CR10440A - Polimorfos de n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-yl)etil]amino]metil]fenil]2e-2-propenamida - Google Patents
Polimorfos de n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-yl)etil]amino]metil]fenil]2e-2-propenamidaInfo
- Publication number
- CR10440A CR10440A CR10440A CR10440A CR10440A CR 10440 A CR10440 A CR 10440A CR 10440 A CR10440 A CR 10440A CR 10440 A CR10440 A CR 10440A CR 10440 A CR10440 A CR 10440A
- Authority
- CR
- Costa Rica
- Prior art keywords
- methyl
- indol
- hydroxy
- phenyl
- ethyl
- Prior art date
Links
- -1 2-METHYL-1H-INDOL-3-YL Chemical class 0.000 title abstract 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 title 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 title 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 title 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000012458 free base Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/20—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
- C07D209/16—Tryptamines
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
-
- 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
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- 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
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Indole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Epidemiology (AREA)
Abstract
Se preparan por varios procedimientos formas polimórficas de base libre de N-hidroxi-3-[4-[[[2-(2-metil-1H-indol-3-il)etil]amino]-metil]fenil]-2E-2-propenamida y sales de la misma.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80451706P | 2006-06-12 | 2006-06-12 | |
| US88322407P | 2007-01-03 | 2007-01-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CR10440A true CR10440A (es) | 2011-08-22 |
Family
ID=38832679
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CR10440A CR10440A (es) | 2006-06-12 | 2008-11-13 | Polimorfos de n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-yl)etil]amino]metil]fenil]2e-2-propenamida |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US7989494B2 (es) |
| EP (2) | EP2086930A2 (es) |
| JP (3) | JP2009540006A (es) |
| KR (4) | KR20160032264A (es) |
| CN (1) | CN102584673B (es) |
| AR (1) | AR061297A1 (es) |
| AU (1) | AU2007257881B2 (es) |
| BR (1) | BRPI0712993A2 (es) |
| CA (1) | CA2650263A1 (es) |
| CL (1) | CL2007001689A1 (es) |
| CR (1) | CR10440A (es) |
| EA (1) | EA017984B1 (es) |
| EC (1) | ECSP088976A (es) |
| GE (1) | GEP20115175B (es) |
| GT (1) | GT200800280A (es) |
| IL (1) | IL195015A (es) |
| MA (1) | MA30511B1 (es) |
| ME (1) | ME00529B (es) |
| MX (1) | MX2008015900A (es) |
| MY (1) | MY149337A (es) |
| NI (1) | NI200800306A (es) |
| NO (1) | NO20090135L (es) |
| PE (1) | PE20080852A1 (es) |
| PH (2) | PH12012501724A1 (es) |
| SM (1) | SMP200900001B (es) |
| TN (1) | TNSN08495A1 (es) |
| TW (2) | TWI515179B (es) |
| UY (1) | UY30406A1 (es) |
| WO (1) | WO2007146716A2 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ572547A (en) * | 2006-06-12 | 2011-06-30 | Novartis Ag | SALTS OF N-HYDROXY-3-[4-[[[2-(2-METHYL-1H-INDOL-3-yl)ETHYL]AMINO]METHYL]PHENYL]-2E-2-PROPENAMIDE |
| AU2008204928B2 (en) * | 2007-01-10 | 2011-03-31 | Novartis Ag | Formulations of deacetylase inhibitors |
| WO2017032281A1 (zh) * | 2015-08-21 | 2017-03-02 | 苏州晶云药物科技有限公司 | 帕比司他乳酸盐的新晶型 |
| CN106866492B (zh) * | 2015-12-10 | 2021-11-26 | 江苏豪森药业集团有限公司 | 帕比司他乳酸盐晶型ii及其制备方法和用途 |
| CN106866491B (zh) * | 2015-12-10 | 2021-12-10 | 江苏豪森药业集团有限公司 | 帕比司他乳酸盐晶型ⅰ及其制备方法和用途 |
| WO2018092151A1 (en) * | 2016-11-21 | 2018-05-24 | Msn Laboratories Private Limited, R&D Center | Process for the preparation of 2-(e)-n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl) ethyl]amino]methyl]phenyl]-2-propenamide 2-hydroxypropanoic acid (1:1) and its polymorphs thereof |
| WO2018163114A1 (en) * | 2017-03-10 | 2018-09-13 | Shilpa Medicare Limited | Amorphous panobinostat and its lactate salt |
| US10537585B2 (en) | 2017-12-18 | 2020-01-21 | Dexcel Pharma Technologies Ltd. | Compositions comprising dexamethasone |
| MX2022001820A (es) * | 2019-08-20 | 2022-03-17 | Ono Pharmaceutical Co | Sal y forma cristalina de un compuesto que tiene actividad agonista para el receptor 5 de esfingosina-1-fosfato [acido (2s,3r,4e)-2-amino-3-hidroxioctadeca-4-enil-1-fosforico (s1p5). |
