MA30268B1 - Derive polycyclique de cinnamide - Google Patents
Derive polycyclique de cinnamideInfo
- Publication number
- MA30268B1 MA30268B1 MA31220A MA31220A MA30268B1 MA 30268 B1 MA30268 B1 MA 30268B1 MA 31220 A MA31220 A MA 31220A MA 31220 A MA31220 A MA 31220A MA 30268 B1 MA30268 B1 MA 30268B1
- Authority
- MA
- Morocco
- Prior art keywords
- cinnamide
- polycyclic derivative
- novel pharmaceutical
- polycyclic
- derivative
- Prior art date
Links
- APEJMQOBVMLION-VOTSOKGWSA-N trans-cinnamamide Chemical class NC(=O)\C=C\C1=CC=CC=C1 APEJMQOBVMLION-VOTSOKGWSA-N 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- DJMJHIKGMVJYCW-UHFFFAOYSA-N 2-aminoethanol 3-[3-[[2-(3,4-dimethylphenyl)-5-methyl-3-oxo-1H-pyrazol-4-yl]diazenyl]-2-hydroxyphenyl]benzoic acid Chemical compound CC1=C(C=C(C=C1)N2C(=O)C(=C(N2)C)N=NC3=CC=CC(=C3O)C4=CC(=CC=C4)C(=O)O)C.C(CO)N.C(CO)N DJMJHIKGMVJYCW-UHFFFAOYSA-N 0.000 abstract 1
- -1 3,4-dimethylphenyl Chemical group 0.000 abstract 1
- 229960001827 eltrombopag olamine Drugs 0.000 abstract 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- C07D403/02—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 two hetero rings
- C07D403/10—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 two hetero rings linked by a carbon chain containing aromatic rings
-
- 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
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurosurgery (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
«Composition pharmaceutique nouvelle» Il est révélé des compositions pharmaceutiques nouvelles contenant de l'acide 3'-[(2Z)-[1-(3,4-diméthylphényl)-1,5-dihydro-3-méthyl-5-oxo-4H-pyrazole-4-ylidène]hydrazino]-2'-hydroxy-[1,1'-biphényl]-3-carboxylique bis-(monoéthanolamine) (eltrombopag olamine) et des procédés pour leur préparation.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US78051706P | 2006-03-09 | 2006-03-09 | |
| JP2006063562 | 2006-03-09 | ||
| US86170206P | 2006-11-30 | 2006-11-30 | |
| JP2006322728 | 2006-11-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30268B1 true MA30268B1 (fr) | 2009-03-02 |
Family
ID=38474999
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31220A MA30268B1 (fr) | 2006-03-09 | 2008-09-08 | Derive polycyclique de cinnamide |
Country Status (15)
| Country | Link |
|---|---|
| EP (1) | EP1992618B1 (fr) |
| KR (1) | KR101464651B1 (fr) |
| AR (1) | AR059955A1 (fr) |
| AU (1) | AU2007223158B2 (fr) |
| CA (1) | CA2643796A1 (fr) |
| CY (1) | CY1112767T1 (fr) |
| EA (1) | EA016464B1 (fr) |
| GE (1) | GEP20115139B (fr) |
| HN (1) | HN2008001374A (fr) |
| HR (1) | HRP20120174T1 (fr) |
| IL (1) | IL193770A (fr) |
| MA (1) | MA30268B1 (fr) |
| MX (1) | MX2008011221A (fr) |
| PL (1) | PL1992618T3 (fr) |
| WO (1) | WO2007102580A1 (fr) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1757591A4 (fr) | 2004-05-26 | 2010-05-05 | Eisai R&D Man Co Ltd | Composé de cinnamide |
| CN100577657C (zh) | 2004-10-26 | 2010-01-06 | 卫材R&D管理有限公司 | 肉桂酰胺化合物的无定形物 |
| TWI370130B (en) | 2005-11-24 | 2012-08-11 | Eisai R&D Man Co Ltd | Two cyclic cinnamide compound |
| MY144960A (en) | 2005-11-24 | 2011-11-30 | Eisai R&D Man Co Ltd | Morpholine type cinnamide compound |
