MX2017000208A - Derivados de quinolizinona como inhibidores de pi3k. - Google Patents
Derivados de quinolizinona como inhibidores de pi3k.Info
- Publication number
- MX2017000208A MX2017000208A MX2017000208A MX2017000208A MX2017000208A MX 2017000208 A MX2017000208 A MX 2017000208A MX 2017000208 A MX2017000208 A MX 2017000208A MX 2017000208 A MX2017000208 A MX 2017000208A MX 2017000208 A MX2017000208 A MX 2017000208A
- Authority
- MX
- Mexico
- Prior art keywords
- pi3k inhibitors
- quinolizinone derivatives
- quinolizinone
- derivatives
- tautomer
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- 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
- A61K31/495—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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Se divulgan compuestos de la fórmula I, sus formas tautoméricas, estereoisómeros y sales farmacéuticamente aceptables de los mismos, en donde R1-R4 y n son como se define en la descripción, las composiciones farmacéuticas incluyen un compuesto, tautómero, estereoisómero o sal del mismo, y métodos para el tratamiento o prevención de enfermedades o trastornos, por ejemplo, cáncer, que son susceptibles de tratamiento o prevención inhibiendo la enzima PI3K de un sujeto.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2182MU2014 | 2014-07-04 | ||
PCT/IB2015/054958 WO2016001855A1 (en) | 2014-07-04 | 2015-07-01 | Quinolizinone derivatives as pi3k inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2017000208A true MX2017000208A (es) | 2017-05-01 |
Family
ID=53716533
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2017000208A MX2017000208A (es) | 2014-07-04 | 2015-07-01 | Derivados de quinolizinona como inhibidores de pi3k. |
Country Status (25)
Country | Link |
---|---|
US (1) | US9944639B2 (es) |
EP (1) | EP3164400A1 (es) |
JP (1) | JP6291601B2 (es) |
KR (1) | KR20170082490A (es) |
CN (1) | CN106470996B (es) |
AP (1) | AP2016009661A0 (es) |
AU (1) | AU2015283671B2 (es) |
BR (1) | BR112017000132A2 (es) |
CA (1) | CA2954231A1 (es) |
CL (1) | CL2017000006A1 (es) |
CO (1) | CO2017000011A2 (es) |
CR (1) | CR20160600A (es) |
CU (1) | CU24428B1 (es) |
EA (1) | EA201692557A1 (es) |
GE (1) | GEP20186934B (es) |
HK (1) | HK1232227A1 (es) |
IL (1) | IL249674B (es) |
MA (1) | MA40250A (es) |
MX (1) | MX2017000208A (es) |
PE (1) | PE20170640A1 (es) |
PH (1) | PH12017500007A1 (es) |
SG (1) | SG11201610770PA (es) |
SV (1) | SV2017005354A (es) |
UA (1) | UA115296C2 (es) |
WO (1) | WO2016001855A1 (es) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2015341186B2 (en) * | 2014-11-01 | 2019-11-14 | Fochon Biosciences, Ltd. | Certain protein kinase inhibitors |
WO2017103825A1 (en) | 2015-12-18 | 2017-06-22 | Lupin Limited | Quinolizinone derivatives as pi3k inhibitors |
US10751339B2 (en) | 2018-01-20 | 2020-08-25 | Sunshine Lake Pharma Co., Ltd. | Substituted aminopyrimidine compounds and methods of use |
JP2021535907A (ja) * | 2018-08-21 | 2021-12-23 | 南京明徳新薬研発有限公司 | ピラゾロピリミジン誘導体及びそのpi3k抑制剤とする適用 |