| GB201913124D0 (en) | 2019-09-11 | 2019-10-23 | Seald As | Compositions and methods for treatment of cholangiocarcinoma |
| GB201913122D0 (en) | 2019-09-11 | 2019-10-23 | Seald As | Compositions and methods for treatment of cholangiocarcinoma |
| GB201913121D0 (en) | 2019-09-11 | 2019-10-23 | Seald As | Compositions and methods for treatment of cholangiocarcinoma |
| AU2021368107A1 (en) * | 2020-10-28 | 2023-06-22 | Viracta Subsidiary, Inc. | Hdac inhibitor solid state forms |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20020354A1 (es) * | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
| ATE352319T1 (de) | 2001-11-06 | 2007-02-15 | Novartis Pharma Gmbh | Kombination cyclooxygenase-2 inhibitor/ histone deacetylase inhibitor |
| AU2002361022A1 (en) | 2001-12-07 | 2003-06-17 | Novartis Ag | Use of alpha-tubulin acetylation levels as a biomarker for protein deacetylase inhibitors |
| MXPA05012464A (es) | 2003-05-21 | 2006-01-30 | Novartis Ag | Combinacion de inhibidores de deacetilasa de histona con agentes quimioterapeuticos. |
| JP2007501775A (ja) | 2003-08-07 | 2007-02-01 | ノバルティス アクチエンゲゼルシャフト | 免疫抑制剤としてのヒストンデアセチラーゼ阻害剤 |
| US20080085902A1 (en) | 2003-09-23 | 2008-04-10 | Guido Bold | Combination Of A Vegf Receptor Inhibitor Or With A Chemotherapeutic Agent |
| NZ572547A (en) | 2006-06-12 | 2011-06-30 | Novartis Ag | SALTS OF N-HYDROXY-3-[4-[[[2-(2-METHYL-1H-INDOL-3-yl)ETHYL]AMINO]METHYL]PHENYL]-2E-2-PROPENAMIDE |
-
2007
- 2007-06-07 ME MEP-2008-876A patent/ME00529B/me unknown
- 2007-06-07 BR BRPI0712993-9A patent/BRPI0712993A2/pt not_active Application Discontinuation
- 2007-06-07 WO PCT/US2007/070561 patent/WO2007146716A2/en not_active Ceased
- 2007-06-07 JP JP2009515573A patent/JP2009540006A/ja active Pending
- 2007-06-07 US US12/302,564 patent/US7989494B2/en active Active
- 2007-06-07 AU AU2007257881A patent/AU2007257881B2/en not_active Ceased
- 2007-06-07 SM SM200900001T patent/SMP200900001B/it unknown
- 2007-06-07 CA CA002650263A patent/CA2650263A1/en not_active Abandoned
- 2007-06-07 EA EA200802383A patent/EA017984B1/ru not_active IP Right Cessation
- 2007-06-07 GE GEAP200711011A patent/GEP20115175B/en unknown
- 2007-06-07 PH PH1/2012/501724A patent/PH12012501724A1/en unknown
- 2007-06-07 EP EP07798194A patent/EP2086930A2/en not_active Withdrawn
- 2007-06-07 KR KR1020167006197A patent/KR20160032264A/ko not_active Ceased
- 2007-06-07 CN CN201210014735.0A patent/CN102584673B/zh active Active
- 2007-06-07 EP EP11183770A patent/EP2409967A1/en not_active Withdrawn
- 2007-06-07 KR KR1020157017416A patent/KR20150082690A/ko not_active Withdrawn
- 2007-06-07 MX MX2008015900A patent/MX2008015900A/es active IP Right Grant
- 2007-06-07 KR KR1020087030229A patent/KR20090015968A/ko not_active Ceased
- 2007-06-07 KR KR1020147030218A patent/KR20140142335A/ko not_active Withdrawn
- 2007-06-07 MY MYPI20084896A patent/MY149337A/en unknown
- 2007-06-08 TW TW103124314A patent/TWI515179B/zh not_active IP Right Cessation
- 2007-06-08 AR ARP070102499A patent/AR061297A1/es not_active Application Discontinuation
- 2007-06-08 TW TW096120847A patent/TWI453196B/zh not_active IP Right Cessation
- 2007-06-08 PE PE2007000724A patent/PE20080852A1/es not_active Application Discontinuation
- 2007-06-11 UY UY30406A patent/UY30406A1/es not_active Application Discontinuation
- 2007-06-11 CL CL200701689A patent/CL2007001689A1/es unknown
-
2008
- 2008-10-30 IL IL195015A patent/IL195015A/en active IP Right Grant
- 2008-11-13 CR CR10440A patent/CR10440A/es not_active Application Discontinuation
- 2008-11-21 NI NI200800306A patent/NI200800306A/es unknown
- 2008-11-28 TN TNP2008000495A patent/TNSN08495A1/en unknown
- 2008-12-10 GT GT200800280A patent/GT200800280A/es unknown
- 2008-12-12 EC EC2008008976A patent/ECSP088976A/es unknown
- 2008-12-12 MA MA31470A patent/MA30511B1/fr unknown
-
2009
- 2009-01-09 NO NO20090135A patent/NO20090135L/no not_active Application Discontinuation
-
2012
- 2012-08-29 PH PH12012501725A patent/PH12012501725A1/en unknown
-
2013
- 2013-04-15 JP JP2013085093A patent/JP2013139476A/ja active Pending
-
2015
- 2015-06-24 JP JP2015127007A patent/JP2015164968A/ja active Pending
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal |