MX2016014197A - 4-fenilpiperidinas sustituidas, su preparacion y uso. - Google Patents

4-fenilpiperidinas sustituidas, su preparacion y uso.

Info

Publication number
MX2016014197A
MX2016014197A MX2016014197A MX2016014197A MX2016014197A MX 2016014197 A MX2016014197 A MX 2016014197A MX 2016014197 A MX2016014197 A MX 2016014197A MX 2016014197 A MX2016014197 A MX 2016014197A MX 2016014197 A MX2016014197 A MX 2016014197A
Authority
MX
Mexico
Prior art keywords
substituted
preparaiton
phenylpiperidines
halogen
alkyl
Prior art date
Application number
MX2016014197A
Other languages
English (en)
Inventor
Cioffi Christopher
Johnson Graham
Zhu Lei
Petrukhin Konstantin
Allikmets Rando
Freeman Emily
Chen Ping
Conlon Michael
Original Assignee
Univ Columbia
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Univ Columbia filed Critical Univ Columbia
Publication of MX2016014197A publication Critical patent/MX2016014197A/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/451Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Ophthalmology & Optometry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

La invención actual proporciona un compuesto que tiene la estructura: (ver Fórmulas) en donde R1, R2, R3, R4, y R5 son cada uno independientemente H, halógeno, CF3 o alquilo C1-C4, en donde dos o más de R1, R2, R3, R4, o R5 son diferentes a H; R6 es H, OH, o halógeno; y B es un heterobiciclo sustituido o no sustituido, en donde cuando R1 es CF3, R2 es H, R3 es F, R4 es H, y R5 es H, o R1 es H, R2 es CF3, R3 es H, R4 es CF3, y R5 es H, o R1 es C1, R2 es H, R3 es H, R4 es F, y R5 es H, o R1 es CF3, R2 es H, R3 es F, R4 es H, y R5 es H, o R1 es CF3, R2 es F, R3 es H,R4 es H, y R5 es H, o R1 es C1,R2 es F, R3 es H,R4 es H, y R5 es H, entonces B es diferente o una sal farmacéuticamente aceptable del mismo.
MX2016014197A 2014-04-30 2015-04-29 4-fenilpiperidinas sustituidas, su preparacion y uso. MX2016014197A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201461986578P 2014-04-30 2014-04-30
PCT/US2015/028293 WO2015168286A1 (en) 2014-04-30 2015-04-29 Substituted 4-phenylpiperidines, their preparaiton and use

Publications (1)

Publication Number Publication Date
MX2016014197A true MX2016014197A (es) 2017-05-03

Family

ID=54354744

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2016014197A MX2016014197A (es) 2014-04-30 2015-04-29 4-fenilpiperidinas sustituidas, su preparacion y uso.

Country Status (15)

Country Link
US (7) US9434727B2 (es)
EP (2) EP3137168B1 (es)
JP (1) JP6676541B2 (es)
KR (1) KR102429220B1 (es)
CN (2) CN106794364B (es)
AU (1) AU2015253232B2 (es)
BR (1) BR112016025356B1 (es)
CA (1) CA2947174C (es)
DK (1) DK3137168T3 (es)
ES (1) ES2909793T3 (es)
HK (1) HK1232169A1 (es)
MX (1) MX2016014197A (es)
PH (1) PH12016502147B1 (es)
SG (1) SG11201608943VA (es)
WO (1) WO2015168286A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9333202B2 (en) 2012-05-01 2016-05-10 The Trustees Of Columbia University In The City Of New York Non-retinoid antagonists for treatment of age-related macular degeneration and stargardt disease
US9938291B2 (en) 2013-03-14 2018-04-10 The Trustess Of Columbia University In The City Of New York N-alkyl-2-phenoxyethanamines, their preparation and use
US9944644B2 (en) 2013-03-14 2018-04-17 The Trustees Of Columbia University In The City Of New York Octahydropyrrolopyrroles their preparation and use
WO2014152018A1 (en) 2013-03-14 2014-09-25 The Trustees Of Columbia University In The City Of New York Octahydrocyclopentapyrroles, their preparation and use
US10273243B2 (en) 2013-03-14 2019-04-30 The Trustees Of Columbia University In The City Of New York 4-phenylpiperidines, their preparation and use
EP3137168B1 (en) 2014-04-30 2022-01-05 The Trustees of Columbia University in the City of New York Substituted 4-phenylpiperidines, their preparation and use
GB201604638D0 (en) * 2016-03-18 2016-05-04 Mission Therapeutics Ltd Novel compounds
WO2018232154A1 (en) * 2017-06-15 2018-12-20 Belite Bio, Inc Methods of treating metabolic diseases with fused bicyclic pyrazoles
US10245259B2 (en) 2017-06-15 2019-04-02 Belite Bio, Inc Methods of treating RBP4 related diseases with triazolopyridines
EP3829575A4 (en) * 2018-08-01 2022-07-20 The Trustees of Columbia University in the City of New York RBP4 ANTAGONISTS FOR THE TREATMENT AND PREVENTION OF NON-ALCOHOLIC LIVER DISEASE AND GOUT
WO2021007172A1 (en) * 2019-07-08 2021-01-14 Belite Bio, Llc Formulations of rbp4 inhibitors and methods of use
KR102399432B1 (ko) 2020-04-20 2022-05-19 주식회사 엘파니 전도성 고분자 구조체 표면에 코팅된 금속 박막 층을 포함하는, 하이브리드 구조체 및 이의 제조 방법

