UY32200A - Pirazolilaminopiridinas como inhibidores de fak - Google Patents

Pirazolilaminopiridinas como inhibidores de fak

Info

Publication number
UY32200A
UY32200A UY32200A UY32200A UY32200A UY 32200 A UY32200 A UY 32200A UY 32200 A UY32200 A UY 32200A UY 32200 A UY32200 A UY 32200A UY 32200 A UY32200 A UY 32200A
Authority
UY
Uruguay
Prior art keywords
pirazolilaminopiridinas
fak inhibitors
present
fak
inhibitors
Prior art date
Application number
UY32200A
Other languages
English (en)
Inventor
Jerry Leroy Adams
Thomas H Faitg
Neil W Johnson
Lin Hong
Original Assignee
Smithkline Beckman Corp
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=UY32200(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Smithkline Beckman Corp filed Critical Smithkline Beckman Corp
Publication of UY32200A publication Critical patent/UY32200A/es

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
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non 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
    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/4353—Heterocyclic 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
    • A61K31/4375—Heterocyclic 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
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/47—Quinolines; Isoquinolines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—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
    • C07D401/02—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
    • C07D401/12—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 chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—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
    • C07D401/14—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 three or more hetero rings
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
    • G01N33/57407—Specifically defined cancers
    • G01N33/57423—Specifically 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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente invención se refiere a un compuesto de fórmula (I): o una sal farmacéuticamente aceptable del mismo, en la que R1, R2, R3, R11,R12, R13,Q, Z y p son como se han descrito en la presente memoria. Los compuestos de la presente invención son útiles para el tratamiento de cánceres.
UY32200A 2008-10-27 2009-10-26 Pirazolilaminopiridinas como inhibidores de fak UY32200A (es)

Applications Claiming Priority (3)

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

Publications (1)

Publication Number Publication Date
UY32200A true UY32200A (es) 2010-05-31

Family

ID=42132177

Family Applications (1)

Application Number Title Priority Date Filing Date
UY32200A UY32200A (es) 2008-10-27 2009-10-26 Pirazolilaminopiridinas como inhibidores de fak

Country Status (36)

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

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
WO2012103276A1 (en) * 2011-01-26 2012-08-02 Glaxo Wellcome Manufacturing Pte Ltd Combinations
CA2827172C (en) 2011-02-17 2019-02-26 Cancer Therapeutics Crc Pty Limited Selective fak inhibitors
US20130324532A1 (en) 2011-02-17 2013-12-05 Cancer Therapeutics Crc Pty Limited Fak inhibitors
WO2013003575A1 (en) * 2011-06-28 2013-01-03 Glaxosmithkline Llc Method of administration and treatment
WO2015054477A1 (en) 2013-10-09 2015-04-16 The General Hospital Corporation Methods of diagnosing and treating b cell acute lymphoblastic leukemia
CN108289892B (zh) 2015-06-29 2021-11-23 维瑞斯特姆股份有限公司 治疗组合物、组合和使用方法
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
CA3093742A1 (en) 2018-03-12 2019-09-19 Inserm (Institut National De La Sante Et De La Recherche Medicale) Use of caloric restriction mimetics for potentiating chemo-immunotherapy for the treatment of cancers
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
US20220040317A1 (en) * 2018-09-27 2022-02-10 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
CA2533320A1 (en) * 2003-08-15 2006-02-24 Novartis Ag 2, 4-pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders
GB0419161D0 (en) * 2004-08-27 2004-09-29 Novartis Ag Organic compounds
GB0419160D0 (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
CA2681015C (en) * 2007-03-16 2016-06-21 The Scripps Research Institute Inhibitors of focal adhesion kinase
EP2249650A4 (en) * 2008-02-19 2012-01-11 Glaxosmithkline Llc ANILINOPYRIDINE AS A FAK HEMMER
CA2726508C (en) * 2008-06-17 2016-06-07 Astrazeneca Ab Pyridine compounds

Also Published As

Publication number Publication date
EP2421537B1 (en) 2015-04-08
PE20110941A1 (es) 2012-02-08
TW201028394A (en) 2010-08-01
WO2010062578A1 (en) 2010-06-03
ZA201102892B (en) 2012-02-29
PT2421537E (pt) 2015-07-03
PL2421537T3 (pl) 2015-08-31
SMT201500157B (it) 2015-09-07
JO3067B1 (ar) 2017-03-15
CA2741760A1 (en) 2010-06-03
HK1161680A1 (en) 2012-08-03
MA32727B1 (fr) 2011-10-02
AR073993A1 (es) 2010-12-15
EA021927B1 (ru) 2015-09-30
JP2012506876A (ja) 2012-03-22
US9012479B2 (en) 2015-04-21
MX2011004369A (es) 2011-05-25
AU2009320144B2 (en) 2013-11-21
DK2421537T3 (da) 2015-06-22
CL2011000933A1 (es) 2011-10-21
BRPI0920053B1 (pt) 2019-11-26
EP2421537A4 (en) 2012-06-13
AU2009320144A1 (en) 2010-06-03
US20140107131A1 (en) 2014-04-17
CR20110264A (es) 2011-10-04
CA2741760C (en) 2016-02-23
US20160095841A1 (en) 2016-04-07
EA201170617A1 (ru) 2011-12-30
KR20110080172A (ko) 2011-07-12
RS54045B1 (en) 2015-10-30
DOP2011000113A (es) 2011-07-15
TWI454467B (zh) 2014-10-01
HRP20150531T1 (hr) 2015-06-19
IL212444A (en) 2015-11-30
KR101512217B1 (ko) 2015-04-15
MY161890A (en) 2017-05-15
BRPI0920053A2 (pt) 2015-12-15
SG195608A1 (en) 2013-12-30
ES2539835T3 (es) 2015-07-06
EP2421537A1 (en) 2012-02-29
JP5642689B2 (ja) 2014-12-17
CY1116399T1 (el) 2017-02-08
IL212444A0 (en) 2011-06-30
US20110269774A1 (en) 2011-11-03
BRPI0920053B8 (pt) 2021-05-25
US20110207743A1 (en) 2011-08-25
SI2421537T1 (sl) 2015-06-30
CO6361929A2 (es) 2012-01-20
US9446034B2 (en) 2016-09-20
US20150265589A1 (en) 2015-09-24
US20100113475A1 (en) 2010-05-06
CN102264371A (zh) 2011-11-30
CN102264371B (zh) 2013-10-02
NZ592477A (en) 2013-01-25

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Legal Events

Date Code Title Description
109 Application deemed to be withdrawn

Effective date: 20180919