KR930006036A - 퓨린 및 피리미딘의 불포화 비환식 포스포네이트 유도체 - Google Patents
퓨린 및 피리미딘의 불포화 비환식 포스포네이트 유도체 Download PDFInfo
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- KR930006036A KR930006036A KR1019920016534A KR920016534A KR930006036A KR 930006036 A KR930006036 A KR 930006036A KR 1019920016534 A KR1019920016534 A KR 1019920016534A KR 920016534 A KR920016534 A KR 920016534A KR 930006036 A KR930006036 A KR 930006036A
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- dihydroxyphosphoryl
- compound
- cytosine
- thymine
- hydroxymethyl
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- 150000003212 purines Chemical class 0.000 title claims abstract 6
- 150000003230 pyrimidines Chemical class 0.000 title claims abstract 5
- -1 Unsaturated acyclic phosphonate derivatives Chemical class 0.000 title claims 5
- 241000700605 Viruses Species 0.000 claims abstract 5
- 230000005740 tumor formation Effects 0.000 claims abstract 4
- 241001430294 unidentified retrovirus Species 0.000 claims abstract 4
- 241000450599 DNA viruses Species 0.000 claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims 20
- OPTASPLRGRRNAP-UHFFFAOYSA-N cytosine Chemical compound NC=1C=CNC(=O)N=1 OPTASPLRGRRNAP-UHFFFAOYSA-N 0.000 claims 14
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims 11
- RWQNBRDOKXIBIV-UHFFFAOYSA-N thymine Chemical compound CC1=CNC(=O)NC1=O RWQNBRDOKXIBIV-UHFFFAOYSA-N 0.000 claims 10
- 229940104302 cytosine Drugs 0.000 claims 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 229940113082 thymine Drugs 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical compound O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 claims 4
- 229930024421 Adenine Natural products 0.000 claims 3
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 claims 3
- 229960000643 adenine Drugs 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 239000003937 drug carrier Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- 229940083251 peripheral vasodilators purine derivative Drugs 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 claims 2
- OYPXTMXCWPHUBO-UHFFFAOYSA-N 5-(6-aminopurin-9-yl)pent-1-enylphosphonic acid Chemical compound NC1=NC=NC2=C1N=CN2CCCC=CP(O)(O)=O OYPXTMXCWPHUBO-UHFFFAOYSA-N 0.000 claims 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 1
- VZCBHEHKHHXKGP-GQCTYLIASA-N [(e)-5-(5-methyl-2,4-dioxopyrimidin-1-yl)pent-1-enyl]phosphonic acid Chemical compound CC1=CN(CCC\C=C\P(O)(O)=O)C(=O)NC1=O VZCBHEHKHHXKGP-GQCTYLIASA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 230000000840 anti-viral effect Effects 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- 230000003612 virological effect Effects 0.000 claims 1
- 239000003443 antiviral agent Substances 0.000 abstract 2
- 125000002015 acyclic group Chemical group 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 abstract 1
Classifications
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- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
- C07F9/65616—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings containing the ring system having three or more than three double bonds between ring members or between ring members and non-ring members, e.g. purine or analogs
-
- 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
- A61P31/12—Antivirals
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
본 발명은 항바이러스제로서 유용한 특정의 퓨린 또는 피리미딘의 신규한 불포화 비환식 포스포네이트 유돛, 이의 제조방법 및 제조에 유용한 중간체, 및 DNA 바이러스, 레트로바이러스 및 종양 형성과 관련된 바이러스에 대해 유효한 항바이러스제로서의 이의 최종-용도에 관한 것이다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (18)
- 다음 일반식(Ⅰ) 또는 (Ⅱ)의 화합물, 이들의 입체이성체, 혼합물 및 호변이성체, 및 약제학적으로 허용되는 이의 염.상기식에서, Y는 -CH2-, -O-CH2- 또는 -CH2-O-이고, Y′는 (CH2)n,-O-CH2-또는-CH2-O 이며, n은 1 또는 2이고, A 및 A′는 독립적으로 H, -CH2OH 또는 OH이며, X1은 H 또는 NH2이고, X2은 OH 또는 NH2이며, X3은 H 또는 CH3이고, X4은 NH 또는 OH이며, 단 Y는 -O-CH2-이고 A가 H인 경우, X1은 NH2가 아니고, 동시에 X2는 OH 가 아니며, 단 Y는 -CH2-O- 인 경우, A가 OH이고, A가 OH인 경우, Y는 -OCH2-가 아니며, A′가 OH인 경우, Y′는 -OCH2-가 아니고, Y가 -CH2-CH2-이고, A가 H인 경우 X1은 NH2가 아니며, 동시에 X2는 OH 가 아니다.
