IN2014MN01756A - - Google Patents
Info
- Publication number
- IN2014MN01756A IN2014MN01756A IN1756MUN2014A IN2014MN01756A IN 2014MN01756 A IN2014MN01756 A IN 2014MN01756A IN 1756MUN2014 A IN1756MUN2014 A IN 1756MUN2014A IN 2014MN01756 A IN2014MN01756 A IN 2014MN01756A
- Authority
- IN
- India
- Prior art keywords
- compounds
- disclosed
- therapy
- thereofs
- subtype
- Prior art date
Links
Classifications
-
- 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
- C07D498/08—Bridged 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
- A61K31/41—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
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/439—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 the ring forming part of a bridged ring system, e.g. quinuclidine
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/22—Bridged ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
- C07D277/56—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
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Abstract
Disclosed is a compound of formula (I) wherein Y Ring D m and R R are as described herein as a modulator of nicotinic acetylcholine receptors particularly the a7 subtype in a subject in need thereof as well as pharmaceutically acceptable salts polymorphs solvates and isomers thereofs for use either alone or in combinations with suitable other medicaments and pharmaceutical compositions containing such compounds. Also disclosed are a process of preparation of the compounds and the intended uses thereof in therapy particularly in the prophylaxis and therapy of disorders such as Alzheimer s disease mild cognitive impairment senile dementia and the like.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN1756MUN2014 IN2014MN01756A (en) | 2012-03-06 | 2013-02-22 |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN236KO2012 | 2012-03-06 | ||
IN235KO2012 | 2012-03-06 | ||
IN237KO2012 | 2012-03-06 | ||
IN1307KO2012 | 2012-11-12 | ||
IN1756MUN2014 IN2014MN01756A (en) | 2012-03-06 | 2013-02-22 | |
PCT/IB2013/051455 WO2013132380A1 (en) | 2012-03-06 | 2013-02-22 | Thiazole derivatives as alpha 7 nachr modulators |
Publications (1)
Publication Number | Publication Date |
---|---|
IN2014MN01756A true IN2014MN01756A (en) | 2015-07-03 |
Family
ID=54261190
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IN1756MUN2014 IN2014MN01756A (en) | 2012-03-06 | 2013-02-22 |
Country Status (8)
Country | Link |
---|---|
US (1) | US9388196B2 (en) |
EP (1) | EP2822946A1 (en) |
AU (1) | AU2013229177B2 (en) |
CA (1) | CA2866015A1 (en) |
IN (1) | IN2014MN01756A (en) |
NZ (1) | NZ629453A (en) |
SG (1) | SG11201405239WA (en) |
WO (1) | WO2013132380A1 (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013178362A1 (en) | 2012-05-31 | 2013-12-05 | Phenex Pharmaceuticals Ag | Carboxamide or sulfonamide substituted thiazoles and related derivatives as modulators for the orphan nuclear receptor ror[gamma] |
WO2014072957A1 (en) * | 2012-11-12 | 2014-05-15 | Lupin Limited | Thiazole derivatives as alpha 7 nachr modulators |
WO2014141091A1 (en) | 2013-03-13 | 2014-09-18 | Lupin Limited | Pyrrole derivatives as alpha 7 nachr modulators |
TW201446243A (en) | 2013-06-03 | 2014-12-16 | Lupin Ltd | 4-(5-(4-chlorophenyl)-2-(2-cyclopropylacetyl)-1,4-dimethyl-1H-pyrrol-3-yl)benzenesulfonamide as alpha 7 nAChR modulator |
EP3010899A1 (en) | 2013-06-17 | 2016-04-27 | Lupin Limited | Pyrrole derivatives as alpha 7 nachr modulators |
CA2954049A1 (en) * | 2014-07-03 | 2016-01-07 | Celgene Quanticel Research, Inc. | Inhibitors of lysine specific demethylase-1 |
CA2971413A1 (en) | 2014-12-16 | 2016-06-23 | Axovant Sciences Gmbh | Geminal substituted quinuclidine amide compounds as agonists of alpha-7 nicotinic acetylcholine receptors |
MX2017016231A (en) | 2015-06-10 | 2018-11-29 | Axovant Sciences Gmbh | Aminobenzisoxazole compounds as agonists of a7-nicotinic acetylcholine receptors. |
