DK0737686T3 - Camthothecinderivat med antitumoraktivitet - Google Patents

Camthothecinderivat med antitumoraktivitet

Info

Publication number
DK0737686T3
DK0737686T3 DK96105661T DK96105661T DK0737686T3 DK 0737686 T3 DK0737686 T3 DK 0737686T3 DK 96105661 T DK96105661 T DK 96105661T DK 96105661 T DK96105661 T DK 96105661T DK 0737686 T3 DK0737686 T3 DK 0737686T3
Authority
DK
Denmark
Prior art keywords
compound
camthothecin
derivatives
antitumor activity
formula
Prior art date
Application number
DK96105661T
Other languages
Danish (da)
English (en)
Inventor
Hirofumi Terasawa
Shinji Kamihara
Kazuaki Kanai
Hiroaki Kitaoka
Original Assignee
Daiichi Seiyaku Co
Yakult Honsha Kk
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 Daiichi Seiyaku Co, Yakult Honsha Kk filed Critical Daiichi Seiyaku Co
Application granted granted Critical
Publication of DK0737686T3 publication Critical patent/DK0737686T3/da

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
    • 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Saccharide Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
DK96105661T 1995-04-10 1996-04-10 Camthothecinderivat med antitumoraktivitet DK0737686T3 (da)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8371795 1995-04-10

Publications (1)

Publication Number Publication Date
DK0737686T3 true DK0737686T3 (da) 1999-11-22

Family

ID=13810270

Family Applications (1)

Application Number Title Priority Date Filing Date
DK96105661T DK0737686T3 (da) 1995-04-10 1996-04-10 Camthothecinderivat med antitumoraktivitet

Country Status (13)

