SG106656A1 - Nucleotide analog composition and synthesis method - Google Patents
Nucleotide analog composition and synthesis methodInfo
- Publication number
- SG106656A1 SG106656A1 SG200200438A SG200200438A SG106656A1 SG 106656 A1 SG106656 A1 SG 106656A1 SG 200200438 A SG200200438 A SG 200200438A SG 200200438 A SG200200438 A SG 200200438A SG 106656 A1 SG106656 A1 SG 106656A1
- Authority
- SG
- Singapore
- Prior art keywords
- pmpa
- composition
- diethyl
- useful
- synthesis method
- Prior art date
Links
- 125000003729 nucleotide group Chemical group 0.000 title 1
- 238000001308 synthesis method Methods 0.000 title 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract 2
- 230000000840 anti-viral effect Effects 0.000 abstract 2
- -1 diethyl PMPA Chemical compound 0.000 abstract 2
- 239000000543 intermediate Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- VCMJCVGFSROFHV-WZGZYPNHSA-N tenofovir disoproxil fumarate Chemical compound OC(=O)\C=C\C(O)=O.N1=CN=C2N(C[C@@H](C)OCP(=O)(OCOC(=O)OC(C)C)OCOC(=O)OC(C)C)C=NC2=C1N VCMJCVGFSROFHV-WZGZYPNHSA-N 0.000 abstract 2
- MJZYTEBKXLVLMY-UHFFFAOYSA-N 1-(6-aminopurin-9-yl)propan-2-ol Chemical compound N1=CN=C2N(CC(O)C)C=NC2=C1N MJZYTEBKXLVLMY-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- ZRGHYSBYGWGKOY-UHFFFAOYSA-N diethyl (4-methylphenyl)sulfonylmethyl phosphate Chemical compound CCOP(=O)(OCC)OCS(=O)(=O)C1=CC=C(C)C=C1 ZRGHYSBYGWGKOY-UHFFFAOYSA-N 0.000 abstract 1
- 239000001530 fumaric acid Substances 0.000 abstract 1
- LZWQNOHZMQIFBX-UHFFFAOYSA-N lithium;2-methylpropan-2-olate Chemical compound [Li+].CC(C)(C)[O-] LZWQNOHZMQIFBX-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- JFVZFKDSXNQEJW-CQSZACIVSA-N tenofovir disoproxil Chemical compound N1=CN=C2N(C[C@@H](C)OCP(=O)(OCOC(=O)OC(C)C)OCOC(=O)OC(C)C)C=NC2=C1N JFVZFKDSXNQEJW-CQSZACIVSA-N 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 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
- 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
-
- 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
-
- 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
- A61P31/14—Antivirals for RNA viruses
-
- 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
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- A61P31/20—Antivirals for DNA viruses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Virology (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Steroid Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US5377797P | 1997-07-25 | 1997-07-25 | |
US08/900,752 US5935946A (en) | 1997-07-25 | 1997-07-25 | Nucleotide analog composition and synthesis method |
Publications (1)
Publication Number | Publication Date |
---|---|
SG106656A1 true SG106656A1 (en) | 2004-10-29 |
Family
ID=26732232
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG200200487A SG106657A1 (en) | 1997-07-25 | 1998-07-23 | Nycleotide analog composition and sythesis method |
SG200200438A SG106656A1 (en) | 1997-07-25 | 1998-07-23 | Nucleotide analog composition and synthesis method |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG200200487A SG106657A1 (en) | 1997-07-25 | 1998-07-23 | Nycleotide analog composition and sythesis method |
Country Status (19)
Country | Link |
---|---|
EP (1) | EP0998480B1 (de) |