Family Cites Families (126)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3926606A1 (de) 1989-08-11 1991-02-14 Hoechst Ag Verfahren zur behandlung der cardialen sowie der vasculaeren hypertrophie und hyperplasie
DE4130514A1 (de) 1991-09-13 1993-03-18 Chemie Linz Deutschland Verfahren zur herstellung reiner n,n'-unsymmetrisch substituierter phenylharnstoffe
US5532243A (en) 1992-02-14 1996-07-02 The Dupont Merck Pharmaceutical Company Antipsychotic nitrogen-containing bicyclic compounds
US5312814A (en) 1992-12-09 1994-05-17 Bristol-Myers Squibb Co. α-phosphonocarboxylate squalene synthetase inhibitors
DE4341403A1 (de) 1993-12-04 1995-06-08 Basf Ag N-substituierte 3-Azabicycloalkan-Derivate, ihre Herstellung und Verwendung
US5523430A (en) 1994-04-14 1996-06-04 Bristol-Myers Squibb Company Protein farnesyl transferase inhibitors
WO1997017954A1 (en) 1995-11-13 1997-05-22 Albany Medical College Analgesic compounds and uses thereof
CA2249601A1 (en) 1996-04-03 1997-10-23 Thorsten E. Fisher Inhibitors of farnesyl-protein transferase
CA2282654C (en) 1997-03-03 2009-02-03 Eisai Co., Ltd. Use of cholinesterase inhibitors to treat attention deficit hyperactivity disorder
CA2319198C (en) 1998-01-27 2011-02-22 Aventis Pharmaceuticals Products Inc. Substituted oxoazaheterocyclyl factor xa inhibitors
EP1087937A1 (en) 1998-06-17 2001-04-04 Du Pont Pharmaceuticals Company Cyclic hydroxamic acids as metalloproteinase inhibitors
CA2346006A1 (en) 1998-10-09 2000-04-20 Merck & Co., Inc. Delta 6 fatty acid desaturase
EP1146790A4 (en) 1999-01-25 2004-03-17 Smithkline Beecham Corp COMPOUNDS AND METHODS
CA2369822A1 (en) 1999-04-14 2000-10-19 Merck & Co., Inc. Novel human voltage-gated potassium channel
KR20020002501A (ko) 1999-05-13 2002-01-09 시오노 요시히코 당뇨병의 예방 또는 치료약
CA2374793A1 (en) 1999-05-24 2000-11-30 Penglie Zhang Inhibitors of factor xa
CN1420882A (zh) 1999-07-28 2003-05-28 阿温蒂斯药物公司 取代的氧代氮杂杂环基化合物
US6372793B1 (en) 1999-08-20 2002-04-16 Florida Agricultural & Mechanical University Method for treatment of a neurological disease characterized by impaired neuromodulator function
MY125533A (en) * 1999-12-06 2006-08-30 Bristol Myers Squibb Co Heterocyclic dihydropyrimidine compounds
DK1311272T3 (da) 2000-03-03 2007-02-26 Eisai R&D Man Co Ltd Hidtil ukendte fremgangsmåder hvor der anvendes cholinesteraseinhibitorer
US20020045613A1 (en) 2000-04-27 2002-04-18 Heinz Pauls 1-aroyl-piperidinyl benzamidines
WO2001087921A2 (en) 2000-05-16 2001-11-22 Merck & Co., Inc. Gene responsible for stargardt-like dominant macular dystrophy
WO2002005819A1 (en) 2000-07-15 2002-01-24 Smithkline Beecham Corporation Compounds and methods
US6962936B2 (en) 2001-04-27 2005-11-08 Vertex Pharmaceuticals Incorporated Triazole-derived kinase inhibitors and uses thereof
JP2004532899A (ja) 2001-07-06 2004-10-28 ニューロサーチ、アクティーゼルスカブ 新規化合物、その製造方法及びその使用方法
WO2003024450A1 (en) 2001-09-20 2003-03-27 Eisai Co., Ltd. Methods for treating prion diseases
WO2003024456A1 (en) 2001-09-20 2003-03-27 Eisai Co., Ltd. Methods for treating and preventing migraines
WO2003032914A2 (en) 2001-10-17 2003-04-24 Eisai Co., Ltd. Methods for treating substance abuse with cholinesterase inhibitors