US20220227747A1 (en) * | 2019-04-23 | 2022-07-21 | Evotec International Gmbh | Modulators of the integrated stress response pathway |
WO2021164789A1 (zh) * | 2020-02-21 | 2021-08-26 | 南京明德新药研发有限公司 | 一种吡唑并嘧啶类化合物的晶型及其应用 |
WO2023018636A1 (en) * | 2021-08-09 | 2023-02-16 | Scorpion Therapeutics, Inc. | Compounds that inhibit pi3k isoform alpha and methods for treating cancer |
Family Cites Families (98)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
US4501728A (en) | 1983-01-06 | 1985-02-26 | Technology Unlimited, Inc. | Masking of liposomes from RES recognition |
US5019369A (en) | 1984-10-22 | 1991-05-28 | Vestar, Inc. | Method of targeting tumors in humans |
US4837028A (en) | 1986-12-24 | 1989-06-06 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
US6667300B2 (en) | 2000-04-25 | 2003-12-23 | Icos Corporation | Inhibitors of human phosphatidylinositol 3-kinase delta |
KR100785363B1 (ko) | 2000-04-25 | 2007-12-18 | 이코스 코포레이션 | 인간 포스파티딜-이노시톨 3-키나제 델타의 억제제 |
US20050054614A1 (en) | 2003-08-14 | 2005-03-10 | Diacovo Thomas G. | Methods of inhibiting leukocyte accumulation |
WO2005016348A1 (en) | 2003-08-14 | 2005-02-24 | Icos Corporation | Method of inhibiting immune responses stimulated by an endogenous factor |
CA2552664A1 (en) | 2004-01-08 | 2005-07-28 | Michigan State University | Methods for treating and preventing hypertension and hypertension-related disorders |
CA2730540A1 (en) | 2004-05-13 | 2005-12-01 | Vanderbilt University | Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis |
CA2566609C (en) | 2004-05-13 | 2012-06-26 | Icos Corporation | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
CA2567883A1 (en) | 2004-05-25 | 2005-12-15 | Icos Corporation | Methods for treating and/or preventing aberrant proliferation of hematopoietic cells |
EP1750715A1 (en) | 2004-06-04 | 2007-02-14 | Icos Corporation | Methods for treating mast cell disorders |
EP1885356A2 (en) | 2005-02-17 | 2008-02-13 | Icos Corporation | Phosphoinositide 3-kinase inhibitors for inhibiting leukocyte accumulation |
US20080032960A1 (en) | 2006-04-04 | 2008-02-07 | Regents Of The University Of California | PI3 kinase antagonists |
CN101605797A (zh) | 2006-11-13 | 2009-12-16 | 伊莱利利公司 | 治疗炎症疾病和癌症的噻吩并嘧啶酮 |
WO2008118454A2 (en) | 2007-03-23 | 2008-10-02 | Amgen Inc. | Derivatives of quinoline or benzopyrazine and their uses for the treatment of (inter alia) inflammatory diseases, autoimmune diseases or various kinds of cancer |
PT2139882E (pt) | 2007-03-23 | 2014-01-30 | Amgen Inc | Derivados de quinolina ou quinoxalina 3-substituídos e sua utilização como inibidores de fosfatidilinositol 3-cinase (pi3k) |
ES2563458T3 (es) | 2007-03-23 | 2016-03-15 | Amgen Inc. | Compuestos heterocíclicos y sus usos |
AU2008321099A1 (en) | 2007-11-13 | 2009-05-22 | Icos Corporation | Inhibitors of human phosphatidyl-inositol 3-kinase delta |
NZ613219A (en) | 2008-01-04 | 2014-11-28 | Intellikine Llc | Heterocyclic containing entities, compositions and methods |
US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