JP (7) | JP4173202B2 (de) |
KR (3) | KR100661153B1 (de) |
CN (2) | CN100383148C (de) |
AT (3) | ATE228526T1 (de) |
AU (1) | AU756793B2 (de) |
BR (1) | BR9811045A (de) |
CA (1) | CA2298059C (de) |
DE (3) | DE69831694T2 (de) |
DK (2) | DK1243593T3 (de) |
ES (3) | ES2249511T3 (de) |
HK (3) | HK1029793A1 (de) |
ID (1) | ID24701A (de) |
IN (1) | IN190780B (de) |
NZ (1) | NZ501287A (de) |
PT (2) | PT1243590E (de) |
SG (2) | SG106657A1 (de) |
TW (2) | TWI224103B (de) |
WO (1) | WO1999005150A1 (de) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69831694T2 (de) * | 1997-07-25 | 2006-07-13 | Gilead Sciences, Inc., Foster City | Nukleotid-Analog Zusamensetzung und Synthese Verfahren |
GB0013407D0 (en) * | 2000-06-02 | 2000-07-26 | Astrazeneca Ab | Forms of a chemical compound |
KR100749160B1 (ko) | 2000-07-21 | 2007-08-14 | 길리애드 사이언시즈, 인코포레이티드 | 포스포네이트 뉴클레오티드 유사체의 전구 약물의 제조방법 |
UA93354C2 (ru) * | 2004-07-09 | 2011-02-10 | Гилиад Сайенсиз, Инк. | Местный противовирусный препарат |
TWI471145B (zh) | 2005-06-13 | 2015-02-01 | Bristol Myers Squibb & Gilead Sciences Llc | 單一式藥學劑量型 |
CN100352823C (zh) * | 2005-08-19 | 2007-12-05 | 浙江车头制药有限公司 | 一种腺嘌呤衍生物的制备方法 |
CN100396689C (zh) * | 2006-03-07 | 2008-06-25 | 中国医学科学院医药生物技术研究所 | 一组具有抑制hiv-1/hbv病毒复制活性的替诺福韦单酯化合物 |
EP2046792B1 (de) | 2006-07-12 | 2015-02-25 | Mylan Laboratories Limited | Verfahren zur Herstellung von Tenofovir |
AU2008253803A1 (en) | 2007-05-22 | 2008-11-27 | Ultimorphix Technolgies B.V. | Tenofovir disoproxil hemi-fumaric acid Co-crystal |
WO2010026603A2 (en) * | 2008-09-05 | 2010-03-11 | Matrix Laboratories Limited | Novel amine salts of tenofovir, process for producing the same and use thereof in production of tenofovir dioproxil |
CN101906119B (zh) * | 2009-06-03 | 2012-12-26 | 中国人民解放军军事医学科学院毒物药物研究所 | 制备替诺福韦的新方法 |
EP2389929A1 (de) | 2010-05-30 | 2011-11-30 | Abdi Ibrahim Ilac Sanayi ve Ticaret Anonim Sirketi | Pharmazeutische Formulierungen von Tenofovir |
CN103282369A (zh) | 2011-04-08 | 2013-09-04 | 劳乐斯实验室私营有限公司 | 抗逆转录病毒化合物与抗氧化酸的固体形式、其制备方法以及其药物组合物 |
CN102295660A (zh) * | 2011-07-04 | 2011-12-28 | 常州大学 | 泰诺福韦的合成工艺 |
PE20141328A1 (es) | 2011-08-16 | 2014-10-04 | Gilead Sciences Inc | Tenofovir alafenamida hemifumarato |
CN103626803B (zh) * | 2012-08-23 | 2017-12-15 | 四川海思科制药有限公司 | 替诺福韦二吡呋酯的固体及其制备方法和用途 |
CN103665043B (zh) | 2012-08-30 | 2017-11-10 | 江苏豪森药业集团有限公司 | 一种替诺福韦前药及其在医药上的应用 |
CN103230404A (zh) * | 2013-05-14 | 2013-08-07 | 福建广生堂药业股份有限公司 | 替诺福韦二吡呋酯或其药用盐的新用途 |
EP2860184B1 (de) | 2013-10-09 | 2018-08-29 | Zentiva, k.s. | Dihydrogenphosphatsalz von Tenofovirdisoproxil |
EP2860185A1 (de) | 2013-10-09 | 2015-04-15 | Zentiva, k.s. | Verbessertes Verfahren zur Herstellung von Tenofovirdisoproxil und dessen pharmazeutisch annehmbare Salze |
CN103483385B (zh) * | 2013-10-11 | 2015-11-18 | 福建广生堂药业股份有限公司 | 替诺福韦单酯富马酸盐的新晶型及其制备方法 |
CN104688747B (zh) * | 2013-12-04 | 2019-04-12 | 重庆药友制药有限责任公司 | 包含富马酸替诺福韦二吡呋酯的药物组合物 |
CN104725423A (zh) * | 2013-12-18 | 2015-06-24 | 山东新时代药业有限公司 | 一种富马酸替诺福韦二吡呋酯的合成方法 |
CN103705478B (zh) * | 2013-12-23 | 2020-02-07 | 浙江华海药业股份有限公司 | 含有富马酸替诺福韦二吡呋酯的口服片剂 |
CN104744512B (zh) * | 2013-12-26 | 2017-01-11 | 成都伊诺达博医药科技有限公司 | 一种“一锅法”制备泰诺福韦的新工艺 |
KR20160003532A (ko) | 2014-07-01 | 2016-01-11 | 한미약품 주식회사 | 테노포비어 디소프록실 인산염과, 비금속염 붕해제 및 비금속염 활택제를 포함하는 약학 조성물 |
