MA30000B1 - Nouvelle forme cristalline d'un derive de pyridazino [4,5-b] indole - Google Patents
Nouvelle forme cristalline d'un derive de pyridazino [4,5-b] indoleInfo
- Publication number
- MA30000B1 MA30000B1 MA30757A MA30757A MA30000B1 MA 30000 B1 MA30000 B1 MA 30000B1 MA 30757 A MA30757 A MA 30757A MA 30757 A MA30757 A MA 30757A MA 30000 B1 MA30000 B1 MA 30000B1
- Authority
- MA
- Morocco
- Prior art keywords
- pyridazino
- crystalline form
- novel crystalline
- indole derivative
- indole
- Prior art date
Links
- LDBZRFQWKQUHFF-UHFFFAOYSA-N 5h-pyridazino[4,5-b]indole Chemical class N1=NC=C2C3=CC=CC=C3NC2=C1 LDBZRFQWKQUHFF-UHFFFAOYSA-N 0.000 title 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 abstract 2
- IUUZMSMGSOUFTO-UHFFFAOYSA-N 2-indol-1-ylacetamide Chemical compound C1=CC=C2N(CC(=O)N)C=CC2=C1 IUUZMSMGSOUFTO-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- 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
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Hospice & Palliative Care (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
L'invention concerne une nouvelle forme cristalline de 7-chloro-N,N,5-triméthyle-4-oxo-3-phényle- 3,5-dihydro-4H-pyridazino[4,5--]indole-1-acétamide, des procédés de préparation de cette forme cristalline de 7-chloro-N,N,5-triméthyle-4-oxo-3-phényle-3,5-dihydro-4H-pyridazino[4,5-o]indole-1-acétamide, des compositions contenant cette forme mélangée à un ou plusieurs excipients acceptables sur le plan pharmaceutique, et utilisations associées.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71215305P | 2005-08-29 | 2005-08-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30000B1 true MA30000B1 (fr) | 2008-12-01 |
Family
ID=37546937
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA30757A MA30000B1 (fr) | 2005-08-29 | 2008-03-17 | Nouvelle forme cristalline d'un derive de pyridazino [4,5-b] indole |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US7683062B2 (fr) |
| EP (1) | EP1924585B1 (fr) |
| JP (1) | JP5063600B2 (fr) |
| KR (2) | KR20080050577A (fr) |
| CN (1) | CN101253176B (fr) |
| AR (1) | AR057099A1 (fr) |
| AT (1) | ATE531717T1 (fr) |
| AU (1) | AU2006285142B2 (fr) |
| BR (1) | BRPI0615259A2 (fr) |
| CA (1) | CA2619284C (fr) |
| CR (1) | CR9723A (fr) |
| CY (1) | CY1112317T1 (fr) |
| DK (1) | DK1924585T3 (fr) |
| EA (1) | EA014164B1 (fr) |
| EC (1) | ECSP088209A (fr) |
| ES (1) | ES2375841T3 (fr) |
| HR (1) | HRP20120073T1 (fr) |
| IL (1) | IL189276A (fr) |
| MA (1) | MA30000B1 (fr) |
| NO (1) | NO20081365L (fr) |
| NZ (1) | NZ566087A (fr) |
| PL (1) | PL1924585T3 (fr) |
| PT (1) | PT1924585E (fr) |
| RS (1) | RS52318B (fr) |
| SI (1) | SI1924585T1 (fr) |
| TN (1) | TNSN08059A1 (fr) |
| TW (1) | TW200813060A (fr) |
| UA (1) | UA91716C2 (fr) |
| UY (1) | UY29771A1 (fr) |
| WO (1) | WO2007027525A1 (fr) |
| ZA (1) | ZA200801890B (fr) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2545968C (fr) * | 2003-11-17 | 2010-03-09 | Merck Eprova Ag | Formes cristallines de dihydrochlorure de (6r)-l-erythro-tetrahydrobiopterine |
