IL104874A - Phytocyanine clot complexes of pharmaceutical preparations containing them and the process for their preparation - Google Patents

Phytocyanine clot complexes of pharmaceutical preparations containing them and the process for their preparation

Info

Publication number: IL104874A
Authority: IL; Israel
Prior art keywords: carbon atoms; formula; germanium; bis; phthalocyanine
Prior art date: 1992-02-27

Application number

IL104874A

Other languages

English (en)

Hebrew (he)

Other versions

IL104874A0 (en

Original Assignee

Ciba Geigy Ag

Priority date (The priority date 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 date listed.)

1992-02-27

Filing date

1993-02-26

Publication date

1998-06-15

1993-02-26 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1993-06-10 Publication of IL104874A0 publication Critical patent/IL104874A0/xx

1998-06-15 Publication of IL104874A publication Critical patent/IL104874A/en

Links

238000000034 method Methods 0.000 title claims description 15
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 title claims description 14
239000008194 pharmaceutical composition Substances 0.000 title claims description 12
238000002360 preparation method Methods 0.000 title claims description 10
239000013522 chelant Substances 0.000 title abstract description 7
206010028980 Neoplasm Diseases 0.000 claims abstract description 18
238000002512 chemotherapy Methods 0.000 claims abstract description 13
KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims abstract description 8
229910052732 germanium Inorganic materials 0.000 claims abstract description 8
GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims abstract description 8
229910052707 ruthenium Inorganic materials 0.000 claims abstract description 8
229910052782 aluminium Inorganic materials 0.000 claims abstract description 4
239000004411 aluminium Substances 0.000 claims abstract description 4
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 73
150000001875 compounds Chemical class 0.000 claims description 60
-1 n-hexadecyloxy, cis-9-octadecenyloxy Chemical group 0.000 claims description 35
125000000217 alkyl group Chemical group 0.000 claims description 20
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 20
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol group Chemical group [C@@H]1(CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)[C@H](C)CCCC(C)C HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 19
125000001931 aliphatic group Chemical class 0.000 claims description 17
239000001257 hydrogen Substances 0.000 claims description 17
229910052739 hydrogen Inorganic materials 0.000 claims description 17
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
125000003545 alkoxy group Chemical group 0.000 claims description 11
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
239000001301 oxygen Substances 0.000 claims description 11
229910052760 oxygen Inorganic materials 0.000 claims description 11
229910052736 halogen Inorganic materials 0.000 claims description 9
125000004414 alkyl thio group Chemical group 0.000 claims description 8
150000002367 halogens Chemical class 0.000 claims description 8
241001465754 Metazoa Species 0.000 claims description 7
125000005103 alkyl silyl group Chemical group 0.000 claims description 7
125000004423 acyloxy group Chemical group 0.000 claims description 5
125000002947 alkylene group Chemical group 0.000 claims description 5
230000000737 periodic effect Effects 0.000 claims description 4
239000003937 drug carrier Substances 0.000 claims description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 3
230000001225 therapeutic effect Effects 0.000 claims description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
125000003302 alkenyloxy group Chemical group 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 2
GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 abstract description 2
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract description 2
229910052733 gallium Inorganic materials 0.000 abstract description 2
