SMT201500157B - Pirazolilaminopiridine come inibitori di fak - Google Patents

Pirazolilaminopiridine come inibitori di fak

Info

Publication number
SMT201500157B
SMT201500157B SM201500157T SM201500157T SMT201500157B SM T201500157 B SMT201500157 B SM T201500157B SM 201500157 T SM201500157 T SM 201500157T SM 201500157 T SM201500157 T SM 201500157T SM T201500157 B SMT201500157 B SM T201500157B
Authority
SM
San Marino
Prior art keywords
pyrazolylaminopyridines
fak inhibitors
fak
inhibitors
Prior art date
Application number
SM201500157T
Other languages
English (en)
Italian (it)
Inventor
Thomas Faitg
Neil W Johnson
Hong Lin
Jiri Kasparec
Mark Mellinger
Ren Xie
Xin Peng
Jerry Leroy Adams
Original Assignee
Glaxosmithkline Llc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=42132177&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SMT201500157(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Glaxosmithkline Llc filed Critical Glaxosmithkline Llc
Publication of SMT201500157B publication Critical patent/SMT201500157B/xx

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/574Immunoassay; Biospecific binding assay; Materials therefor for cancer
    • G01N33/57407Specifically defined cancers
    • G01N33/57423Specifically defined cancers of lung

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Urology & Nephrology (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Hematology (AREA)
  • Biochemistry (AREA)
  • Food Science & Technology (AREA)
  • Oncology (AREA)
  • Biotechnology (AREA)
  • Cell Biology (AREA)
  • Hospice & Palliative Care (AREA)
  • Microbiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
SM201500157T 2008-10-27 2015-07-03 Pirazolilaminopiridine come inibitori di fak SMT201500157B (it)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US10856808P 2008-10-27 2008-10-27
US17851709P 2009-05-15 2009-05-15
US24243209P 2009-09-15 2009-09-15
PCT/US2009/062163 WO2010062578A1 (en) 2008-10-27 2009-10-27 Pyrazolylaminopyridines as inhibitors of fak

Publications (1)

Publication Number Publication Date
SMT201500157B true SMT201500157B (it) 2015-09-07

Family

ID=42132177

Family Applications (1)

Application Number Title Priority Date Filing Date
SM201500157T SMT201500157B (it) 2008-10-27 2015-07-03 Pirazolilaminopiridine come inibitori di fak

Country Status (36)

