NO970293L - Substituerte camptothecinderivater og fremgangsmåte for deres fremstilling - Google Patents

Substituerte camptothecinderivater og fremgangsmåte for deres fremstilling

Info

Publication number
NO970293L
NO970293L NO970293A NO970293A NO970293L NO 970293 L NO970293 L NO 970293L NO 970293 A NO970293 A NO 970293A NO 970293 A NO970293 A NO 970293A NO 970293 L NO970293 L NO 970293L
Authority
NO
Norway
Prior art keywords
alkyl
hydrogen
optionally substituted
phenyl
cycloalkyl
Prior art date
Application number
NO970293A
Other languages
English (en)
Other versions
NO970293D0 (no
Inventor
Walter Cabri
Ilaria Candiani
Angelo Bedeschi
Franco Zarini
Sergio Penco
Original Assignee
Pharmacia & Upjohn Spa
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.)
Filing date
Publication date
Application filed by Pharmacia & Upjohn Spa filed Critical Pharmacia & Upjohn Spa
Publication of NO970293D0 publication Critical patent/NO970293D0/no
Publication of NO970293L publication Critical patent/NO970293L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/22Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Saccharide Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Substituerte camptothecinderivater av formel (I) hvor symbolet representerer en enkelt- eller dobbeltbinding; (I) substituert benzoyl, fenyl-Ci¿C^-alkanoyl, 'Ry, R2 OS ^3 ^i" som definert tinder (a) eller (b) nedenfor: (a) Ry og Rg er, hver uavhengig, hydrogen; C]^-C4-alkyl; C3-C7- cykloalkyl; fenyl-Cj^¿C(j-alkyl; en eventuelt substituert fenylrlng; -NR^Rfj hvor en av R5 og Rj, er hydrogen, Cy¿C(^- alkyl eller benzyl og den andre er hydrogen, Cj^-C^j-alkanoyl, en eventuelt substituert Cj-C^-alkoksykarbonyl, en eventuelt en eventuelt substituert C;i-C5-alkoksykarbonyl, en eventuelt substituert fenoksykarbonyl eller fenyl-Cj^-C^-alkoksykarbonyl, eller Rg og R^, 1 kombinasjon med det nltrogenatan til hvilket de er bundet, danner en 4-7-leddet, mettet, eventuelt substituert, heteromono- cyklisk rlngrest; COORs hvor Rg er hydrogen, C^-C^-alkyl, C3-C7-cykloalkyl eller fenyl-C^-C^j-alkyl; eller CORg, hvor Rg er Cj^-C^-alkyl, Cgr-Cy-cykloalkyl, fenyl-Cj-C^j-alkyl, en eventuelt substituert fenylrlng eller ^10^11 hvor RyQ og Ryy hver uavhengig er hydrogen eller Cj^-C(,-alkyl; og R3 er hydrogen, Cj¿C^-alkyl eller en eventuelt substituert fenylrlng; eller (b) R-y og R3, 1 kombinasjon, danner en 5-8-leddet, eventuelt substituert, karbonionoc.vkllsk ring; og R2 er hydrogen, C]^-C4-alkyl eller C3-C7-cykloalkyl; R4 er hydrogen, C]^-C(,-alkyl, C3-C7-cykloalkyl eller fenyl-Cj^-C(,-alkyl; X er hydrogen, C^-C(,-alkyl, C3-C7-cykloalkyl, C^-C^-alkoksy, C3-C7-cykloalkoksy, Cj-C^-alkanoyloksy, benzoyloksy, amino, hydroksy, nitro, halogen eller den er en metylendloksygruppe bundet til stillingene 10 og 11 1 molekylet, og de farmasoytisk akseptable saltene derav. Disse forbindelsene er nyttige 1 terapi som antltumormldler.
NO970293A 1995-05-26 1997-01-23 Substituerte camptothecinderivater og fremgangsmåte for deres fremstilling NO970293L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9510716.5A GB9510716D0 (en) 1995-05-26 1995-05-26 Substituted camptothecin derivatives and process for their preparation
PCT/EP1996/002008 WO1996037496A1 (en) 1995-05-26 1996-05-10 Substituted camptothecin derivatives and process for their preparation

Publications (2)

Publication Number Publication Date
NO970293D0 NO970293D0 (no) 1997-01-23
NO970293L true NO970293L (no) 1997-03-06

Family

ID=10775098

Family Applications (1)

Application Number Title Priority Date Filing Date
NO970293A NO970293L (no) 1995-05-26 1997-01-23 Substituerte camptothecinderivater og fremgangsmåte for deres fremstilling

Country Status (18)