229910052738 indium Inorganic materials 0.000 abstract description 2
APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 abstract description 2
229910052718 tin Inorganic materials 0.000 abstract description 2
LKKPNUDVOYAOBB-UHFFFAOYSA-N naphthalocyanine Chemical compound N1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)N3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 LKKPNUDVOYAOBB-UHFFFAOYSA-N 0.000 abstract 1
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 53
239000000203 mixture Substances 0.000 description 34
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 33
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 28
239000000243 solution Substances 0.000 description 22
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
239000002904 solvent Substances 0.000 description 20
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 18
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
238000010992 reflux Methods 0.000 description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 12
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 11
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 10
239000007858 starting material Substances 0.000 description 10
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 9
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
239000013078 crystal Substances 0.000 description 8
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
238000001816 cooling Methods 0.000 description 7
239000000706 filtrate Substances 0.000 description 7
239000002244 precipitate Substances 0.000 description 7
239000011541 reaction mixture Substances 0.000 description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
238000001035 drying Methods 0.000 description 6
238000009472 formulation Methods 0.000 description 6
239000000047 product Substances 0.000 description 6
125000001424 substituent group Chemical group 0.000 description 6
229910052786 argon Inorganic materials 0.000 description 5
OLLFKUHHDPMQFR-UHFFFAOYSA-N dihydroxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](O)(O)C1=CC=CC=C1 OLLFKUHHDPMQFR-UHFFFAOYSA-N 0.000 description 5
238000001704 evaporation Methods 0.000 description 5
230000008020 evaporation Effects 0.000 description 5
239000002502 liposome Substances 0.000 description 5
239000012074 organic phase Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
PCHWMZGABVKUSP-UHFFFAOYSA-N 16,16-diphenylhexadecoxy(hydroxy)silane Chemical compound C=1C=CC=CC=1C(CCCCCCCCCCCCCCCO[SiH2]O)C1=CC=CC=C1 PCHWMZGABVKUSP-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
241000699670 Mus sp. Species 0.000 description 4
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000012267 brine Substances 0.000 description 4
YCITZMJNBYYMJO-UHFFFAOYSA-N chloro(diphenyl)silicon Chemical compound C=1C=CC=CC=1[Si](Cl)C1=CC=CC=C1 YCITZMJNBYYMJO-UHFFFAOYSA-N 0.000 description 4
235000012000 cholesterol Nutrition 0.000 description 4
239000012043 crude product Substances 0.000 description 4
238000001914 filtration Methods 0.000 description 4
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 4
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 4
239000000741 silica gel Substances 0.000 description 4
229910002027 silica gel Inorganic materials 0.000 description 4
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 4
SLNYBUIEAMRFSZ-UHFFFAOYSA-N 2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol Chemical compound COCCOCCOCCOCCOCCO SLNYBUIEAMRFSZ-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000004480 active ingredient Substances 0.000 description 3
239000003153 chemical reaction reagent Substances 0.000 description 3
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 3
150000002431 hydrogen Chemical group 0.000 description 3
239000008101 lactose Substances 0.000 description 3
WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 3
239000000843 powder Substances 0.000 description 3
VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 3
238000000746 purification Methods 0.000 description 3