CN104288118A (zh) * | 2014-07-08 | 2015-01-21 | 南京卡文迪许生物工程技术有限公司 | 富马酸替诺福韦二吡呋酯片剂及其制备方法 |
JP2017535520A (ja) * | 2014-09-30 | 2017-11-30 | ハンミ・ファイン・ケミカル・カンパニー・リミテッドHanmi Fine Chemical Co., Ltd. | 高純度の(r)−9−[2−(ホスホノメトキシ)プロピル]アデニンの製造方法 |
CN106046055A (zh) * | 2016-05-27 | 2016-10-26 | 湖北丽益医药科技有限公司 | R‑9‑(2‑膦酰甲氧基丙基)‑腺嘌呤一水合物晶体及制备、富马酸替诺福韦二吡呋酯制备 |
KR101909570B1 (ko) | 2016-12-05 | 2018-10-19 | (주) 성운파마코피아 | 고순도 테노포비어 디소프록실 제조방법 |
CN108358968B (zh) * | 2018-04-03 | 2020-09-15 | 科兴生物制药股份有限公司 | 一种替诺福韦的制备方法 |
CN109942634A (zh) * | 2019-01-24 | 2019-06-28 | 深圳科兴药业有限公司 | 一种富马酸替诺福韦二吡呋酯的晶型i及制备方法和应用 |
CN110507625A (zh) * | 2019-09-19 | 2019-11-29 | 苏州东瑞制药有限公司 | 一种新型富马酸替诺福韦酯片及其制备方法 |
CN111939134B (zh) * | 2020-08-24 | 2023-02-17 | 山东罗欣药业集团股份有限公司 | 一种抗病毒药物组合物 |
KR20220141457A (ko) | 2021-04-13 | 2022-10-20 | 경동제약 주식회사 | 신규 결정형의 테노포비어 알라펜아미드 말레산염 및 이를 포함하는 약제학적 조성물 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CS263951B1 (en) * | 1985-04-25 | 1989-05-12 | Antonin Holy | 9-(phosponylmethoxyalkyl)adenines and method of their preparation |
US6057305A (en) * | 1992-08-05 | 2000-05-02 | Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic | Antiretroviral enantiomeric nucleotide analogs |
EP0632048B1 (de) * | 1993-06-29 | 2001-03-21 | Mitsubishi Chemical Corporation | Phosphonat-Nukleotid Ester-Derivate |
WO1998004569A1 (en) * | 1996-07-26 | 1998-02-05 | Gilead Sciences, Inc. | Nucleotide analogs |
DE69831694T2 (de) * | 1997-07-25 | 2006-07-13 | Gilead Sciences, Inc., Foster City | Nukleotid-Analog Zusamensetzung und Synthese Verfahren |
-
1998
- 1998-07-23 DE DE69831694T patent/DE69831694T2/de not_active Expired - Lifetime
- 1998-07-23 AT AT98937022T patent/ATE228526T1/de active
- 1998-07-23 DE DE69809750T patent/DE69809750T2/de not_active Expired - Lifetime
- 1998-07-23 AU AU85827/98A patent/AU756793B2/en not_active Expired
- 1998-07-23 CA CA002298059A patent/CA2298059C/en not_active Expired - Lifetime
- 1998-07-23 JP JP51006799A patent/JP4173202B2/ja not_active Expired - Lifetime
- 1998-07-23 KR KR1020007000636A patent/KR100661153B1/ko not_active IP Right Cessation
- 1998-07-23 ES ES02010677T patent/ES2249511T3/es not_active Expired - Lifetime
- 1998-07-23 KR KR1020067001297A patent/KR100707505B1/ko not_active IP Right Cessation
- 1998-07-23 PT PT02010678T patent/PT1243590E/pt unknown
- 1998-07-23 CN CNB988074354A patent/CN100383148C/zh not_active Ceased
- 1998-07-23 DK DK02010677T patent/DK1243593T3/da active
- 1998-07-23 PT PT98937022T patent/PT998480E/pt unknown
- 1998-07-23 DK DK98937022T patent/DK0998480T3/da active
- 1998-07-23 WO PCT/US1998/015254 patent/WO1999005150A1/en not_active Application Discontinuation
- 1998-07-23 SG SG200200487A patent/SG106657A1/en unknown
- 1998-07-23 ES ES98937022T patent/ES2187989T3/es not_active Expired - Lifetime
- 1998-07-23 SG SG200200438A patent/SG106656A1/en unknown
- 1998-07-23 EP EP98937022A patent/EP0998480B1/de not_active Expired - Lifetime
- 1998-07-23 BR BR9811045-4A patent/BR9811045A/pt not_active Application Discontinuation
- 1998-07-23 ID IDW991548A patent/ID24701A/id unknown
- 1998-07-23 AT AT02010678T patent/ATE288914T1/de active
- 1998-07-23 DE DE69829010T patent/DE69829010T2/de not_active Expired - Lifetime
- 1998-07-23 CN CNB200410046290XA patent/CN1251679C/zh not_active Expired - Lifetime
