HUE027846T2 - Pyrimidine derivatives as FAK inhibitors - Google Patents

Pyrimidine derivatives as FAK inhibitors Download PDF

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Publication number
HUE027846T2
HUE027846T2 HUE11743438A HUE11743438A HUE027846T2 HU E027846 T2 HUE027846 T2 HU E027846T2 HU E11743438 A HUE11743438 A HU E11743438A HU E11743438 A HUE11743438 A HU E11743438A HU E027846 T2 HUE027846 T2 HU E027846T2
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Hungary
Prior art keywords
compounds
diseases
compound
denotes
treatment
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HUE11743438A
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English (en)
Hungarian (hu)
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Timo Heinrich
Christina Esdar
Hartmut Greiner
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Merck Patent Gmbh
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Publication of HUE027846T2 publication Critical patent/HUE027846T2/en

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    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/42—One nitrogen atom
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    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
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    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Hematology (AREA)
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  • Urology & Nephrology (AREA)
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  • Obesity (AREA)
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  • Endocrinology (AREA)
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  • Pain & Pain Management (AREA)
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HUE11743438A 2010-08-18 2011-07-19 Pyrimidine derivatives as FAK inhibitors HUE027846T2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102010034699A DE102010034699A1 (de) 2010-08-18 2010-08-18 Pyrimidinderivate

Publications (1)

Publication Number Publication Date
HUE027846T2 true HUE027846T2 (en) 2016-11-28

Family

ID=44504442

Family Applications (1)

Application Number Title Priority Date Filing Date
HUE11743438A HUE027846T2 (en) 2010-08-18 2011-07-19 Pyrimidine derivatives as FAK inhibitors

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Country Link
US (1) US8906916B2 (enExample)
EP (1) EP2606034B1 (enExample)
JP (2) JP6049617B2 (enExample)
CN (1) CN103052627B (enExample)
AR (1) AR082722A1 (enExample)
AU (1) AU2011291110B2 (enExample)
CA (1) CA2808540C (enExample)
DE (1) DE102010034699A1 (enExample)
DK (1) DK2606034T3 (enExample)
ES (1) ES2572740T3 (enExample)
HR (1) HRP20160562T1 (enExample)
HU (1) HUE027846T2 (enExample)
IL (1) IL224751A (enExample)
PL (1) PL2606034T3 (enExample)
RS (1) RS54882B1 (enExample)
SI (1) SI2606034T1 (enExample)
WO (1) WO2012022408A1 (enExample)

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JP5937111B2 (ja) 2011-02-17 2016-06-22 カンサー・セラピューティクス・シーアールシー・プロプライエタリー・リミテッドＣａｎｃｅｒ Ｔｈｅｒａｐｅｕｔｉｃｓ Ｃｒｃ Ｐｔｙ Ｌｉｍｉｔｅｄ Ｆａｋ阻害剤
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WO2014027199A1 (en) * 2012-08-14 2014-02-20 Cancer Therapeutics Crc Pty Ltd Fak and flt3 inhibitors
CN104736533B (zh) * 2012-08-17 2016-12-07 癌症治疗合作研究中心有限公司 Vegfr3抑制剂
HK1209104A1 (en) 2012-08-17 2016-03-24 Cancer Therapeutics Crc Pty Limited Vegfr3 inhibitors
TW201412740A (zh) * 2012-09-20 2014-04-01 Bayer Pharma AG 經取代之吡咯并嘧啶胺基苯并噻唑酮
JPWO2014174745A1 (ja) * 2013-04-26 2017-02-23 国立大学法人京都大学 Ｅｇ５阻害剤
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WO2016033100A1 (en) * 2014-08-25 2016-03-03 Salk Institute For Biological Studies Novel ulk1 inhibitors and methods using same
WO2019117813A1 (en) * 2017-12-15 2019-06-20 National University Of Singapore Focal adhesion kinase targeted therapeutics for the treatment of glaucoma and fibrosis
TW202508595A (zh) 2023-05-04 2025-03-01 美商銳新醫藥公司 用於ｒａｓ相關疾病或病症之組合療法
WO2025034702A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 for use in the treatment of ras protein-related disease or disorder
WO2025080946A2 (en) 2023-10-12 2025-04-17 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
WO2025240847A1 (en) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Ras inhibitors

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