Country Link
US (1) US5856333A (no)
EP (1) EP0777670B1 (no)
JP (1) JPH10503220A (no)
CN (1) CN1159192A (no)
AR (1) AR003126A1 (no)
AT (1) ATE262532T1 (no)
AU (1) AU5817996A (no)
BR (1) BR9606396A (no)
CA (1) CA2194700A1 (no)
DE (1) DE69631943D1 (no)
GB (1) GB9510716D0 (no)
HU (1) HUP9702400A3 (no)
IL (1) IL118410A0 (no)
NO (1) NO970293L (no)
NZ (1) NZ308514A (no)
PL (1) PL318279A1 (no)
WO (1) WO1996037496A1 (no)
ZA (1) ZA964138B (no)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6096336A (en) * 1996-01-30 2000-08-01 The Stehlin Foundation For Cancer Research Liposomal prodrugs comprising derivatives of camptothecin and methods of treating cancer using these prodrugs
GB9702807D0 (en) 1997-02-12 1997-04-02 Pharmacia & Upjohn Spa Alkynyl-substituted camptothecins and process for their preparation
EP1017675B1 (en) * 1997-02-14 2006-06-14 Bionumerik Pharmaceuticals, Inc. Highly lipophilic camptothecin derivatives
CA2289625A1 (en) 1997-05-15 1998-11-19 Charles Van Jackson Antithrombotic compound
HUP9701554D0 (en) * 1997-09-18 1997-11-28 Human Oltoanyagtermeloe Gyogys Pharmaceutical composition containing plazma proteins
US6228855B1 (en) 1999-08-03 2001-05-08 The Stehlin Foundation For Cancer Research Aromatic esters of camptothecins and methods to treat cancers
US6352996B1 (en) 1999-08-03 2002-03-05 The Stehlin Foundation For Cancer Research Liposomal prodrugs comprising derivatives of camptothecin and methods of treating cancer using these prodrugs
WO2001024763A2 (en) 1999-10-01 2001-04-12 Immunogen, Inc. Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents
US6288072B1 (en) 1999-12-29 2001-09-11 Monroe E. Wall Camptothecin β-alanine esters with topoisomerase I inhibition
NZ520593A (en) 2000-02-28 2004-10-29 Aventis Pharma S A composition comprising camptothecin and a pyrimidine derivative for the treatment of cancer
US6548488B2 (en) 2000-03-17 2003-04-15 Aventis Pharma S.A. Composition comprising camptothecin or a camptothecin derivative and an alkylating agent for the treatment of cancer
US6545010B2 (en) 2000-03-17 2003-04-08 Aventis Pharma S.A. Composition comprising camptothecin or a camptothecin derivative and a platin derivative for the treatment of cancer
US6486320B2 (en) 2000-09-15 2002-11-26 Aventis Pharma S.A. Preparation of camptothecin and of its derivatives
SK5122003A3 (en) 2000-10-27 2003-12-02 Aventis Pharma Sa A combination comprising camptothecin and a stilbene derivative for the treatment of cancer
TW200408621A (en) 2002-04-08 2004-06-01 Glaxo Group Ltd Compounds
GB0225548D0 (en) 2002-11-01 2002-12-11 Glaxo Group Ltd Compounds
CN100406460C (zh) * 2003-11-10 2008-07-30 中国科学院上海药物研究所 喜树碱的新衍生物、制备方法和用途
WO2006069344A2 (en) 2004-12-22 2006-06-29 Rutgers, The State University Of New Jersey Controlled release hydrogels
WO2012050591A1 (en) 2010-10-15 2012-04-19 Rutgers, The State University Of New Jersey Hydrogel formulation for dermal and ocular delivery
KR101394768B1 (ko) 2006-03-30 2014-05-21 드라이스 파마슈티컬스 아이엔씨 캄토테신-세포 투과 펩티드 결합체 및 이를 포함하는 약학 조성물
CN101880285B (zh) * 2010-06-24 2012-07-04 华东师范大学 一种烯丙基取代喜树碱化合物的合成方法
CN104774209B (zh) * 2014-01-15 2018-06-19 上海海和药物研究开发有限公司 一种9-烯丙基喜树碱衍生物的合成方法
UY39743A (es) 2021-04-29 2022-11-30 Abbvie Inc Conjugados de anticuerpo anti-c-met y fármaco

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5364858A (en) * 1987-03-31 1994-11-15 Research Triangle Institute Camptothecin analogs as potent inhibitors of topoisomerase I
US5122606A (en) * 1987-04-14 1992-06-16 Research Triangle Institute 10,11-methylenedioxy camptothecins
US5340817A (en) * 1987-04-14 1994-08-23 Research Triangle Institute Method of treating tumors with anti-tumor effective camptothecin compounds
US5004758A (en) * 1987-12-01 1991-04-02 Smithkline Beecham Corporation Water soluble camptothecin analogs useful for inhibiting the growth of animal tumor cells
JPH0615547B2 (ja) * 1988-01-20 1994-03-02 株式会社ヤクルト本社 新規なカンプトテシン誘導体
WO1991004260A2 (en) * 1989-09-15 1991-04-04 Research Triangle Institute 10,11-methylenedioxy-20(rs)-camptothecin and 10,11-methylenedioxy-20(s)-camptothecin analogs
GB9319944D0 (en) * 1993-09-28 1993-11-17 Erba Carlo Spa Process for the preparation of 9-amino camptothecin
GB9402934D0 (en) * 1994-02-16 1994-04-06 Erba Carlo Spa Camptothecin derivatives and process for their preparation

Also Published As

Publication number Publication date
US5856333A (en) 1999-01-05
GB9510716D0 (en) 1995-07-19
ATE262532T1 (de) 2004-04-15
ZA964138B (en) 1996-11-27
NZ308514A (en) 1998-06-26
PL318279A1 (en) 1997-06-09
JPH10503220A (ja) 1998-03-24
CN1159192A (zh) 1997-09-10
BR9606396A (pt) 1997-10-14
AU5817996A (en) 1996-12-11
AR003126A1 (es) 1998-07-08
HUP9702400A2 (hu) 1998-06-29
CA2194700A1 (en) 1996-11-28
IL118410A0 (en) 1996-09-12
HUP9702400A3 (en) 1998-07-28
DE69631943D1 (de) 2004-04-29
EP0777670B1 (en) 2004-03-24
WO1996037496A1 (en) 1996-11-28
NO970293D0 (no) 1997-01-23
EP0777670A1 (en) 1997-06-11

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