WO2010036380A1 (en) | 2008-09-26 | 2010-04-01 | Intellikine, Inc. | Heterocyclic kinase inhibitors |
EA019499B1 (ru) | 2009-03-24 | 2014-04-30 | ГИЛИЭД КАЛИСТОГА ЭлЭлСи | Производные атропоизомеров 2-пуринил-3-толилхиназолинона и способы применения |
SG175259A1 (en) | 2009-04-20 | 2011-11-28 | Gilead Calistoga Llc | Methods of treatment for solid tumors |
EP2427195B1 (en) | 2009-05-07 | 2019-05-01 | Intellikine, LLC | Heterocyclic compounds and uses thereof |
US20100331306A1 (en) | 2009-06-25 | 2010-12-30 | Amgen Inc. | Heterocyclic compounds and their uses |
AU2010266064A1 (en) * | 2009-06-25 | 2012-01-19 | Amgen Inc. | 4H - pyrido [1, 2 - a] pyrimidin - 4 - one derivatives as PI3 K inhibitors |
TW201111376A (en) | 2009-06-25 | 2011-04-01 | Amgen Inc | Heterocyclic compounds and their uses |
PL2448938T3 (pl) * | 2009-06-29 | 2014-11-28 | Incyte Holdings Corp | Pirymidynony jako inhibitory PI3K |
WO2011011550A1 (en) | 2009-07-21 | 2011-01-27 | Calistoga Pharmaceuticals Inc. | Treatment of liver disorders with pi3k inhibitors |
GB0918249D0 (en) | 2009-10-19 | 2009-12-02 | Respivert Ltd | Compounds |
CN105801550B (zh) | 2009-11-05 | 2019-06-14 | 理森制药股份公司 | 新型苯并吡喃激酶调节剂 |
WO2011058112A1 (en) | 2009-11-12 | 2011-05-19 | Ucb Pharma S.A. | Fused bicyclic pyrazole derivatives as kinase inhibitors |
WO2011075643A1 (en) | 2009-12-18 | 2011-06-23 | Incyte Corporation | Substituted heteroaryl fused derivatives as pi3k inhibitors |
WO2011075628A1 (en) | 2009-12-18 | 2011-06-23 | Amgen Inc. | Heterocyclic compounds and their uses |
UY33304A (es) | 2010-04-02 | 2011-10-31 | Amgen Inc | Compuestos heterocíclicos y sus usos |
EP2558463A1 (en) | 2010-04-14 | 2013-02-20 | Incyte Corporation | Fused derivatives as i3 inhibitors |
ES2593256T3 (es) | 2010-05-21 | 2016-12-07 | Infinity Pharmaceuticals, Inc. | Compuestos químicos, composiciones y métodos para las modulaciones de cinasas |
US20110306622A1 (en) | 2010-06-11 | 2011-12-15 | Calitoga Pharmaceuticals, Inc. | Methods of treating hematological disorders with quinazolinone compounds in selected subjects |
JP2013533883A (ja) | 2010-06-30 | 2013-08-29 | アムジエン・インコーポレーテツド | PI3Kδ阻害剤としての含窒素複素環化合物 |
MX2012014983A (es) | 2010-06-30 | 2013-04-24 | Amgen Inc | Quinolinas como inhibidores pi3k. |
JP2013530238A (ja) | 2010-07-01 | 2013-07-25 | アムジエン・インコーポレーテツド | Pi3k活性の阻害剤としての複素環化合物及びその使用 |
MX2012014996A (es) | 2010-07-01 | 2013-03-21 | Amgen Inc | Compuestos heterociclicos y su uso como inhibidores de la actividad pi3k. |
MX2012015134A (es) | 2010-07-02 | 2013-05-06 | Amgen Inc | Compuestos heterociclicos y su uso como inhibidores de actividad de pi3k. |
US20130324561A1 (en) | 2010-09-24 | 2013-12-05 | Gilead Calistroga Llc. | Atropisomers of p13k-inhibiting compounds |
UY33337A (es) | 2010-10-18 | 2011-10-31 | Respivert Ltd | DERIVADOS SUSTITUIDOS DE 1H-PIRAZOL[ 3,4-d]PIRIMIDINA COMO INHIBIDORES DE LAS FOSFOINOSITIDA 3-QUINASAS |
WO2012061696A1 (en) | 2010-11-04 | 2012-05-10 | Amgen Inc. | 5 -cyano-4, 6 -diaminopyrimidine or 6 -aminopurine derivatives as pi3k- delta inhibitors |
CA2817577A1 (en) | 2010-11-10 | 2012-05-18 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
MX2013005567A (es) | 2010-11-17 | 2013-10-30 | Amgen Inc | Derivados de quinolina como inhibidores de pik3. |
AU2011349669A1 (en) | 2010-12-23 | 2013-07-11 | Amgen Inc. | Heterocyclic compounds and their uses |
UA115767C2 (uk) | 2011-01-10 | 2017-12-26 | Інфініті Фармасьютікалз, Інк. | Способи отримання ізохінолінонів і тверді форми ізохінолінонів |
EA201391263A1 (ru) | 2011-03-11 | 2014-06-30 | Джилид Калистога Ллс | Комбинированные терапии гематологических опухолей |
WO2012125629A1 (en) | 2011-03-14 | 2012-09-20 | Incyte Corporation | Substituted diamino-pyrimidine and diamino-pyridine derivatives as pi3k inhibitors |
EP2518070A1 (en) | 2011-04-29 | 2012-10-31 | Almirall, S.A. | Pyrrolotriazinone derivatives as PI3K inhibitors |
EA201391606A1 (ru) * | 2011-04-29 | 2016-01-29 | Экселиксис, Инк. | Способ лечения лимфомы посредством пиридопиримидиноновых ингибиторов pi3k/mtor |
TW201306842A (zh) * | 2011-06-15 | 2013-02-16 | Exelixis Inc | 使用pi3k/mtor吡啶並嘧啶酮抑制劑及苯達莫司汀及/或利妥昔單抗治療惡性血液疾病之組合療法 |
CN102838600A (zh) | 2011-06-24 | 2012-12-26 | 山东亨利医药科技有限责任公司 | 苯基喹唑啉类PI3Kδ抑制剂 |
CN102838601A (zh) | 2011-06-24 | 2012-12-26 | 山东亨利医药科技有限责任公司 | 选择性磷酰肌醇3-激酶δ抑制剂 |
US9056877B2 (en) | 2011-07-19 | 2015-06-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US8969363B2 (en) | 2011-07-19 | 2015-03-03 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
PE20141371A1 (es) | 2011-08-29 | 2014-10-13 | Infinity Pharmaceuticals Inc | Compuestos heterociclicos y usos de los mismos |
WO2013052699A2 (en) | 2011-10-04 | 2013-04-11 | Gilead Calistoga Llc | Novel quinoxaline inhibitors of pi3k |
WO2013082540A1 (en) | 2011-12-02 | 2013-06-06 | Gilead Calistoga Llc | Compositions and methods of treating a proliferative disease with a quinazolinone derivative |
WO2013116562A1 (en) | 2012-02-03 | 2013-08-08 | Gilead Calistoga Llc | Compositions and methods of treating a disease with (s)-4 amino-6-((1-(5-chloro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)ethyl)amino)pyrimidine-5-carbonitrile |
NZ627963A (en) | 2012-03-13 | 2015-08-28 | Respivert Ltd | Dry powder pharmaceutical formulations for inhalation of a compound that inhibits pi3 kinase |
EA201491823A1 (ru) | 2012-04-04 | 2015-01-30 | Эмджен Инк. | Гетероциклические соединения и их использование |
US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
MX357043B (es) | 2012-07-04 | 2018-06-25 | Rhizen Pharmaceuticals Sa | Inhibidores selectivos de pi3k delta. |
WO2014015523A1 (en) | 2012-07-27 | 2014-01-30 | Hutchison Medipharma Limited | Novel heteroaryl and heterocycle compounds, compositions and methods |
SG10202003090VA (en) | 2012-08-08 | 2020-05-28 | Kbp Biosciences Co Ltd | PI3K δ INHIBITOR |
JP2015529195A (ja) | 2012-08-14 | 2015-10-05 | ギリアード カリストガ エルエルシー | 癌を処置するための組合せ治療 |
WO2014060432A1 (en) | 2012-10-16 | 2014-04-24 | Almirall, S.A. | Pyrrolotriazinone derivatives as pi3k inhibitors |