WO2003066581A1 (en) 2002-02-05 2003-08-14 Eli Lilly And Company Urea linker derivatives for use as ppar modulators
US20030195192A1 (en) 2002-04-05 2003-10-16 Fortuna Haviv Nicotinamides having antiangiogenic activity
IL164007A0 (en) 2002-03-13 2005-12-18 Janssen Pharmaceutica Nv New inhibitors of histone deacetylase
AU2003228796A1 (en) 2002-05-01 2003-11-17 Eisai Co., Ltd. Cholinesterase inhibitors to prevent injuries caused by chemicals
AU2003298514A1 (en) 2002-05-17 2004-05-04 Eisai Co., Ltd. Methods and compositions using cholinesterase inhibitors
EP2508204B1 (en) 2002-06-26 2014-09-24 Ono Pharmaceutical Co., Ltd. Remedies for diseases caused by vascular contraction or dilation
MXPA05000947A (es) 2002-07-25 2005-05-16 Pharmacia Italia Spa Biciclo-pirazoles activos como inhibidores de cinasa, procedimiento para su preparacion y composiciones farmaceuticas que los contienen.
WO2004010942A2 (en) 2002-07-31 2004-02-05 Smithkline Beecham Corporation Substituted heterocyclic compounds as modulators of the ccr5 receptor
AU2003255845A1 (en) 2002-08-22 2004-03-11 Piramed Limited Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents
US7196082B2 (en) 2002-11-08 2007-03-27 Merck & Co. Inc. Ophthalmic compositions for treating ocular hypertension
US7501405B2 (en) * 2003-04-11 2009-03-10 High Point Pharmaceuticals, Llc Combination therapy using an 11β-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent for the treatment of metabolic syndrome and related diseases and disorders
JP2006522750A (ja) 2003-04-11 2006-10-05 ノボ ノルディスク アクティーゼルスカブ 代謝性症候群ならびに関連の疾患および障害を治療するために、11β−ヒドロキシステロイドデヒドロゲナーゼ1型阻害剤および抗高血圧剤を使用する併用療法
US7700583B2 (en) * 2003-04-11 2010-04-20 High Point Pharmaceuticals, Llc 11β-hydroxysteroid dehydrogenase type 1 active compounds
US20060287394A1 (en) 2003-05-30 2006-12-21 Konstantin Petrukhin Composition and method for treating macular disorders
WO2004110996A1 (en) 2003-06-19 2004-12-23 Pfizer Products Inc. Nk1 antagonist
FR2857363B1 (fr) * 2003-07-10 2007-09-07 Aventis Pharma Sa 4,5,6,7-tetrahydro-1h-pyrazolo[3,4-c] pyridines substituees compositions les contenant et utilisation
AR045037A1 (es) 2003-07-10 2005-10-12 Aventis Pharma Sa Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion.
WO2005074535A2 (en) 2004-01-30 2005-08-18 Eisai Co., Ltd. Cholinesterase inhibitors for spinal cord disorders
US7435831B2 (en) 2004-03-03 2008-10-14 Chemocentryx, Inc. Bicyclic and bridged nitrogen heterocycles
WO2005087226A1 (en) 2004-03-05 2005-09-22 Eisai Co., Ltd. Cadasil treatment with cholinesterase inhibitors
BRPI0511295A (pt) 2004-05-18 2007-12-04 Schering Corp 2-quinolil-oxazóis substituìdos úteis como inibidores de pde4
FR2872416B1 (fr) 2004-07-01 2006-09-22 Oreal Utilisation de derives de piperidine pour lutter contre les rides
JPWO2006004201A1 (ja) 2004-07-01 2008-04-24 エーザイ・アール・アンド・ディー・マネジメント株式会社 神経再生促進剤
WO2006015737A1 (de) 2004-08-02 2006-02-16 Schwarz Pharma Ag Carboxamide des indolizins und seiner aza- und diazaderivate
JP2006077006A (ja) 2004-08-13 2006-03-23 Eisai Co Ltd 加齢に伴う過活動膀胱治療薬
WO2006033734A2 (en) 2004-08-18 2006-03-30 Sirion Therapeutics, Inc. Combination compositions comprising 13-cis-retinyl derivatives and uses thereof to treat opthalmic disorders
