JP2000506168A - Ｃｃ―１０６５及びデュオカマイシンのｍｃｂｉ類似体 - Google Patents

Ｃｃ―１０６５及びデュオカマイシンのｍｃｂｉ類似体

Info

Publication number
JP2000506168A
JP2000506168A JP9531987A JP53198797A JP2000506168A JP 2000506168 A JP2000506168 A JP 2000506168A JP 9531987 A JP9531987 A JP 9531987A JP 53198797 A JP53198797 A JP 53198797A JP 2000506168 A JP2000506168 A JP 2000506168A
Authority
JP
Japan
Prior art keywords
mcbi
pyrrolidine ring
substituted pyrrolidine
hours
dna
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
JP9531987A
Other languages
English (en)
Japanese (ja)
Other versions
JP2000506168A5 (enExample
Inventor
デイル エル ボガー
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Scripps Research Institute
Original Assignee
Scripps Research Institute
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 Scripps Research Institute filed Critical Scripps Research Institute
Publication of JP2000506168A publication Critical patent/JP2000506168A/ja
Publication of JP2000506168A5 publication Critical patent/JP2000506168A5/ja
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/58—[b]- or [c]-condensed
    • C07D209/60—Naphtho [b] pyrroles; Hydrogenated naphtho [b] pyrroles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/58—[b]- or [c]-condensed
    • C07D209/70—[b]- or [c]-condensed containing carbocyclic rings other than six-membered

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Electrotherapy Devices (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Auxiliary Devices For And Details Of Packaging Control (AREA)
  • Dc Digital Transmission (AREA)
  • Silicon Polymers (AREA)
  • Saccharide Compounds (AREA)
JP9531987A 1996-03-08 1997-03-07 Ｃｃ―１０６５及びデュオカマイシンのｍｃｂｉ類似体 Ceased JP2000506168A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US1302496P 1996-03-08 1996-03-08
US60/013,024 1996-03-08
PCT/US1997/003641 WO1997032850A1 (en) 1996-03-08 1997-03-07 Mcbi analogs of cc-1065 and the duocarmycins

Publications (2)

Publication Number Publication Date
JP2000506168A true JP2000506168A (ja) 2000-05-23
JP2000506168A5 JP2000506168A5 (enExample) 2004-12-02

Family

ID=21757922

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9531987A Ceased JP2000506168A (ja) 1996-03-08 1997-03-07 Ｃｃ―１０６５及びデュオカマイシンのｍｃｂｉ類似体

Country Status (9)

Country Link
US (1) US5985908A (enExample)
EP (1) EP0888301B1 (enExample)
JP (1) JP2000506168A (enExample)
AT (1) ATE301639T1 (enExample)
AU (1) AU711974B2 (enExample)
CA (1) CA2246783C (enExample)
DE (1) DE69733942T2 (enExample)
ES (1) ES2244991T3 (enExample)
WO (1) WO1997032850A1 (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004511466A (ja) * 2000-09-19 2004-04-15 大鵬薬品工業株式会社 Ｃｃ−１０６５およびデュオカルマイシンのアキラルアナログの組成物およびその使用方法
WO2005087762A1 (ja) * 2004-03-13 2005-09-22 Tmrc Co., Ltd. Ｄｎａの特定塩基配列をアルキル化する新規インドール誘導体ならびにそれを用いたアルキル化剤および薬剤