- 1998-07-23 AT AT02010677T patent/ATE305009T1/de active
- 1998-07-23 ES ES02010678T patent/ES2236389T3/es not_active Expired - Lifetime
- 1998-07-23 NZ NZ501287A patent/NZ501287A/en not_active IP Right Cessation
- 1998-07-23 KR KR1020067001298A patent/KR100617608B1/ko not_active IP Right Cessation
- 1998-07-24 TW TW087112168A patent/TWI224103B/zh not_active IP Right Cessation
- 1998-07-24 IN IN2174DE1998 patent/IN190780B/en unknown
- 1998-07-24 TW TW093112403A patent/TWI242561B/zh not_active IP Right Cessation
-
2000
- 2000-11-10 HK HK00107207A patent/HK1029793A1/xx not_active IP Right Cessation
-
2003
- 2003-03-25 HK HK03102166.1A patent/HK1051373B/zh not_active IP Right Cessation
- 2003-03-25 HK HK03102167.0A patent/HK1051360B/zh not_active IP Right Cessation
-
2008
- 2008-03-07 JP JP2008058798A patent/JP4628437B2/ja not_active Expired - Lifetime
-
2010
- 2010-08-04 JP JP2010175808A patent/JP5398662B2/ja not_active Expired - Lifetime
-
2013
- 2013-07-22 JP JP2013151752A patent/JP2013213071A/ja not_active Withdrawn
-
2015
- 2015-07-10 JP JP2015138309A patent/JP2015199773A/ja not_active Withdrawn
-
2017
- 2017-01-06 JP JP2017000870A patent/JP2017057233A/ja not_active Withdrawn
- 2017-10-31 JP JP2017210439A patent/JP2018016645A/ja not_active Withdrawn
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SG106656A1 (en) | Nucleotide analog composition and synthesis method | |
JP4169365B2 (ja) | 不能症を処置するための、cGMP−ホスフォジエステラーゼインヒビターの用途 | |
ES8800157A1 (es) | Un procedimiento para preparar derivados de tironina | |
HU195657B (en) | Process for production of carbocyclic pirin nucleorids and medical compounds containing them | |
EP0034473A3 (en) | Substituted imidazoles, their preparation, pharmaceutical compositions containing the same and their use in therapy | |
AU1428801A (en) | Novel (1,2,3)-triazolo(4,5-D)pyrimidine compounds | |
ES8105980A1 (es) | Un procedimiento para la preparacion de nuevos derivados de 1-fenil-3-(4-piperidil)-1-propanona | |
Murakami et al. | Escherichia coli mediated biosynthesis and in vitro anti-HIV activity of lipophilic 6-halo-2', 3'-dideoxypurine nucleosides | |
KR880012628A (ko) | 치료학적인 뉴클레오시드 | |
HUP0003577A2 (hu) | Tetrahidro-gamma-karbolinok, eljárás előállításukra, alkalmazásuk és az ezeket tartalmazó gyógyszerkészítmények | |
US4315920A (en) | Adenosine deaminase inhibitors | |
ES8400428A1 (es) | Un procedimiento para la preparacion de nuevos derivados de 2-piperazino primidina. | |
Wojtkowski et al. | . beta.-Thionolactam analogs of cephalosporins and penicillins | |
MY103569A (en) | Novel 2, 5-disubstituted dithianes having pesticidal activity, methods for their production and for their use | |
CA2605226A1 (en) | Nucleotide analog composition and synthesis method | |
GB2084152A (en) | Antiviral agents their preparation and use | |
EP0936911B1 (de) | Adenosine deaminase inhibitoren | |
AU6826700A (en) | Ceramide analogs, process for their preparation and their use as antitumor agents | |
ATE34176T1 (de) | 2'-chloropentostatin, eine diese verbindung enthaltende pharmazeutische zusammensetzung und ein mikroorganismus zur herstellung dieser verbindung. | |
Bienkowski et al. | Synthesis of malondialdehyde‐1, 2, 3‐14C3 via ethyl vinyl‐[1, 2‐14C2] ether |