239000011877 solvent mixture Substances 0.000 description 3
WODLURYTHKQUET-UHFFFAOYSA-N 1-[2-(2-chloroethoxy)ethoxy]-2-methoxyethane Chemical compound COCCOCCOCCCl WODLURYTHKQUET-UHFFFAOYSA-N 0.000 description 2
YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 2
208000030507 AIDS Diseases 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
241000700159 Rattus Species 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
241000700605 Viruses Species 0.000 description 2
RNZDACWUXZHQMI-PCHCLZCRSA-N [(8s,9s,10r,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] 4-methylbenzenesulfonate Chemical compound C([C@H]1[C@@H]2CC[C@@H]([C@]2(CC[C@@H]1[C@@]1(C)CC2)C)[C@H](C)CCCC(C)C)C=C1CC2OS(=O)(=O)C1=CC=C(C)C=C1 RNZDACWUXZHQMI-PCHCLZCRSA-N 0.000 description 2
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000000304 alkynyl group Chemical group 0.000 description 2
238000009835 boiling Methods 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
SPWVRYZQLGQKGK-UHFFFAOYSA-N dichloromethane;hexane Chemical compound ClCCl.CCCCCC SPWVRYZQLGQKGK-UHFFFAOYSA-N 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
239000003814 drug Substances 0.000 description 2
FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
ONTXANRUPSHTPK-KTKRTIGZSA-N hydroxy-[(z)-octadec-9-enoxy]-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](O)(OCCCCCCCC\C=C/CCCCCCCC)C1=CC=CC=C1 ONTXANRUPSHTPK-KTKRTIGZSA-N 0.000 description 2
IKSRMYRCWBAVIQ-UHFFFAOYSA-N hydroxy-octadecoxy-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](O)(OCCCCCCCCCCCCCCCCCC)C1=CC=CC=C1 IKSRMYRCWBAVIQ-UHFFFAOYSA-N 0.000 description 2
239000005457 ice water Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 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
QYIXCDOBOSTCEI-RZOVDRORSA-N (5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-ol Chemical compound C([C@@H]1CC2)C(O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CC1 QYIXCDOBOSTCEI-RZOVDRORSA-N 0.000 description 1
XXXFZKQPYACQLD-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl acetate Chemical compound CC(=O)OCCOCCO XXXFZKQPYACQLD-UHFFFAOYSA-N 0.000 description 1
HUHXLHLWASNVDB-UHFFFAOYSA-N 2-(oxan-2-yloxy)oxane Chemical group O1CCCCC1OC1OCCCC1 HUHXLHLWASNVDB-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
MPAIWVOBMLSHQA-UHFFFAOYSA-N 3,6-dihydroxybenzene-1,2-dicarbonitrile Chemical compound OC1=CC=C(O)C(C#N)=C1C#N MPAIWVOBMLSHQA-UHFFFAOYSA-N 0.000 description 1
ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 description 1
208000002874 Acne Vulgaris Diseases 0.000 description 1
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
206010003210 Arteriosclerosis Diseases 0.000 description 1
238000011725 BALB/c mouse Methods 0.000 description 1
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201000009030 Carcinoma Diseases 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
241000282412 Homo Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
208000007766 Kaposi sarcoma Diseases 0.000 description 1
238000005684 Liebig rearrangement reaction Methods 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
201000004681 Psoriasis Diseases 0.000 description 1
206010039491 Sarcoma Diseases 0.000 description 1
206010070834 Sensitisation Diseases 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
CKLZCJHXRHNZFB-UHFFFAOYSA-N [4-(2-methoxyethyl)phenyl]methanesulfonic acid Chemical compound COCCC1=CC=C(CS(O)(=O)=O)C=C1 CKLZCJHXRHNZFB-UHFFFAOYSA-N 0.000 description 1
210000000683 abdominal cavity Anatomy 0.000 description 1
206010000496 acne Diseases 0.000 description 1
125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
125000004466 alkoxycarbonylamino group Chemical group 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
125000004419 alkynylene group Chemical group 0.000 description 1
125000005133 alkynyloxy group Chemical group 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
238000010171 animal model Methods 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
229960000271 arbutin Drugs 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
