MA34771B1 - Formes cristallines - Google Patents
Formes cristallinesInfo
- Publication number
- MA34771B1 MA34771B1 MA36066A MA36066A MA34771B1 MA 34771 B1 MA34771 B1 MA 34771B1 MA 36066 A MA36066 A MA 36066A MA 36066 A MA36066 A MA 36066A MA 34771 B1 MA34771 B1 MA 34771B1
- Authority
- MA
- Morocco
- Prior art keywords
- varieties
- modulation
- sensitive
- cells
- determining
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- 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
- C07D403/12—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 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)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Abstract
La présente invention concerne des formes cristallines spécifiques de la 5 -chloro-n-(2-isopropoxy-5-méthyl-4-(pipéridin-4-ylphényl)-n-2-(isopropylsulfonyl)phényl)-2,4-diamine. La présente invention concerne en outre des procédés de préparation desdites formes cristallines, des compositions pharmaceutiques comprenant lesdites formes cristallines, et des procédés d'utilisation desdites formes cristallines et des compositions pharmaceutiques pour traiter une maladie.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201061424194P | 2010-12-17 | 2010-12-17 | |
PCT/US2011/065030 WO2012082972A1 (fr) | 2010-12-17 | 2011-12-15 | Formes cristallines de la 5-chloro-n2-(2-isopropoxy-5-méthyl-4-pipéridin-4-yl-phényl)-n4[2-(propane-2-sulfonyl)-phényl]-pyrimidine-2,4-diamine |
Publications (1)
Publication Number | Publication Date |
---|---|
MA34771B1 true MA34771B1 (fr) | 2013-12-03 |
Family
ID=45464892
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA36066A MA34771B1 (fr) | 2010-12-17 | 2013-06-28 | Formes cristallines |
Country Status (35)
Country | Link |
---|---|
US (2) | US9309229B2 (fr) |
EP (3) | EP3121171B1 (fr) |
JP (1) | JP5916752B2 (fr) |
KR (4) | KR20190022903A (fr) |
CN (7) | CN114989139A (fr) |
AR (2) | AR084309A1 (fr) |
AU (1) | AU2011343775B2 (fr) |
BR (1) | BR112013015000A2 (fr) |
CA (1) | CA2821102C (fr) |
CL (1) | CL2013001723A1 (fr) |
CO (1) | CO6801792A2 (fr) |
CY (2) | CY1119474T1 (fr) |
DK (2) | DK3121171T3 (fr) |
EC (1) | ECSP13012770A (fr) |
ES (3) | ES2696526T3 (fr) |
GT (1) | GT201300153A (fr) |
HR (2) | HRP20171477T1 (fr) |
HU (1) | HUE041845T2 (fr) |
IL (1) | IL226474A (fr) |
LT (2) | LT2651918T (fr) |
MA (1) | MA34771B1 (fr) |
MX (1) | MX338210B (fr) |
MY (2) | MY164810A (fr) |
NZ (1) | NZ610713A (fr) |
PE (1) | PE20140698A1 (fr) |
PL (2) | PL2651918T3 (fr) |
PT (2) | PT3121171T (fr) |
RS (1) | RS57771B1 (fr) |
RU (2) | RU2599785C3 (fr) |
SG (2) | SG190856A1 (fr) |
SI (2) | SI3121171T1 (fr) |
TN (1) | TN2013000216A1 (fr) |
TW (2) | TWI576343B (fr) |
WO (1) | WO2012082972A1 (fr) |
ZA (1) | ZA201303599B (fr) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG190856A1 (en) * | 2010-12-17 | 2013-07-31 | Novartis Ag | Crystalline forms of 5-chloro-n2-(2-isopropoxy-5-methyl-4-piperidin-4-yl-phenyl)-n4[2-(propane-2-sulfonyl)-phenyl]-pyrimidine-2,4-diamine |