JP4639696B2 (ja) 2004-08-31 2011-02-23 Jsr株式会社 磁性体複合粒子およびその製造方法
WO2006034446A2 (en) 2004-09-20 2006-03-30 Xenon Pharmaceuticals Inc. Pyridine derivatives for inhibiting human stearoyl-coa-desaturase
MX2007003332A (es) 2004-09-20 2007-06-05 Xenon Pharmaceuticals Inc Derivados heterociclicos y su uso como inhibidores de estearoil-coa-desaturasa.
BRPI0517378A (pt) 2004-10-27 2008-10-07 Janssen Pharmaceutica Nv moduladores de tetraidro piridinil pirazol canabinóide
EP1807103A4 (en) 2004-11-04 2009-02-11 Sirion Therapeutics Inc MODULATORS OF A COMPLEX RETINOL-RETINOL-BINDING PROTEIN-TRANSTHYRETINE FORMATION
MX2007006178A (es) 2004-11-23 2007-06-20 Ptc Therapeutics Inc Fenoles substituidos como agentes activos que inhiben la produccion del factor de crecimiento endotelial vascular.
JP2006176503A (ja) 2004-11-26 2006-07-06 Tohoku Univ 脳血管障害を伴うアルツハイマー病治療薬
EA011154B1 (ru) 2004-12-08 2009-02-27 Сирион Терапьютикс, Инк. Композиции для лечения ретинол-ассоциированных заболеваний
WO2006066879A2 (en) * 2004-12-21 2006-06-29 Devgen N.V. Compounds with kv4 ion channel activity
GB0503056D0 (en) 2005-02-14 2005-03-23 Smithkline Beecham Corp Chemical compounds
WO2006094235A1 (en) 2005-03-03 2006-09-08 Sirtris Pharmaceuticals, Inc. Fused heterocyclic compounds and their use as sirtuin modulators
AU2006244074B2 (en) 2005-05-09 2012-12-13 Hydra Biosciences, Inc. Compounds for modulating TRPV3 function
US7632837B2 (en) 2005-06-17 2009-12-15 Bristol-Myers Squibb Company Bicyclic heterocycles as cannabinoid-1 receptor modulators
UA81382C2 (en) 2005-07-11 2007-12-25 Composition for treating retinol-related diseases by modulation of retinol binding
RU2422442C2 (ru) * 2005-07-29 2011-06-27 Ф. Хоффманн-Ля Рош Аг Производные индол-3-ил-карбонил-пиперидина и пиперазина
EP1923388A4 (en) 2005-08-12 2011-03-09 Takeda Pharmaceutical BRAIN / NERVE CELL PROTECTION AND THERAPEUTIC FOR SLEEP DISORDERS
US20090258862A1 (en) 2005-08-29 2009-10-15 Colletti Steven L Niacin receptor agonists, compositions containing such compounds and methods of treatment
EP2407453A1 (en) 2005-09-27 2012-01-18 Shionogi & Co., Ltd. PGD2 receptor antagonist
US7576106B2 (en) 2005-10-11 2009-08-18 Chemocentryx, Inc. Piperidine derivatives and methods of use
DE102005049954A1 (de) * 2005-10-19 2007-05-31 Sanofi-Aventis Deutschland Gmbh Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen
ES2407115T3 (es) 2005-11-18 2013-06-11 Ono Pharmaceutical Co., Ltd. Compuesto que contiene un grupo básico y uso del mismo
WO2007086584A1 (ja) 2006-01-30 2007-08-02 Meiji Seika Kaisha, Ltd. 新規FabKおよびFabI/K阻害剤
US20070254911A1 (en) 2006-03-27 2007-11-01 Mingde Xia Tetrahydro-Pyrazolo[3,4-c]Pyridine Cannabinoid Modulators
CA2647545C (en) 2006-04-03 2016-02-23 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Amide substituted indazole and benzotriazole derivatives as poly(adp-ribose)polymerase (parp) inhibitors
EP2027132B1 (en) 2006-05-18 2010-09-15 F. Hoffmann-La Roche AG Thiazolo-pyramidine / pyridine urea derivatives as adenosine a2b receptor antagonists
CA2665195C (en) 2006-10-11 2011-08-09 Amgen Inc. Imidazo- and triazolo-pyridine compounds and methods of use thereof
ES2371784T3 (es) 2006-12-08 2012-01-10 F. Hoffmann-La Roche Ag Indoles.