208000011775 arteriosclerosis disease Diseases 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
230000037396 body weight Effects 0.000 description 1
244000309464 bull Species 0.000 description 1
201000011510 cancer Diseases 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
WZQSBCHNVPAYOC-UHFFFAOYSA-N chloro(trihexyl)silane Chemical compound CCCCCC[Si](Cl)(CCCCCC)CCCCCC WZQSBCHNVPAYOC-UHFFFAOYSA-N 0.000 description 1
GZGREZWGCWVAEE-UHFFFAOYSA-N chloro-dimethyl-octadecylsilane Chemical compound CCCCCCCCCCCCCCCCCC[Si](C)(C)Cl GZGREZWGCWVAEE-UHFFFAOYSA-N 0.000 description 1
150000004292 cyclic ethers Chemical class 0.000 description 1
OSXYHAQZDCICNX-UHFFFAOYSA-N dichloro(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](Cl)(Cl)C1=CC=CC=C1 OSXYHAQZDCICNX-UHFFFAOYSA-N 0.000 description 1
230000008034 disappearance Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000007429 general method Methods 0.000 description 1
150000002291 germanium compounds Chemical class 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
NYMPGSQKHIOWIO-UHFFFAOYSA-N hydroxy(diphenyl)silicon Chemical compound C=1C=CC=CC=1[Si](O)C1=CC=CC=C1 NYMPGSQKHIOWIO-UHFFFAOYSA-N 0.000 description 1
CUUJVBDPSUOTIQ-UHFFFAOYSA-N hydroxy-dimethyl-octadecylsilane Chemical compound CCCCCCCCCCCCCCCCCC[Si](C)(C)O CUUJVBDPSUOTIQ-UHFFFAOYSA-N 0.000 description 1
230000002779 inactivation Effects 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000007912 intraperitoneal administration Methods 0.000 description 1
238000001990 intravenous administration Methods 0.000 description 1
150000002632 lipids Chemical class 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
238000012544 monitoring process Methods 0.000 description 1
QXHRJCQMYAREHW-UHFFFAOYSA-N n,n-dimethylformamide;tetrachlorogermane Chemical compound CN(C)C=O.Cl[Ge](Cl)(Cl)Cl QXHRJCQMYAREHW-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
238000002428 photodynamic therapy Methods 0.000 description 1
230000002165 photosensitisation Effects 0.000 description 1
XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
JUJWROOIHBZHMG-RALIUCGRSA-N pyridine-d5 Chemical compound [2H]C1=NC([2H])=C([2H])C([2H])=C1[2H] JUJWROOIHBZHMG-RALIUCGRSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000012552 review Methods 0.000 description 1
208000017520 skin disease Diseases 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
241000894007 species Species 0.000 description 1
125000005415 substituted alkoxy group Chemical group 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
IEXRMSFAVATTJX-UHFFFAOYSA-N tetrachlorogermane Chemical compound Cl[Ge](Cl)(Cl)Cl IEXRMSFAVATTJX-UHFFFAOYSA-N 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1
238000002054 transplantation Methods 0.000 description 1
JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
NLSXASIDNWDYMI-UHFFFAOYSA-N triphenylsilanol Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(O)C1=CC=CC=C1 NLSXASIDNWDYMI-UHFFFAOYSA-N 0.000 description 1
230000004614 tumor growth Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/069—Aluminium compounds without C-aluminium linkages
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
- C07F15/0053—Ruthenium compounds without a metal-carbon linkage
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/003—Compounds containing elements of Groups 3 or 13 of the Periodic Table without C-Metal linkages
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/003—Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0836—Compounds with one or more Si-OH or Si-O-metal linkage
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H23/00—Compounds containing boron, silicon, or a metal, e.g. chelates, vitamin B12
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J43/00—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton
- C07J43/003—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton not condensed
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J51/00—Normal steroids with unmodified cyclopenta(a)hydrophenanthrene skeleton not provided for in groups C07J1/00 - C07J43/00