BR112015010221B1 (pt) | 2012-11-06 | 2022-09-13 | Shanghai Fochon Pharmaceutical Co., Ltd. | Inibidores de quinase alk, seus usos, composição farmacêutica, e método para fabricação de medicamento |
KR101656382B1 (ko) * | 2014-02-28 | 2016-09-09 | 한국화학연구원 | 피리미딘-2,4-디아민 유도체 및 이를 유효성분으로 함유하는 항암용 약학적 조성물 |
CN105272921A (zh) * | 2014-06-09 | 2016-01-27 | 江苏奥赛康药业股份有限公司 | 一种制备Ceritinib的方法及其中间体化合物 |
CN105294649B (zh) * | 2014-07-30 | 2019-05-14 | 江苏奥赛康药业股份有限公司 | 一种Ceritinib化合物及其药物组合物 |
CN105294650A (zh) * | 2014-08-01 | 2016-02-03 | 江苏奥赛康药业股份有限公司 | 一种Ceritinib化合物及其药物组合物 |
KR102331856B1 (ko) | 2014-10-21 | 2021-11-29 | 다케다 야쿠힌 고교 가부시키가이샤 | 결정 형태의 5-클로로-n4-[2-(디메틸포스포릴)페닐]-n2-{2-메톡시-4-[4-(4-메틸피페라진-1-일)피페리딘-1-일]피리미딘-2,4-디아민 |
WO2016081538A1 (fr) | 2014-11-18 | 2016-05-26 | Teva Pharmaceuticals International Gmbh | Formes solides de ceritinib et sels de ceux-ci |
CN105601614A (zh) * | 2014-11-21 | 2016-05-25 | 奥浦顿(上海)医药科技有限公司 | 一种色瑞替尼晶型及其制备方法 |
WO2016082795A1 (fr) * | 2014-11-28 | 2016-06-02 | 苏州晶云药物科技有限公司 | Forme cristalline i du ceritinib et son procédé de préparation |
CN105622577A (zh) * | 2014-11-29 | 2016-06-01 | 江苏先声药业有限公司 | 一种色瑞替尼的新晶型及其制备方法 |
WO2016108123A2 (fr) * | 2014-12-17 | 2016-07-07 | Dr. Reddy’S Laboratories Limited | Forme amorphe pure et dispersion solide amorphe de céritinib |
WO2016098042A1 (fr) * | 2014-12-19 | 2016-06-23 | Novartis Ag | Utilisation du céritinib (ldk -378) dans le traitement de troubles médiés par fes ou fer, en particulier des troubles prolifératifs |
WO2016098070A1 (fr) | 2014-12-19 | 2016-06-23 | Novartis Ag | Forme cristalline de la 5-chloro-n2-(2-isopropoxy-5-méthyl-4-pipéridin-4-yl-phényl)-n4-[2-(propane-2-sulfonyl)-phényl]-pyrimidine-2,4-diamine |
WO2017016529A1 (fr) | 2015-07-28 | 2017-02-02 | Zentiva, K.S. | Formes solides de ceritinib base libre |
CN105061397B (zh) * | 2015-08-07 | 2018-01-02 | 武汉英普瑞医药科技有限公司 | 一种色瑞替尼的c型晶型及其制备方法与应用 |
CN106699743B (zh) | 2015-11-05 | 2020-06-12 | 湖北生物医药产业技术研究院有限公司 | 嘧啶类衍生物及其用途 |
WO2017152858A1 (fr) * | 2016-03-11 | 2017-09-14 | 苏州晶云药物科技有限公司 | Forme cristalline de céritinib et procédé pour sa préparation |
WO2017158619A1 (fr) | 2016-03-15 | 2017-09-21 | Natco Pharma Limited | Procédé modifié pour la préparation de céritinib et de forme amorphe de céritinib |
JP2019196359A (ja) * | 2019-06-17 | 2019-11-14 | ノバルティス アーゲー | ピリミジン誘導体およびそれらの中間体を調製する化学的方法 |
GB201915618D0 (en) | 2019-10-28 | 2019-12-11 | Univ Oslo | ALK inhibitors for treatment of ALK-negative cancer and antibody-mediated diseases |
EP4092021A4 (fr) * | 2020-01-17 | 2023-01-25 | Shandong Xuanzhu Pharma Co., Ltd. | Forme cristalline d'un inhibiteur de kinase du lymphome anaplasique polycyclique |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0206215D0 (en) | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
CA2533320A1 (fr) * | 2003-08-15 | 2006-02-24 | Novartis Ag | 2, 4-pyrimidine diamines utiles dans le cadre du traitement de maladies neoplasiques, de troubles inflammatoires et de troubles du systeme immunitaire |
GB0419161D0 (en) * | 2004-08-27 | 2004-09-29 | Novartis Ag | Organic compounds |
