AU760964B2 - 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activityand for use in cancer chemotherapy - Google Patents
3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activityand for use in cancer chemotherapy Download PDFInfo
- Publication number
- AU760964B2 AU760964B2 AU22215/00A AU2221500A AU760964B2 AU 760964 B2 AU760964 B2 AU 760964B2 AU 22215/00 A AU22215/00 A AU 22215/00A AU 2221500 A AU2221500 A AU 2221500A AU 760964 B2 AU760964 B2 AU 760964B2
- Authority
- AU
- Australia
- Prior art keywords
- cancer
- well
- cells
- indolinone
- pct
- 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
Links
Classifications
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11431398P | 1998-12-31 | 1998-12-31 | |
US60/114313 | 1998-12-31 | ||
PCT/US1999/031232 WO2000038519A1 (en) | 1998-12-31 | 1999-12-30 | 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activity and for use in cancer chemotherapy |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2221500A AU2221500A (en) | 2000-07-31 |
AU760964B2 true AU760964B2 (en) | 2003-05-22 |
Family
ID=22354480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU22215/00A Ceased AU760964B2 (en) | 1998-12-31 | 1999-12-30 | 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activityand for use in cancer chemotherapy |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP1139754A4 (es) |
JP (1) | JP2002533360A (es) |
KR (1) | KR20010108063A (es) |
CN (1) | CN1356872A (es) |
AU (1) | AU760964B2 (es) |
BR (1) | BR9916735A (es) |
CA (1) | CA2357042A1 (es) |
IL (1) | IL143920A0 (es) |
MX (1) | MXPA01006742A (es) |
WO (1) | WO2000038519A1 (es) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6569868B2 (en) | 1998-04-16 | 2003-05-27 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
PT1233943E (pt) * | 1999-11-24 | 2011-09-01 | Sugen Inc | Formulações para agentes farmacêuticos ionizáveis como ácidos livres ou bases livres |
US6878733B1 (en) | 1999-11-24 | 2005-04-12 | Sugen, Inc. | Formulations for pharmaceutical agents ionizable as free acids or free bases |
NZ520640A (en) * | 2000-02-15 | 2005-04-29 | Upjohn Co | Pyrrole substituted 2-indolinone protein kinase inhibitors |
PL363110A1 (en) * | 2000-02-28 | 2004-11-15 | Aventis Pharma S.A. | A composition comprising camptothecin and a pyrimidine derivative for the treatment of cancer |
TWI270545B (en) | 2000-05-24 | 2007-01-11 | Sugen Inc | Mannich base prodrugs of 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives |
CA2410509A1 (en) | 2000-06-02 | 2001-12-13 | Sugen, Inc. | Indolinone derivatives as protein kinase/phosphatase inhibitors |
BRPI0207961B8 (pt) | 2001-03-14 | 2021-05-25 | Bristol Myers Squibb Co | uso de análogos de epotilona e capecitabina para fabricar medicamento para tratar tumores cancerosos sólidos e kit compreendendo os referidos compostos. |
AU2002303892A1 (en) | 2001-05-30 | 2002-12-09 | Jingrong Cui | 5-aralkylsulfonyl-3- (pyrrol-2-ylmethylidene)-2-indolinone derivatives as kinase inhibitors |
AR038957A1 (es) * | 2001-08-15 | 2005-02-02 | Pharmacia Corp | Terapia de combinacion para el tratamiento del cancer |
WO2003035619A1 (en) * | 2001-10-25 | 2003-05-01 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
WO2003035616A2 (en) * | 2001-10-25 | 2003-05-01 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
WO2003035614A2 (en) * | 2001-10-25 | 2003-05-01 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
MXPA04004804A (es) * | 2001-11-21 | 2005-02-17 | Sugen Inc | Formulaciones farmaceuticas que comprenden derivados de indolinona. |
US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
US6797825B2 (en) | 2001-12-13 | 2004-09-28 | Abbott Laboratories | Protein kinase inhibitors |
RU2316554C2 (ru) | 2001-12-27 | 2008-02-10 | Тереванс, Инк. | Производные индолина, используемые как ингибиторы протеинкиназы |
EP1515680A4 (en) * | 2002-06-25 | 2005-09-21 | Wyeth Corp | USE OF THIO-OXINDOLE DERIVATIVES IN THE TREATMENT OF SKIN DISORDERS |
