WO2016029002A3 - Growth factor receptor inhibitors - Google Patents
Growth factor receptor inhibitors Download PDFInfo
- Publication number
- WO2016029002A3 WO2016029002A3 PCT/US2015/046089 US2015046089W WO2016029002A3 WO 2016029002 A3 WO2016029002 A3 WO 2016029002A3 US 2015046089 W US2015046089 W US 2015046089W WO 2016029002 A3 WO2016029002 A3 WO 2016029002A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- growth factor
- factor receptor
- receptor inhibitors
- formula
- salt
- Prior art date
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
- A61K31/495—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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- 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
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Compounds of formula (I) or salts thereof as IGF-1R/INSR inhibitors are provided. The compounds may be used in method of treating cancer. Pharmaceutical compositions containing a compound of formula (I) or a salt thereof and a pharmaceutical acceptable excipient are also provided, as are kits containing a compound of formula (I) or a salt thereof and instructions for use, e.g., in a method of treating cancer.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201462040625P | 2014-08-22 | 2014-08-22 | |
US62/040,625 | 2014-08-22 | ||
US201462081300P | 2014-11-18 | 2014-11-18 | |
US62/081,300 | 2014-11-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2016029002A2 WO2016029002A2 (en) | 2016-02-25 |
WO2016029002A3 true WO2016029002A3 (en) | 2016-04-14 |
Family
ID=55351379
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2015/046089 WO2016029002A2 (en) | 2014-08-22 | 2015-08-20 | Growth factor receptor inhibitors |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2016029002A2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL245861A0 (en) | 2016-05-25 | 2016-09-04 | Yeda Res & Dev | Use of agents for treating drug resistant tumors |
CN106243044A (en) * | 2016-06-30 | 2016-12-21 | 浙江大学 | Pyridine derivatives containing halo acrylamide side chain and preparation and application |
CN106831730B (en) * | 2017-01-11 | 2019-11-26 | 温州医科大学 | A kind of substituted diaminopyrimidines and its preparing the purposes in anti-malignant tumor medicine |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090018141A1 (en) * | 2007-06-12 | 2009-01-15 | Robert Shoemaker | Kinase inhibitors, compositions thereof, and methods of use therewith |
WO2009127642A2 (en) * | 2008-04-15 | 2009-10-22 | Cellzome Limited | Use of lrrk2 inhibitors for neurodegenerative diseases |
US20110098280A1 (en) * | 2003-08-15 | 2011-04-28 | Novartis Ag | 2,4-pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders |
US20110190271A1 (en) * | 2003-08-07 | 2011-08-04 | Rigel Pharmaceuticals, Inc. | 2,4-Pyrimidinediamine Compounds and Uses as Anti-Proliferative Agents |
US20110201606A1 (en) * | 2003-03-14 | 2011-08-18 | Novartis Ag | Pyrimidine derivatives |
US20130190320A1 (en) * | 2012-01-13 | 2013-07-25 | Acea Biosciences, Inc. | Heterocyclic compounds and uses as anticancer agents |
US20130267530A1 (en) * | 2012-03-15 | 2013-10-10 | Celgene Avilomics Research, Inc. | Solid forms of an epidermal growth factor receptor kinase inhibitor |
WO2014066606A2 (en) * | 2012-10-25 | 2014-05-01 | Glaxosmithkline Llc | Combination |
WO2014123476A1 (en) * | 2013-02-05 | 2014-08-14 | Stenman Göran | Improved treatment for adenoid cystic carcinoma |
-
2015
- 2015-08-20 WO PCT/US2015/046089 patent/WO2016029002A2/en active Application Filing
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20110201606A1 (en) * | 2003-03-14 | 2011-08-18 | Novartis Ag | Pyrimidine derivatives |
