NO954072L - Vannopplöselige camptotecinderivater, fremgangsmåte for deres fremstilling og deres anvendelse som antitumormidler - Google Patents
Vannopplöselige camptotecinderivater, fremgangsmåte for deres fremstilling og deres anvendelse som antitumormidlerInfo
- Publication number
- NO954072L NO954072L NO954072A NO954072A NO954072L NO 954072 L NO954072 L NO 954072L NO 954072 A NO954072 A NO 954072A NO 954072 A NO954072 A NO 954072A NO 954072 L NO954072 L NO 954072L
- Authority
- NO
- Norway
- Prior art keywords
- alkyl
- blend
- hydrogen
- antitumor agents
- group
- Prior art date
Links
- 239000002246 antineoplastic agent Substances 0.000 title abstract 2
- VSJKWCGYPAHWDS-FQEVSTJZSA-N camptothecin Chemical class C1=CC=C2C=C(CN3C4=CC5=C(C3=O)COC(=O)[C@]5(O)CC)C4=NC2=C1 VSJKWCGYPAHWDS-FQEVSTJZSA-N 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- -1 benzoyloxy, amino, hydroxy Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910052717 sulfur Chemical group 0.000 abstract 1
- 239000011593 sulfur Chemical group 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic 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
- C07D491/22—Heterocyclic 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
Nye camptoteclnderivat av formel (I) B fl. hvor B er en gruppe B' eller B" *'^R' l B1 M ° (y) B" hvor hver av (x) og (y) er en enkelt- eller dobbeltblnding, R! og R2 er hver uavhengig hydrogen, q-C^alkyl, Cg-C7-cykloalkyl, fenyl-C^-alkyl eller en usubetltuert eller substituert fenylrlng, R3 og R4 er (a) hver uavhengig, substltuenter som har samte betydning son RI og Rgt eller (b) l kombinasjon sanmen med nltrogenatomet til hvilket de er bundet danner en 3-7-leddet mettet, usubstituert eller ! substituert heteranonocykllsk ring, son ytterligere kan Inneholde et annet heteroatoa valgt fra nitrogen, oksygen og svovel, og ! A" er et farmasøytisk akseptabelt anion av en farmasøytisk akseptabel uorganisk eller organisk syre, forutsatt at (i) når (i) er en dobbeltblndlng, så er (y) en enkeltblndlng og når (y) er en dobbeltblndlng, så er (T) en enkelt- blndlng, og ! (11) når B er en gruppe B', så er en av R2, R3 og fy fraværende; R£ er hydrogen eller Ci-C^-alkyl; X er hydrogen, q-^-alkyl, q-Ct-alkoksy, Ci-Cft-acyloksy, Cs-Cy-cykloalkyl, Cg^-cykloalkoksy, benzoyloksy, amino, hydroksy, nltro, et halogenatom eller en metylendioksygruppe bundet til stilling 10 og 11 i molekylet; og de farmasøy- tisk akseptable saltene derav. Disse caqptoteclnderlvatene er nyttige l terapi som antitumonnidler.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9402934A GB9402934D0 (en) | 1994-02-16 | 1994-02-16 | Camptothecin derivatives and process for their preparation |
| PCT/EP1995/000393 WO1995022549A1 (en) | 1994-02-16 | 1995-02-03 | Water-soluble camptothecin derivatives, process for their preparation and their use as antitumor agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO954072D0 NO954072D0 (no) | 1995-10-13 |
| NO954072L true NO954072L (no) | 1995-12-11 |
Family
ID=10750430
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO954072A NO954072L (no) | 1994-02-16 | 1995-10-13 | Vannopplöselige camptotecinderivater, fremgangsmåte for deres fremstilling og deres anvendelse som antitumormidler |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US5602141A (no) |
| EP (1) | EP0694035B1 (no) |
| JP (1) | JPH08509244A (no) |
| KR (1) | KR960701878A (no) |
| CN (1) | CN1123548A (no) |
| AT (1) | ATE220681T1 (no) |
| AU (1) | AU681941B2 (no) |
| CA (1) | CA2158855C (no) |
| DE (1) | DE69527400T2 (no) |
| ES (1) | ES2180625T3 (no) |
| FI (1) | FI954898A0 (no) |
| GB (1) | GB9402934D0 (no) |
| HU (1) | HUT73423A (no) |
| IL (1) | IL112622A (no) |
| MX (1) | MX9504287A (no) |