Country Link
US (2) US6504029B1 (fr)
EP (1) EP0737686B1 (fr)
KR (1) KR100400941B1 (fr)
CN (1) CN1050131C (fr)
AT (1) ATE181919T1 (fr)
CA (1) CA2173671A1 (fr)
DE (1) DE69603117T2 (fr)
DK (1) DK0737686T3 (fr)
EA (1) EA000036B1 (fr)
ES (1) ES2136338T3 (fr)
GR (1) GR3031400T3 (fr)
NO (1) NO314085B1 (fr)
TW (1) TW382630B (fr)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CZ298259B6 (cs) 2000-02-28 2007-08-08 Aventis Pharma S. A. Farmaceutická kombinace k lécení rakoviny obsahující CPT-11 a capecitabin
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
AR030207A1 (es) * 2000-04-07 2003-08-13 Daiichi Seiyaku Co Composicion farmaceutica que contiene un derivado de camptotecina y procedimiento de preparacion de la misma
US6486320B2 (en) 2000-09-15 2002-11-26 Aventis Pharma S.A. Preparation of camptothecin and of its derivatives
EP1333820A2 (fr) 2000-10-27 2003-08-13 Aventis Pharma S.A. Combinaison de camptothecine et d'un derive de stilbene pour le traitement du cancer
WO2006069344A2 (fr) 2004-12-22 2006-06-29 Rutgers, The State University Of New Jersey Hydrogels a liberation regulee
CA2658015A1 (fr) 2006-03-30 2007-10-11 Diatos S.A. Conjugues camptotechine/peptide et compositions pharmaceutiques les comportant
US8173621B2 (en) 2008-06-11 2012-05-08 Gilead Pharmasset Llc Nucleoside cyclicphosphates
WO2010075517A2 (fr) 2008-12-23 2010-07-01 Pharmasset, Inc. Analogues de nucléoside
CL2009002207A1 (es) 2008-12-23 2011-02-18 Gilead Pharmasset Llc Compuestos derivados de 3-hidroxi-5-(9h-purin-9-il)tetrahidrofuran-2-il, inhibidor de la replicacion de arn viral dependiente de arn; composicion farmaceutica; uso para el tratamiento de hepatitis c.
SG172363A1 (en) 2008-12-23 2011-07-28 Pharmasset Inc Synthesis of purine nucleosides
AP3515A (en) 2010-03-31 2016-01-11 Gilead Pharmasset Llc Nucleoside phosphoramidates
US20140086975A1 (en) 2010-10-15 2014-03-27 Rutgers, The State University Of New Jersey Hydrogel formulation for dermal and ocular delivery
CN115960111A (zh) 2012-10-11 2023-04-14 第一三共株式会社 抗体－药物偶联物
US9872924B2 (en) 2012-10-19 2018-01-23 Daiichi Sankyo Company, Limited Antibody-drug conjugate produced by binding through linker having hydrophilic structure
KR102088169B1 (ko) 2013-12-25 2020-03-12 다이이찌 산쿄 가부시키가이샤 항 trop2 항체-약물 컨쥬게이트
JP5998289B2 (ja) 2014-01-31 2016-09-28 第一三共株式会社 抗ｈｅｒ２抗体−薬物コンジュゲート
WO2015155998A1 (fr) 2014-04-10 2015-10-15 Daiichi Sankyo Company, Limited Conjugué médicament-anticorps anti-her3
JP6612738B2 (ja) 2014-04-10 2019-11-27 第一三共株式会社 抗ｈｅｒ２抗体−薬物コンジュゲート
JP6787890B2 (ja) 2015-06-29 2020-11-18 第一三共株式会社 抗体−薬物コンジュゲートの選択的製造方法
JPWO2018110515A1 (ja) 2016-12-12 2019-10-24 第一三共株式会社 抗体−薬物コンジュゲートと免疫チェックポイント阻害剤の組み合わせ
WO2018135501A1 (fr) 2017-01-17 2018-07-26 第一三共株式会社 Anticorps anti-gpr20 et conjugué anticorps-médicament anti-gpr20
TWI794230B (zh) 2017-05-15 2023-03-01 日商第一三共股份有限公司 抗ｃｄｈ６抗體及抗ｃｄｈ６抗體-藥物結合物、以及其製造方法
AU2018327170B2 (en) 2017-08-31 2021-03-11 Daiichi Sankyo Company, Limited Novel method for producing antibody-drug conjugate
KR20200041993A (ko) 2017-08-31 2020-04-22 다이이찌 산쿄 가부시키가이샤 항체-약물 콘주게이트의 개량 제조 방법
SG11202010496WA (en) 2018-05-18 2020-12-30 Daiichi Sankyo Co Ltd Anti-muc1 antibody-drug conjugate
BR112021004656A2 (pt) 2018-09-26 2021-06-01 Jiangsu Hengrui Medicine Co., Ltd. conjugado fármaco-ligante de análogo exatecano, método para preparar o mesmo e aplicação do mesmo
MX2021003446A (es) 2018-09-30 2021-06-15 Jiangsu Hansoh Pharmaceutical Group Co Ltd Conjugado analogo del anticuerpo anti-bth3 y exatecan, y uso medicinal del mismo.
CN118221763A (zh) 2019-03-29 2024-06-21 免疫医疗有限公司 化合物及其缀合物
EP3996749A1 (fr) 2019-07-10 2022-05-18 Cybrexa 3, Inc. Conjugués peptidiques d'agents de ciblage de microtubules en tant qu'agents thérapeutiques
TW202116778A (zh) 2019-07-10 2021-05-01 美商斯布雷克薩二號公司 作為治療劑之細胞毒素之肽結合物
CN118403182A (zh) 2019-12-12 2024-07-30 江苏恒瑞医药股份有限公司 抗密蛋白抗体药物偶联物及其医药用途
WO2021147993A1 (fr) 2020-01-22 2021-07-29 江苏恒瑞医药股份有限公司 Conjugué anticorps anti-trop-2-analogue d'exatécan et son utilisation médicale
CN115103691A (zh) 2020-03-25 2022-09-23 江苏恒瑞医药股份有限公司 一种含抗体药物偶联物的药物组合物及其用途
AU2021243080A1 (en) 2020-03-25 2022-09-22 Jiangsu Hengrui Pharmaceuticals Co., Ltd. Preparation method for antibody medicament conjugate
US20230140397A1 (en) 2020-03-25 2023-05-04 Jiangsu Hengrui Pharmaceuticals Co., Ltd. Anti-psma antibody-exatecan analogue conjugate and medical use thereof
WO2023030364A1 (fr) * 2021-09-01 2023-03-09 上海弼领生物技术有限公司 Composé camptothécine, son procédé de préparation et son utilisation
WO2024149193A1 (fr) * 2023-01-09 2024-07-18 四川科伦博泰生物医药股份有限公司 Procédé de préparation d'un composé cyclique fusionné contenant de l'azote

