ZA200107204B - Cyclic Protein Tyrosine Kinase Inhibitors. - Google Patents

Cyclic Protein Tyrosine Kinase Inhibitors. Download PDF

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Publication number
ZA200107204B
ZA200107204B ZA200107204A ZA200107204A ZA200107204B ZA 200107204 B ZA200107204 B ZA 200107204B ZA 200107204 A ZA200107204 A ZA 200107204A ZA 200107204 A ZA200107204 A ZA 200107204A ZA 200107204 B ZA200107204 B ZA 200107204B
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South Africa
Prior art keywords
thiazolecarboxamide
methyl
amino
trimethylphenyl
chloro
Prior art date
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ZA200107204A
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English (en)
Inventor
Jagabandhu Das
Ping Chen
Arthur M P Doweyko
John Wityak
Ramesh Padmanabha
Derek J Norris
Joel C Barrish
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Bristol Myers Squibb Co
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22440334&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ZA200107204(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of ZA200107204B publication Critical patent/ZA200107204B/en

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    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07C237/40Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to a carbon atom of a six-membered aromatic ring
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
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  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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ZA200107204A 1999-04-15 2001-08-30 Cyclic Protein Tyrosine Kinase Inhibitors. ZA200107204B (en)

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US12951099P 1999-04-15 1999-04-15

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US (12) US6596746B1 (enExample)
EP (3) EP2308833A3 (enExample)
JP (1) JP3989175B2 (enExample)
KR (2) KR100722344B1 (enExample)
CN (2) CN1348370A (enExample)
AU (1) AU779089B2 (enExample)
BR (2) BR0009721A (enExample)
CA (1) CA2366932C (enExample)
CY (2) CY1113312T1 (enExample)
CZ (1) CZ302788B6 (enExample)
DK (1) DK1169038T3 (enExample)
ES (1) ES2391550T3 (enExample)
FR (1) FR13C0003I2 (enExample)
HK (2) HK1042433B (enExample)
HU (1) HUP0202708A3 (enExample)
ID (1) ID30460A (enExample)
IL (2) IL144910A0 (enExample)
LU (1) LU92146I2 (enExample)
MX (1) MXPA01010292A (enExample)
NO (3) NO322470B1 (enExample)
NZ (1) NZ513639A (enExample)
PL (1) PL215901B1 (enExample)
PT (1) PT1169038E (enExample)
RU (2) RU2312860C2 (enExample)
TR (1) TR200102969T2 (enExample)
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ZA (1) ZA200107204B (enExample)

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US20020058286A1 (en) * 1999-02-24 2002-05-16 Danishefsky Samuel J. Synthesis of epothilones, intermediates thereto and analogues thereof
EP2308833A3 (en) * 1999-04-15 2011-09-28 Bristol-Myers Squibb Company Cyclic protein tyrosine kinase inhibitors
US7125875B2 (en) * 1999-04-15 2006-10-24 Bristol-Myers Squibb Company Cyclic protein tyrosine kinase inhibitors
US6114365A (en) * 1999-08-12 2000-09-05 Pharmacia & Upjohn S.P.A. Arylmethyl-carbonylamino-thiazole derivatives, process for their preparation, and their use as antitumor agents
ATE309241T1 (de) 1999-09-10 2005-11-15 Merck & Co Inc Tyrosin kinase inhibitoren
JP2003520854A (ja) 2000-01-27 2003-07-08 サイトビア インコーポレイテッド カスパーゼのアクチベーターおよびアポトーシスのインデューサーとしての置換ニコチンアミドおよび類似物およびそれらの使用
GB0001930D0 (en) * 2000-01-27 2000-03-22 Novartis Ag Organic compounds
CA2417500C (en) * 2000-07-28 2008-11-18 Georgetown University Medical Center Erbb-2 selective small molecule kinase inhibitors
HUP0303038A2 (hu) 2000-09-21 2003-12-29 Bristol-Myers Squibb Co. Szubsztituált azolszármazékok mint kortikotropin releasing faktor inhibitorok, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk
US20020137755A1 (en) 2000-12-04 2002-09-26 Bilodeau Mark T. Tyrosine kinase inhibitors
SI1347971T1 (sl) * 2000-12-21 2006-06-30 Bristol Myers Squibb Co Tiazolilni inhibitorji tirozin kinaz Tec druzine
HUP0303538A2 (hu) 2000-12-21 2005-02-28 Bristol-Myers Squibb Co. Tirozin kinázok Tec családjának tiazolil-vegyület inhibitorai és ezeket tartalmazó gyógyszerkészítmények
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