SG10201901977XA - Hydrochloride salt form for ezh2 inhibition - Google Patents
Hydrochloride salt form for ezh2 inhibitionInfo
- Publication number
- SG10201901977XA SG10201901977XA SG10201901977XA SG10201901977XA SG10201901977XA SG 10201901977X A SG10201901977X A SG 10201901977XA SG 10201901977X A SG10201901977X A SG 10201901977XA SG 10201901977X A SG10201901977X A SG 10201901977XA SG 10201901977X A SG10201901977X A SG 10201901977XA
- Authority
- SG
- Singapore
- Prior art keywords
- salt form
- hydrochloride salt
- ezh2 inhibition
- methyl
- ezh2
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
HYDROCHLORIDE SALT FORM FOR EZH2 INHIBITION Provided herein are novel solid forms of N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-5 - (ethyl (tetrahydro-2H-pyran-4-yl)amino)-4-methyl-4'-(morpholinomethyl)-[1,1'-biphenyl]-3- carboxamide hydrochloride, and related compositions and methods. [Figure 3]
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361891786P | 2013-10-16 | 2013-10-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG10201901977XA true SG10201901977XA (en) | 2019-04-29 |
Family
ID=52828660
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG10201901977XA SG10201901977XA (en) | 2013-10-16 | 2014-10-15 | Hydrochloride salt form for ezh2 inhibition |
SG11201602269QA SG11201602269QA (en) | 2013-10-16 | 2014-10-15 | Hydrochloride salt form for ezh2 inhibition |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201602269QA SG11201602269QA (en) | 2013-10-16 | 2014-10-15 | Hydrochloride salt form for ezh2 inhibition |
Country Status (24)
Country | Link |
---|---|
US (3) | US10040782B2 (en) |
EP (2) | EP4324525A2 (en) |
JP (2) | JP6608812B2 (en) |
KR (1) | KR102142177B1 (en) |
CN (1) | CN105829302B (en) |
AU (2) | AU2014337300B2 (en) |
CA (1) | CA2925889C (en) |
CL (1) | CL2016000866A1 (en) |
DK (1) | DK3057962T3 (en) |
EA (1) | EA038869B1 (en) |
ES (1) | ES2960953T3 (en) |
FI (1) | FI3057962T3 (en) |
HU (1) | HUE063984T2 (en) |
IL (1) | IL244787B (en) |
LT (1) | LT3057962T (en) |
MA (1) | MA38949A1 (en) |
MX (1) | MX2016004703A (en) |
MY (1) | MY179802A (en) |
PE (1) | PE20161273A1 (en) |
PL (1) | PL3057962T3 (en) |
PT (1) | PT3057962T (en) |
SG (2) | SG10201901977XA (en) |
SI (1) | SI3057962T1 (en) |
WO (1) | WO2015057859A1 (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP4190777A1 (en) | 2012-04-13 | 2023-06-07 | Epizyme, Inc. | Hbr salt form for ezh2 inhibition |
MY179802A (en) | 2013-10-16 | 2020-11-16 | Eisai R&D Man Co Ltd | Hydrochloride salt form for ezh2 inhibition |
EP3076977B1 (en) | 2013-12-06 | 2021-03-03 | Epizyme, Inc. | Combination therapy for treating cancer |
PL3157527T3 (en) | 2014-06-17 | 2023-08-07 | Epizyme, Inc. | Ezh2 inhibitors for treating lymphoma |
AU2015331729A1 (en) | 2014-10-16 | 2017-04-13 | Epizyme, Inc. | Method for treating cancer |
MX2017006089A (en) * | 2014-11-17 | 2017-12-11 | Epizyme Inc | Method for treating cancer. |
US10456407B2 (en) | 2015-04-20 | 2019-10-29 | Epizyme, Inc. | Combination therapy for treating cancer |
WO2016201328A1 (en) | 2015-06-10 | 2016-12-15 | Epizyme, Inc. | Ezh2 inhibitors for treating lymphoma |
US10493076B2 (en) | 2015-08-24 | 2019-12-03 | Epizyme, Inc. | Method for treating cancer |
US11951108B2 (en) | 2016-01-29 | 2024-04-09 | Epizyme, Inc. | Combination therapy for treating cancer |
CA3025933A1 (en) | 2016-06-01 | 2017-12-07 | Epizyme, Inc. | Use of ezh2 inhibitors for treating cancer |
MA45406A (en) | 2016-06-17 | 2019-04-24 | Epizyme Inc | EZH2 INHIBITORS TO TREAT CANCER |
TW201831181A (en) | 2017-01-19 | 2018-09-01 | 日商第一三共股份有限公司 | Therapeutic agent for htlv-1-associated myelopathy |
WO2018183885A1 (en) | 2017-03-31 | 2018-10-04 | Epizyme, Inc. | Combination therapy for treating cancer |
JP2020522687A (en) | 2017-06-02 | 2020-07-30 | エピザイム,インコーポレイティド | Use of EZH2 inhibitors for treating cancer |
US11452727B2 (en) | 2017-09-05 | 2022-09-27 | Epizyme, Inc. | Combination therapy for treating cancer |
WO2020011607A1 (en) | 2018-07-09 | 2020-01-16 | Fondation Asile Des Aveugles | Inhibition of prc2 subunits to treat eye disorders |
WO2021035194A1 (en) | 2019-08-22 | 2021-02-25 | Juno Therapeutics, Inc. | Combination therapy of a t cell therapy and an enhancer of zeste homolog 2 (ezh2) inhibitor and related methods |
WO2023209591A1 (en) | 2022-04-27 | 2023-11-02 | Daiichi Sankyo Company, Limited | Combination of antibody-drug conjugate with ezh1 and/or ezh2 inhibitor |
Family Cites Families (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0733729A (en) | 1993-07-26 | 1995-02-03 | Kirin Brewery Co Ltd | Production of n-cyano-n'-substituted-arylcarboxyimidamide compound |
WO1995018097A1 (en) | 1993-12-27 | 1995-07-06 | Eisai Co., Ltd. | Anthranilic acid derivative |
DE19516776A1 (en) | 1995-05-10 | 1996-11-14 | Boehringer Ingelheim Int | Chromatin regulatory genes |
US5741819A (en) | 1995-06-07 | 1998-04-21 | 3-Dimensional Pharmaceuticals, Inc. | Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors |
JP3906935B2 (en) | 1995-12-18 | 2007-04-18 | 杏林製薬株式会社 | N-substituted dioxothiazolidylbenzamide derivative and process for producing the same |
AU6060099A (en) | 1998-09-30 | 2000-04-17 | Procter & Gamble Company, The | 2-substituted ketoamides |
UA71587C2 (en) | 1998-11-10 | 2004-12-15 | Шерінг Акцієнгезелльшафт | Anthranilic acid amides and use thereof as medicaments |
US6710058B2 (en) | 2000-11-06 | 2004-03-23 | Bristol-Myers Squibb Pharma Company | Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors |
CA2433158C (en) | 2000-12-28 | 2011-05-10 | Shionogi & Co., Ltd. | Pyridone derivatives having a binding activity to the cannabinoid type 2 receptor |
US7700293B2 (en) | 2001-08-02 | 2010-04-20 | The Regents Of The University Of Michigan | Expression profile of prostate cancer |
JPWO2003070277A1 (en) | 2002-02-19 | 2005-06-09 | 塩野義製薬株式会社 | Antipruritic agent |
TW200306155A (en) | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
US7442685B2 (en) | 2003-06-13 | 2008-10-28 | The University Of North Carolina At Chapel Hill | DOT1 histone methyltransferases as a target for identifying therapeutic agents for leukemia |
JP5160885B2 (en) | 2004-06-01 | 2013-03-13 | ザ・ユニヴァーシティ・オヴ・ノース・キャロライナ・アト・チャペル・ヒル | Reconstituted histone methyltransferase complex and method for identifying modulators thereof |
JO2787B1 (en) | 2005-04-27 | 2014-03-15 | امجين إنك, | Substituted Amid derivatives & methods of use |
US7923219B2 (en) | 2005-06-02 | 2011-04-12 | The University Of North Carolina At Chapel Hill | Ubiquitin E3 ligase |
FR2889526B1 (en) | 2005-08-04 | 2012-02-17 | Aventis Pharma Sa | SUBSTITUTED 7-AZA-INDAZOLES, COMPOSITIONS CONTAINING SAME, PROCESS FOR PRODUCTION AND USE |
PL1940821T3 (en) | 2005-10-19 | 2013-08-30 | Gruenenthal Gmbh | Novel vanilloid receptor ligands and their use for producing medicaments |
ATE510822T1 (en) | 2005-10-21 | 2011-06-15 | Merck Sharp & Dohme | POTASSIUM CHANNEL INHIBITORS |
EP1941060B1 (en) | 2005-10-28 | 2012-02-29 | The University of North Carolina At Chapel Hill | Protein demethylases comprising a jmjc domain |
AU2006325746A1 (en) | 2005-12-14 | 2007-06-21 | Bristol-Myers Squibb Company | Six-membered heterocycles useful as serine protease inhibitors |
AU2006336552B2 (en) | 2006-01-20 | 2012-12-20 | The University Of North Carolina At Chapel Hill | Diagnostic and therapeutic targets for leukemia |
CN101443007A (en) | 2006-05-15 | 2009-05-27 | Irm责任有限公司 | TEREPHTHALAMATE compounds and compositions, and their use as HIV integrase inhibitors |
EP2040711A2 (en) | 2006-05-18 | 2009-04-01 | Amphora Discovery Corporation | 2-oxo-1,2-dihydroquinoline derivatives, compositions, and uses thereof as antiproliferative agents |
WO2008108825A2 (en) | 2006-10-10 | 2008-09-12 | Burnham Institute For Medical Research | Neuroprotective compositions and methods |
AU2008219166B2 (en) | 2007-02-16 | 2013-05-16 | Amgen Inc. | Nitrogen-containing heterocyclyl ketones and their use as c-Met inhibitors |
WO2008104077A1 (en) | 2007-02-28 | 2008-09-04 | Methylgene Inc. | Small molecule inhibitors of protein arginine methyltransferases (prmts) |
WO2008113006A1 (en) | 2007-03-14 | 2008-09-18 | Xenon Pharmaceuticals Inc. | Methods of using quinolinone compounds in treating sodium channel-mediated diseases or conditions |
DE102007017884A1 (en) | 2007-04-13 | 2008-10-16 | Grünethal GmbH | Novel vanilloid receptor ligands and their use in the preparation of medicines |
US20090012031A1 (en) | 2007-07-03 | 2009-01-08 | The Regents Of The University Of Michigan | EZH2 Cancer Markers |
JP2011502148A (en) | 2007-10-31 | 2011-01-20 | メルク・シャープ・エンド・ドーム・コーポレイション | P2X3 receptor antagonist for the treatment of pain |
AU2008337286B2 (en) | 2007-12-19 | 2014-08-07 | Cancer Research Technology Limited | Pyrido[2,3-b]pyrazine-8-substituted compounds and their use |
WO2009124137A2 (en) | 2008-04-01 | 2009-10-08 | Mount Sinai School Of Medicine Of New York University | Method of suppressing gene transcription through histone lysine methylation |
US20100113415A1 (en) | 2008-05-29 | 2010-05-06 | Rajapakse Hemaka A | Epha4 rtk inhibitors for treatment of neurological and neurodegenerative disorders and cancer |
EP2335779A1 (en) | 2008-08-08 | 2011-06-22 | New York Blood Center | Small Molecule Inhibitors of Retroviral Assembly & Maturation |
FR2934995B1 (en) | 2008-08-14 | 2010-08-27 | Sanofi Aventis | POLYSUBSTITUTED AZETIDINE COMPOUNDS, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF |
JP2012522013A (en) | 2009-03-27 | 2012-09-20 | ザ ユーエービー リサーチ ファウンデーション | Regulated IRES-mediated translation |
WO2011011366A2 (en) | 2009-07-20 | 2011-01-27 | Constellation Pharmaceuticals | Agents for stimulating activity of methyl modifying enzymes and methods of use thereof |