BR0312054A (pt) * | 2002-06-25 | 2005-10-18 | Wyeth Corp | Uso de derivados de tio-oxindol na preparação de medicamentos úteis no tratamento de condições relacionadas com hormÈnio, e kit farmacêutico |
BRPI0313165B8 (pt) | 2002-08-02 | 2021-05-25 | Ab Science | 2-(3-aminoaril)amino-4-aril-tiazóis e sua utilização como inibidores de c-kit |
US8450302B2 (en) | 2002-08-02 | 2013-05-28 | Ab Science | 2-(3-aminoaryl) amino-4-aryl-thiazoles and their use as c-kit inhibitors |
WO2004045617A1 (en) * | 2002-11-15 | 2004-06-03 | Warner-Lambert Company Llc | Combination chemotherapy comprising a mek inhibitor and capecitabine for treating cancer |
PL1684750T3 (pl) | 2003-10-23 | 2010-10-29 | Ab Science | 2-Aminoarylooksazole jako inhibitory kinazy tyrozynowej |
CN100432071C (zh) * | 2004-11-05 | 2008-11-12 | 中国科学院上海药物研究所 | 取代1h-吲哚-2-酮类化合物及其制备方法和用途 |
CA2603826C (en) | 2005-04-04 | 2013-03-12 | Ab Science | Substituted oxazole derivatives and their use as tyrosine kinase inhibitors |
US8246966B2 (en) | 2006-08-07 | 2012-08-21 | University Of Georgia Research Foundation, Inc. | Trypanosome microsome system and uses thereof |
WO2008066755A2 (en) | 2006-11-22 | 2008-06-05 | University Of Georgia Research Foundation, Inc. | Tyrosine kinase inhibitors as anti-kinetolastid and anti-apicomplexan agents |
PT2780011T (pt) * | 2011-11-11 | 2018-05-14 | Lilly Co Eli | Terapia de combinação para cancro do ovário |
JP7041515B2 (ja) | 2015-01-08 | 2022-03-24 | ザ ボード オブ トラスティーズ オブ ザ レランド スタンフォード ジュニア ユニバーシティー | 骨、骨髄、及び軟骨の誘導を提供する因子及び細胞 |
MD3288940T2 (ro) | 2015-04-29 | 2021-08-31 | Janssen Pharmaceutica Nv | Azabenzimidazoli și utilizarea lor ca modulatori ai receptorilor AMPA |
CN105585558A (zh) * | 2015-12-15 | 2016-05-18 | 贵州大学 | 双烷氧基嘧啶拼接3-烯键氧化吲哚衍生物及其制备方法及应用 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996040116A1 (en) * | 1995-06-07 | 1996-12-19 | Sugen, Inc. | Indolinone compounds for the treatment of disease |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2264220A1 (en) * | 1996-08-23 | 1998-02-26 | Sugen, Inc. | Indolinone combinatorial libraries and related products and methods for the treatment of disease |
-
1999
- 1999-12-30 BR BR9916735-2A patent/BR9916735A/pt not_active IP Right Cessation
- 1999-12-30 JP JP2000590484A patent/JP2002533360A/ja not_active Withdrawn
- 1999-12-30 IL IL14392099A patent/IL143920A0/xx unknown
- 1999-12-30 CA CA002357042A patent/CA2357042A1/en not_active Abandoned
- 1999-12-30 AU AU22215/00A patent/AU760964B2/en not_active Ceased
- 1999-12-30 KR KR1020017008453A patent/KR20010108063A/ko not_active Application Discontinuation
- 1999-12-30 CN CN99816376A patent/CN1356872A/zh active Pending
- 1999-12-30 WO PCT/US1999/031232 patent/WO2000038519A1/en not_active Application Discontinuation
- 1999-12-30 EP EP99966725A patent/EP1139754A4/en not_active Withdrawn
- 1999-12-30 MX MXPA01006742A patent/MXPA01006742A/es unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996040116A1 (en) * | 1995-06-07 | 1996-12-19 | Sugen, Inc. | Indolinone compounds for the treatment of disease |
US5792783A (en) * | 1995-06-07 | 1998-08-11 | Sugen, Inc. | 3-heteroaryl-2-indolinone compounds for the treatment of disease |
US5886020A (en) * | 1995-06-07 | 1999-03-23 | Sugen, Inc. | 3-(4'-dimethylaminobenzylidenyl)-2-indolinone and analogues thereof for the treatment of disease |
Also Published As
Publication number | Publication date |
---|---|
BR9916735A (pt) | 2001-09-25 |
AU2221500A (en) | 2000-07-31 |
KR20010108063A (ko) | 2001-12-07 |
WO2000038519A1 (en) | 2000-07-06 |
EP1139754A1 (en) | 2001-10-10 |
EP1139754A4 (en) | 2002-12-18 |
MXPA01006742A (es) | 2004-04-21 |
CN1356872A (zh) | 2002-07-03 |
CA2357042A1 (en) | 2000-07-06 |
IL143920A0 (en) | 2002-04-21 |
JP2002533360A (ja) | 2002-10-08 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FGA | Letters patent sealed or granted (standard patent) |