WO2017011920A1 (en) * | 2015-07-22 | 2017-01-26 | The Royal Institution For The Advancement Of Learning/Mcgill University | Compounds and uses thereof in the treatment of cancers and other medical conditions |
JP2018523707A (en) | 2015-08-12 | 2018-08-23 | アクソバント サイエンシズ ゲーエムベーハー | Geminal-substituted aminobenzisoxazole compounds as agonists of α7-nicotinic acetylcholine receptors |
CN108101860B (en) * | 2018-02-08 | 2021-11-23 | 苏州敬业医药化工有限公司 | Preparation method of cis-2, 6-dimethyl morpholine |
Family Cites Families (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3953596A (en) | 1973-06-14 | 1976-04-27 | Ici United States Inc. | 8-Oxa-3-azabicyclo(3.2.1)octane analgesic compositions and method of alleviating pain in animals |
US4235871A (en) | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
US4501728A (en) | 1983-01-06 | 1985-02-26 | Technology Unlimited, Inc. | Masking of liposomes from RES recognition |
US5019369A (en) | 1984-10-22 | 1991-05-28 | Vestar, Inc. | Method of targeting tumors in humans |
US4837028A (en) | 1986-12-24 | 1989-06-06 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
EP0772606A1 (en) * | 1994-07-27 | 1997-05-14 | G.D. SEARLE & CO. | Substituted thiazoles for the treatment of inflammation |
US5608082A (en) | 1994-07-28 | 1997-03-04 | Agouron Pharmaceuticals, Inc. | Compounds useful as antiproliferative agents and GARFT inhibitors |
CA2301742C (en) | 1997-09-12 | 2004-05-18 | Richard Friesen | 2,3,5-trisubstituted pyridines as inhibitors of cyclooxygenase-2 |
JP4415216B2 (en) | 2002-02-01 | 2010-02-17 | 大日本住友製薬株式会社 | 2-furancarboxylic acid hydrazide compound and pharmaceutical composition containing the same |
FR2840303B1 (en) | 2002-05-31 | 2005-07-15 | Rhodia Chimie Sa | PROCESS FOR ARYLATION OR VINYLATION OR ALKYLATION OF A NUCLEOPHILIC COMPOUND |
SE0201938D0 (en) | 2002-06-20 | 2002-06-20 | Astrazeneca Ab | New process |
DE10244810A1 (en) | 2002-09-26 | 2004-04-08 | Bayer Ag | New morpholine-bridged indazole derivatives |
US7129235B2 (en) | 2003-07-11 | 2006-10-31 | Abbott Laboratories | Amides useful for treating pain |
US7442805B2 (en) | 2003-09-25 | 2008-10-28 | Wyeth | Substituted sulfonamide-indoles |
GB0403038D0 (en) | 2004-02-11 | 2004-03-17 | Novartis Ag | Organic compounds |
BRPI0507296A (en) | 2004-03-29 | 2007-07-03 | Neurosearch As | urea derivative, pharmaceutical composition, use of a urea derivative, and method of treatment, prevention or alleviation of a disease or disorder or condition of a living animal body |
ITTO20040264A1 (en) | 2004-04-28 | 2004-07-28 | Rotta Res Lab Spa | NEW PYROLIC DERIVATIVES WITH ANGIOTENSIN-II ANTAGONIST ACTIVITY |
KR20070106969A (en) | 2004-09-09 | 2007-11-06 | 추가이 세이야쿠 가부시키가이샤 | Novel imidazolidine derivative and use thereof |
US20060142349A1 (en) | 2004-12-23 | 2006-06-29 | Pfizer Inc | Methods of modulating the activities of alpha-7 nicotinic acetylcholine receptor |
DE602006016926D1 (en) | 2005-02-16 | 2010-10-28 | Neurosearch As | NEW DIAZABICYCLIC ARYL DERIVATIVES AND MEDICAL USE THEREOF |
FR2885616B1 (en) | 2005-05-12 | 2007-06-22 | Servier Lab | NOVEL PHENYLPYRIDINYLPIPERAZINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
CA2617788A1 (en) | 2005-08-04 | 2007-02-15 | Apogee Biotechnology Corporation | Sphingosine kinase inhibitors and methods of their use |
CN101263130B (en) | 2005-09-13 | 2011-03-09 | 詹森药业有限公司 | 2-aniline-4-aryl substituted thiazole derivatives |
US7863302B2 (en) | 2006-02-03 | 2011-01-04 | Eli Lilly And Company | Compounds and methods for modulating FX-receptors |
ATE455114T1 (en) | 2006-02-16 | 2010-01-15 | Neurosearch As | ENANTIOMER PURE CHINUCLIDINYLOXY-PYRIDAZINE AND THEIR USE AS NICOTINE-ACETYLCHOLINE RECEPTOR LIGANDS |
JO3019B1 (en) | 2006-04-19 | 2016-09-05 | Janssen Pharmaceutica Nv | Trisubstituted 1,2,4-Triazoles |