| US20070249827A1 (en) * | 2004-06-02 | 2007-10-25 | Sandoz Ag | Meropenem Intermediatein in Crystalling Form |
| EA018698B1 (ru) * | 2005-09-21 | 2013-10-30 | 4Сц Аг | Сульфонилпирролгидрохлориды как ингибиторы гистондезацетилазы |
| EP2404911A1 (fr) * | 2005-10-31 | 2012-01-11 | Janssen Pharmaceutica NV | Nouveaux procédés pour la préparation de dérivés de pipérazinyle et diazépanyle benzamide |
| MX2008016008A (es) * | 2006-06-16 | 2009-01-16 | Lundbeck & Co As H | Formas cristalinas de 4-[2-(4-metilfenilsulfonil)-fenil] piperidina con inhibicion combinada de la recaptacion de serotonina y norepinefrina para el tratamiento del dolor neuropatico. |
| NZ576347A (en) * | 2006-10-27 | 2011-10-28 | Signal Pharm Llc | Solid forms comprising 4-[9-(tetrahydro-furan-3-yl)-8-(2,4,6-trifluoro-phenylamino)-9h-purin-2-ylamino]-cyclohexan-1-ol, compositions thereof, and use therewith |
| EP2085397A1 (fr) * | 2008-01-21 | 2009-08-05 | Esteve Quimica, S.A. | Forme cristalline d'abacavir |
| US7935817B2 (en) * | 2008-03-31 | 2011-05-03 | Apotex Pharmachem Inc. | Salt form and cocrystals of adefovir dipivoxil and processes for preparation thereof |
| AR071318A1 (es) * | 2008-04-15 | 2010-06-09 | Basilea Pharmaceutica Ag | Benzhidril ester del acido (6r,7r)-7-{2-(5-amino-[1,2,4]tiadiazol-3-il)-2-[(z)-tritiloxiimino]-acetilamino}-3-[(r)-1'-terc-butoxicarbonil-2-oxo-[1,3']bipirrolidinil-(3e)-ilidenometil]-8-oxo-5-tia-1-aza-biciclo[4.2.0]oct-2-eno-2-carboxilico cristalino; su elaboracion y uso |
| US8097719B2 (en) * | 2008-07-15 | 2012-01-17 | Genesen Labs | Meropenem intermediate in novel crystalline form and a method of manufacture of meropenem |
| AU2009283039A1 (en) * | 2008-08-18 | 2010-02-25 | Sanofi-Aventis U.S. Llc | Process for preparing polymorph of 7-chloro-N, N,5-trimethyl-4-oxo-3-phenyl-3,5-dihydr0-4H-pyridazin0[4,5-b]indole-1-acetamide |
| NZ601967A (en) | 2010-03-12 | 2015-03-27 | Omeros Corp | Pde10 inhibitors and related compositions and methods |
| KR20130101524A (ko) * | 2010-09-01 | 2013-09-13 | 아레나 파마슈티칼스, 인크. | 5-ht2c 아고니스트의 비-흡습성 염 |
| WO2013044816A1 (fr) * | 2011-09-30 | 2013-04-04 | Sunshine Lake Pharma Co., Ltd. | Formes cristalline d'azilsartan et leur préparation et leurs utilisations |
| NZ716462A (en) * | 2014-04-28 | 2017-11-24 | Omeros Corp | Optically active pde10 inhibitor |
| NZ630810A (en) | 2014-04-28 | 2016-03-31 | Omeros Corp | Processes and intermediates for the preparation of a pde10 inhibitor |
| CA2980801A1 (fr) | 2015-04-24 | 2016-10-27 | Omeros Corporation | Inhibiteurs de pde10 ainsi que compositions et procedes associes |
| CA3003611C (fr) | 2015-11-04 | 2022-11-01 | Omeros Corporation | Formes solides d'un inhibiteur de pde10 |
| US20210393621A1 (en) | 2018-10-26 | 2021-12-23 | The Research Foundation For The State University Of New York | Combination serotonin specific reuptake inhibitor and serotonin 1a receptor partial agonist for reducing l-dopa-induced dyskinesia |