CA2784899A1 (en) | 2009-12-30 | 2011-07-07 | Avon Products, Inc. | Topical lightening composition and uses thereof |
WO2011140325A1 (en) | 2010-05-07 | 2011-11-10 | Glaxosmithkline Llc | Indazoles |
WO2012005805A1 (en) | 2010-05-07 | 2012-01-12 | Glaxosmithkline Llc | Azaindazoles |
WO2011140324A1 (en) | 2010-05-07 | 2011-11-10 | Glaxosmithkline Llc | Indoles |
US9175331B2 (en) | 2010-09-10 | 2015-11-03 | Epizyme, Inc. | Inhibitors of human EZH2, and methods of use thereof |
US8895245B2 (en) | 2010-09-10 | 2014-11-25 | Epizyme, Inc. | Inhibitors of human EZH2 and methods of use thereof |
WO2012068589A2 (en) | 2010-11-19 | 2012-05-24 | Constellation Pharmaceuticals | Modulators of methyl modifying enzymes, compositions and uses thereof |
WO2012075080A1 (en) | 2010-12-01 | 2012-06-07 | Glaxosmithkline Llc | Indoles |
RU2013130253A (en) | 2010-12-03 | 2015-01-10 | Эпизайм, Инк. | 7-DEAZAPURINE HISTONIC METHYL TRANSFERASES AND WAYS OF THEIR APPLICATION |
JP2014511389A (en) | 2011-02-28 | 2014-05-15 | エピザイム インコーポレイテッド | Substituted 6,5-fused bicyclic heteroaryl compounds |
JO3438B1 (en) | 2011-04-13 | 2019-10-20 | Epizyme Inc | Aryl- or heteroaryl-substituted benzene compounds |
TWI598336B (en) | 2011-04-13 | 2017-09-11 | 雅酶股份有限公司 | Substituted benzene compounds |
KR102587175B1 (en) | 2012-03-12 | 2023-10-06 | 에피자임, 인코포레이티드 | Inhibitors of human ezh2, and methods of use thereof |
BR112014025506B1 (en) | 2012-04-13 | 2024-02-06 | Epizyme, Inc | COMPOSITION COMPRISING EZH2 INHIBITOR COMPOUND, THERAPEUTIC USE THEREOF AND IN VITRO METHOD OF INHIBITING THE PROLIFERATION OF CANCER CELLS |
EP4190777A1 (en) | 2012-04-13 | 2023-06-07 | Epizyme, Inc. | Hbr salt form for ezh2 inhibition |
US9562041B2 (en) | 2012-05-16 | 2017-02-07 | Glaxosmithkline Llc | Enhancer of zeste homolog 2 inhibitors |
CA2888021A1 (en) | 2012-10-15 | 2014-04-24 | Epizyme, Inc. | Substituted n-((2-oxo-1,2-dihydropyridin-3-yl)-methyl)-benzamide compounds and their use in the treatment of ezh2-mediated disorders |
PL2908823T3 (en) | 2012-10-15 | 2020-03-31 | Epizyme, Inc. | Methods of treating cancer |
CA2894216A1 (en) | 2012-12-21 | 2014-06-26 | Epizyme, Inc. | 1,4-pyridone compounds |
WO2014100665A1 (en) | 2012-12-21 | 2014-06-26 | Epizyme, Inc. | 1,4-pyridone bicyclic heteroaryl compounds |
EP2970306A4 (en) | 2013-03-15 | 2016-08-03 | Epizyme Inc | Substituted 6,5-fused bicyclic heteroaryl compounds |
CA2903572A1 (en) | 2013-03-15 | 2014-10-23 | Epizyme, Inc. | Substituted benzene compounds |
US9624205B2 (en) | 2013-07-19 | 2017-04-18 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
EP3022184B1 (en) | 2013-07-19 | 2017-09-27 | Epizyme, Inc. | Substituted benzene compounds |
MY179802A (en) | 2013-10-16 | 2020-11-16 | Eisai R&D Man Co Ltd | Hydrochloride salt form for ezh2 inhibition |
-
2014
- 2014-10-15 MY MYPI2016000542A patent/MY179802A/en unknown
- 2014-10-15 LT LTEPPCT/US2014/060724T patent/LT3057962T/en unknown
- 2014-10-15 US US15/029,848 patent/US10040782B2/en active Active
- 2014-10-15 EP EP23203529.5A patent/EP4324525A2/en active Pending
- 2014-10-15 CN CN201480056428.6A patent/CN105829302B/en active Active
- 2014-10-15 SI SI201432051T patent/SI3057962T1/en unknown
- 2014-10-15 EP EP14854272.3A patent/EP3057962B1/en active Active
- 2014-10-15 MX MX2016004703A patent/MX2016004703A/en active IP Right Grant