| TWI378091B (en) | 2006-03-09 | 2012-12-01 | Eisai R&D Man Co Ltd | Multi-cyclic cinnamide derivatives |
| AR062095A1 (es) | 2006-07-28 | 2008-10-15 | Eisai R&D Man Co Ltd | Profarmaco de compuesto cinamida |
| WO2008097538A1 (fr) * | 2007-02-08 | 2008-08-14 | Merck & Co., Inc. | Agents thérapeutiques |
| TW200848054A (en) | 2007-02-28 | 2008-12-16 | Eisai R&D Man Co Ltd | Two cyclic oxomorpholine derivatives |
| CA2686754C (fr) | 2007-05-11 | 2014-10-28 | F. Hoffmann-La Roche Ag | Hetarylanilines en tant que modulateurs de l'amyloide beta |
| EP2152695A2 (fr) * | 2007-06-01 | 2010-02-17 | Schering Corporation | Modulateurs de sécrétase gamma |
| US7935815B2 (en) * | 2007-08-31 | 2011-05-03 | Eisai R&D Management Co., Ltd. | Imidazoyl pyridine compounds and salts thereof |
| MY150507A (en) | 2007-08-31 | 2014-01-30 | Eisai R&D Man Co Ltd | Polycyclic compound |
| WO2009061699A1 (fr) * | 2007-11-05 | 2009-05-14 | Schering Corporation | Modulateurs de gamma-secrétase |
| US20100298372A1 (en) * | 2007-12-11 | 2010-11-25 | Schering Corporation | Gamma secretase modulators |
| WO2009086277A1 (fr) | 2007-12-20 | 2009-07-09 | Envivo Pharmaceuticals, Inc. | Benzènes tétrasubstitués |
| BRPI0821141A2 (pt) | 2007-12-21 | 2015-06-16 | Hoffmann La Roche | Derivados de heteroarila como antagonistas do receptor de orexina |
| US7923450B2 (en) | 2008-01-11 | 2011-04-12 | Hoffmann-La Roche Inc. | Modulators for amyloid beta |
| MX2010008700A (es) | 2008-02-22 | 2010-08-30 | Hoffmann La Roche | Moduladores de beta-amiloide. |
| EP2324009A1 (fr) * | 2008-08-27 | 2011-05-25 | Eisai R&D Management Co., Ltd. | Procédé de préparation de certains composés de cinnamide |
| EP2334665B1 (fr) | 2008-10-09 | 2013-07-10 | F. Hoffmann-La Roche AG | Modulateurs pour l'amyloïde bêta |
| US20110263529A1 (en) * | 2008-11-06 | 2011-10-27 | Ruo Xu | Gamma secretase modulators |
| AU2009313527A1 (en) * | 2008-11-06 | 2010-05-14 | Merck Sharp & Dohme Corp. | Gamma secretase modulators |
| CN102209537A (zh) | 2008-11-10 | 2011-10-05 | 弗·哈夫曼-拉罗切有限公司 | 杂环γ分泌酶调节剂 |
| CA2742472A1 (fr) * | 2008-11-13 | 2010-05-20 | Schering Corporation | Modulateurs de gamma secretase |
| JP2012513399A (ja) | 2008-12-22 | 2012-06-14 | シェーリング コーポレイション | γ−セクレターゼ調節剤 |
| TW201030002A (en) | 2009-01-16 | 2010-08-16 | Bristol Myers Squibb Co | Bicyclic compounds for the reduction of beta-amyloid production |
| CA2749702A1 (fr) | 2009-02-26 | 2010-09-02 | Eisai R&D Management Co., Ltd. | Sel de derive de tetrahydrotriazolopyridine et ses cristaux |
| JP2012051805A (ja) | 2009-02-26 | 2012-03-15 | Eisai R & D Management Co Ltd | テトラヒドロトリアゾロピリジン誘導体の製造方法 |
| JP2012051807A (ja) * | 2009-02-26 | 2012-03-15 | Eisai R & D Management Co Ltd | アリールイミダゾール化合物 |
| JP2012121809A (ja) * | 2009-02-26 | 2012-06-28 | Eisai R & D Management Co Ltd | 多環式化合物の製造法およびその中間体 |
| US8754100B2 (en) * | 2009-02-26 | 2014-06-17 | Eisai R&D Management Co., Ltd. | Nitrogen-containing fused heterocyclic compounds and their use as beta amyloid production inhibitors |
| WO2011007756A1 (fr) | 2009-07-13 | 2011-01-20 | 武田薬品工業株式会社 | Composé hétérocyclique et son utilisation |