US20110190271A1 (en) * | 2003-08-07 | 2011-08-04 | Rigel Pharmaceuticals, Inc. | 2,4-Pyrimidinediamine Compounds and Uses as Anti-Proliferative Agents |
US20110098280A1 (en) * | 2003-08-15 | 2011-04-28 | Novartis Ag | 2,4-pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders |
US20090018141A1 (en) * | 2007-06-12 | 2009-01-15 | Robert Shoemaker | Kinase inhibitors, compositions thereof, and methods of use therewith |
WO2009127642A2 (en) * | 2008-04-15 | 2009-10-22 | Cellzome Limited | Use of lrrk2 inhibitors for neurodegenerative diseases |
US20130190320A1 (en) * | 2012-01-13 | 2013-07-25 | Acea Biosciences, Inc. | Heterocyclic compounds and uses as anticancer agents |
US20130267530A1 (en) * | 2012-03-15 | 2013-10-10 | Celgene Avilomics Research, Inc. | Solid forms of an epidermal growth factor receptor kinase inhibitor |
WO2014066606A2 (en) * | 2012-10-25 | 2014-05-01 | Glaxosmithkline Llc | Combination |
WO2014123476A1 (en) * | 2013-02-05 | 2014-08-14 | Stenman Göran | Improved treatment for adenoid cystic carcinoma |
Also Published As
Publication number | Publication date |
---|---|
WO2016029002A2 (en) | 2016-02-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PH12019501321B1 (en) | Use of pyrazolopyrimidine derivatives for the treatment of pi3k-delta related disorders | |
PH12018502102A1 (en) | Pyrrolotriazine compounds as tam inhibitors | |
WO2014105958A3 (en) | Fused pyrimidine compounds and use thereof | |
PH12017500367B1 (en) | Compounds that inhibit mcl-1 protein | |
MA39986A (en) | Purine derivatives as cd73 inhibitors for the treatment of cancer | |
TN2018000119A1 (en) | Dihydroimidazopyrazinone derivatives useful in the treatment of cancer | |
WO2017075629A3 (en) | Wee 1 kinase inhibitors and methods of making and using the same | |
WO2016130920A3 (en) | Lrrk2 inhibitors and methods of making and using the same | |
CN106536480A8 (en) | The derovatives of pyrrolidines 2,5, pharmaceutical composition and the method as IDO1 inhibitor | |
UA117976C2 (en) | Aminopyrimidinyl compounds as jak inhibitors | |
EA201692095A1 (en) | IMIDAZO [4,5-C] QUINOLIN-2-NEW COMPOUNDS AND THEIR APPLICATION IN CANCER TREATMENT | |
MY192521A (en) | Bicyclic-fused heteroaryl or aryl compounds and their use as irak4 inhibitors | |
WO2015200680A8 (en) | Prmt5 inhibitors and uses thereof | |
PH12016500169A1 (en) | Polymorph of syk inhibitors | |
MD4820C1 (en) | Substituted dihydroisoquinolinone compounds | |
NZ729037A (en) | Carboxylic acid compound, method for preparation thereof, and use thereof | |
TW201613864A (en) | Novel compounds | |
CA2922375C (en) | Alpha-tea salt forms: compositions and uses for treating disease | |
WO2016183120A8 (en) | Inhibitors of influenza viruses replication | |
WO2016029002A3 (en) | Growth factor receptor inhibitors | |
WO2016164295A3 (en) | Fused pyridines as adaptor associated kinase 1 (aak1) inhibitors | |
WO2017095950A3 (en) | Compounds for treating proliferative diseases | |
SG11201903463PA (en) | Quinolyl-substituted carboxylic acid compound or pharmaceutically acceptable salt thereof, pharmaceutical composition of the same, and use of the same | |
MX2015012600A (en) | Tetrahydroisoquinolin-2-yl-(quinazolin-4-yl) methanone compounds as cancer cell growth inhibitors. | |
MX2019005723A (en) | Fgfr4 inhibitor and preparation method and use thereof. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 15833065 Country of ref document: EP Kind code of ref document: A2 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 15833065 Country of ref document: EP Kind code of ref document: A2 |