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6087746A (ja) * 1983-10-17 1985-05-17 Hakubakumai Kk 即席麺ないしは焼そば用蒸し麺の製造方法
US4939255A (en) * 1987-06-24 1990-07-03 Daiichi Pharmaceutical Co., Ltd. Hexa-cyclic camptothecin derivatives
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
JP3008226B2 (ja) * 1991-01-16 2000-02-14 第一製薬株式会社 六環性化合物
US5658920A (en) * 1991-01-16 1997-08-19 Daiichi Pharmaceutical Co., Ltd. Substituted 1H,12H-benz-[DE]pyrano[3',4':6,7] indolizino[1,2-B]quinoline-10,13(9H,15H)-dione compound
JP3359955B2 (ja) * 1992-07-16 2002-12-24 第一製薬株式会社 抗腫瘍剤
IS4152A (is) * 1993-04-29 1994-10-30 Glaxo Inc. Vatnsuppleysanlegar Camptothecin afleiður og aðferð til framleiðslu þeirra
GB9319944D0 (en) * 1993-09-28 1993-11-17 Erba Carlo Spa Process for the preparation of 9-amino camptothecin

Also Published As

Publication number Publication date
NO314085B1 (no) 2003-01-27
ES2136338T3 (es) 1999-11-16
US6504029B1 (en) 2003-01-07
US20010034446A1 (en) 2001-10-25
EP0737686A1 (fr) 1996-10-16
DE69603117D1 (de) 1999-08-12
AU5056696A (en) 1996-10-24
CA2173671A1 (fr) 1996-10-11
AU692078B2 (en) 1998-05-28
TW382630B (en) 2000-02-21
GR3031400T3 (en) 2000-01-31
ATE181919T1 (de) 1999-07-15
EA000036B1 (ru) 1998-02-26
NO961405L (no) 1996-10-11
KR960037682A (ko) 1996-11-19
KR100400941B1 (ko) 2003-12-24
DE69603117T2 (de) 1999-10-28
US6552197B2 (en) 2003-04-22
EA199600018A2 (ru) 1996-10-01
CN1050131C (zh) 2000-03-08
NO961405D0 (no) 1996-04-09
EA199600018A3 (ru) 1997-03-31
EP0737686B1 (fr) 1999-07-07
CN1133290A (zh) 1996-10-16

Similar Documents

Publication Publication Date Title
DK0737686T3 (da) Camthothecinderivat med antitumoraktivitet
DE69327567D1 (de) Verfahren zur Herstellung von Alanylglutamin
FR2383907A1 (fr) Procede de preparation de derives de l'acide acetique et derives obtenus par ce procede
NO882588L (no) Fremgangsmaate ved fremstilling av substituerte inololinonderivater.
BG95145A (bg) Метод за получаване на 9-заместени гуанинови производни
KR880700793A (ko) 퀴놀린 카복실산의 제조 방법
DE69809888D1 (de) Verfahren zur Herstellung von alpha-Aminoketonen
DK159432C (da) Fremgangsmaade til fremstilling af 4-amino-5-dialkoxymethylpyrimidinderivater
ATE18208T1 (de) N-(4-hydroxyphenyl)essigsaeureamid-estern aus 5benzoyl-1-methylpyrrol-2-essigsaeure.
PL326563A1 (en) Method of obtaining derivatives of methoxyiminophenyglyoxalic acid
ATE159519T1 (de) Verfahren zur herstellung von n-phenyl-n-(4- piperidinyl)amid-derivaten
SE8503811D0 (sv) Novel process for the preparation of an aminolactone
ATE100105T1 (de) Physiologisch aktive substanz fa-4283, derivate und ihre herstellung.