| US8871760B2 (en) * | 2009-09-21 | 2014-10-28 | Roche Palo Alto Llc | [1,2,4]triazolo[3,4-C][1,4]oxazines as P2X7 modulators |
| EP2523955B1 (fr) | 2010-01-15 | 2014-07-16 | Janssen Pharmaceuticals, Inc. | Nouveaux dérivés de triazole en tant que modulateurs de la secrétase gamma |
| US8486967B2 (en) | 2010-02-17 | 2013-07-16 | Hoffmann-La Roche Inc. | Heteroaryl substituted piperidines |
| US8513230B2 (en) | 2010-03-05 | 2013-08-20 | Karyopharm Therapeutics, Inc. | Nuclear transport modulators and uses thereof |
| US8901309B2 (en) * | 2010-09-02 | 2014-12-02 | Takeda Pharmaceutical Company Limited | Fused triazoles for the treatment or prophylaxis of mild cognitive impairment |
| JP2014012641A (ja) * | 2010-10-29 | 2014-01-23 | Dainippon Sumitomo Pharma Co Ltd | 新規ピリジン誘導体 |
| JP6106605B2 (ja) * | 2011-01-17 | 2017-04-05 | カリオファーム セラピューティクス,インコーポレイテッド | オレフィン含有核輸送調節剤およびその使用 |
| CN110372673B (zh) | 2011-07-29 | 2023-10-03 | 卡尔约药物治疗公司 | 含酰肼的核运输调节剂及其用途 |
| SG10201609097PA (en) | 2011-07-29 | 2016-12-29 | Karyopharm Therapeutics Inc | Nuclear transport modulators and uses thereof |
| WO2013055793A1 (fr) | 2011-10-12 | 2013-04-18 | University Of Pittsburg-Of The Commonwealth System Of Higher Education | Petites molécules ciblant la localisation et/ou le niveau nucléaire des récepteurs de l'androgène dans le cancer de la prostate |
| SG11201407268SA (en) | 2012-05-09 | 2015-01-29 | Karyopharm Therapeutics Inc | Nuclear transport modulators and uses thereof |
| CN104583208B (zh) | 2012-05-16 | 2016-09-28 | 杨森制药公司 | 可用于治疗(尤其是)阿尔茨海默病的取代的3,4-二氢-2H-吡啶并[1,2-a]吡嗪-1,6-二酮衍生物 |
| EP2687528A1 (fr) * | 2012-07-17 | 2014-01-22 | Ares Trading S.A. | Dérivés de triazole fusionnés comme modulateurs de gamma-sécrétase |
| WO2014096212A1 (fr) | 2012-12-20 | 2014-06-26 | Janssen Pharmaceutica Nv | Dérivés d'un nouveau type de 3,4-dihydro-2h-pyrido[1,2-α]pyrazine-1,6-dione tricyclique en tant que modulateurs de la gamma sécrétase |
| KR102171710B1 (ko) | 2013-01-17 | 2020-10-30 | 얀센 파마슈티카 엔.브이. | 감마 세크레타제 조절 인자로서의 신규 치환 피리도-피페라지논 유도체 |
| EP2968278B8 (fr) | 2013-03-15 | 2019-05-22 | Karyopharm Therapeutics Inc. | Procédés de promotion de la cicatrisation d'une plaie à l'aide d'inhibiteurs de crm1 |
| ES2724275T3 (es) | 2013-06-21 | 2019-09-09 | Karyopharm Therapeutics Inc | 1,2,4-triazoles como moduladores del transporte nuclear y usos de los mismos |
| CA2924527C (fr) | 2013-09-20 | 2022-07-12 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Composes destines au traitement du cancer de la prostate |
| US20160257657A1 (en) | 2013-09-20 | 2016-09-08 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Small molecule inhibitors of the nuclear translocation of androgen receptor for the treatment of castration-resistant prostate cancer |
| US10562897B2 (en) | 2014-01-16 | 2020-02-18 | Janssen Pharmaceutica Nv | Substituted 3,4-dihydro-2H-pyrido[1,2-a]pyrazine-1,6-diones as gamma secretase modulators |
| KR102608259B1 (ko) | 2014-08-15 | 2023-11-29 | 카리오팜 쎄라퓨틱스, 인코포레이티드 | 셀리넥소의 다형태 |
| EP3397633A1 (fr) | 2015-12-31 | 2018-11-07 | Karyopharm Therapeutics, Inc. | Modulateurs de transport nucléaire et leurs utilisations |