| CN111303230B (zh) * | 2020-03-09 | 2021-07-13 | 中国食品药品检定研究院 | 一种黄体酮共晶物及其制备方法和用途 |
| WO2026130526A1 (fr) * | 2024-12-20 | 2026-06-25 | 杭州百新生物医药科技有限公司 | Composé tricyclique et utilisation médicale de celui-ci |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2766823B1 (fr) * | 1997-07-30 | 1999-10-08 | Synthelabo | Derives de 4-oxo-3,5-dihydro-4h-pyridazino[4,5-b] indole-1-acetamide, leur preparation et leur application en therapeutique |
| FR2788696B1 (fr) * | 1999-01-26 | 2004-03-05 | Synthelabo | Utilisation de derives de pyridazino [4,5-b] indole-1-acetamide pour la preparation de medicaments destines aux maladies du systeme nerveux central |
| FR2829939B3 (fr) | 2001-09-21 | 2003-11-28 | Sanofi Synthelabo | Utilisation du 7-chloro-n,n,5-trimethyl-4-oxo-3-phenyl-3,5- dihydro-4h-pyridazino(4,5-b)indole-1-acetamide pour la preparation de medicaments destines au traitement de la polyarthrite rhumatoide |
| US20050220881A1 (en) | 2003-10-10 | 2005-10-06 | Bvm Holding Co. | Pharmaceutical composition |
-
2006
- 2006-08-24 PT PT06813757T patent/PT1924585E/pt unknown
- 2006-08-24 KR KR1020087004953A patent/KR20080050577A/ko not_active Abandoned
- 2006-08-24 AU AU2006285142A patent/AU2006285142B2/en not_active Ceased
- 2006-08-24 EP EP06813757A patent/EP1924585B1/fr active Active
- 2006-08-24 EA EA200800716A patent/EA014164B1/ru not_active IP Right Cessation
- 2006-08-24 WO PCT/US2006/033254 patent/WO2007027525A1/fr not_active Ceased
- 2006-08-24 JP JP2008529130A patent/JP5063600B2/ja not_active Expired - Fee Related
- 2006-08-24 KR KR1020137018636A patent/KR20130087059A/ko not_active Ceased
- 2006-08-24 ES ES06813757T patent/ES2375841T3/es active Active
- 2006-08-24 CN CN2006800314750A patent/CN101253176B/zh not_active Expired - Fee Related
- 2006-08-24 AT AT06813757T patent/ATE531717T1/de active
- 2006-08-24 HR HRP20120073TT patent/HRP20120073T1/hr unknown
- 2006-08-24 PL PL06813757T patent/PL1924585T3/pl unknown
- 2006-08-24 DK DK06813757.9T patent/DK1924585T3/da active
- 2006-08-24 BR BRPI0615259-7A patent/BRPI0615259A2/pt not_active IP Right Cessation
- 2006-08-24 UA UAA200803953A patent/UA91716C2/ru unknown
- 2006-08-24 SI SI200631252T patent/SI1924585T1/sl unknown
- 2006-08-24 ZA ZA200801890A patent/ZA200801890B/xx unknown
- 2006-08-24 RS RS20120032A patent/RS52318B/sr unknown
- 2006-08-24 CA CA2619284A patent/CA2619284C/fr not_active Expired - Fee Related
- 2006-08-24 NZ NZ566087A patent/NZ566087A/en not_active IP Right Cessation
- 2006-08-28 AR ARP060103740A patent/AR057099A1/es not_active Application Discontinuation
- 2006-08-29 TW TW095131681A patent/TW200813060A/zh unknown
- 2006-08-29 UY UY29771A patent/UY29771A1/es unknown
-
2008
- 2008-02-04 IL IL189276A patent/IL189276A/en not_active IP Right Cessation
- 2008-02-06 TN TNP2008000059A patent/TNSN08059A1/en unknown