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Biochemistry (AREA)
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Pharmacology & Pharmacy (AREA)
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Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
General Chemical & Material Sciences (AREA)
Steroid Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Diaphragms For Electromechanical Transducers (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Medicines Containing Plant Substances (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polyethers (AREA)

IL104874A 1992-02-27 1993-02-26 Phytocyanine clot complexes of pharmaceutical preparations containing them and the process for their preparation IL104874A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH60092		1992-02-27

Publications (2)

Publication Number	Publication Date
IL104874A0 IL104874A0 (en)	1993-06-10
IL104874A true IL104874A (en)	1998-06-15

Family

ID=4190744

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL104874A IL104874A (en)	1992-02-27	1993-02-26	Phytocyanine clot complexes of pharmaceutical preparations containing them and the process for their preparation

Country Status (22)

Country	Link
US (3)	US5358940A (no)
EP (1)	EP0558449B1 (no)
JP (1)	JPH0656839A (no)
KR (1)	KR100270284B1 (no)
CN (1)	CN1044476C (no)
AT (1)	ATE196143T1 (no)
AU (1)	AU662800B2 (no)
CA (1)	CA2090772A1 (no)
DE (1)	DE59310096D1 (no)
DK (1)	DK0558449T3 (no)
ES (1)	ES2151502T3 (no)
FI (1)	FI930831A (no)
GR (1)	GR3034887T3 (no)
HU (1)	HUT64075A (no)
IL (1)	IL104874A (no)
MX (1)	MX9301083A (no)
NO (1)	NO930719L (no)
NZ (1)	NZ247000A (no)
PT (1)	PT558449E (no)
SG (1)	SG49615A1 (no)
TW (1)	TW235298B (no)
ZA (1)	ZA931382B (no)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
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US5484778C1 (en) *	1990-07-17	2001-05-08	Univ Cleveland Hospitals	Phthalocynine photosensitizers for photodynamic therapy and methods for their use
US5179120A (en) *	1991-06-28	1993-01-12	Cytopharm, Inc.	Porphycene compounds for photodynamic therapy
GB9123814D0 (en) *	1991-11-08	1992-01-02	Johnson Matthey Plc	Photosensitizers
TW235298B (no) *	1992-02-27	1994-12-01	Ciba Geigy
GB9405970D0 (en) *	1994-03-25	1994-05-11	Secr Defence	Substituted phthalocyanines
RU2106146C1 (ru) *	1995-07-17	1998-03-10	Институт элементоорганических соединений РАН	Средство для подавления опухолевого роста
US5763602A (en) *	1996-10-01	1998-06-09	Li; Ying-Syi	Methods of syntheses of phthalocyanine compounds
US5872248A (en) *	1997-03-28	1999-02-16	Case Western Reserve University	Methods for inserting silicon into phthalocyanines and naphthalocyanines
IL121440A0 (en)	1997-07-31	1998-01-04	Yeda Res & Dev	The use of 1,3,4,6-tetrahydroxy-helianthrone and its derivatives in photodynamic therapy and certain such novel derivatives
AU3507900A (en) *	1999-03-05	2000-09-21	Case Western Reserve University	Hydrophobic liquid photobleaches
US8211883B2 (en) *	2004-04-01	2012-07-03	Case Western Reserve University	Topical delivery of phthalocyanines
US7153956B2 (en) *	2004-08-09	2006-12-26	Silverbrook Research Pty Ltd	Cyanine dye having multifunctional peripheral groups
JP2010163473A (ja) *	2009-01-13	2010-07-29	Konica Minolta Business Technologies Inc	インクジェット記録用シアンインク
US8440641B2 (en) *	2009-03-20	2013-05-14	Case Western Reserve University	Phthalocyanine salt formulations
EP2976347B1 (en)	2013-03-15	2022-01-19	McFarland, Sherri Ann	Metal-based coordination complexes as photodynamic compounds and their use
JP6767695B2 (ja) *	2018-03-29	2020-10-14	パナソニックＩｐマネジメント株式会社	組成物、近赤外光電変換素子および撮像装置
WO2019188118A1 (ja) *	2018-03-29	2019-10-03	パナソニックＩｐマネジメント株式会社	組成物、光電変換素子および撮像装置

