MA37896A1 - Azahétérocycles utilisés comme inhibiteurs de bir2 et/ou bir3 - Google Patents
Azahétérocycles utilisés comme inhibiteurs de bir2 et/ou bir3Info
- Publication number
- MA37896A1 MA37896A1 MA37896A MA37896A MA37896A1 MA 37896 A1 MA37896 A1 MA 37896A1 MA 37896 A MA37896 A MA 37896A MA 37896 A MA37896 A MA 37896A MA 37896 A1 MA37896 A1 MA 37896A1
- Authority
- MA
- Morocco
- Prior art keywords
- azaheterocycles
- bir2
- bir3
- inhibitors
- compounds
- Prior art date
Links
- 101100111639 Caenorhabditis elegans bir-2 gene Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/4035—Isoindoles, e.g. phthalimide
-
- 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
- A61K31/47—Quinolines; Isoquinolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
- C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur 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
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0806—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La présente invention concerne des composés de formule (i) ou leurs sels de qualité pharmaceutique, dans laquelle r
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261683253P | 2012-08-15 | 2012-08-15 | |
| PCT/EP2013/066458 WO2014026882A1 (fr) | 2012-08-15 | 2013-08-06 | Azahétérocycles utilisés comme inhibiteurs de bir2 et/ou bir3 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA37896A1 true MA37896A1 (fr) | 2016-09-30 |
Family
ID=48948413
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA37896A MA37896A1 (fr) | 2012-08-15 | 2013-08-06 | Azahétérocycles utilisés comme inhibiteurs de bir2 et/ou bir3 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US9422332B2 (fr) |
| EP (1) | EP2885275A1 (fr) |
| JP (1) | JP6203261B2 (fr) |
| KR (1) | KR20150042792A (fr) |
| CN (1) | CN104540806B (fr) |
| AU (1) | AU2013304214A1 (fr) |
| BR (1) | BR112015003201A2 (fr) |
| CA (1) | CA2878106A1 (fr) |
| CL (1) | CL2015000333A1 (fr) |
| CO (1) | CO7180196A2 (fr) |
| CR (1) | CR20150041A (fr) |
| EA (1) | EA201590347A1 (fr) |
| IL (1) | IL237063A0 (fr) |
| MA (1) | MA37896A1 (fr) |
| MX (1) | MX2015001905A (fr) |
| PE (1) | PE20150674A1 (fr) |
| PH (1) | PH12015500185A1 (fr) |
| SG (1) | SG11201500581WA (fr) |
| WO (1) | WO2014026882A1 (fr) |
| ZA (1) | ZA201500342B (fr) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016079527A1 (fr) | 2014-11-19 | 2016-05-26 | Tetralogic Birinapant Uk Ltd | Polythérapie |
| WO2016097773A1 (fr) | 2014-12-19 | 2016-06-23 | Children's Cancer Institute | Antagonistes des iap thérapeutiques pour traiter des troubles prolifératifs |
| CN109476631B (zh) * | 2016-03-22 | 2021-04-06 | 国家健康与医学研究院 | 新衍生物及其作为胱天蛋白酶-2的选择性抑制剂的用途 |
| WO2017194390A1 (fr) * | 2016-05-09 | 2017-11-16 | F. Hoffmann-La Roche Ag | Composés dimères |
| CN106265764B (zh) | 2016-08-18 | 2018-03-16 | 广州威溶特医药科技有限公司 | Iap抑制剂和溶瘤病毒在制备抗肿瘤药物中的应用 |
| TW202500133A (zh) * | 2023-03-14 | 2025-01-01 | 美商賽堤爾醫療公司 | 3﹐4-稠合雙環吡咯啶及3﹐4-稠合雙環吡咯啶酮化合物 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0513310A (pt) * | 2004-07-12 | 2008-05-06 | Idun Pharmaceuticals Inc | análogos de tetrapeptìdeo |
| CN101094833A (zh) * | 2004-07-12 | 2007-12-26 | 伊邓药品公司 | 四肽类似物 |
| CA2789879A1 (fr) * | 2009-10-28 | 2011-05-19 | Joyant Pharmaceuticals, Inc. | Mimetiques dimeres de smac |
-
2013
- 2013-08-06 PE PE2015000194A patent/PE20150674A1/es not_active Application Discontinuation
- 2013-08-06 MX MX2015001905A patent/MX2015001905A/es unknown
- 2013-08-06 MA MA37896A patent/MA37896A1/fr unknown
- 2013-08-06 EA EA201590347A patent/EA201590347A1/ru unknown
- 2013-08-06 US US14/419,288 patent/US9422332B2/en not_active Expired - Fee Related
- 2013-08-06 SG SG11201500581WA patent/SG11201500581WA/en unknown
- 2013-08-06 CA CA2878106A patent/CA2878106A1/fr not_active Abandoned
- 2013-08-06 EP EP13745838.6A patent/EP2885275A1/fr not_active Withdrawn
- 2013-08-06 AU AU2013304214A patent/AU2013304214A1/en not_active Abandoned
- 2013-08-06 KR KR20157003782A patent/KR20150042792A/ko not_active Withdrawn
- 2013-08-06 CN CN201380035682.3A patent/CN104540806B/zh not_active Expired - Fee Related
- 2013-08-06 JP JP2015526932A patent/JP6203261B2/ja not_active Expired - Fee Related
- 2013-08-06 WO PCT/EP2013/066458 patent/WO2014026882A1/fr not_active Ceased
- 2013-08-06 BR BR112015003201A patent/BR112015003201A2/pt active Search and Examination
-
2015
- 2015-01-16 ZA ZA2015/00342A patent/ZA201500342B/en unknown
- 2015-01-28 CO CO15017272A patent/CO7180196A2/es unknown
- 2015-01-28 PH PH12015500185A patent/PH12015500185A1/en unknown
- 2015-01-29 CR CR20150041A patent/CR20150041A/es unknown
- 2015-02-02 IL IL237063A patent/IL237063A0/en unknown
- 2015-02-11 CL CL2015000333A patent/CL2015000333A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP6203261B2 (ja) | 2017-09-27 |
| IL237063A0 (en) | 2015-03-31 |
| WO2014026882A1 (fr) | 2014-02-20 |
| CA2878106A1 (fr) | 2014-02-20 |
| BR112015003201A2 (pt) | 2017-07-04 |
| KR20150042792A (ko) | 2015-04-21 |
| SG11201500581WA (en) | 2015-04-29 |
| CR20150041A (es) | 2015-03-13 |
| AU2013304214A1 (en) | 2015-02-12 |
| US20150210739A1 (en) | 2015-07-30 |
| HK1209427A1 (en) | 2016-04-01 |
| MX2015001905A (es) | 2015-06-05 |
| CO7180196A2 (es) | 2015-02-09 |
| PH12015500185B1 (en) | 2015-04-20 |
| US9422332B2 (en) | 2016-08-23 |
| PE20150674A1 (es) | 2015-05-06 |
| CL2015000333A1 (es) | 2015-11-06 |
| CN104540806A (zh) | 2015-04-22 |
| PH12015500185A1 (en) | 2015-04-20 |
| ZA201500342B (en) | 2017-09-27 |
| JP2015526436A (ja) | 2015-09-10 |
| CN104540806B (zh) | 2017-05-03 |
| EP2885275A1 (fr) | 2015-06-24 |
| EA201590347A1 (ru) | 2015-05-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA37142A3 (fr) | Dérivés de dihydro-benzo-oxazine et de dihydro-pyrido-oxazine | |
| MA34644B1 (fr) | Dérivés de pyrazole aminopyrimidine en tant que modulateurs du lrrk2 | |
| EA201201663A1 (ru) | Производные 2-(ариламино)-3н-имидазо[4,5-b]пиридин-6-карбоксамида и их применение в качестве ингибиторов mpges-1 | |
| MA38050A1 (fr) | Inhibiteurs de gdf-8 | |
| MA39172A1 (fr) | Dérivés bicycliques hétérocycliques comme inhibiteurs de bromodomaines | |
| MA35089B1 (fr) | Inhibiteurs de la production de leucotrienes de type benzodioxane | |
| EA201590224A1 (ru) | Имидазотриазинкарбонитрилы, используемые в качестве ингибиторов киназы | |
| UA110612C2 (uk) | Похідні 1-аміно-2-циклопропілетилборонової кислоти | |
| MA33492B1 (fr) | Inhibiteurs de bace | |
| EA201290632A1 (ru) | Производные бетулина | |
| EA201590879A1 (ru) | Арилконденсированные и гетероарилконденсированные лактамы | |
| EA201490493A1 (ru) | Пирано[3,2-d][1,3]тиазол в качестве ингибиторов гликозидазы | |
| BR112013016595A2 (pt) | inibidores de neprilisina | |
| EA201400412A1 (ru) | ЗАМЕЩЕННЫЕ БЕНЗИЛИНДАЗОЛЫ ДЛЯ ПРИМЕНЕНИЯ В КАЧЕСТВЕ ИНГИБИТОРОВ Bub1 КИНАЗЫ ДЛЯ ЛЕЧЕНИЯ ГИПЕРПРОЛИФЕРАТИВНЫХ ЗАБОЛЕВАНИЙ | |
| EA201492287A1 (ru) | Дейтерированные производные руксолитиниба | |
| EA201300684A1 (ru) | Производные 6-амино-2-фениламино-1н-бензимидазол-5-карбоксамида и их применение в качестве ингибиторов микросомной простагландин-е2-синтазы-1 | |
| EA201291073A1 (ru) | Производные транилципромина в качестве ингибиторов гистон деметилаз lsd1 и/или lsd2 | |
| MX390726B (es) | Procesos para preparar compuestos de quinolina y composiciones farmaceuticas que contienen tales compuestos. | |
| EA201491936A1 (ru) | Азотсодержащее гетероциклическое соединение | |
| MA39152B1 (fr) | Cyclopentanes substitués en 1,2 utilisés comme antagonistes du récepteur d'orexine | |
| MA38645A1 (fr) | Nouveaux inhibiteurs de cyp17/antiandrogènes | |
| PH12013502516A1 (en) | Derivatives of 1-phenyl-2-pyridinyl alkyl alcohols as phosphodiesterase inhibitors | |
| EA201170997A1 (ru) | Производные индола в качестве противораковых агентов | |
| EA201300282A1 (ru) | Производные триазолопиразина | |
| BR112015012825A2 (pt) | piridopirazinas substituídas como inibidores de syk |