- 2008-02-11 CR CR9723A patent/CR9723A/es unknown
- 2008-02-14 US US12/031,243 patent/US7683062B2/en not_active Expired - Fee Related
- 2008-02-20 EC EC2008008209A patent/ECSP088209A/es unknown
- 2008-03-14 NO NO20081365A patent/NO20081365L/no not_active Application Discontinuation
- 2008-03-17 MA MA30757A patent/MA30000B1/fr unknown
-
2012
- 2012-01-26 CY CY20121100092T patent/CY1112317T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TNSN08059A1 (en) | Novel crystalline form of a pyridazino [4,5-b] indole derivative | |
| HUP0301892A2 (hu) | Szexuális zavarok kezelésére szolgáló gyógyszerkészítmények és előállításuk | |
| BRPI0418112A (pt) | inibidores de p-38 quinase bicìclico heterocìclicos | |
| MY129348A (en) | Stable polymorph of n-(3-ethynylphenyl)-6, 7-bis (2-methoxyethoxy)-4- quinazolinamine hydrochloride, methods of production, and pharmaceutical uses thereof | |
| DE60015153D1 (de) | Isomere kondensierte pyrrolocarbazole und isoindolone | |
| DE60326060D1 (de) | Nichtvernetzende pyrroloä2,1-cüä1,4übenzodiazepine als potentielle antitumor-agentien und ihre herstellung | |
| MXPA06001494A (es) | Compuestos de piramidina condensados como inhibidores de canales ionicos gatillados por tension. | |
| MXPA05010137A (es) | Derivados de tetrahidroisoquinolil acetamida para usarse como antagonistas del receptor de orexina. | |
| PL1776349T3 (pl) | Pochodne 2-amino-chinazoliny użyteczne jako inhibitory beta-sekretazy (BACE) | |
| EE200000048A (et) | Uudsed ühendid | |
| IL159289A0 (en) | Oxytocin agonists | |
| TW200716583A (en) | Crystal forms of {[(2R)-7-(2,6-dichlorophenyl)-5-fluoro-2,3-dihydro-1-benzofuran-2-yl]methyl}amine hydrochloride | |
| ATE389651T1 (de) | Als inhibitoren von c-met geeignete pyrrolzusammensetzungen | |
| AU5764496A (en) | Cyclohexyl dihydrobenzofuranes | |
| PL1966198T3 (pl) | Pochodne 2-amino-3,4-dihydropirydo[3,4-d]pirymidyny do zastosowania jako inhibitory beta-sekretazy (BACE) | |
| YU62504A (sh) | Triciklična 2-pirimidonska jedinjenja korisna kao inhibitori hiv reverzne transkriptoze | |
| MXPA04000358A (es) | Hexahidroazepino (4,5-g) indoles e indolinas como ligandos del receptor 5-ht. | |
| MXPA04000779A (es) | 7-aza[2.2.1]bicicloheptanos sustituidos con arilo para el tratamiento de enfermedades. | |
| NO20061575L (no) | Fremgangsmate for fremstilling av renzapride og mellomprodukter derav | |
| MA27944A1 (fr) | N-[3-(3-substituees-pyrazolo [1,5-a] pyrimidin-7-yl) - phenyl] - sulfonamides et compositions et methodes rapportees. | |
| TW200710091A (en) | (1,10B-dihydro-2-(aminoalkyl-phenyl)-5H-pyrazolo [1,5-c][1,3]benzoxazin-5-yl)phenyl methanone derivatives as HIV viral replication inhibitors | |
| TW200518742A (en) | Entry inhibitors | |
| YU3203A (sh) | Jedinjenja tricikličnog 2-piridona koja se koriste kao inhibitori hiv reverznih transkriptaza | |
| MY136138A (en) | Hexacyclic compounds | |
| WO2004014294A3 (fr) | Indoles 4,7-disubstitues et procede de preparation |