLI等: "Focus on cyclo(His-Pro): history and perspectives as antioxidant peptide", 《AMINO ACIDS》 * |
ALBA MINELLI等: "Cyclo(His-Pro) exerts anti-inflammatory effects by modulating NF- B and Nrf2 signalling", 《THE INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY》 * |
ALBA MINELLI等: "Cyclo(His-Pro) promotes cytoprotection by activating Nrf2-mediated up-regulation of antioxidant defence", 《J. CELL. MOL. MED.》 * |
ALBA MINELLI等: "Phosphoproteomic analysis of the effect of cyclo-[His-Pro] dipeptide on PC12 cells", 《PEPTIDES》 * |
ILARIA BELLEZZA等: "Neuroinflammation and endoplasmic reticulum stress are coregulated by cyclo(His-Pro) to prevent LPS neurotoxicity", 《THE INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY》 * |
KOO, KWANG BON等: "Protective Effect of Cyclo(His-Pro) on Streptozotocin-Induced Cytotoxicity and Apoptosis In Vitro", 《J. MICROBIOL. BIOTECHNOL.》 * |
Also Published As
Publication number | Publication date |
---|---|
CN109476701A (zh) | 2019-03-15 |
US20210161998A1 (en) | 2021-06-03 |
KR102179736B1 (ko) | 2020-11-18 |
CN109476701B (zh) | 2022-02-25 |
CN113368248B (zh) | 2022-09-16 |
JP6750087B2 (ja) | 2020-09-02 |
KR20190104921A (ko) | 2019-09-11 |
US20220331396A1 (en) | 2022-10-20 |
JP2019530638A (ja) | 2019-10-24 |
EP3486252A1 (en) | 2019-05-22 |
KR102012554B1 (ko) | 2019-08-23 |
KR20180008305A (ko) | 2018-01-24 |
JP7128880B2 (ja) | 2022-08-31 |
US20190290720A1 (en) | 2019-09-26 |
EP3486252B1 (en) | 2023-06-07 |
EP3486252A4 (en) | 2020-05-27 |
US10918693B2 (en) | 2021-02-16 |
EP3797788A1 (en) | 2021-03-31 |
US11890317B2 (en) | 2024-02-06 |
JP2021046435A (ja) | 2021-03-25 |
US11433114B2 (en) | 2022-09-06 |
JP2020128411A (ja) | 2020-08-27 |
JP6929413B2 (ja) | 2021-09-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN113368248B (zh) | 包含环组氨酸-脯氨酸作为有效成分的用于保护细胞的组合物 | |
US11938123B2 (en) | Use of 2,3,5-substituted thiophene compound to prevent, ameliorate, or treat breast cancers | |
JP2010106019A (ja) | リマプロストを含有してなる癌化学療法に起因する末梢神経障害予防、治療および/または症状軽減剤 | |
CN112089710A (zh) | 4-羟基异亮氨酸在制备抗肿瘤药物中的应用 | |
CN103965274A (zh) | 一种芹菜素-7-o-β-D-葡萄糖醛酸苷制备方法及用途 | |
WO2018012901A1 (ko) | 사이클로 히스티딘-프롤린을 유효성분으로 포함하는 세포 보호용 조성물 | |
JP2007520431A (ja) | 血糖降下用組成物 | |
KR101965591B1 (ko) | 키토올리고당을 함유하는 아밀레이즈 활성 저해용 조성물 | |
CN106822152B (zh) | 一种药物组合物及其应用 | |
CN113304139B (zh) | Viniferifuran在制备黄嘌呤氧化酶抑制药物中的应用 | |
KR20130071664A (ko) | 바이러스 억제 활성을 갖는 플라보노이드 화합물 | |
US20240009211A1 (en) | Pharmaceutical composition for treatment of lung cancer comprising cannabidiol and anticancer agent as active ingredients, and use thereof | |
CN105748589A (zh) | 一种治疗腹泻的中西药复方兽药及其制备方法和用途 | |
TW201907939A (zh) | 南洋山蘇水萃物的用途 | |
KR101899086B1 (ko) | 간손상 예방, 개선 또는 치료용 조성물 | |
EP4121035A1 (en) | Use of bucillamine in the treatment of infectious diseases | |
CN116392476A (zh) | 协同抑制胰脂肪酶的组合物及其应用 | |
CN117064936A (zh) | 一种药物组合物及在抑菌药物制备中的应用 | |
WO2017015777A1 (zh) | 表没食子儿茶素没食子酸酯、其类似物和它们的转化产物及其各自可药用盐的应用 | |
CN112137996A (zh) | 一种预防钩吻中毒的药物 | |
CN107648586A (zh) | 一种治疗脂肪肝的药物及其制备方法 | |
TW201909909A (zh) | 南洋山蘇水萃物的用途 | |
KR20180029317A (ko) | 간손상 예방, 개선 또는 치료용 조성물 | |
WO2008007450A1 (fr) | Aliment, boisson et composition médicinale ayant un effet antitumoral |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |