SG11201702082VA - Benzyl substituted indazoles as bub1 inhibitors - Google Patents
Benzyl substituted indazoles as bub1 inhibitorsInfo
- Publication number
- SG11201702082VA SG11201702082VA SG11201702082VA SG11201702082VA SG11201702082VA SG 11201702082V A SG11201702082V A SG 11201702082VA SG 11201702082V A SG11201702082V A SG 11201702082VA SG 11201702082V A SG11201702082V A SG 11201702082VA SG 11201702082V A SG11201702082V A SG 11201702082VA
- Authority
- SG
- Singapore
- Prior art keywords
- benzyl substituted
- substituted indazoles
- bub1 inhibitors
- bub1
- inhibitors
- Prior art date
Links
Classifications
-
- 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
-
- 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
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP14185604 | 2014-09-19 | ||
EP15176903 | 2015-07-15 | ||
PCT/EP2015/071340 WO2016042084A1 (en) | 2014-09-19 | 2015-09-17 | Benzyl substituted indazoles as bub1 inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11201702082VA true SG11201702082VA (en) | 2017-04-27 |
Family
ID=54140475
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201702082VA SG11201702082VA (en) | 2014-09-19 | 2015-09-17 | Benzyl substituted indazoles as bub1 inhibitors |
Country Status (27)
Country | Link |
---|---|
US (1) | US10350206B2 (de) |
EP (1) | EP3194379A1 (de) |
JP (1) | JP6664385B2 (de) |
KR (1) | KR20170049604A (de) |
CN (1) | CN107001331A (de) |
AP (1) | AP2017009803A0 (de) |
AU (1) | AU2015316796A1 (de) |
BR (1) | BR112017005444A2 (de) |
CA (1) | CA2961589A1 (de) |
CL (1) | CL2017000654A1 (de) |
CO (1) | CO2017002532A2 (de) |
CR (1) | CR20170100A (de) |
CU (1) | CU20170029A7 (de) |
DO (1) | DOP2017000078A (de) |
EA (1) | EA032401B1 (de) |
EC (1) | ECSP17016797A (de) |
IL (1) | IL251071A0 (de) |
MA (1) | MA39484A (de) |
MX (1) | MX2017003664A (de) |
NI (1) | NI201700034A (de) |
PE (1) | PE20170697A1 (de) |
PH (1) | PH12017500509A1 (de) |
SG (1) | SG11201702082VA (de) |
TN (1) | TN2017000092A1 (de) |
TW (1) | TW201615636A (de) |
UY (1) | UY36311A (de) |
WO (1) | WO2016042084A1 (de) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA111754C2 (uk) | 2011-10-06 | 2016-06-10 | Байєр Фарма Акцієнгезелльшафт | Заміщені бензиліндазоли для застосування як інгібіторів bub1-кінази для лікування гіперпроліферативних захворювань |
PL3176170T3 (pl) | 2012-06-13 | 2019-05-31 | Incyte Holdings Corp | Podstawione związki tricykliczne jako inhibitory fgfr |
CA2909207C (en) | 2013-04-19 | 2021-11-02 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
CA2916116A1 (en) | 2013-06-21 | 2014-12-24 | Bayer Pharma Aktiengesellschaft | Substituted benzylpyrazoles |
EP3010901B1 (de) | 2013-06-21 | 2017-09-13 | Bayer Pharma Aktiengesellschaft | Heteroarylsubstituierte pyrazole |
JP2016536311A (ja) | 2013-10-30 | 2016-11-24 | バイエル ファーマ アクチエンゲゼルシャフト | ヘテロアリール置換ピラゾール類 |
CA2938169C (en) | 2014-02-06 | 2022-03-15 | Heptares Therapeutics Limited | Bicyclic aza compounds as muscarinic m1 receptor agonists |
UY36175A (es) | 2014-06-17 | 2016-01-29 | Bayer Pharma AG | 3-amino-1,5,6,7-tetrahidro-4h-indol-4-onas |
CN107001331A (zh) | 2014-09-19 | 2017-08-01 | 拜耳制药股份公司 | 作为bub1抑制剂的苄基取代的吲唑 |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
EP3617205B1 (de) | 2015-02-20 | 2021-08-04 | Incyte Corporation | Bicyclische heterocyclen als fgfr-inhibitoren |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
TWI794171B (zh) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Hdac抑制劑與pd-l1抑制劑之組合治療 |
WO2018122168A1 (en) | 2016-12-29 | 2018-07-05 | Bayer Pharma Aktiengesellschaft | Combinations of bub1 kinase and parp inhibitors |
WO2018158175A1 (en) | 2017-02-28 | 2018-09-07 | Bayer Pharma Aktiengesellschaft | Combination of bub1 inhibitors |
KR102615821B1 (ko) | 2017-04-11 | 2023-12-21 | 선샤인 레이크 파르마 컴퍼니 리미티드 | 불소-치환된 인다졸 화합물 및 이의 용도 |
WO2018206547A1 (en) | 2017-05-12 | 2018-11-15 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and atr inhibitors |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
WO2018215282A1 (en) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and pi3k inhibitors |
WO2019213506A1 (en) | 2018-05-04 | 2019-11-07 | Incyte Corporation | Salts of an fgfr inhibitor |
CA3099287A1 (en) | 2018-05-04 | 2019-11-07 | Incyte Corporation | Solid forms of an fgfr inhibitor and processes for preparing the same |
US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
KR20220100879A (ko) | 2019-10-14 | 2022-07-18 | 인사이트 코포레이션 | Fgfr 저해제로서의 이환식 헤테로사이클 |
US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
EP4069696A1 (de) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclische heterocyclen als fgfr-inhibitoren |
MX2022006691A (es) | 2019-12-04 | 2022-09-19 | Incyte Corp | Derivados de un inhibidor de receptores del factor de crecimiento de fibroblastos (fgfr). |
US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
WO2022261160A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
Family Cites Families (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
US5470862A (en) | 1995-02-03 | 1995-11-28 | Ohmeda Pharmaceutical Products Division Inc. | Substituted pyrazolyl compounds and methods employing such compounds |
DE59713007D1 (de) | 1996-10-14 | 2009-06-25 | Bayer Healthcare Ag | Neue heterocyclylmethyl-substituierte pyrazolderivate und ihre verwendung in der behandlung von herz-kreislauf-erkrankungen |
DE19834047A1 (de) | 1998-07-29 | 2000-02-03 | Bayer Ag | Substituierte Pyrazolderivate |
DE19846514A1 (de) | 1998-10-09 | 2000-04-20 | Bayer Ag | Neue Heterocyclyl-methyl-substituierte Pyrazole |
US7569592B2 (en) | 2001-12-18 | 2009-08-04 | Merck & Co., Inc. | Heteroaryl substituted pyrazole modulators of metabotropic glutamate receptor-5 |
US7166293B2 (en) | 2002-03-29 | 2007-01-23 | Carlsbad Technology, Inc. | Angiogenesis inhibitors |
CA2498460A1 (en) | 2002-09-10 | 2004-03-25 | Scios Inc. | Inhibitors of tfg.beta. |
DE10244810A1 (de) | 2002-09-26 | 2004-04-08 | Bayer Ag | Neue Morpholin-überbrückte Indazolderivate |
WO2007038613A2 (en) | 2005-09-26 | 2007-04-05 | The Regents Of The University Of California | Selective serine/threonine kinase inhibitors |
US20080242681A1 (en) | 2004-01-22 | 2008-10-02 | Altana Pharma Ag | N-4-(6-(Hetero)Aryl-Pyrimidin-4-Ylaminophenyl)-Benzenesulfonamides as Kinase Inhibitors |
WO2007065010A2 (en) | 2005-12-02 | 2007-06-07 | Hif Bio, Inc. | Anti-angiogenesis compounds |
DE102006043443A1 (de) | 2006-09-15 | 2008-03-27 | Bayer Healthcare Ag | Neue aza-bicyclische Verbindungen und ihre Verwendung |
KR20100016617A (ko) | 2007-05-18 | 2010-02-12 | 바이엘 쉐링 파마 악티엔게젤샤프트 | 과증식성 장애 및 혈관형성 관련 질환의 치료에 유용한 저산소증 유도성 인자 (hif)의 억제제 |
JP2010111624A (ja) | 2008-11-06 | 2010-05-20 | Shionogi & Co Ltd | Ttk阻害作用を有するインダゾール誘導体 |
WO2010069966A1 (en) | 2008-12-18 | 2010-06-24 | Nerviano Medical Sciences S.R.L. | Substituted indazole derivatives active as kinase inhibitors |
CN102666537A (zh) | 2009-10-20 | 2012-09-12 | 艾格尔生物制药股份有限公司 | 治疗黄病毒科病毒感染的氮杂吲唑 |
EA036422B1 (ru) | 2009-11-27 | 2020-11-09 | Адверио Фарма Гмбх | Способ получения метил-{4,6-диамино-2-[1-(2-фторбензил)-1h-пиразоло[3,4-b]пиридин-3-ил]пиримидин-5-ил}метилкарбамата |
WO2011115804A1 (en) | 2010-03-17 | 2011-09-22 | Ironwood Pharmaceuticals, Inc. | Sgc stimulators |
SG184243A1 (en) | 2010-03-30 | 2012-10-30 | Verseon Corp | Multisubstituted aromatic compounds as inhibitors of thrombin |
AU2011272800B2 (en) | 2010-06-30 | 2016-11-03 | Cyclerion Therapeutics, Inc. | sGC stimulators |
UA111754C2 (uk) | 2011-10-06 | 2016-06-10 | Байєр Фарма Акцієнгезелльшафт | Заміщені бензиліндазоли для застосування як інгібіторів bub1-кінази для лікування гіперпроліферативних захворювань |
CA2859779A1 (en) | 2011-12-21 | 2013-06-27 | Bayer Intellectual Property Gmbh | Substituted benzylpyrazoles |
CA2861804C (en) | 2011-12-27 | 2021-10-26 | Ironwood Pharmaceuticals, Inc. | 2-benzyl,3(pyrimidin-2-yl)substituted pyrazoles useful as sgc stimulators |
ES2620316T3 (es) | 2012-05-11 | 2017-06-28 | Bayer Pharma Aktiengesellschaft | Cicloalquenopirazoles sustituidos como inhibidores de BUB1 para el tratamiento del cáncer |
WO2014047111A1 (en) | 2012-09-18 | 2014-03-27 | Ironwood Pharmaceuticals, Inc. | Sgc stimulators |
CA2885645A1 (en) | 2012-09-19 | 2014-03-27 | Ironwood Pharmaceuticals, Inc. | Sgc stimulators |
US9738610B2 (en) | 2012-09-24 | 2017-08-22 | Whitehead Institute For Biomedical Research | Indazole derivatives and uses thereof |
US20160046610A1 (en) | 2013-03-21 | 2016-02-18 | Bayer Pharma Aktiengesellschaft | 3-heteroaryl substituted indazoles |
JP2016514717A (ja) | 2013-03-21 | 2016-05-23 | バイエル ファーマ アクチエンゲゼルシャフト | ジアミノヘテロアリール置換インダゾール |
CA2907594A1 (en) | 2013-03-21 | 2014-09-25 | Bayer Pharma Aktiengesellschaft | Heteroaryl substituted indazoles |
EP3010901B1 (de) | 2013-06-21 | 2017-09-13 | Bayer Pharma Aktiengesellschaft | Heteroarylsubstituierte pyrazole |
EP3010907A1 (de) | 2013-06-21 | 2016-04-27 | Bayer Pharma Aktiengesellschaft | Diaminoheteroarylsubstituierte pyrazole |
CA2916116A1 (en) | 2013-06-21 | 2014-12-24 | Bayer Pharma Aktiengesellschaft | Substituted benzylpyrazoles |
CA2916109A1 (en) | 2013-06-21 | 2014-12-24 | Bayer Pharma Aktiengesellschaft | Heteroaryl substituted pyrazoles |
JP2016526540A (ja) | 2013-06-21 | 2016-09-05 | バイエル ファーマ アクチエンゲゼルシャフト | 置換ベンジルピラゾール |
JP2016536311A (ja) | 2013-10-30 | 2016-11-24 | バイエル ファーマ アクチエンゲゼルシャフト | ヘテロアリール置換ピラゾール類 |
CN111909130B (zh) | 2014-09-19 | 2023-10-31 | 福马治疗股份有限公司 | 作为突变型异柠檬酸脱氢酶抑制剂的吡啶-2(1h)-酮喹啉酮衍生物 |
US20170305882A1 (en) | 2014-09-19 | 2017-10-26 | Bayer Pharma Aktiengesellschaft | Benzyl substituted indazoles as bub1 kinase inhibitors |
BR112017003548A2 (pt) | 2014-09-19 | 2017-12-12 | Nestec Sa | tratamento de câncer com inibidor de alfa-amilase para animais de estimação |
CN107001331A (zh) | 2014-09-19 | 2017-08-01 | 拜耳制药股份公司 | 作为bub1抑制剂的苄基取代的吲唑 |
CA2961745A1 (en) | 2014-09-19 | 2016-03-24 | Glaxosmithkline Intellectual Property Development Limited | Novel soluble guanylate cyclase activators and their use |
CA2961570A1 (en) | 2014-09-19 | 2016-03-24 | Lars Barfacker | Benzyl substituted indazoles |
WO2016042081A1 (en) | 2014-09-19 | 2016-03-24 | Bayer Pharma Aktiengesellschaft | Benzyl substituted indazoles as bub1 kinase inhibitors |
WO2017148995A1 (en) | 2016-03-04 | 2017-09-08 | Bayer Pharma Aktiengesellschaft | 1-(pyrimidin-2-yl)-1h-indazoles having bub1 kinase inhibiting activity |
WO2017157992A1 (en) | 2016-03-18 | 2017-09-21 | Bayer Pharma Aktiengesellschaft | Annulated pyrazoles as bub1 kinase inhibitors for treating proliferative disorders |
WO2017157991A1 (en) | 2016-03-18 | 2017-09-21 | Bayer Pharma Aktiengesellschaft | 1-alkyl-pyrazoles and -indazoles as bub1 inhibitors for the treatment of hyperproliferative diseases |
WO2018122168A1 (en) | 2016-12-29 | 2018-07-05 | Bayer Pharma Aktiengesellschaft | Combinations of bub1 kinase and parp inhibitors |
WO2018158175A1 (en) | 2017-02-28 | 2018-09-07 | Bayer Pharma Aktiengesellschaft | Combination of bub1 inhibitors |
WO2018206547A1 (en) | 2017-05-12 | 2018-11-15 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and atr inhibitors |
WO2018215282A1 (en) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and pi3k inhibitors |
-
2015
- 2015-09-17 CN CN201580062951.4A patent/CN107001331A/zh active Pending
- 2015-09-17 PE PE2017000480A patent/PE20170697A1/es unknown
- 2015-09-17 JP JP2017514825A patent/JP6664385B2/ja not_active Expired - Fee Related
- 2015-09-17 SG SG11201702082VA patent/SG11201702082VA/en unknown
- 2015-09-17 MX MX2017003664A patent/MX2017003664A/es unknown
- 2015-09-17 BR BR112017005444A patent/BR112017005444A2/pt not_active IP Right Cessation
- 2015-09-17 CU CUP2017000029A patent/CU20170029A7/xx unknown
- 2015-09-17 AU AU2015316796A patent/AU2015316796A1/en not_active Abandoned
- 2015-09-17 MA MA039484A patent/MA39484A/fr unknown
- 2015-09-17 TN TN2017000092A patent/TN2017000092A1/en unknown
- 2015-09-17 EP EP15763619.2A patent/EP3194379A1/de not_active Withdrawn
- 2015-09-17 CR CR20170100A patent/CR20170100A/es unknown
- 2015-09-17 US US15/512,494 patent/US10350206B2/en not_active Expired - Fee Related
- 2015-09-17 KR KR1020177010425A patent/KR20170049604A/ko unknown
- 2015-09-17 WO PCT/EP2015/071340 patent/WO2016042084A1/en active Application Filing