| WO2017117535A1 (fr) | 2015-12-31 | 2017-07-06 | Karyopharm Therapeutics Inc. | Modulateurs de transport nucléaire et leurs utilisations |
| CN113332292A (zh) * | 2016-02-23 | 2021-09-03 | 辉瑞公司 | 6,7-二氢-5H-吡唑并[5,1-b][1,3]噁嗪-2-甲酰胺化合物 |
| US10980806B2 (en) | 2016-03-24 | 2021-04-20 | University of Pittsburgh—of the Commonwealth System of Higher Education | Small molecule inhibitors of the nuclear translocation of androgen receptor for the treatment of castration-resistant prostate cancer |
| WO2018098472A1 (fr) | 2016-11-28 | 2018-05-31 | Karyopharm Therapeutics Inc. | Inhibiteurs de crm1 pour le traitement de l'épilepsie |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ525917A (en) * | 2000-12-04 | 2005-11-25 | F | Phenylethenyl or phenylethinyl derivatives as glutamate receptor antagonists and their use in treating mGLuR5 receptor mediated disorders |
| US20040192743A1 (en) * | 2003-02-12 | 2004-09-30 | Mjalli Adnan M.M. | Substituted azole derivatives as therapeutic agents |
| AU2005214349B2 (en) * | 2004-02-12 | 2011-11-03 | Transtech Pharma, Inc. | Substituted azole derivatives, compositions, and methods of use |
| EP1757591A4 (fr) * | 2004-05-26 | 2010-05-05 | Eisai R&D Man Co Ltd | Composé de cinnamide |
-
2007
- 2007-03-08 AR ARP070100958A patent/AR059955A1/es not_active Application Discontinuation
- 2007-03-08 MX MX2008011221A patent/MX2008011221A/es active IP Right Grant
- 2007-03-08 GE GEAP200710893A patent/GEP20115139B/en unknown
- 2007-03-08 CA CA002643796A patent/CA2643796A1/fr not_active Abandoned
- 2007-03-08 EA EA200870336A patent/EA016464B1/ru not_active IP Right Cessation
- 2007-03-08 KR KR1020087023309A patent/KR101464651B1/ko not_active Expired - Fee Related
- 2007-03-08 AU AU2007223158A patent/AU2007223158B2/en not_active Ceased
- 2007-03-08 HR HR20120174T patent/HRP20120174T1/hr unknown
- 2007-03-08 WO PCT/JP2007/054532 patent/WO2007102580A1/fr not_active Ceased
- 2007-03-08 PL PL07738023T patent/PL1992618T3/pl unknown
- 2007-03-08 EP EP07738023A patent/EP1992618B1/fr active Active
-
2008
- 2008-08-28 IL IL193770A patent/IL193770A/en not_active IP Right Cessation
- 2008-09-05 HN HN2008001374A patent/HN2008001374A/es unknown
- 2008-09-08 MA MA31220A patent/MA30268B1/fr unknown
-
2012
- 2012-02-16 CY CY20121100165T patent/CY1112767T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GEP20115139B (en) | 2011-01-10 |
| AU2007223158B2 (en) | 2012-04-12 |
| EA016464B1 (ru) | 2012-05-30 |
| IL193770A0 (en) | 2009-05-04 |
| IL193770A (en) | 2012-10-31 |
| AU2007223158A1 (en) | 2007-09-13 |
| KR101464651B1 (ko) | 2014-11-24 |
| CY1112767T1 (el) | 2016-02-10 |
| HN2008001374A (es) | 2011-03-15 |
| WO2007102580A1 (fr) | 2007-09-13 |
| CA2643796A1 (fr) | 2007-09-13 |
| PL1992618T3 (pl) | 2012-06-29 |
| AR059955A1 (es) | 2008-05-14 |
| EP1992618A1 (fr) | 2008-11-19 |
| HK1122027A1 (en) | 2009-05-08 |
| EA200870336A1 (ru) | 2009-02-27 |
| KR20080108481A (ko) | 2008-12-15 |
| EP1992618B1 (fr) | 2012-01-18 |
| HRP20120174T1 (hr) | 2012-03-31 |
| EP1992618A4 (fr) | 2010-11-10 |
| HK1128085A1 (en) | 2009-10-16 |
| MX2008011221A (es) | 2008-09-11 |
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