Country Link
US (6) US20110207743A1 (xx)
EP (1) EP2421537B1 (xx)
JP (1) JP5642689B2 (xx)
KR (1) KR101512217B1 (xx)
CN (1) CN102264371B (xx)
AR (1) AR073993A1 (xx)
AU (1) AU2009320144B2 (xx)
BR (1) BRPI0920053B8 (xx)
CA (1) CA2741760C (xx)
CL (1) CL2011000933A1 (xx)
CO (1) CO6361929A2 (xx)
CR (1) CR20110264A (xx)
CY (1) CY1116399T1 (xx)
DK (1) DK2421537T3 (xx)
DO (1) DOP2011000113A (xx)
EA (1) EA021927B1 (xx)
ES (1) ES2539835T3 (xx)
HK (1) HK1161680A1 (xx)
HR (1) HRP20150531T1 (xx)
IL (1) IL212444A (xx)
JO (1) JO3067B1 (xx)
MA (1) MA32727B1 (xx)
MX (1) MX2011004369A (xx)
MY (1) MY161890A (xx)
NZ (1) NZ592477A (xx)
PE (1) PE20110941A1 (xx)
PL (1) PL2421537T3 (xx)
PT (1) PT2421537E (xx)
RS (1) RS54045B1 (xx)
SG (1) SG195608A1 (xx)
SI (1) SI2421537T1 (xx)
SM (1) SMT201500157B (xx)
TW (1) TWI454467B (xx)
UY (1) UY32200A (xx)
WO (1) WO2010062578A1 (xx)
ZA (1) ZA201102892B (xx)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8338441B2 (en) 2009-05-15 2012-12-25 Gilead Sciences, Inc. Inhibitors of human immunodeficiency virus replication
US20120244141A1 (en) 2010-09-28 2012-09-27 Boehringer Ingelheim International Gmbh Stratification of cancer patients for susceptibility to therapy with PTK2 inhibitors
EP2667871A4 (en) * 2011-01-26 2014-07-09 Glaxosmithkline Intellectual Property Ltd SUITS
CA2827172C (en) 2011-02-17 2019-02-26 Cancer Therapeutics Crc Pty Limited Selective fak inhibitors
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
EP2726079A4 (en) 2011-06-28 2014-12-17 Glaxosmithkline Ip No 2 Ltd METHOD OF ADMINISTRATION AND TREATMENT
US10106834B2 (en) 2013-10-09 2018-10-23 The General Hospital Corporation Methods of diagnosing and treating B cell acute lymphoblastic leukemia
JP2018519327A (ja) 2015-06-29 2018-07-19 ベラステム・インコーポレーテッドVerastem,Inc. 治療用組成物、組合せ物および使用の方法
CN108948019B (zh) * 2017-05-18 2022-07-08 广东东阳光药业有限公司 黏着斑激酶抑制剂及其用途
WO2019117813A1 (en) * 2017-12-15 2019-06-20 National University Of Singapore Focal adhesion kinase targeted therapeutics for the treatment of glaucoma and fibrosis
JP2021517589A (ja) 2018-03-12 2021-07-26 アンセルム(アンスティチュート・ナシオナル・ドゥ・ラ・サンテ・エ・ドゥ・ラ・ルシェルシュ・メディカル) 癌の治療のための化学免疫療法を増強するためのカロリー制限模倣物の使用
CN108912095B (zh) * 2018-08-09 2019-08-20 广州安岩仁医药科技有限公司 苯并咪唑类化合物及其制备方法和应用
AU2019348011A1 (en) * 2018-09-27 2021-02-11 Dana-Farber Cancer Institute, Inc. Degradation of FAK or FAK and ALK by conjugation of FAK and ALK inhibitors with E3 ligase ligands and methods of use
CN113387947B (zh) * 2021-07-12 2022-07-01 中国科学院成都生物研究所 调节雌激素受体合成活性的吡唑并吡啶衍生物

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US166139A (en) * 1875-07-27 Improvement in dental pluggers
EP1109823B1 (en) 1998-09-08 2005-11-16 Agouron Pharmaceuticals, Inc. Modifications of the vegf receptor-2 protein and methods of use
US7102009B2 (en) * 2001-01-12 2006-09-05 Amgen Inc. Substituted amine derivatives and methods of use
JP4607879B2 (ja) * 2003-08-15 2011-01-05 ノバルティス アーゲー 新生物疾患、炎症および免疫障害の処置に有用な2,4−ピリミジンジアミン
GB0419160D0 (en) * 2004-08-27 2004-09-29 Novartis Ag Organic compounds
GB0419161D0 (en) * 2004-08-27 2004-09-29 Novartis Ag Organic compounds
EP1746096A1 (en) * 2005-07-15 2007-01-24 4Sc Ag 2-Arylbenzothiazole analogues and uses thereof in the treatment of cancer
DK2134689T3 (da) * 2007-03-16 2014-06-30 Scripps Research Inst Inhibitorer af fokal adhæsionskinase
WO2009105498A1 (en) * 2008-02-19 2009-08-27 Smithkline Beecham Corporation Anilinopyridines as inhibitors of fak
BRPI0914927B8 (pt) * 2008-06-17 2021-05-25 Astrazeneca Ab composto, composição farmacêutica e uso de um composto

Also Published As

Publication number Publication date
KR20110080172A (ko) 2011-07-12
NZ592477A (en) 2013-01-25
HRP20150531T1 (hr) 2015-06-19
EP2421537A1 (en) 2012-02-29
CR20110264A (es) 2011-10-04
JP5642689B2 (ja) 2014-12-17
US9446034B2 (en) 2016-09-20
WO2010062578A1 (en) 2010-06-03
AU2009320144B2 (en) 2013-11-21
MY161890A (en) 2017-05-15
MA32727B1 (fr) 2011-10-02
CN102264371B (zh) 2013-10-02
ZA201102892B (en) 2012-02-29
CA2741760C (en) 2016-02-23
IL212444A (en) 2015-11-30
BRPI0920053A2 (pt) 2015-12-15
JP2012506876A (ja) 2012-03-22
CY1116399T1 (el) 2017-02-08
SI2421537T1 (sl) 2015-06-30
BRPI0920053B8 (pt) 2021-05-25
US20100113475A1 (en) 2010-05-06
CN102264371A (zh) 2011-11-30
SG195608A1 (en) 2013-12-30
US20160095841A1 (en) 2016-04-07
US9012479B2 (en) 2015-04-21
RS54045B1 (en) 2015-10-30
KR101512217B1 (ko) 2015-04-15
US20110207743A1 (en) 2011-08-25
IL212444A0 (en) 2011-06-30
EA201170617A1 (ru) 2011-12-30
US20150265589A1 (en) 2015-09-24
UY32200A (es) 2010-05-31
AR073993A1 (es) 2010-12-15
PE20110941A1 (es) 2012-02-08
US20140107131A1 (en) 2014-04-17
CL2011000933A1 (es) 2011-10-21
TW201028394A (en) 2010-08-01
AU2009320144A1 (en) 2010-06-03
EP2421537B1 (en) 2015-04-08
PT2421537E (pt) 2015-07-03
PL2421537T3 (pl) 2015-08-31
HK1161680A1 (en) 2012-08-03
CO6361929A2 (es) 2012-01-20
JO3067B1 (ar) 2017-03-15
TWI454467B (zh) 2014-10-01
CA2741760A1 (en) 2010-06-03
BRPI0920053B1 (pt) 2019-11-26
EP2421537A4 (en) 2012-06-13
EA021927B1 (ru) 2015-09-30
DK2421537T3 (da) 2015-06-22
ES2539835T3 (es) 2015-07-06
MX2011004369A (es) 2011-05-25
DOP2011000113A (es) 2011-07-15
US20110269774A1 (en) 2011-11-03

Similar Documents

Publication Publication Date Title
CY2020023I1 (el) Αναστολεiς βητα-λακταμασων
CY2017042I2 (el) Ενωσεις πυρρολοπυριμιδινης ως αναστολεις cdk
CY2017016I1 (el) Αναστολεις πρωτεασωματος
SMT201500157B (it) Pirazolilaminopiridine come inibitori di fak
SMT201600008B (it) Composti di piridazinone
SMT201600311B (it) Inibitori di cdk
SMT201500043B (it) Indazoli ossazolo-sostituiti come inibitori di pi13-chinasi
SMT201600104B (it) Inibitore di bromodominio benzodiazepinico
SMT201600081B (it) Inibitore di bromodominio di benzodiazepina
SMT201500271B (it) Inibitori di neprilisina
DK2421825T3 (da) Azetidinyldiamider som monoacylglycerollipase-inhibitorer
BRPI0907376A8 (pt) fotobiorreator
DK2288375T3 (da) Pegylerede insulin-lispro-forbindelser
DK2634232T3 (da) Sammensætninger
BRPI0920707A2 (pt) compostos
DK2242759T3 (da) Forbindelser
BRPI0918564A2 (pt) inibidores
DK2323972T3 (da) C7-fluor-substituerede tetracylinforbindelser
DK2297162T3 (da) Forbindelser
DK2300238T3 (da) Skyggebillede-sikkerhedstræk
BRPI0916432A2 (pt) compostos
BRPI0912152A2 (pt) umbilical
BRPI0923592A2 (pt) composto
DK2240506T3 (da) IAP inhibitorer
DK2206698T3 (da) Ethynylindolforbindelser