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US3094535A (en) *	1961-01-03	1963-06-18	Malcolm E Kenney	Germanium phthalocyanines
US3094536A (en) *	1961-01-03	1963-06-18	Malcolm E Kenney	Silicon phthalocyanines
CA1337194C (en) *	1988-04-07	1995-10-03	Koichi Kamijima	Tetraazaporphin, process for producing the same, as well as optical recording media using the same and production processes thereof
US5109016A (en) *	1988-05-23	1992-04-28	Georgia State University Foundation, Inc.	Method for inhibiting infection or replication of human immunodeficiency virus with porphyrin and phthalocyanine antiviral compositions
DE3829851A1 (de) *	1988-09-02	1990-03-08	Basf Ag	Tetraazaporphyrine sowie strahlungsempfindliche beschichtungsfilme
US5457195A (en) *	1989-12-21	1995-10-10	Board Of Regents, The University Of Texas System	Sapphyrin derivatives and conjugates
DE59102143D1 (de) *	1990-04-03	1994-08-18	Ciba Geigy Ag	Parenteral applizierbare Liposomenformulierung aus synthetischen Lipiden.
WO1991018007A1 (en) *	1990-05-15	1991-11-28	Diatron Corporation	Phthalocyanatopolyethylene glycol, and phthalocyanato saccharides as fluorescent digoxin reagents
DE69132750T2 (de) *	1990-05-15	2002-06-20	Hyperion, Inc.	Fluoreszierende porphyrin- und fluoreszierende phthalocyanin-polyethylenglykol-, polyol- und saccharidderivate als fluoreszierende sonden
US5120649A (en) *	1990-05-15	1992-06-09	New York Blood Center, Inc.	Photodynamic inactivation of viruses in blood cell-containing compositions
US5166197A (en) *	1990-07-17	1992-11-24	Kenney Malcolm E	Phthalocyanine photosensitizers for photodynamic therapy
DE69130054T2 (de) *	1990-07-23	1999-01-07	Hitachi Chemical Co., Ltd., Tokio/Tokyo	Perfluoralkyliertes naphthalocyaninderivat, seine herstellung sowie ein optisches aufzeichnungsmedium
GB9123814D0 (en) *	1991-11-08	1992-01-02	Johnson Matthey Plc	Photosensitizers
TW235298B (no) *	1992-02-27	1994-12-01	Ciba Geigy

1993
- 1993-02-04 TW TW082100745A patent/TW235298B/zh active
- 1993-02-18 SG SG1996001068A patent/SG49615A1/en unknown
- 1993-02-18 ES ES93810100T patent/ES2151502T3/es not_active Expired - Lifetime
- 1993-02-18 DK DK93810100T patent/DK0558449T3/da active
- 1993-02-18 AT AT93810100T patent/ATE196143T1/de not_active IP Right Cessation
- 1993-02-18 DE DE59310096T patent/DE59310096D1/de not_active Expired - Fee Related
- 1993-02-18 EP EP93810100A patent/EP0558449B1/de not_active Expired - Lifetime
- 1993-02-18 PT PT93810100T patent/PT558449E/pt unknown
- 1993-02-24 FI FI930831A patent/FI930831A/fi unknown
- 1993-02-24 AU AU33768/93A patent/AU662800B2/en not_active Ceased
- 1993-02-25 US US08/022,246 patent/US5358940A/en not_active Expired - Fee Related
- 1993-02-25 CA CA002090772A patent/CA2090772A1/en not_active Abandoned
- 1993-02-25 NZ NZ247000A patent/NZ247000A/en unknown
- 1993-02-26 HU HU9300554A patent/HUT64075A/hu unknown
- 1993-02-26 JP JP5038723A patent/JPH0656839A/ja active Pending
- 1993-02-26 ZA ZA931382A patent/ZA931382B/xx unknown
- 1993-02-26 KR KR1019930002814A patent/KR100270284B1/ko not_active IP Right Cessation
- 1993-02-26 NO NO93930719A patent/NO930719L/no unknown
- 1993-02-26 CN CN93102147A patent/CN1044476C/zh not_active Expired - Fee Related
- 1993-02-26 IL IL104874A patent/IL104874A/en not_active IP Right Cessation
- 1993-02-26 MX MX9301083A patent/MX9301083A/es not_active IP Right Cessation
1994
- 1994-06-30 US US08/269,290 patent/US5670491A/en not_active Expired - Fee Related
1995
- 1995-12-15 US US08/573,102 patent/US5686439A/en not_active Expired - Fee Related
2000
- 2000-11-22 GR GR20000402576T patent/GR3034887T3/el not_active IP Right Cessation