DE102006060598A1 (de) 2006-12-21 2008-06-26 Merck Patent Gmbh Tetrahydrobenzoisoxazole
DK2170340T3 (en) 2007-06-21 2016-03-14 Neuronascent Inc Methods and compositions for Stimulating neurogenesis and inhibition of neuronal degeneration BY USING ISOTHIAZOLOPYRIMIDINONER
US20120121540A1 (en) 2007-08-10 2012-05-17 Franz Ulrich Schmitz Certain Nitrogen Containing Bicyclic Chemical Entities For Treating Viral Infections
US7973079B2 (en) 2007-09-27 2011-07-05 Revision Therapeutics, Inc. Methods and compounds for treating retinol-related diseases
WO2009042444A2 (en) 2007-09-27 2009-04-02 Sirion Therapeutics, Inc. Methods and compounds for treating retinol-related diseases
WO2009051244A1 (ja) 2007-10-18 2009-04-23 Takeda Pharmaceutical Company Limited 複素環化合物
EP2085398A1 (en) 2008-02-01 2009-08-05 Merz Pharma GmbH & Co. KGaA Pyrazolopyrimidines, a process for their preparation and their use as medicine
EP2295406B1 (en) 2008-05-30 2014-04-23 Takeda Pharmaceutical Company Limited Heterocyclic compound
WO2014097304A1 (en) 2012-12-22 2014-06-26 Maytronics Ltd. Autonomous pool cleaning robot
MX2011002263A (es) 2008-09-10 2011-05-23 Kalypsys Inc Aminopirimidinas como inhibidores de receptores de histamina para el tratamiento de enfermedades.
US20100168080A1 (en) 2008-12-17 2010-07-01 Khamrai Uttam Novel compounds useful as cc chemokine receptor ligands
JP6062633B2 (ja) 2009-01-28 2017-01-18 カラ セラピューティクス インコーポレイテッド 二環式ピラゾロ複素環類
US20100204265A1 (en) 2009-02-09 2010-08-12 Genelabs Technologies, Inc. Certain Nitrogen Containing Bicyclic Chemical Entities for Treating Viral Infections
JP5642661B2 (ja) * 2009-03-05 2014-12-17 塩野義製薬株式会社 Npyy5受容体拮抗作用を有するピペリジンおよびピロリジン誘導体
TW201041868A (en) 2009-03-20 2010-12-01 Intervet Int Bv Anthelmintic agents and their use
WO2010108268A1 (en) 2009-03-23 2010-09-30 Merck Frosst Canada Ltd. Heterocyclic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase
JP2012523461A (ja) 2009-04-13 2012-10-04 アイアールエム・リミテッド・ライアビリティ・カンパニー レチノール結合タンパク質4(rbp4)へのレチノールの結合を調節するための組成物および方法
BRPI1013763A2 (pt) 2009-04-16 2015-08-25 Takeda Pharmaceutical Composto ou sal do mesmo, prodroga, composição farmacêutica, agente diminuidor da proteína de ligação de retinol 4, agente para a profilaxia ou tratamento de diabetes, e, uso de um composto
MX2011012584A (es) 2009-05-26 2012-02-21 Exelixis Inc Benzoxazepinas como inhibidores de pi3k/m tor, metodos para su uso y fabricación.
US8102887B2 (en) 2009-05-26 2012-01-24 Corning Incorporated Edge bonded optical packages
AR076928A1 (es) 2009-05-28 2011-07-20 Otsuka Pharma Co Ltd Derivados de 3h-pirido[4, 3-d]pirimidin-4-ona, un metodo para su preparacion, composiciones farmaceuticas que los comprenden y su uso en la manufactura de un medicamento para el tratamiento o prevencion de enfermedades relacionadas con el estres.
ES2540547T3 (es) 2009-09-16 2015-07-10 The University Of Edinburgh Compuestos de (4-fenil-piperidin-1-il)-[5-(1H-pirazol-4-il)-tiofen-3-il]-metanona y su uso
WO2011059881A1 (en) 2009-11-12 2011-05-19 The Trustees Of Columbia University In The City Of New York Treatment of ophthalmic conditions with fluorenone derivatives
CA2781888C (en) 2009-12-11 2019-06-18 Nono Inc. Agents and methods for treating ischemic and other diseases