- 제1항에 있어서, 일반식(Ⅰ)의 화합물.
- 제1항에 있어서, 일반식(Ⅱ)의 화합물.
- 제1항에 있어서, E-1-[5-(디하이드록시포스포릴)펜트-4-엔일]시토신 ; E-1-[5-(디하이드록시포스포릴)펜트-4-엔일]티민 ; E-1-[3-(디하이드록시포스포릴)부트-4-엔일]시토신 ; E-1-[4-(디하이드록시포스포릴)부트-4-엔일]티민 ; E-1-[4-(디하이드록시포스포릴)프로프-2-엔일옥시]-메틸-시토신 ; E-9-[(3-(디하이드록시포스포릴-2-프로프페닐옥시)메틸]아데닌 ; E-1-[3-(디하이드록시포스포릴)부트-4-엔일]시토신 ; E-1-[4-(디하이드록시포스포릴)부트-4-엔일]티민 ; E-9-[5-(디하이드록시포스포릴)-3-하이드로옥시메틸-4-페테닐]구아닌 ; (R,S)-E-9-[5-(디하이드록시포스포릴)-3-(하이드로옥시메틸)-4-페테닐]아데닌 ; (R,S)-E-1-5-(디하이드록시포스포릴-3-하이드록시메틸-4-페테닐)시토신 ; (R,S)-E-1-5-(디하이드록시포스포릴-3-하이드록시메틸-4-페테닐)티민 ; (R,S)-E-9-[(3-디하이드록시포스포릴-1-하이드록시메틸-2-프로페닐옥시)메틸]구아닌 ; (R,S)-E-9-[(3-디하이드록시포스포릴-1-하이드록시메틸-2-프로페닐옥시)메틸]아데닌 ; (R,S)-E-1-[(3-디하이드록시포스포릴-1-하이드록시메틸-2-프로페닐옥시)메틸]시토신 ; (R,S)-E-1-[(3-디하이드록시포스포릴-1-하이드록시메틸-2-프로페닐옥시)메틸]티민 ; (R,S)-E-1-[4-(디하이드록시포스포릴)-2-(하이드록시메틸)-3-부테닐]시토신 ; (R,S)-E-1-[4-(디하이드록시포스포릴)-2-하이드록시메틸-3-부테닐]티민 ; (R,S)-E-1-[4-(디하이드록시포스포릴)-2-하이드록시메틸-부트-3-엔일옥시]시토신 ; (R,S)-E-1-[4-(디하이드록시포스포릴)-2-하이드록시메틸-부트-3-엔일옥시]티민 ; (R,S)-E-9-(4-디하이드록시포스포릴-2-하이드로록시-3-부테닐)-구아닌 ; (R,S)-E-9-(4-디하이드록시포스포릴-2-하이드로록시-3-부테닐)-아데닌 ; (R,S)-E-1-(4-디하이드록시포스포릴-2-하이드로록시-3-부테닐)-티민 ; (R,S)-E-1-(4-디하이드록시포스포릴-2-하이드로록시-3-부테닐)-시토신 ; (R,S)-E-9-(5-디하이드록시포스포릴-3-하이드로록시-4-펜테닐)-구아닌 ; (R,S)-E-9-(5-디하이드록시포스포릴-3-하이드로록시-4-펜테닐)-아데닌 ; (R,S)-E-1-(5-디하이드록시포스포릴-3-하이드로록시-4-펜테닐)-티민 ; (R,S)-E-1-(5-디하이드록시포스포릴-3-하이드로록시-4-펜테닐)-시토신 ; (R,S)-E-9-(4-디하이드록시포스포릴-3-하이드로록시부틸-3-엔일옥시)-구아닌 ; (R,S)-E-9-(4-디하이드록시포스포릴-3-하이드로록시부트-3-엔일옥시)-아데닌 ; (R,S)-E-1-(4-디하이드록시포스포릴-3-하이드로록시부트-3-엔일옥시)-티민 ; (R,S)-E-1-(4-디하이드록시포스포릴-3-하이드로록시부트-3-엔일)-시토신 ; 또는 [5-(6-아미노-9h-퓨린-9-일)-1-펜테닐]포스폰산인 화합물.