| NO (1) | NO954072L (no) |
| NZ (1) | NZ279813A (no) |
| PL (1) | PL311122A1 (no) |
| WO (1) | WO1995022549A1 (no) |
| ZA (1) | ZA951227B (no) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9319944D0 (en) * | 1993-09-28 | 1993-11-17 | Erba Carlo Spa | Process for the preparation of 9-amino camptothecin |
| US5965566A (en) * | 1993-10-20 | 1999-10-12 | Enzon, Inc. | High molecular weight polymer-based prodrugs |
| US5880131A (en) * | 1993-10-20 | 1999-03-09 | Enzon, Inc. | High molecular weight polymer-based prodrugs |
| GB9402934D0 (en) * | 1994-02-16 | 1994-04-06 | Erba Carlo Spa | Camptothecin derivatives and process for their preparation |
| GB9410388D0 (en) * | 1994-05-24 | 1994-07-13 | Erba Carlo Spa | Method for the preparation of 9-amino camptothecin |
| GB9510716D0 (en) * | 1995-05-26 | 1995-07-19 | Pharmacia Spa | Substituted camptothecin derivatives and process for their preparation |
| GB9601779D0 (en) * | 1996-01-30 | 1996-04-03 | Pharmacia Spa | 9, 10 Disubstituted camptothecin derivatives |
| 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 |
| GB9715821D0 (en) * | 1997-07-25 | 1997-10-01 | Pharmacia & Upjohn Spa | Amidino-camptothecin derivatives |
| US6043367A (en) * | 1998-09-30 | 2000-03-28 | Roffler; Steve | Proactive antitumor compounds |
| 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 |
| CA2385528C (en) | 1999-10-01 | 2013-12-10 | Immunogen, Inc. | Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents |
| ATE398131T1 (de) * | 2001-11-30 | 2008-07-15 | Chugai Pharmaceutical Co Ltd | Kondensierte camptothecine als antitumormittel |
| US7563810B2 (en) | 2002-11-06 | 2009-07-21 | Celgene Corporation | Methods of using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myeloproliferative diseases |
| US8034831B2 (en) | 2002-11-06 | 2011-10-11 | Celgene Corporation | Methods for the treatment and management of myeloproliferative diseases using 4-(amino)-2-(2,6-Dioxo(3-piperidyl)-isoindoline-1,3-dione in combination with other therapies |
| CZ299329B6 (cs) * | 2003-08-26 | 2008-06-18 | Pliva-Lachema A.S. | Zpusob výroby 7-ethyl-10-[ 4-(1-piperidino)-1-piperidino]karbonyloxykamptothecinu |
| CZ299593B6 (cs) * | 2003-12-16 | 2008-09-10 | Pliva-Lachema A. S. | Zpusob výroby 7-ethyl-10-hydroxykamptothecinu |
| UA88008C2 (en) | 2004-04-09 | 2009-09-10 | Чугей Сейяку Кабусики Кайся | Water-soluble prodrugs |
| TW200744603A (en) | 2005-08-22 | 2007-12-16 | Chugai Pharmaceutical Co Ltd | Novel anticancer concomitant drug |
| JP5126900B2 (ja) * | 2009-02-24 | 2013-01-23 | 株式会社渡辺オイスター研究所 | カキ肉エキス顆粒の製造方法。 |
| CN101555250B (zh) * | 2009-05-19 | 2011-05-18 | 重庆泰濠制药有限公司 | 盐酸拓扑替康的制备方法 |
| BR112023024433A2 (pt) * | 2021-05-27 | 2024-02-20 | Zymeworks Bc Inc | Análogos, conjugados e métodos de uso de camptotecina |
| MX2024003496A (es) | 2021-10-15 | 2024-04-05 | Kunshan Xinyunda Biotech Co Ltd | Composicion que contiene un farmaco antitumoral, metodo de preparacion y uso de este. |
| IL315393A (en) * | 2022-03-25 | 2024-11-01 | Zymeworks Bc Inc | Antibody preparations for drugs targeting alpha acid receptor and methods of use |
| TW202421137A (zh) * | 2022-10-19 | 2024-06-01 | 加拿大商酵活英屬哥倫比亞有限公司 | 靶向NaPi2b之抗體—藥物結合物及使用方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4399276A (en) * | 1981-01-09 | 1983-08-16 | Kabushiki Kaisha Yakult Honsha | 7-Substituted camptothecin derivatives |
| JPS6019790A (ja) * | 1983-07-14 | 1985-01-31 | Yakult Honsha Co Ltd | 新規なカンプトテシン誘導体 |
| US4981968A (en) * | 1987-03-31 | 1991-01-01 | Research Triangle Institute | Synthesis of camptothecin and analogs thereof |
| US5227380A (en) * | 1987-03-31 | 1993-07-13 | Research Triangle Institute | Pharmaceutical compositions and methods employing camptothecins |
