MA38949A1 - Forme saline d'hydrochlorure pour inhibition d'ezh2 - Google Patents
Forme saline d'hydrochlorure pour inhibition d'ezh2Info
- Publication number
- MA38949A1 MA38949A1 MA38949A MA38949A MA38949A1 MA 38949 A1 MA38949 A1 MA 38949A1 MA 38949 A MA38949 A MA 38949A MA 38949 A MA38949 A MA 38949A MA 38949 A1 MA38949 A1 MA 38949A1
- Authority
- MA
- Morocco
- Prior art keywords
- dgat1
- ezh2
- hydrochloride
- inhibition
- saline form
- Prior art date
Links
Classifications
-
- 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
-
- 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
-
- 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)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
L'invention concerne de nouveaux composés qui sont des inhibiteurs d'acyl-coenzyme a: diacylglycérol transférase 1 (dgat1), des compositions pharmaceutiques les contenant, des procédés pour leur préparation, ainsi que leur utilisation en thérapie, seuls ou en combinaison avec des thérapies de gestion du poids ou autre thérapie de diminution des triglycérides pour la prévention ou le traitement de maladies liées à un dysfonctionnement de dgat1 ou dans lesquelles une modulation de l'activité de dgat1 peut avoir un bénéfice thérapeutique.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361891786P | 2013-10-16 | 2013-10-16 | |
PCT/US2014/060724 WO2015057859A1 (fr) | 2013-10-16 | 2014-10-15 | Forme saline d'hydrochlorure pour inhibition d'ezh2 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA38949A1 true MA38949A1 (fr) | 2017-07-31 |
Family
ID=52828660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA38949A MA38949A1 (fr) | 2013-10-16 | 2014-10-15 | Forme saline d'hydrochlorure pour inhibition d'ezh2 |
Country Status (24)
Country | Link |
---|---|
US (3) | US10040782B2 (fr) |
EP (2) | EP4324525A3 (fr) |
JP (2) | JP6608812B2 (fr) |
KR (1) | KR102142177B1 (fr) |
CN (1) | CN105829302B (fr) |
AU (2) | AU2014337300B2 (fr) |
CA (1) | CA2925889C (fr) |
CL (1) | CL2016000866A1 (fr) |
DK (1) | DK3057962T3 (fr) |
EA (1) | EA038869B1 (fr) |
ES (1) | ES2960953T3 (fr) |
FI (1) | FI3057962T3 (fr) |
HU (1) | HUE063984T2 (fr) |
IL (1) | IL244787B (fr) |
LT (1) | LT3057962T (fr) |
MA (1) | MA38949A1 (fr) |
MX (1) | MX2016004703A (fr) |
MY (1) | MY179802A (fr) |
PE (1) | PE20161273A1 (fr) |
PL (1) | PL3057962T3 (fr) |
PT (1) | PT3057962T (fr) |
SG (2) | SG11201602269QA (fr) |
SI (1) | SI3057962T1 (fr) |
WO (1) | WO2015057859A1 (fr) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2745016T3 (es) | 2012-04-13 | 2020-02-27 | Epizyme Inc | Bromhidrato de N-((4,6-dimetil-2-oxo-L,2-dihidropiridin-3-il)metil)-5-(etil(tetrahidro-2H-piran-4-il)amino)-4-metil-4'-(morfolinometil)-[L,1'-bifenil]-3-carboxamida para su uso en el tratamiento de un trastorno proliferativo celular del sistema hematológico |
JP6608812B2 (ja) | 2013-10-16 | 2019-11-20 | エピザイム,インコーポレイティド | Ezh2阻害のための塩酸塩形 |
CA2931263A1 (fr) | 2013-12-06 | 2015-06-11 | Epizyme, Inc. | Polytherapie pour le traitement du cancer |
SG10201811128RA (en) | 2014-06-17 | 2019-01-30 | Epizyme Inc | Ezh2 inhibitors for treating lymphoma |
AU2015331729A1 (en) | 2014-10-16 | 2017-04-13 | Epizyme, Inc. | Method for treating cancer |
CA2967664A1 (fr) * | 2014-11-17 | 2016-05-26 | Epizyme, Inc. | Formulations pharmaceutiques comprenant des inhibiteurs de l'histone methyltransferase ezh2 humain |
AU2016252546A1 (en) | 2015-04-20 | 2017-11-02 | Epizyme, Inc. | Combination therapy for treating cancer |
US20180311251A1 (en) | 2015-06-10 | 2018-11-01 | Epizyme, Inc. | Ezh2 inhibitors for treating lymphoma |
AU2016312514A1 (en) | 2015-08-24 | 2018-03-15 | Epizyme, Inc. | Method for treating cancer |
AU2017211331A1 (en) | 2016-01-29 | 2018-06-07 | Epizyme, Inc. | Combination therapy for treating cancer |
US11786533B2 (en) | 2016-06-01 | 2023-10-17 | Epizyme, Inc. | Use of EZH2 inhibitors for treating cancer |
WO2017218953A1 (fr) | 2016-06-17 | 2017-12-21 | Epizyme, Inc. | Inhibiteurs d'ezh2 pour traiter le cancer |
TW201831181A (zh) | 2017-01-19 | 2018-09-01 | 日商第一三共股份有限公司 | 用以用於治療htlv-1相關脊髓病之醫藥組成物 |
US11642346B2 (en) | 2017-03-31 | 2023-05-09 | Epizyme, Inc. | Combination therapy for treating cancer |
JP2020522687A (ja) | 2017-06-02 | 2020-07-30 | エピザイム,インコーポレイティド | 癌を処置するためのezh2阻害剤の使用 |
CN111093660A (zh) | 2017-09-05 | 2020-05-01 | Epizyme股份有限公司 | 用于治疗癌症的组合疗法 |
WO2020011607A1 (fr) | 2018-07-09 | 2020-01-16 | Fondation Asile Des Aveugles | Inhibition de sous-unités de prc2 permettant de traiter des troubles oculaires |
US20220298222A1 (en) | 2019-08-22 | 2022-09-22 | Juno Therapeutics, Inc. | Combination therapy of a t cell therapy and an enhancer of zeste homolog 2 (ezh2) inhibitor and related methods |
TW202400140A (zh) | 2022-04-27 | 2024-01-01 | 日商第一三共股份有限公司 | 抗體-藥物結合物與ezh1及/或ezh2抑制劑之組合 |
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CN1118595A (zh) | 1993-12-27 | 1996-03-13 | 卫材株式会社 | 氨茴酸衍生物 |
DE19516776A1 (de) | 1995-05-10 | 1996-11-14 | Boehringer Ingelheim Int | Chromatin-Regulatorgene |
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WO2006130720A2 (fr) | 2005-06-02 | 2006-12-07 | University Of North Carolina At Chapel Hill | Purification, caracterisation et reconstitution d'une ubiquitine e3 ligase |
FR2889526B1 (fr) | 2005-08-04 | 2012-02-17 | Aventis Pharma Sa | 7-aza-indazoles substitues, compositions les contenant, procede de fabrication et utilisation |
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US9562041B2 (en) | 2012-05-16 | 2017-02-07 | Glaxosmithkline Llc | Enhancer of zeste homolog 2 inhibitors |
EP2906538A4 (fr) | 2012-10-15 | 2016-05-11 | Epizyme Inc | Composés de benzène substitué |
CN105142642B (zh) | 2012-10-15 | 2019-10-18 | Epizyme股份有限公司 | 癌症治疗方法 |
US20150344427A1 (en) | 2012-12-21 | 2015-12-03 | Epizyme, Inc. | 1,4-pyridone compounds |
WO2014100665A1 (fr) | 2012-12-21 | 2014-06-26 | Epizyme, Inc. | Composés hétéroaryles bicycliques 1,4-pyridone |
EP2970306A4 (fr) | 2013-03-15 | 2016-08-03 | Epizyme Inc | Composés hétéroaryles bicycliques substitués condensés en 6,5 |
EP2970281A4 (fr) | 2013-03-15 | 2016-08-03 | Epizyme Inc | Composés de benzène substitués |
WO2015010078A2 (fr) | 2013-07-19 | 2015-01-22 | Epizyme, Inc. | Composés hétéroaryles bicycliques substitués condensés en 6,5 |
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-
2014
- 2014-10-15 JP JP2016519378A patent/JP6608812B2/ja active Active
- 2014-10-15 SI SI201432051T patent/SI3057962T1/sl unknown
- 2014-10-15 CN CN201480056428.6A patent/CN105829302B/zh active Active
- 2014-10-15 EP EP23203529.5A patent/EP4324525A3/fr active Pending
- 2014-10-15 ES ES14854272T patent/ES2960953T3/es active Active
- 2014-10-15 PT PT148542723T patent/PT3057962T/pt unknown
- 2014-10-15 KR KR1020167011534A patent/KR102142177B1/ko active IP Right Grant
- 2014-10-15 WO PCT/US2014/060724 patent/WO2015057859A1/fr active Application Filing
- 2014-10-15 PL PL14854272.3T patent/PL3057962T3/pl unknown
- 2014-10-15 MY MYPI2016000542A patent/MY179802A/en unknown
- 2014-10-15 SG SG11201602269QA patent/SG11201602269QA/en unknown
- 2014-10-15 PE PE2016000506A patent/PE20161273A1/es unknown
- 2014-10-15 AU AU2014337300A patent/AU2014337300B2/en active Active
- 2014-10-15 FI FIEP14854272.3T patent/FI3057962T3/fi active
- 2014-10-15 DK DK14854272.3T patent/DK3057962T3/da active
- 2014-10-15 EA EA201690650A patent/EA038869B1/ru unknown
- 2014-10-15 MX MX2016004703A patent/MX2016004703A/es active IP Right Grant
- 2014-10-15 HU HUE14854272A patent/HUE063984T2/hu unknown
- 2014-10-15 EP EP14854272.3A patent/EP3057962B1/fr active Active
- 2014-10-15 CA CA2925889A patent/CA2925889C/fr active Active
- 2014-10-15 MA MA38949A patent/MA38949A1/fr unknown
- 2014-10-15 SG SG10201901977XA patent/SG10201901977XA/en unknown
- 2014-10-15 US US15/029,848 patent/US10040782B2/en active Active
- 2014-10-15 LT LTEPPCT/US2014/060724T patent/LT3057962T/lt unknown
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2016
- 2016-03-28 IL IL244787A patent/IL244787B/en unknown
- 2016-04-13 CL CL2016000866A patent/CL2016000866A1/es unknown
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2018
- 2018-06-05 US US16/000,539 patent/US10710987B2/en active Active
- 2018-12-11 JP JP2018231817A patent/JP2019052181A/ja 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
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