- 제1항에 있어서, X1이 H이고 X2가 NH2인 화합물.
- 제1항에 있어서, X1이 NH2이고 X2가 NH2인 화합물.
- 제1항에 있어서, X1이 NH2이고 X2가 OH인 화합물.
- 제1항에 있어서, X1이 H이고 X2가 OH인 화합물.
- 제1항에 있어서, X4이 NH2이고 X3이 H인 화합물.
- 제1항에 있어서, X4이 OH이고 X3가 CH2인 화합물.
- 제1항에 있어서, -CH2CH2-이고 Y′가 (CH2)n인 화합물
- 약제학적 활성 화합물로서 사용하기 위한, 제1항에 따르는 화합물.
- DNA 바이러스, 레트로바이러스 또는 종양 형성과 관련된 바이러스에 의해 야기된 질병의 치료에 사용하기위한, 제1항에 따르는 화합물.
- 제1항에 따르는 화합물을 약제학적으로 허용되는 담체와 임의로 혼합하여 함유하는 약제학적 조성물.
- DNA 바이러스, 레트로바이러스 또는 종양 형성과 관련된 바이러스에 의해 야기된 질병의 치료하기위한, 제14항에 따르는 화합물.
- DNA 바이러스, 레트로바이러스 또는 종양 형성과 관련된 바이러스에 의해 야기된 질병의 치료하는 약제학적 조성물을 제조하기 위한, 약제학적으로 허용되는 담체와 임의로 혼합한 제1항에 따르는 화합물의 용도.
- 다음 일반식(6), (7) 또는 (8)의 화합물을 각각 유기 용매의 존재하에 1-하이드록시 피리미딘 유도체 또는 9-하이드록시 퓨린 유도체 및 적당한 촉합제 ; 유기 용매의 존재하에 피리미딘 유도체 또는 퓨린 유도체의 염 형태 ; 및 불활성 대기 중의 유기 용매의 존재하에 피리미딘 유도체 또는 퓨린유도체의 실릴화 유도체(여기서, 피리미딘 유도체 또는 퓨린 유도체는 하기 일반식을 갖는다)와 반응시키고, 이로써 제조된 화합물을 임의로 탈보호시킨 다음, 반응영역으로부터 목적 생성물을 회수함을 포함하여, 일반식(Ⅰ) 또는 (Ⅱ)의 화합물, 이들의 입체이성체 및 혼합물 및 호변이성체, 및 약제학적으로 허용되는 이의 염을 제조하는 방법.상기식에서, Y는 -CH2-CH2-, -O-CH2- 또는 -CH2-O-이고, Y′는 (CH2)n,-O-CH2- 또는 -CH2-O 이며, n은 1 또는 2이고, A 및 A′는 독립적으로 H, -CH2OH 또는 OH이며, X1은 H 또는 NH2이고, X2은 OH 또는 NH2이며, X3은 CH3이고, X4은 NH2또는 OH이며, 단 Y는 -O-CH2-이고 A가 H인 경우, X1은 NH2가 아니고, 동시에 X2는 OH가 아니며, A′가 OH인 경우, Y′는 -OCH2-가 아니고, Y가 -CH2CH2-이고 A가 H인 경우, X1가 NH2인 경우, 동시에 X2는 OH 가 아니며 m은 0.1 또는 2이고 R은 알킬이며, Pg는 A가 OH 또는 인 경우 적당한 보호 그룹이며 Lg는 적당한 이탈 그룹이고, 피리미딘 및 퓨린 유도체에서 점선을 결합부분을 나타낸다.