- 2014-10-15 EA EA201690650A patent/EA038869B1/en unknown
- 2014-10-15 PT PT148542723T patent/PT3057962T/en unknown
- 2014-10-15 WO PCT/US2014/060724 patent/WO2015057859A1/en active Application Filing
- 2014-10-15 SG SG10201901977XA patent/SG10201901977XA/en unknown
- 2014-10-15 ES ES14854272T patent/ES2960953T3/en active Active
- 2014-10-15 CA CA2925889A patent/CA2925889C/en active Active
- 2014-10-15 FI FIEP14854272.3T patent/FI3057962T3/en active
- 2014-10-15 SG SG11201602269QA patent/SG11201602269QA/en unknown
- 2014-10-15 AU AU2014337300A patent/AU2014337300B2/en active Active
- 2014-10-15 PE PE2016000506A patent/PE20161273A1/en unknown
- 2014-10-15 JP JP2016519378A patent/JP6608812B2/en active Active
- 2014-10-15 KR KR1020167011534A patent/KR102142177B1/en active IP Right Grant
- 2014-10-15 PL PL14854272.3T patent/PL3057962T3/en unknown
- 2014-10-15 HU HUE14854272A patent/HUE063984T2/en unknown
- 2014-10-15 DK DK14854272.3T patent/DK3057962T3/en active
- 2014-10-15 MA MA38949A patent/MA38949A1/en unknown
-
2016
- 2016-03-28 IL IL244787A patent/IL244787B/en unknown
- 2016-04-13 CL CL2016000866A patent/CL2016000866A1/en unknown
-
2018
- 2018-06-05 US US16/000,539 patent/US10710987B2/en active Active
- 2018-12-11 JP JP2018231817A patent/JP2019052181A/en active Pending
-
2019
- 2019-04-02 AU AU2019202246A patent/AU2019202246A1/en not_active Abandoned
-
2020
- 2020-06-03 US US16/891,427 patent/US20210017163A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SG10201901977XA (en) | Hydrochloride salt form for ezh2 inhibition | |
MX362339B (en) | Salt form of a human hi stone methyltransf erase ezh2 inhibitor. | |
DK3220916T3 (en) | METHOD FOR TREATMENT OF CANCER WITH N-((4,6-DIMETHYL-2-OXO-1,2-DIHYDROPYRIDIN-3-YL)METHYL)-5-(ETHYL(TETRAHYDRO-2H-PYRAN-4-YL)AMINO) -4-METHYL-4'-(MORPHOLINOMETHYL)-[1,1'-BIPHENYL]-3-CARBOXAMIDE | |
EA201991884A2 (en) | G12C KRAS INHIBITORS | |
EA201690752A1 (en) | INHIBITORS G12C KRAS | |
EA201891191A1 (en) | 2-SUBSTITUTED HINAZOLIN COMPOUNDS CONTAINING A SUBSTITUTED HETEROCYCLIC GROUP AND METHODS OF THEIR APPLICATION | |
PH12018500777A1 (en) | Farnesoid x receptor modulators | |
PH12015500719A1 (en) | Gdf-8-inhibitors | |
EP4219465A3 (en) | Prmt5 inhibitors and uses thereof | |
GEP20166432B (en) | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh | |
MX2019009501A (en) | Amino pyrimidine compounds useful as ssao inhibitors. | |
JO3452B1 (en) | Aminoheteroaryl benzamides as kinase inhibitors | |
EA201590748A1 (en) | ANTI-VIRUS CONNECTIONS AGAINST RSV | |
GEP201706699B (en) | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh | |
MX2015012850A (en) | Arginine methyltransferase inhibitors and uses thereof. | |
GEP20166474B (en) | Pyrazolospiroketone derivatives for use as acetyl-coa carboxylase inhibitors | |
EA201490471A1 (en) | PYRIDAZINOUS COMPOUNDS AND THEIR APPLICATION AS DAAO INHIBITORS | |
EA029499B9 (en) | Rorc2 inhibitors and methods of use thereof | |
IL273974B1 (en) | Amine-substituted heterocyclic compounds as ehmt2 inhibitors, salts thereof, and methods of synthesis thereof | |
MY198008A (en) | Crystal of benzofuran derivative free base and preparation method | |
EA201391299A1 (en) | PEPTIDDEFORMILASE INHIBITORS | |
IN2013MU03565A (en) |