JP2003525872A5 - - Google Patents

Download PDF

Info

Publication number
JP2003525872A5
JP2003525872A5 JP2001544731A JP2001544731A JP2003525872A5 JP 2003525872 A5 JP2003525872 A5 JP 2003525872A5 JP 2001544731 A JP2001544731 A JP 2001544731A JP 2001544731 A JP2001544731 A JP 2001544731A JP 2003525872 A5 JP2003525872 A5 JP 2003525872A5
Authority
JP
Japan
Prior art keywords
methyl
mammal
pharmaceutically acceptable
pharmaceutical composition
compound according
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.)
Pending
Application number
JP2001544731A
Other languages
English (en)
Japanese (ja)
Other versions
JP2003525872A (ja
Filing date
Publication date
Priority claimed from US09/464,511 external-priority patent/US6262096B1/en
Priority claimed from US09/616,629 external-priority patent/US6214852B1/en
Application filed filed Critical
Publication of JP2003525872A publication Critical patent/JP2003525872A/ja
Publication of JP2003525872A5 publication Critical patent/JP2003525872A5/ja
Pending legal-status Critical Current

Links

JP2001544731A 1999-12-15 2000-12-07 サイクリン依存性キナーゼのn−[5−[[[5−アルキル−2−オキサゾリル]メチル]チオ−2−チアゾリル]カルボキサミドインヒビター Pending JP2003525872A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US09/464,511 1999-12-15
US09/464,511 US6262096B1 (en) 1997-11-12 1999-12-15 Aminothiazole inhibitors of cyclin dependent kinases
US09/616,629 US6214852B1 (en) 1998-10-21 2000-07-26 N-[5-[[[5-alkyl-2-oxazolyl]methyl]thio]-2-thiazolyl]-carboxamide inhibitors of cyclin dependent kinases
US09/616,629 2000-07-26
PCT/US2000/033113 WO2001044241A1 (en) 1999-12-15 2000-12-07 N-[5-[[[5-alkyl-2-oxazolyl]methyl]thio]-2-thiazolyl]-carboxamide inhibitors of cyclin dependent kinases

Publications (2)

Publication Number Publication Date
JP2003525872A JP2003525872A (ja) 2003-09-02
JP2003525872A5 true JP2003525872A5 (enExample) 2008-01-31

Family

ID=27041009

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001544731A Pending JP2003525872A (ja) 1999-12-15 2000-12-07 サイクリン依存性キナーゼのn−[5−[[[5−アルキル−2−オキサゾリル]メチル]チオ−2−チアゾリル]カルボキサミドインヒビター

Country Status (22)