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2255703A1 (en) * 1996-05-31 1997-12-04 Dale L. Boger Analogs of cc-1065 and the duocarmycins
ATE310725T1 (de) * 1996-09-12 2005-12-15 Auckland Uniservices Ltd Kondensierte n-acylindole als antitumormittel
US6130237A (en) * 1996-09-12 2000-10-10 Cancer Research Campaign Technology Limited Condensed N-aclyindoles as antitumor agents
WO1998025900A1 (en) * 1996-12-13 1998-06-18 Shionogi & Co., Ltd. Compounds having antitumor activity
JP3649617B2 (ja) 1999-03-26 2005-05-18 独立行政法人科学技術振興機構 ２本鎖ｄｎａを切断できる化合物及びその使用方法
US7626026B2 (en) 2001-02-22 2009-12-01 University Of Bradford Pyrrolo-indole and pyrrolo-quinoline derivatives as prodrugs for tumour treatment
JP4862120B2 (ja) * 2001-02-22 2012-01-25 ユニヴァーシティ オブ ブラッドフォード 腫瘍治療のためのプロドラッグとしてのベンズ−インドールおよびベンゾ−キノリン誘導体
KR20030033007A (ko) * 2001-05-31 2003-04-26 코울터 파머수티컬, 인코포레이티드 세포독소, 약물전구체, 링커 및 이에 유용한 안정화제
JP2006505571A (ja) * 2002-10-15 2006-02-16 リゲル ファーマシューテイカルズ、インコーポレイテッド 置換されたインドール及びｈｃｖ阻害剤としてのその使用
US7691962B2 (en) * 2004-05-19 2010-04-06 Medarex, Inc. Chemical linkers and conjugates thereof
BRPI0510909A2 (pt) 2004-05-19 2008-12-16 Medarex Inc composto de ligaÇço fÁrmaco-ligante citotàxico, formulaÇço farmacÊutica, mÉtodo para matar uma cÉlula e mÉtodo para retardar ou interromper o crescimento de tumor
US7714016B2 (en) 2005-04-08 2010-05-11 Medarex, Inc. Cytotoxic compounds and conjugates with cleavable substrates
BRPI0619331A2 (pt) * 2005-10-26 2011-09-27 Medarex Inc método para fazer um composto para preparar um análogo de cbi cc-1065, método para preparar um análogo de cbi cc-1065 e composto
WO2007059404A2 (en) 2005-11-10 2007-05-24 Medarex, Inc. Duocarmycin derivatives as novel cytotoxic compounds and conjugates
TWI412367B (zh) 2006-12-28 2013-10-21 梅達雷克斯有限責任公司 化學鏈接劑與可裂解基質以及其之綴合物
JP2010519310A (ja) 2007-02-21 2010-06-03 メダレックス インコーポレイテッド 単一のアミノ酸を有する化学リンカーおよびその複合体
US9901567B2 (en) 2007-08-01 2018-02-27 Syntarga B.V. Substituted CC-1065 analogs and their conjugates
HUE035798T2 (en) 2008-11-03 2018-05-28 Syntarga Bv CC-1065 analogues and conjugates
NO3056203T3 (enExample) 2010-04-21 2018-05-12
EP2762472B1 (en) * 2011-09-28 2017-05-24 Industry-Academia Cooperation Group of Sejong University Selenophene-fused aromatic compound and manufacturing method thereof
US10131682B2 (en) 2012-11-24 2018-11-20 Hangzhou Dac Biotech Co., Ltd. Hydrophilic linkers and their uses for conjugation of drugs to a cell binding molecules
KR20210132742A (ko) 2012-12-21 2021-11-04 알트루바이오 인코퍼레이티드 친수성 자기-희생 링커 및 그것의 포합체
TR201810856T4 (tr) 2014-01-10 2018-08-27 Synthon Biopharmaceuticals Bv CYS'le bağlı antikor-ilaç konjugatlarını saflaştırmak için usul.
JP6417421B2 (ja) 2014-02-28 2018-11-07 ハンジョウ ディーエーシー バイオテック シーオー．，エルティディ．Ｈａｎｇｚｈｏｕ Ｄａｃ Ｂｉｏｔｅｃｈ Ｃｏ．，Ｌｔｄ． 荷電連結体及び共役体のためのその使用
KR20170020868A (ko) 2014-06-20 2017-02-24 바이오얼라이언스 씨.브이. 항-폴레이트 수용체 알파 (fra) 항체-약물 컨쥬게이트 및 그것의 사용 방법
CA2991973C (en) 2015-07-12 2021-12-07 Suzhou M-Conj Biotech Co., Ltd. Bridge linkers for conjugation of a cell-binding molecule
US9839687B2 (en) 2015-07-15 2017-12-12 Suzhou M-Conj Biotech Co., Ltd. Acetylenedicarboxyl linkers and their uses in specific conjugation of a cell-binding molecule
WO2017120534A1 (en) 2016-01-08 2017-07-13 Bioalliance C.V. Tetravalent anti-psgl-1 antibodies and uses thereof
KR20220147719A (ko) 2016-11-14 2022-11-03 항저우 디에이씨 바이오테크 씨오, 엘티디 결합 링커, 그러한 결합 링커를 함유하는 세포 결합 분자-약물 결합체, 링커를 갖는 그러한 결합체의 제조 및 사용
KR102894542B1 (ko) 2020-01-30 2025-12-03 (주)에임드바이오 벤조셀레노펜계 화합물, 이를 포함하는 약학적 조성물 및 항체-약물 결합체
CN117980327A (zh) 2021-11-03 2024-05-03 杭州多禧生物科技有限公司 抗体的特异性偶联