MX2009006081A (es) * | 2006-12-08 | 2009-06-17 | Irmc Llc | Compuestos y composiciones como inhibidores de cinasa de proteina. |
SI2091918T1 (sl) * | 2006-12-08 | 2015-01-30 | Irm Llc | Spojine in sestavki kot inhibitorji protein-kinaze |
KR101174201B1 (ko) * | 2007-08-28 | 2012-08-16 | 아이알엠 엘엘씨 | 키나제 억제제로서의 2-비페닐아미노-4-아미노피리미딘 유도체 |
WO2009032694A1 (fr) * | 2007-08-28 | 2009-03-12 | Dana Farber Cancer Institute | Pyrimidine substituée par amino, dérivés de pyrollopyridine et de pyrazolopyrimidine utilisés en tant qu'inhibiteurs de la kinase et dans le traitement de troubles prolifératifs et de maladies liées à l'angiogenèse |
CA2720946C (fr) | 2008-04-07 | 2013-05-28 | Irm Llc | Composes et compositions comme inhibiteurs de la proteine kinase |
HUE035029T2 (en) * | 2008-05-21 | 2018-03-28 | Ariad Pharma Inc | Kinase inhibitor phosphorus derivatives |
WO2010142766A2 (fr) * | 2009-06-10 | 2010-12-16 | Cellzome Limited | Dérivés de pyrimidine comme inhibiteurs de la zap-70 |
TWI481607B (zh) | 2009-12-17 | 2015-04-21 | Lundbeck & Co As H | 作為pde10a酵素抑制劑的2-芳基咪唑衍生物 |
NZ612788A (en) | 2010-12-17 | 2015-10-30 | Reata Pharmaceuticals Inc | Pyrazolyl and pyrimidinyl tricyclic enones as antioxidant inflammation modulators |
SG190856A1 (en) * | 2010-12-17 | 2013-07-31 | Novartis Ag | Crystalline forms of 5-chloro-n2-(2-isopropoxy-5-methyl-4-piperidin-4-yl-phenyl)-n4[2-(propane-2-sulfonyl)-phenyl]-pyrimidine-2,4-diamine |
EP2651219A2 (fr) | 2010-12-17 | 2013-10-23 | E.I. Du Pont De Nemours And Company | Amides azocycliques fongicides |
CN105294650A (zh) | 2014-08-01 | 2016-02-03 | 江苏奥赛康药业股份有限公司 | 一种Ceritinib化合物及其药物组合物 |
WO2016081538A1 (fr) | 2014-11-18 | 2016-05-26 | Teva Pharmaceuticals International Gmbh | Formes solides de ceritinib et sels de ceux-ci |
DE112015005255B4 (de) | 2014-11-21 | 2023-10-26 | Joyson Safety Systems Acquisition Llc | Airbagmodul |
CN105622577A (zh) | 2014-11-29 | 2016-06-01 | 江苏先声药业有限公司 | 一种色瑞替尼的新晶型及其制备方法 |
JP2017537927A (ja) | 2014-12-04 | 2017-12-21 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | がん(骨髄腫)を処置するための抗cs1および抗pd1抗体の併用 |
WO2016098070A1 (fr) | 2014-12-19 | 2016-06-23 | Novartis Ag | Forme cristalline de la 5-chloro-n2-(2-isopropoxy-5-méthyl-4-pipéridin-4-yl-phényl)-n4-[2-(propane-2-sulfonyl)-phényl]-pyrimidine-2,4-diamine |
WO2017016529A1 (fr) | 2015-07-28 | 2017-02-02 | Zentiva, K.S. | Formes solides de ceritinib base libre |
CN105061397B (zh) | 2015-08-07 | 2018-01-02 | 武汉英普瑞医药科技有限公司 | 一种色瑞替尼的c型晶型及其制备方法与应用 |
-
2011
- 2011-12-15 SG SG2013039342A patent/SG190856A1/en unknown
- 2011-12-15 PL PL11806079T patent/PL2651918T3/pl unknown
- 2011-12-15 CN CN202210792464.5A patent/CN114989139A/zh active Pending
- 2011-12-15 WO PCT/US2011/065030 patent/WO2012082972A1/fr active Application Filing
- 2011-12-15 HU HUE16167355A patent/HUE041845T2/hu unknown
- 2011-12-15 SG SG10201510082XA patent/SG10201510082XA/en unknown
- 2011-12-15 SI SI201131583T patent/SI3121171T1/sl unknown
- 2011-12-15 AU AU2011343775A patent/AU2011343775B2/en active Active
- 2011-12-15 ES ES16167355T patent/ES2696526T3/es active Active