Country Link
US (1) US6214852B1 (enExample)
EP (1) EP1240165B1 (enExample)
JP (1) JP2003525872A (enExample)
KR (1) KR20020067547A (enExample)
CN (1) CN1433415A (enExample)
AT (1) ATE294800T1 (enExample)
AU (1) AU774381B2 (enExample)
CA (1) CA2394544A1 (enExample)
CO (1) CO5251464A1 (enExample)
CZ (1) CZ20022013A3 (enExample)
DE (1) DE60019964T2 (enExample)
DK (1) DK1240165T3 (enExample)
EE (1) EE200200306A (enExample)
ES (1) ES2241678T3 (enExample)
HU (1) HUP0300974A3 (enExample)
PE (1) PE20010932A1 (enExample)
PL (1) PL364884A1 (enExample)
PT (1) PT1240165E (enExample)
SI (1) SI20975B (enExample)
TW (1) TWI265930B (enExample)
UY (1) UY26480A1 (enExample)
WO (1) WO2001044241A1 (enExample)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6262096B1 (en) 1997-11-12 2001-07-17 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
US6414156B2 (en) 1998-10-21 2002-07-02 Bristol-Myers Squibb Company Process for preparing azacycloalkanoylaminothiazoles
US6515004B1 (en) 1999-12-15 2003-02-04 Bristol-Myers Squibb Company N-[5-[[[5-alkyl-2-oxazolyl]methyl]thio]-2-thiazolyl]-carboxamide inhibitors of cyclin dependent kinases
US6392053B2 (en) * 1999-12-15 2002-05-21 Bristol-Myers Squibb Company Process for preparing arylacetylaminothiazoles
US6534531B2 (en) * 2000-04-27 2003-03-18 Bristol-Myers Squibb Company Methods for preventing and treating alopecia induced by chemotherapy or radiotherapy
EP1724270A3 (en) * 2001-07-19 2007-01-03 Pfizer Italia S.r.l. Phenylacetamido-thiazole derivatives, process for their preparation and their use as antitumor agents
WO2003008365A2 (en) * 2001-07-19 2003-01-30 Pharmacia Italia S.P.A. Phenylacetamido-thiazole derivatives, process for their preparation and their use as antitumor agents
ES2183734B1 (es) * 2001-08-02 2004-06-16 Consejo Sup. Investigaciones Cientificas Derivados de 4-4'-bipiridil-2-2'-bisoxazoles y 4-4'-bipiridil-2-2'-bistiazoles como agentes antineoplasicos.
CN1547574A (zh) * 2001-08-03 2004-11-17 ŵ��Ų�ڿ˹�˾ 新型2,4-二氨基噻唑衍生物
MXPA04000906A (es) * 2001-08-03 2004-11-22 Novo Nordisk As Nuevos derivados de 2,4-diaminotiazol.
TW200401638A (en) * 2002-06-20 2004-02-01 Bristol Myers Squibb Co Heterocyclic inhibitors of kinases
DE10300124A1 (de) * 2003-01-07 2004-07-15 Bayer Ag Verfahren zur Herstellung von Arylalkinen
AU2004262369A1 (en) * 2003-07-29 2005-02-10 Bristol-Myers Squibb Company Biomarkers of cyclin-dependent kinase modulation
US7888504B2 (en) * 2006-07-06 2011-02-15 Bristol-Myers Squibb Company Glucokinase activators and methods of using same
WO2008049856A2 (en) * 2006-10-25 2008-05-02 Ingenium Pharmaceuticals Gmbh Methods of treating pain using cdk inhibitors
EP2937345B1 (en) 2009-12-29 2018-03-21 Dana-Farber Cancer Institute, Inc. Type ii raf kinase inhibitors
EP2760860B8 (en) * 2011-09-28 2017-03-08 Euro-Celtique S.A. Nitrogen mustard derivatives
WO2013074986A1 (en) 2011-11-17 2013-05-23 Dana-Farber Cancer Institute, Inc. Inhibitors of c-jun-n-terminal kinase (jnk)
AR092790A1 (es) 2012-02-01 2015-05-06 Euro Celtique Sa Derivados bencimidazolicos del acido hidroxamico
US10112927B2 (en) 2012-10-18 2018-10-30 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
US9758522B2 (en) 2012-10-19 2017-09-12 Dana-Farber Cancer Institute, Inc. Hydrophobically tagged small molecules as inducers of protein degradation
WO2015058140A1 (en) 2013-10-18 2015-04-23 Dana-Farber Cancer Institute, Inc. Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7)
WO2015058126A1 (en) 2013-10-18 2015-04-23 Syros Pharmaceuticals, Inc. Heteroaromatic compounds useful for the treatment of prolferative diseases
GB201409485D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201409488D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
GB201409471D0 (en) 2014-05-28 2014-07-09 Euro Celtique Sa Pharmaceutical composition
AU2015371251B2 (en) 2014-12-23 2020-06-11 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
CN107427521B (zh) 2015-03-27 2021-08-03 达纳-法伯癌症研究所股份有限公司 细胞周期蛋白依赖性激酶的抑制剂
EP3307728A4 (en) 2015-06-12 2019-07-17 Dana Farber Cancer Institute, Inc. COMBINATION THERAPY OF TRANSCRIPTION INHIBITORS AND CHINESE INHIBITORS
JP7028766B2 (ja) * 2015-09-09 2022-03-02 ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド サイクリン依存性キナーゼの阻害剤
AU2016426574B2 (en) 2016-10-11 2023-07-13 Euro-Celtique S.A. Hodgkin lymphoma therapy
GB201709403D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating sarcoma
GB201709405D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating ovarian cancer
GB201709406D0 (en) 2017-06-13 2017-07-26 Euro-Cletique S A Compounds for treating TNBC
GB201709402D0 (en) 2017-06-13 2017-07-26 Euro Celtique Sa Compounds for treating t-pll
JP7590185B2 (ja) 2018-06-25 2024-11-26 ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド Taireファミリーキナーゼインヒビターおよびそれらの使用
WO2020128913A1 (en) 2018-12-18 2020-06-25 Mundipharma International Corporation Limited Compounds for treating multiple myeloma
WO2020140098A1 (en) 2018-12-28 2020-07-02 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 and uses thereof
CN117049976A (zh) * 2023-08-16 2023-11-14 四川伊诺达博医药科技有限公司 一种n-乙基-2-(4-甲酰基苯基)乙酰胺的制备方法