CA2647601A1 (en) | 2006-06-27 | 2008-01-03 | Abbott Laboratories | Pyrrole derivatives and their methods of use |
EP2038278A2 (en) | 2006-06-27 | 2009-03-25 | Abbott Laboratories | Thiazoline and oxazoline derivatives and their methods of use |
AU2007318058A1 (en) | 2006-11-02 | 2008-05-15 | Merck Sharp & Dohme Corp. | Heterocyclyl-substituted anti-hypercholesterolemic compounds |
US20080287479A1 (en) | 2006-12-20 | 2008-11-20 | Pfizer Inc | Inhibitors of serine palmitoyltransferase |
CN101796034A (en) | 2007-08-08 | 2010-08-04 | 神经研究公司 | Novel 1,2,3-triazole derivatives useful as modulators of nicotinic acetylcholine receptors |
GB0718735D0 (en) | 2007-09-25 | 2007-11-07 | Prolysis Ltd | Antibacterial agents |
ES2443290T3 (en) | 2007-10-04 | 2014-02-18 | F. Hoffmann-La Roche Ag | Tetrazol substituted arylamide derivatives and uses thereof |
MX2010003155A (en) | 2007-10-04 | 2010-04-01 | Hoffmann La Roche | Cyclopropyl aryl amide derivatives and uses thereof. |
JO2784B1 (en) | 2007-10-18 | 2014-03-15 | شركة جانسين فارماسوتيكا ان. في | 1,3,5-trisubstitued triazole derivative |
US8778974B2 (en) | 2008-03-19 | 2014-07-15 | Janssen Pharmaceutica Nv | Trisubstituted 1,2,4 triazoles |
US7786171B2 (en) | 2008-04-04 | 2010-08-31 | Abbott Laboratories | Amide derivatives as positive allosteric modulators and methods of use thereof |
ES2392796T3 (en) | 2008-04-17 | 2012-12-13 | Proximagen Limited | Indole modulators of the nicotinic acetylcholine alpha-7 receptor |
BRPI0912196A2 (en) | 2008-05-09 | 2015-10-06 | Janssen Pharmaceutica Nv | trisubstituted pyrazoles as acetylcholine receptor modulators. |
EP2387575B1 (en) | 2009-01-15 | 2013-09-04 | Anvyl, LLC | Alpha7 nicotinic acetylcholine receptor allosteric modulators, their derivatives and uses thereof |
WO2010120854A1 (en) | 2009-04-15 | 2010-10-21 | Glaxosmithkline Llc | Chemical compounds |
US20120071469A1 (en) | 2009-05-14 | 2012-03-22 | Neurosearch A/S | Novel 1,4-diaza-bicyclo[3.2.1]octane derivatives useful as nicotinic acetylcholine receptor modulators |
TWI558398B (en) | 2009-09-22 | 2016-11-21 | 諾華公司 | Use of nicotinic acetylcholine receptor alpha 7 activators |
JO3078B1 (en) * | 2009-11-27 | 2017-03-15 | Janssen Pharmaceutica Nv | Morpholinothiazoles as alpha 7 positive allosteric modulators |
WO2012104782A1 (en) | 2011-02-03 | 2012-08-09 | Lupin Limited | Pyrrole derivatives used as modulators of alpha7 nachr |
GEP20156318B (en) | 2011-02-23 | 2015-07-10 | Lupin Ltd | Heteroaryl derivatives as alpha7 nachr modulators |
WO2012131576A1 (en) | 2011-03-31 | 2012-10-04 | Lupin Limited | Pyrrole derivatives as nicotinic acetylcholine receptor modulators for use in the treatment of neurodegenerative disorders such as alzheimer's and parkinson's disease |
ES2606043T3 (en) | 2011-07-05 | 2017-03-17 | Lupin Limited | Biaryl derivatives as nAChR modulators |
-
2013
- 2013-02-22 WO PCT/IB2013/051455 patent/WO2013132380A1/en active Application Filing
- 2013-02-22 CA CA2866015A patent/CA2866015A1/en not_active Abandoned
- 2013-02-22 US US14/379,134 patent/US9388196B2/en not_active Expired - Fee Related
- 2013-02-22 NZ NZ629453A patent/NZ629453A/en not_active IP Right Cessation
- 2013-02-22 SG SG11201405239WA patent/SG11201405239WA/en unknown
- 2013-02-22 AU AU2013229177A patent/AU2013229177B2/en not_active Expired - Fee Related
- 2013-02-22 EP EP13711972.3A patent/EP2822946A1/en not_active Withdrawn
- 2013-02-22 IN IN1756MUN2014 patent/IN2014MN01756A/en unknown
Also Published As
Publication number | Publication date |
---|---|
CA2866015A1 (en) | 2013-09-12 |
AU2013229177B2 (en) | 2017-03-23 |
US9388196B2 (en) | 2016-07-12 |
EP2822946A1 (en) | 2015-01-14 |
SG11201405239WA (en) | 2014-09-26 |
AU2013229177A1 (en) | 2014-09-18 |
NZ629453A (en) | 2016-04-29 |
WO2013132380A1 (en) | 2013-09-12 |
US20150291617A1 (en) | 2015-10-15 |
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