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004511466A (ja) * 2000-09-19 2004-04-15 大鵬薬品工業株式会社 Ｃｃ−１０６５およびデュオカルマイシンのアキラルアナログの組成物およびその使用方法
WO2005087762A1 (ja) * 2004-03-13 2005-09-22 Tmrc Co., Ltd. Ｄｎａの特定塩基配列をアルキル化する新規インドール誘導体ならびにそれを用いたアルキル化剤および薬剤
US7745473B2 (en) 2004-03-13 2010-06-29 Kyoto University Indole derivative for alkylating specific base sequence of DNA and alkylating agent and drug containing the derivative

Also Published As

Publication number Publication date
WO1997032850A1 (en) 1997-09-12
ATE301639T1 (de) 2005-08-15
DE69733942T2 (de) 2006-06-08
AU1990297A (en) 1997-09-22
EP0888301A4 (en) 2002-05-08
AU711974B2 (en) 1999-10-28
CA2246783A1 (en) 1997-09-12
ES2244991T3 (es) 2005-12-16
US5985908A (en) 1999-11-16
DE69733942D1 (de) 2005-09-15
CA2246783C (en) 2006-07-11
EP0888301A1 (en) 1999-01-07
EP0888301B1 (en) 2005-08-10

Similar Documents

Publication Publication Date Title
US5985908A (en) MCBI analogs of CC-1065 and the duocarmycins
EP0711280B1 (fr) Derives de perhydroisoindole comme antagonistes de la substance p
FR2676442A1 (fr) Nouveau derives de perhydroisoindole, leur preparation et les compositions pharmaceutiques qui les contiennent.
FR2689888A1 (fr) Nouveaux dérivés de pérhydroisoindole, leur préparation et les compositions pharmaceutiques qui les contiennent.
JPH11513391A (ja) Ｃｃ−１０６５ 及びズオカーマイシンのｃｂｉ 類縁体
FR2698873A1 (fr) Benzocycloheptènes, benzoxépines et benzothiépines activateurs des canaux potassiques, procédé de préparation, composition pharmaceutique les contenant.
EP0708774B1 (fr) DERIVES D'IMIDAZO[1,2-a]PYRAZIN-4-ONE ANTAGONISTES DES RECEPTEURS AMPA ET NMDA
JPH09510728A (ja) ５Ｈ−インデン［１，２−ｂ］ピラジン−２，３−ジオン誘導体、それらの製造方法およびそれらを含有する医薬製品
FR2669029A1 (fr) Nouveaux derives de la n-benzoyl proline, leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
EP0011059B1 (fr) Procédé de préparation de la (+,-) vincadifformine et d'autres dérivés pentacycliques apparentés
FR2620700A1 (fr) Procede de synthese d'alpha amino acides n alkyles et leurs esters. application a la synthese de carboxyalkyl dipeptides
JPH09510726A (ja) インデノ［１，２−ｅ］ピラジン−４−オン、その製造およびそれを含む医薬品
JPH09510727A (ja) イミダゾ（１，２−ａ）−インデノ（１，２−ｅ）ピラジン−４−オン誘導体およびそれを含む医薬組成物
EP0658557B1 (fr) Nouveaux analogues de l'éburnane, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent
BE881862A (fr) Composes antibacteriens et inhibiteurs de beta-lactamase, procede pour les preparer et leur usage comme medicaments
EP0233800B1 (fr) Dérivés d'imidazo[1,2-a]quinoléines, leur préparation et leur application en thérapeutique
EP0926145A1 (fr) Composés naphtaléniques, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent
CA2061065A1 (fr) Composes derives de beta-carbolines ligands du recepteur des benzodia zepines, ayant un effet agoniste inverse et antagoniste vis-a-vis des benzodiazepines, et medicaments en contenant
EP0820985B1 (fr) Nouveaux dérivés de bis-imides, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent
EP0043811B1 (fr) Nouvelles indolonaphtyridines et leur utilisation en tant que médicaments
EP0172041A1 (fr) Acides dihydro-5,6-4H-cyclopenta [b] thiophènecarboxyliques-6, procédés de préparation et médicaments les contenant
EP1196418B1 (fr) PROCEDE DE PREPARATION DE 1,4]DIAZEPINO 6,7,1- i hi /i ]INDOL-4-ONES SUBSTITUEES
CH633290A5 (en) Process for preparing derivatives of 7-oxo-1,3-diazabicyclo[3.2.0]heptane-2-carboxylic acid
BE884145R (fr) Composes indoliques nouveaux
FR2727681A1 (fr) Procede de preparation de derives de pyrrolizine

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20040308

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20040308

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20071127

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20080227

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20080414

A313 Final decision of rejection without a dissenting response from the applicant

Free format text: JAPANESE INTERMEDIATE CODE: A313

Effective date: 20080708

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20080902