- 바이러스성 질환을 치료할 필요가 있는 환자에게 항바이러스성 유효량의 제1항의 화합물을 투여함을 포함하는 상기 환자의 치료방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP91402427A EP0531597A1 (en) | 1991-09-12 | 1991-09-12 | Novel unsaturated acyclic phosphonate derivatives of purine and pyrimidine |
EP91-402427.8 | 1991-09-12 |
Publications (1)
Publication Number | Publication Date |
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KR930006036A true KR930006036A (ko) | 1993-04-20 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019920016534A KR930006036A (ko) | 1991-09-12 | 1992-09-09 | 퓨린 및 피리미딘의 불포화 비환식 포스포네이트 유도체 |
Country Status (9)
Country | Link |
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EP (2) | EP0531597A1 (ko) |
JP (1) | JPH05247070A (ko) |
KR (1) | KR930006036A (ko) |
AU (1) | AU646758B2 (ko) |
CA (1) | CA2078030A1 (ko) |
FI (1) | FI924077A (ko) |
HU (1) | HUT62009A (ko) |
IL (1) | IL103125A0 (ko) |
NO (1) | NO923539L (ko) |
Families Citing this family (37)
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US5817647A (en) * | 1993-04-01 | 1998-10-06 | Merrell Pharmaceuticals Inc. | Unsaturated acetylene phosphonate derivatives of purines |
EP0618214A1 (en) * | 1993-04-01 | 1994-10-05 | Merrell Dow Pharmaceuticals Inc. | Unsaturated phosphonate derivatives of purines and pyrimidines |
CA2171868A1 (en) * | 1993-09-17 | 1995-03-23 | Petr Alexander | Method for dosing therapeutic compounds |
US5798340A (en) | 1993-09-17 | 1998-08-25 | Gilead Sciences, Inc. | Nucleotide analogs |
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DE69116750T2 (de) * | 1990-07-04 | 1996-11-14 | Merrell Dow Pharma | 9-Purinyl-Phosphonsäurederivate |
WO1992001698A1 (en) * | 1990-07-19 | 1992-02-06 | Beecham Group Plc | Antiviral phosphono-alken derivatives of purines |
-
1991
- 1991-09-12 EP EP91402427A patent/EP0531597A1/en not_active Withdrawn
-
1992
- 1992-09-08 AU AU22197/92A patent/AU646758B2/en not_active Ceased
- 1992-09-09 KR KR1019920016534A patent/KR930006036A/ko not_active Application Discontinuation
- 1992-09-10 IL IL103125A patent/IL103125A0/xx unknown
- 1992-09-11 CA CA002078030A patent/CA2078030A1/en not_active Abandoned
- 1992-09-11 FI FI924077A patent/FI924077A/fi unknown
- 1992-09-11 JP JP4267791A patent/JPH05247070A/ja active Pending
- 1992-09-11 HU HU9202924A patent/HUT62009A/hu unknown
- 1992-09-11 EP EP92402487A patent/EP0532423A1/en not_active Withdrawn
- 1992-09-11 NO NO92923539A patent/NO923539L/no unknown
Also Published As
Publication number | Publication date |
---|---|
AU2219792A (en) | 1993-03-18 |
EP0532423A1 (en) | 1993-03-17 |
HUT62009A (en) | 1993-03-29 |
HU9202924D0 (en) | 1992-11-30 |
JPH05247070A (ja) | 1993-09-24 |
CA2078030A1 (en) | 1993-03-13 |
AU646758B2 (en) | 1994-03-03 |
FI924077A0 (fi) | 1992-09-11 |
NO923539D0 (no) | 1992-09-11 |
FI924077A (fi) | 1993-03-13 |
IL103125A0 (en) | 1993-02-21 |
NO923539L (no) | 1993-03-15 |
EP0531597A1 (en) | 1993-03-17 |
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