Also Published As

Publication number	Publication date
IL104874A0 (en)	1993-06-10
CN1044476C (zh)	1999-08-04
JPH0656839A (ja)	1994-03-01
KR930017912A (ko)	1993-09-20
FI930831A (fi)	1993-08-28
KR100270284B1 (ko)	2000-10-16
ES2151502T3 (es)	2001-01-01
PT558449E (pt)	2001-02-28
US5670491A (en)	1997-09-23
NZ247000A (en)	1995-07-26
TW235298B (no)	1994-12-01
US5686439A (en)	1997-11-11
MX9301083A (es)	1993-09-01
EP0558449A1 (de)	1993-09-01
HUT64075A (en)	1993-11-29
AU3376893A (en)	1993-09-02
AU662800B2 (en)	1995-09-14
ATE196143T1 (de)	2000-09-15
EP0558449B1 (de)	2000-09-06
CN1075966A (zh)	1993-09-08
NO930719L (no)	1993-08-30
GR3034887T3 (en)	2001-02-28
DE59310096D1 (de)	2000-10-12
FI930831A0 (fi)	1993-02-24
US5358940A (en)	1994-10-25
CA2090772A1 (en)	1993-08-28
HU9300554D0 (en)	1993-05-28
NO930719D0 (no)	1993-02-26
ZA931382B (en)	1993-08-31
DK0558449T3 (da)	2001-01-02
SG49615A1 (en)	2001-01-16

Publication	Publication Date	Title
IL104874A (en)	1998-06-15	Phytocyanine clot complexes of pharmaceutical preparations containing them and the process for their preparation
KR950006153B1 (ko)	1995-06-09	탁솔 유도체, 그 제법 및 그들을 함유한 약제학적 조성물
CA2259621C (en)	2007-09-18	Isocoumarin derivatives and their use in medicines
JPS6089474A (ja)	1985-05-20	モルフイナン誘導体，その製造方法，及び該化合物を含有する抗腫瘍剤
JP2015504075A (ja)	2015-02-05	７−置換ハンファンギチンｂ誘導体、その調製方法及び使用
US4585589A (en)	1986-04-29	Water-soluble alkanoyloxy and alkoxycarbonyloxy rifampicin derivatives, process for its preparation, intermediates, and its pharmaceutical composition as antibacterials
CN111362998A (zh)	2020-07-03	氮杂20(r)-人参二醇衍生物及其抗肿瘤应用
JPS6041670B2 (ja)	1985-09-18	２，６−ジメチル−１，４−ジヒドロピリジン−３，５−ジカルボン酸エステルおよびその製造方法
JP4348475B2 (ja)	2009-10-21	新規なジテルペン化合物
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FI56371C (fi)	1980-01-10	Foerfarande foer framstaellning av terapeutiskt anvaendbara bensoylestrar av 1,8,9-trihydroxiantracen
EP0258655B1 (en)	1991-11-06	Complexes of platinum (ii) 2,3-dinitrilo-2-butene-2,3-dithiolate, a process for preparing them and pharmaceutical compositions containing them
US5753695A (en)	1998-05-19	Flavilium compounds and method of using
CN115583890B (zh)	2023-06-06	一种治疗血脂异常的药物及其用途
JPH03223289A (ja)	1991-10-02	チエノキノリン誘導体、チエノナフチリジン誘導体およびそれらの塩
JPH0370700B2 (no)	1991-11-08
CN118319907B (zh)	2024-08-20	一种噁二唑化合物的新用途
US5496854A (en)	1996-03-05	Metallocenes as anti-tumor drugs
KR810001697B1 (ko)	1981-10-27	이소부티라미드 유도체의 신규한 제조방법
KR840000910B1 (ko)	1984-06-28	술포늄 화합물의 제조방법
JPH1129471A (ja)	1999-02-02	クマリン誘導体を薬効成分として含有する肝疾患治療剤
US3595879A (en)	1971-07-27	Naphthoquinone derivatives,preparation thereof and chemotherapeutic compositions therewith and their administration
KR810000473B1 (ko)	1981-05-09	N-2,6-디클로로페닐-2-아미노피리미딘의 제법
CN112300187A (zh)	2021-02-02	一种斑蝥素衍生物、其药物组合物及其应用
JPS6332359B2 (no)	1988-06-29

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