| US5364858A (en) * | 1987-03-31 | 1994-11-15 | Research Triangle Institute | Camptothecin analogs as potent inhibitors of topoisomerase I |
| US5180722A (en) * | 1987-04-14 | 1993-01-19 | Research Triangle Institute | 10,11-methylenedioxy-20(RS)-camptothecin and 10,11-methylenedioxy-20(S)-camptothecin analogs |
| US4943579A (en) * | 1987-10-06 | 1990-07-24 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Water soluble prodrugs of camptothecin |
| 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 |
| DK0418099T3 (da) * | 1989-09-15 | 2002-04-02 | Res Triangle Inst | Fremgangsmåde til fremstilling af 10,11-methylendioxy-20(RS)-camptothecin og 10,11-methylendioxy-20(S)-camptothecinanaloger |
| JP2848958B2 (ja) * | 1990-09-28 | 1999-01-20 | スミスクライン・ビーチャム・コーポレイション | 水溶性カンプトテシン類似体、方法および手段 |
| US5162532A (en) * | 1990-12-20 | 1992-11-10 | North Carolina State University | Intermediates and method of making camptothecin and camptothecin analogs |
| US5342947A (en) * | 1992-10-09 | 1994-08-30 | Glaxo Inc. | Preparation of water soluble camptothecin derivatives |
| GB9402934D0 (en) * | 1994-02-16 | 1994-04-06 | Erba Carlo Spa | Camptothecin derivatives and process for their preparation |
-
1994
- 1994-02-16 GB GB9402934A patent/GB9402934D0/en active Pending
-
1995
- 1995-02-03 CA CA002158855A patent/CA2158855C/en not_active Expired - Fee Related
- 1995-02-03 KR KR1019950704455A patent/KR960701878A/ko not_active Withdrawn
- 1995-02-03 DE DE69527400T patent/DE69527400T2/de not_active Expired - Fee Related
- 1995-02-03 PL PL95311122A patent/PL311122A1/xx unknown
- 1995-02-03 AU AU17056/95A patent/AU681941B2/en not_active Ceased
- 1995-02-03 NZ NZ279813A patent/NZ279813A/en unknown
- 1995-02-03 JP JP7521541A patent/JPH08509244A/ja not_active Ceased
- 1995-02-03 AT AT95908901T patent/ATE220681T1/de active
- 1995-02-03 EP EP95908901A patent/EP0694035B1/en not_active Expired - Lifetime
- 1995-02-03 MX MX9504287A patent/MX9504287A/es unknown
- 1995-02-03 HU HU9503273A patent/HUT73423A/hu unknown
- 1995-02-03 WO PCT/EP1995/000393 patent/WO1995022549A1/en not_active Ceased
- 1995-02-03 ES ES95908901T patent/ES2180625T3/es not_active Expired - Lifetime
- 1995-02-03 CN CN95190093A patent/CN1123548A/zh active Pending
- 1995-02-13 IL IL112622A patent/IL112622A/xx not_active IP Right Cessation
- 1995-02-15 US US08/389,190 patent/US5602141A/en not_active Expired - Fee Related
- 1995-02-15 ZA ZA951227A patent/ZA951227B/xx unknown
- 1995-10-13 FI FI954898A patent/FI954898A0/fi not_active Application Discontinuation
- 1995-10-13 NO NO954072A patent/NO954072L/no unknown
-
1996
- 1996-08-20 US US08/697,125 patent/US5801167A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE69527400T2 (de) | 2003-03-06 |
| CN1123548A (zh) | 1996-05-29 |
| CA2158855C (en) | 2006-01-31 |
| CA2158855A1 (en) | 1995-08-24 |
| HUT73423A (en) | 1996-07-29 |
| PL311122A1 (en) | 1996-02-05 |
| IL112622A (en) | 1997-09-30 |
| FI954898A7 (fi) | 1995-10-13 |
| US5801167A (en) | 1998-09-01 |
| ZA951227B (en) | 1996-01-19 |
| NO954072D0 (no) | 1995-10-13 |
| EP0694035B1 (en) | 2002-07-17 |
| AU681941B2 (en) | 1997-09-11 |
| GB9402934D0 (en) | 1994-04-06 |
| FI954898A0 (fi) | 1995-10-13 |
| KR960701878A (ko) | 1996-03-28 |
| EP0694035A1 (en) | 1996-01-31 |
| MX9504287A (es) | 1997-05-31 |
| AU1705695A (en) | 1995-09-04 |
| IL112622A0 (en) | 1995-05-26 |
| US5602141A (en) | 1997-02-11 |
| HU9503273D0 (en) | 1996-01-29 |
| WO1995022549A1 (en) | 1995-08-24 |
| JPH08509244A (ja) | 1996-10-01 |
| NZ279813A (en) | 1996-10-28 |
| ES2180625T3 (es) | 2003-02-16 |
| DE69527400D1 (de) | 2002-08-22 |
| ATE220681T1 (de) | 2002-08-15 |
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