WO2014060431A1 (en) | 2012-10-16 | 2014-04-24 | Almirall, S.A. | Pyrrolotriazinone derivatives as pi3k inhibitors |
HUE040126T2 (hu) | 2012-11-01 | 2019-02-28 | Infinity Pharmaceuticals Inc | Rákok kezelése PI3 kináz izoform modulátorok alkalmazásával |
US20140120060A1 (en) | 2012-11-01 | 2014-05-01 | Infinity Pharmaceuticals, Inc. | Treatment of rheumatoid arthritis and asthma using pi3 kinase inhibitors |
PT2941426T (pt) | 2012-12-21 | 2018-07-18 | Gilead Calistoga Llc | Quinazolinonas aminoalquis de pirimidina substituída como inibidores de fosfatidilinositol 3-quinase |
ES2685568T3 (es) | 2012-12-21 | 2018-10-10 | Gilead Calistoga Llc | Inhibidores de la isoquinolinona o quinazolinona fosfatidilinositol 3-quinasa |
WO2014106800A2 (en) | 2013-01-04 | 2014-07-10 | Aurigene Discovery Technologies Limited | Substituted 2-amino pyrimidine derivatives as kinase inhibitors |
TW201446767A (zh) | 2013-02-15 | 2014-12-16 | Almirall Sa | 作為磷脂肌醇3-激酶抑製劑之吡咯並三嗪衍生物 |
WO2014128612A1 (en) | 2013-02-20 | 2014-08-28 | Novartis Ag | Quinazolin-4-one derivatives |
JO3279B1 (ar) | 2013-03-15 | 2018-09-16 | Respivert Ltd | مشتقات 2-((4- امينو -3- (3- فلورو-5- هيدروكسي فينيل)-h1- بيرازولو [d-3,4] بيرمدين-1-يل )ميثيل )- 3- (2- تراي فلورو ميثيل ) بينزيل ) كوينازولين -4 (h3)- واحد واستخدامها كمثبطات فوسفواينوسيتايد 3- كاينيز |
US9216985B2 (en) | 2013-03-28 | 2015-12-22 | Scifluor Life Sciences, Inc. | 3-aryl-2-((arylamino)methyl)quinazolin-4-(3H)-ones |
SI3008053T1 (en) | 2013-06-14 | 2018-06-29 | Gilead Calistoga Llc | PHOSPHATIDYLINOSITOL 3-KINATE INHIBITORS |
CN111153905A (zh) | 2013-07-02 | 2020-05-15 | 理森制药股份公司 | PI3K蛋白激酶抑制剂,特别是δ抑制剂和/或γ抑制剂 |
CN104513235B (zh) | 2013-09-02 | 2017-12-05 | 广东东阳光药业有限公司 | 取代的氨基嘧啶类化合物及其使用方法和用途 |
CA2920059A1 (en) | 2013-09-22 | 2015-03-26 | Calitor Sciences, Llc | Substituted aminopyrimidine compounds and methods of use |
DK3119397T3 (da) | 2014-03-19 | 2022-03-28 | Infinity Pharmaceuticals Inc | Heterocykliske forbindelser til anvendelse i behandling af PI3K-gamma-medierede lidelser |
WO2015168079A1 (en) | 2014-04-29 | 2015-11-05 | Infinity Pharmaceuticals, Inc. | Pyrimidine or pyridine derivatives useful as pi3k inhibitors |
CN105130966B (zh) | 2014-05-07 | 2019-05-24 | 广东东阳光药业有限公司 | 炔基化合物及其使用方法和用途 |
WO2015175579A1 (en) | 2014-05-15 | 2015-11-19 | Calitor Sciences, Llc | Alkynyl compounds and methods of use |
CA2952037A1 (en) | 2014-06-13 | 2015-12-17 | Gilead Sciences, Inc. | Phosphatidylinositol 3-kinase inhibitors |
CA2952012A1 (en) | 2014-06-13 | 2015-12-17 | Gilead Sciences, Inc. | Phosphatidylinositol 3-kinase inhibitors |
EA201692267A1 (ru) | 2014-06-13 | 2017-06-30 | Джилид Сайэнс, Инк. | Ингибиторы фосфатидилинозитол-3-киназы |
JP6391718B2 (ja) | 2014-06-24 | 2018-09-19 | ギリアード サイエンシーズ, インコーポレイテッド | ホスファチジルイノシトール3−キナーゼ阻害剤 |
AU2015341186B2 (en) * | 2014-11-01 | 2019-11-14 | Fochon Biosciences, Ltd. | Certain protein kinase inhibitors |
CN105130984B (zh) | 2015-09-23 | 2017-03-29 | 前湾医药科技(深圳)有限公司 | 一种咪唑并吡啶类化合物与在制备pi3k抑制剂中的应用 |
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2015
- 2015-07-01 CU CU2016000195A patent/CU24428B1/es unknown
- 2015-07-01 EP EP15739683.9A patent/EP3164400A1/en not_active Withdrawn
- 2015-07-01 AU AU2015283671A patent/AU2015283671B2/en not_active Ceased
- 2015-07-01 JP JP2016575554A patent/JP6291601B2/ja not_active Expired - Fee Related
- 2015-07-01 EA EA201692557A patent/EA201692557A1/ru unknown
- 2015-07-01 BR BR112017000132A patent/BR112017000132A2/pt not_active Application Discontinuation
- 2015-07-01 SG SG11201610770PA patent/SG11201610770PA/en unknown
- 2015-07-01 MA MA040250A patent/MA40250A/fr unknown
- 2015-07-01 MX MX2017000208A patent/MX2017000208A/es unknown
- 2015-07-01 US US15/323,565 patent/US9944639B2/en not_active Expired - Fee Related
- 2015-07-01 CR CR20160600A patent/CR20160600A/es unknown
- 2015-07-01 GE GEAP201514408A patent/GEP20186934B/en unknown
- 2015-07-01 CN CN201580036482.9A patent/CN106470996B/zh not_active Expired - Fee Related
- 2015-07-01 PE PE2016002810A patent/PE20170640A1/es unknown
- 2015-07-01 CA CA2954231A patent/CA2954231A1/en not_active Abandoned
- 2015-07-01 UA UAA201701013A patent/UA115296C2/uk unknown
- 2015-07-01 KR KR1020177003196A patent/KR20170082490A/ko unknown
- 2015-07-01 AP AP2016009661A patent/AP2016009661A0/en unknown
- 2015-07-01 WO PCT/IB2015/054958 patent/WO2016001855A1/en active Application Filing
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2016
- 2016-12-20 IL IL249674A patent/IL249674B/en not_active IP Right Cessation
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2017
- 2017-01-03 PH PH12017500007A patent/PH12017500007A1/en unknown
- 2017-01-03 SV SV2017005354A patent/SV2017005354A/es unknown
- 2017-01-03 CL CL2017000006A patent/CL2017000006A1/es unknown
- 2017-01-03 CO CONC2017/0000011A patent/CO2017000011A2/es unknown
- 2017-06-16 HK HK17106009.7A patent/HK1232227A1/zh unknown
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Publication number | Publication date |
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US20170137421A1 (en) | 2017-05-18 |
AU2015283671A1 (en) | 2017-02-02 |
AU2015283671B2 (en) | 2018-07-05 |
HK1232227A1 (zh) | 2018-01-05 |
PH12017500007A1 (en) | 2017-05-15 |
IL249674B (en) | 2019-06-30 |
CA2954231A1 (en) | 2016-01-07 |
KR20170082490A (ko) | 2017-07-14 |
EA201692557A1 (ru) | 2017-05-31 |
CU20160195A7 (es) | 2017-05-10 |
MA40250A (fr) | 2017-05-10 |
CU24428B1 (es) | 2019-06-04 |
CR20160600A (es) | 2017-03-07 |
UA115296C2 (uk) | 2017-10-10 |
SG11201610770PA (en) | 2017-01-27 |
CN106470996B (zh) | 2019-02-22 |
SV2017005354A (es) | 2018-10-05 |
JP2017519786A (ja) | 2017-07-20 |
AP2016009661A0 (en) | 2016-12-31 |
JP6291601B2 (ja) | 2018-03-14 |
CL2017000006A1 (es) | 2017-06-02 |
BR112017000132A2 (pt) | 2018-01-09 |
CO2017000011A2 (es) | 2017-04-10 |
WO2016001855A1 (en) | 2016-01-07 |
US9944639B2 (en) | 2018-04-17 |
CN106470996A (zh) | 2017-03-01 |
EP3164400A1 (en) | 2017-05-10 |
PE20170640A1 (es) | 2017-05-26 |
GEP20186934B (en) | 2018-12-10 |
IL249674A0 (en) | 2017-02-28 |
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