- 2011-12-15 CA CA2821102A patent/CA2821102C/fr active Active
- 2011-12-15 EP EP16167355.3A patent/EP3121171B1/fr active Active
- 2011-12-15 CN CN201410457562.9A patent/CN104262324A/zh active Pending
- 2011-12-15 LT LTEP11806079.7T patent/LT2651918T/lt unknown
- 2011-12-15 MX MX2013006952A patent/MX338210B/es active IP Right Grant
- 2011-12-15 DK DK16167355.3T patent/DK3121171T3/en active
- 2011-12-15 PL PL16167355T patent/PL3121171T3/pl unknown
- 2011-12-15 KR KR1020197005138A patent/KR20190022903A/ko active Search and Examination
- 2011-12-15 EP EP11806079.7A patent/EP2651918B1/fr not_active Revoked
- 2011-12-15 NZ NZ610713A patent/NZ610713A/en not_active IP Right Cessation
- 2011-12-15 KR KR1020137018605A patent/KR20130130022A/ko not_active Application Discontinuation
- 2011-12-15 ES ES11806079.7T patent/ES2643016T3/es active Active
- 2011-12-15 CN CN202011050061.0A patent/CN112125884A/zh active Pending
- 2011-12-15 MY MYPI2013001848A patent/MY164810A/en unknown
- 2011-12-15 PE PE2013001425A patent/PE20140698A1/es not_active Application Discontinuation
- 2011-12-15 RU RU2013132947A patent/RU2599785C3/ru active Protection Beyond IP Right Term
- 2011-12-15 PT PT16167355T patent/PT3121171T/pt unknown
- 2011-12-15 CN CN201180060435XA patent/CN103282359A/zh active Pending
- 2011-12-15 LT LTEP16167355.3T patent/LT3121171T/lt unknown
- 2011-12-15 PT PT118060797T patent/PT2651918T/pt unknown
- 2011-12-15 SI SI201131289T patent/SI2651918T1/sl unknown
- 2011-12-15 JP JP2013544762A patent/JP5916752B2/ja active Active
- 2011-12-15 KR KR1020187007996A patent/KR20180032680A/ko not_active Application Discontinuation
- 2011-12-15 EP EP18186197.2A patent/EP3453708B8/fr active Active
- 2011-12-15 RU RU2016136823A patent/RU2746159C2/ru active
- 2011-12-15 CN CN201710063792.0A patent/CN106831716A/zh active Pending
- 2011-12-15 AR ARP110104703A patent/AR084309A1/es not_active Application Discontinuation
- 2011-12-15 CN CN201710063793.5A patent/CN107056751A/zh active Pending
- 2011-12-15 MY MYPI2016001551A patent/MY177742A/en unknown
- 2011-12-15 RS RS20181240A patent/RS57771B1/sr unknown
- 2011-12-15 KR KR1020207009828A patent/KR102325775B1/ko active IP Right Grant
- 2011-12-15 BR BR112013015000A patent/BR112013015000A2/pt not_active Application Discontinuation
- 2011-12-15 US US13/993,217 patent/US9309229B2/en active Active
- 2011-12-15 CN CN201610217386.0A patent/CN106008462A/zh active Pending
- 2011-12-15 DK DK11806079.7T patent/DK2651918T3/en active
- 2011-12-15 ES ES18186197T patent/ES2905973T3/es active Active
- 2011-12-16 TW TW100146987A patent/TWI576343B/zh active
- 2011-12-16 TW TW105112710A patent/TWI576344B/zh active
-
2013
- 2013-05-17 ZA ZA2013/03599A patent/ZA201303599B/en unknown
- 2013-05-17 TN TNP2013000216A patent/TN2013000216A1/fr unknown
- 2013-05-20 IL IL226474A patent/IL226474A/en active IP Right Grant
- 2013-06-14 CL CL2013001723A patent/CL2013001723A1/es unknown
- 2013-06-17 GT GT201300153A patent/GT201300153A/es unknown
- 2013-06-28 MA MA36066A patent/MA34771B1/fr unknown