- 2015-09-17 CA CA2961589A patent/CA2961589A1/en not_active Abandoned
- 2015-09-17 AP AP2017009803A patent/AP2017009803A0/en unknown
- 2015-09-17 EA EA201790649A patent/EA032401B1/ru not_active IP Right Cessation
- 2015-09-18 TW TW104131025A patent/TW201615636A/zh unknown
- 2015-09-18 UY UY0001036311A patent/UY36311A/es not_active Application Discontinuation
-
2017
- 2017-03-09 IL IL251071A patent/IL251071A0/en unknown
- 2017-03-16 PH PH12017500509A patent/PH12017500509A1/en unknown
- 2017-03-17 EC ECIEPI201716797A patent/ECSP17016797A/es unknown
- 2017-03-17 CL CL2017000654A patent/CL2017000654A1/es unknown
- 2017-03-17 DO DO2017000078A patent/DOP2017000078A/es unknown
- 2017-03-17 CO CONC2017/0002532A patent/CO2017002532A2/es unknown
- 2017-03-17 NI NI201700034A patent/NI201700034A/es unknown
Also Published As
Publication number | Publication date |
---|---|
KR20170049604A (ko) | 2017-05-10 |
AP2017009803A0 (en) | 2017-03-31 |
UY36311A (es) | 2016-04-29 |
US10350206B2 (en) | 2019-07-16 |
TN2017000092A1 (en) | 2018-07-04 |
CN107001331A (zh) | 2017-08-01 |
CL2017000654A1 (es) | 2017-12-11 |
JP2017530962A (ja) | 2017-10-19 |
NI201700034A (es) | 2017-06-16 |
IL251071A0 (en) | 2017-04-30 |
BR112017005444A2 (pt) | 2018-04-24 |
PE20170697A1 (es) | 2017-06-24 |
EA032401B1 (ru) | 2019-05-31 |
US20170273980A1 (en) | 2017-09-28 |
EP3194379A1 (de) | 2017-07-26 |
DOP2017000078A (es) | 2017-06-30 |
CO2017002532A2 (es) | 2017-07-11 |
EA201790649A1 (ru) | 2017-09-29 |
WO2016042084A1 (en) | 2016-03-24 |
CR20170100A (es) | 2017-04-24 |
PH12017500509A1 (en) | 2017-08-30 |
ECSP17016797A (es) | 2017-05-31 |
JP6664385B2 (ja) | 2020-03-13 |
MA39484A (fr) | 2016-03-24 |
TW201615636A (zh) | 2016-05-01 |
MX2017003664A (es) | 2017-07-13 |
CU20170029A7 (es) | 2017-08-08 |
AU2015316796A1 (en) | 2017-03-30 |
CA2961589A1 (en) | 2016-03-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL251071A0 (en) | Benzyl-substituted indazoles as bub1 inhibitors | |
IL287113A (en) | smyd inhibitors | |
HK1244792B (zh) | 壞死抑制劑 | |
IL246785A0 (en) | Benzimidazole-2-amines as midh1 inhibitors | |
IL251420A0 (en) | Triazolopyrazinones as pde1 inhibitors | |
HK1243415A1 (zh) | 溴結構域抑制劑 | |
HK1226398A1 (zh) | 作為midh1抑制劑的苯並咪唑-2-胺 | |
EP3116503A4 (de) | Hptp-beta-hemmer | |
IL248895A0 (en) | Phosphatidylinositol 3-kinase inhibitors | |
HK1244480A1 (zh) | 細胞壞死抑制劑 | |
IL246400A0 (en) | Neprilysin inhibitors | |
ZA201606174B (en) | Tetrazolone-substituted dihydropyridinone mgat2 inhibitors | |
IL265139B (en) | Dopamine-b-hydroxylase inhibitors | |
IL258870A (en) | Substituted indazole compounds as rorgammat inhibitors and uses thereof | |
IL250306A0 (en) | indazoles | |
GB201612860D0 (en) | Inhibitors | |
GB201501004D0 (en) | Inhibitors | |
EP3628374C0 (de) | Bcl-3-inhibitoren | |
PT3151658T (pt) | Ferradura | |
HK1232214A1 (zh) | 作為 抑制劑的六氫呋喃並吡咯 | |
GB201400299D0 (en) | Corrosion inhibitors | |
GB201401005D0 (en) | Inhibitor | |
GB201520949D0 (en) | Inhibitors | |
EP3180003A4 (de) | Pkc-epsilon-inhibitoren | |
GB201418154D0 (en) | Inhibitors |