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1088049A (en) 1975-06-03 1980-10-21 Takashi Masugi 3-substituted-7-substituted alkanamido-3-cephem-4- carboxylic acid compounds and processes for preparation thereof
CA1201431A (en) 1981-12-17 1986-03-04 Daiei Tunemoto .beta.-LACTAM COMPOUNDS, PROCESS FOR THE PREPARATION THEREOF AND INTERMEDIATE PRODUCTS FOR THE PREPARATION THEREOF
TW205041B (enExample) 1989-08-07 1993-05-01 Fujisawa Pharmaceutical Co
US5491157A (en) 1993-05-10 1996-02-13 Eastman Kodak Company Method and composition for the prevention, control and amelioration of soilborne fungi and disease caused thereby
IL112721A0 (en) 1994-03-10 1995-05-26 Zeneca Ltd Azole derivatives
JPH10510258A (ja) 1994-12-09 1998-10-06 藤沢薬品工業株式会社 セフェム化合物およびその医薬用途
IL117620A0 (en) 1995-03-27 1996-07-23 Fujisawa Pharmaceutical Co Heterocyclic compounds processes for the preparation thereof and pharmaceutical compositions containing the same
AUPN801196A0 (en) 1996-02-12 1996-03-07 Fujisawa Pharmaceutical Co., Ltd. New cephem compounds and pharmaceutical use thereof
UA66810C2 (uk) 1997-10-27 2004-06-15 Агорон Фармацевтикалз Інк. Похідні 4-амінотіазолу та композиції на їх основі як інгібітори циклінозалежних кіназ
US6040321A (en) 1997-11-12 2000-03-21 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
GB9823871D0 (en) 1998-10-30 1998-12-23 Pharmacia & Upjohn Spa 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents

Similar Documents

Publication Publication Date Title
SI20975B (sl) N-/5-///5-alkil-2-oksazolil/metil/tio/-2-tiazolil/-karboksamidni inhibitorji ciklodekstrin odvisne kinaze
US9187465B2 (en) Oxazole tyrosine kinase inhibitors
JP2019077725A5 (enExample)
RU2005109561A (ru) Новые производные аминоиндазолов в качестве лекарственных средств и содержащие их фармацевтические композиции
JP2022096662A5 (enExample)
RU2386630C2 (ru) Соединения и композиции в качестве ингибиторов протеинтирозинкиназы
RU2005121897A (ru) Производные аминоиндазолов и их применение в качестве ингибиторов киназ
JP2024540445A5 (enExample)
RU2017121044A (ru) Производные амидотиадиазола в качестве ингибиторов надфн-оксидазы
JP2005524660A5 (enExample)
JP2010533158A5 (enExample)
JP2014511869A5 (enExample)
RU2012143689A (ru) Спироциклические соединения и их применение в качестве терапевтических агентов и диагностических зондов
IL196129A (en) Human protein tyrosine phosphatase inhibitors, compositions comprising such compounds and uses thereof in the preparation of medicaments for regulating angiogenesis
US20130096149A1 (en) Heteroaryl compounds and compositions as protein kinase inhibitors
RU2003118448A (ru) Производные замещенного триазолдиамина и их применение в качестве ингибиторов киназы
JP2008516986A5 (enExample)
CA2610888A1 (en) Inhibitors of akt activity
RU2002119016A (ru) N-[5-[[[5-алкил-2-оксазолил]метил]тио]-2-тиазолил]карбоксамидные ингибиторы циклин-зависимых киназ
JP2003511384A5 (enExample)
JP2006503081A5 (enExample)
HRP20100714T1 (hr) Derivati 5-(benz-(z)-iliden)-tiazolidin-4-ona kao imunosupresivna sredstva
MX2010004176A (es) Derivado de triazol 1,3,5-trisustituido.
JP2014523400A5 (enExample)
RU2000100935A (ru) Производные ароил-пиперазина, их получение и их использование в качестве антагонистов тахикинина