- 2013-07-04 CO CO13158446A patent/CO6801792A2/es not_active Application Discontinuation
- 2013-07-16 EC ECSP13012770 patent/ECSP13012770A/es unknown
-
2016
- 2016-03-02 US US15/058,489 patent/US20160175305A1/en not_active Abandoned
-
2017
- 2017-10-03 HR HRP20171477TT patent/HRP20171477T1/hr unknown
- 2017-10-11 CY CY20171101064T patent/CY1119474T1/el unknown
-
2018
- 2018-10-22 HR HRP20181737TT patent/HRP20181737T1/hr unknown
- 2018-11-09 CY CY181101192T patent/CY1121017T1/el unknown
-
2021
- 2021-03-19 AR ARP210100698A patent/AR122395A2/es unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA34771B1 (fr) | Formes cristallines | |
MA32351B1 (fr) | Derives d'aminodihydrothiazine a titre d'inhibiteurs de bace pour le traitement de la maladie d'alzheimer | |
TW200634006A (en) | Tetrahydroquinoline analogues as muscarinic agonists | |
MA33450B1 (fr) | Dérivés d'oxazine et leur utilisation en tant qu'inhibiteurs de bace pour le traitement de troubles neurologiques | |
MA34299B1 (fr) | Dérivés d'aminopyrimidine au titre de modulateurs de lrrk2 | |
MA31433B1 (fr) | Inhibiteurs de la p70 s6 kinase | |
EA201100691A1 (ru) | Антагонисты рецепторов лизофосфатидной кислоты | |
WO2007120689A3 (fr) | Procédés d'utilisation du récepteur gpr119 pour identifier des composés utiles pour augmenter la masse osseuse chez un individu | |
MA33492B1 (fr) | Inhibiteurs de bace | |
EA201001680A1 (ru) | Соединения бензолсульфонамидтиазола и оксазола | |
EA200970612A1 (ru) | Производные индола в качестве агонистов рецептора s1p1 | |
MA30672B1 (fr) | Utilisation de derives de l'azabicyclo hexane | |
EA201070148A1 (ru) | Соединения и способы модулирования фарнезоидного рецептора x (fxr) | |
EA200800727A1 (ru) | Введение ингибиторов дипептидилпептидазы | |
MX2009007337A (es) | Indazoles sustituidos con 5-piridinona. | |
WO2006102308A3 (fr) | Antagonistes de bêta-lactamyl vasopressine v1b | |
ATE486601T1 (de) | Verwendung von 3- (4-amino-1-oxo-1,3-dihydro- isoindol-2-yl)-piperidin--2,6-dion zur behandlung von mantelzelllymphomen | |
MA35716B1 (fr) | Formulations pharmaceutiques | |
EA200970532A1 (ru) | Фумаратная соль (альфа s, бета r)-6-бром-альфа-[2-(диметиламино)этил]-2-метокси-альфа-1-нафталенил-бета-фенил-3-хинолинэтанола | |
WO2009089263A3 (fr) | Nouvelles compositions et procédés d'utilisation | |
MY167575A (en) | Heterocyclic compounds and use thereof as modulators of type iii receptor tyrosine kinases | |
MA33679B1 (fr) | Derives de 2-oxo-1-pyrrolidinyle imidazothiadiazole | |
MA39163A1 (fr) | Forme cristalline de (s)-(2-(6-chloro-7-methyl-1h-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1 -yl)(5-methoxy-2-(2h-1,2,3-triazol-2-yl)phenyl)methanone et utilisation de celle-ci en tant qu'antagonistes des recepteurs de l'orexine | |
MA33839B1 (fr) | Compositions et procédés destinés à diagnostiquer et à traiter des tumeurs | |
MA39164A1 (fr) | Forme de sel cristalline de (s)-(2-(6-chloro-7-méthyl-1 h-benzo[d]imidazol- 2-yl)-2-méthylpyrrolidin-1-yl)(5-méthoxy-2-(2h-1,2,3-triazol-2-yl)phényl)méthanone comme antagoniste des récepteurs à l'oréxine |