RU2581367C2 (ru) 2010-03-01 2016-04-20 Джи Ти Икс, ИНК. Соединения для лечения рака
WO2011116356A2 (en) 2010-03-19 2011-09-22 Sanford-Burnham Medical Research Institute Positive allosteric modulators of group ii mglurs
WO2011116123A1 (en) 2010-03-19 2011-09-22 Irm Llc Tafamidis for the treatment of ophthalmic diseases
WO2011149993A2 (en) 2010-05-25 2011-12-01 Abbott Laboratories SUBSTITUTED OCTAHYDROCYCLOPENTA[c]PYRROLES AS CALCIUM CHANNEL MODULATORS
WO2011156632A2 (en) 2010-06-09 2011-12-15 Georgetown University Compositions and methods of treatment for tumors in the nervous system
CA2803009A1 (en) * 2010-07-01 2012-01-05 Amgen Inc. Heterocyclic compounds and their use as inhibitors of pi3k activity
BR112013004623A2 (pt) 2010-08-27 2016-07-05 Novartis Ag "inibidores de desacetilases com base em hidroxamato."
EP2642998B1 (en) 2010-11-24 2020-09-16 The Trustees of Columbia University in the City of New York A non-retinoid rbp4 antagonist for treatment of age-related macular degeneration and stargardt disease
US9290453B2 (en) 2010-12-23 2016-03-22 Merck Sharp & Dohme Corp. Quinolines and aza-quinolines as CRTH2 receptor modulators
US9295676B2 (en) 2011-03-17 2016-03-29 The Trustees Of The University Of Pennsylvania Mutation mimicking compounds that bind to the kinase domain of EGFR
WO2012158844A1 (en) 2011-05-17 2012-11-22 Shionogi & Co., Ltd. Heterocyclic compounds
WO2013166041A1 (en) 2012-05-01 2013-11-07 The Trustees Of Columbia University In The City Of New York Transthyretin ligands capable of inhibiting retinol-dependent rbp4-ttr interaction for treatment of age-related macular
US9333202B2 (en) 2012-05-01 2016-05-10 The Trustees Of Columbia University In The City Of New York Non-retinoid antagonists for treatment of age-related macular degeneration and stargardt disease
WO2013166040A1 (en) 2012-05-01 2013-11-07 The Trustees Of Columbia University In The City Of New York S-fta and s-fta analogues capable of inhibiting retinol-dependent rbp4-ttr interaction for treatment of age-related macular degeneration, stargardt disease, and other retinal disease characterized by excessive lipofuscin accumulation
TW201501713A (zh) * 2013-03-01 2015-01-16 Kyowa Hakko Kirin Co Ltd 眼炎症性疾病之預防及/或治療劑
WO2014152018A1 (en) 2013-03-14 2014-09-25 The Trustees Of Columbia University In The City Of New York Octahydrocyclopentapyrroles, their preparation and use
US9938291B2 (en) 2013-03-14 2018-04-10 The Trustess Of Columbia University In The City Of New York N-alkyl-2-phenoxyethanamines, their preparation and use
US9944644B2 (en) 2013-03-14 2018-04-17 The Trustees Of Columbia University In The City Of New York Octahydropyrrolopyrroles their preparation and use
US20160030422A1 (en) 2013-03-14 2016-02-04 Konstantin Petrukhin Rbp4 antagonists for the treatment of age-related macular degeneration and stargardt disease
US10273243B2 (en) 2013-03-14 2019-04-30 The Trustees Of Columbia University In The City Of New York 4-phenylpiperidines, their preparation and use
EP3137168B1 (en) * 2014-04-30 2022-01-05 The Trustees of Columbia University in the City of New York Substituted 4-phenylpiperidines, their preparation and use

Also Published As

Publication number Publication date
ES2909793T3 (es) 2022-05-10
JP6676541B2 (ja) 2020-04-08
CN106794364A (zh) 2017-05-31
US20180030060A1 (en) 2018-02-01
WO2015168286A8 (en) 2016-11-17
AU2015253232A1 (en) 2016-11-24
BR112016025356A2 (pt) 2017-08-15
NZ726053A (en) 2023-10-27
HK1232169A1 (zh) 2018-01-05
PH12016502147A1 (en) 2017-01-16
CN106794364B (zh) 2019-12-24
US20180354957A1 (en) 2018-12-13
WO2015168286A1 (en) 2015-11-05
CA2947174A1 (en) 2015-11-05
BR112016025356B1 (pt) 2023-04-18
JP2017514822A (ja) 2017-06-08
AU2015253232B2 (en) 2020-10-01
US9777010B2 (en) 2017-10-03
KR102429220B1 (ko) 2022-08-04
US10913746B2 (en) 2021-02-09
EP4036094A1 (en) 2022-08-03
US20190382409A1 (en) 2019-12-19
US10407433B2 (en) 2019-09-10
CN111393434A (zh) 2020-07-10
US11649240B2 (en) 2023-05-16
SG11201608943VA (en) 2016-11-29
EP3137168A1 (en) 2017-03-08
US20230312585A1 (en) 2023-10-05
US20150315197A1 (en) 2015-11-05
US9434727B2 (en) 2016-09-06
BR112016025356A8 (pt) 2021-07-06
US10072016B2 (en) 2018-09-11
PH12016502147B1 (en) 2017-01-16
KR20160147037A (ko) 2016-12-21
EP3137168B1 (en) 2022-01-05
US20210214360A1 (en) 2021-07-15
CN111393434B (zh) 2022-11-04
CA2947174C (en) 2023-02-28
EP3137168A4 (en) 2017-12-20
US20160368925A1 (en) 2016-12-22
DK3137168T3 (da) 2022-03-21

Similar Documents

Publication Publication Date Title
PH12016502147A1 (en) Substituted 4-phenylpiperidines, their preparation and use
PH12018501151A1 (en) Tank-binding kinase inhibitor compounds
PH12017500408B1 (en) Heteroaryl compounds as btk inhibitors and uses thereof
MX2016015862A (es) Compuestos inhibidores de la cinasa de union a tank.
MX2017006266A (es) Compuestos de heteroarilo como inhibidores de cinasas asociadas al receptor de interleucina 1(irak) y sus usos.
PH12018500457A1 (en) New phenoxymethyl derivatives
PH12015502031A1 (en) Tetrahydropyrrolothiazine compounds
PH12017501523A1 (en) Selective bace1 inhibitors
MX2017003930A (es) Derivados de aminotriazina utiles como compuestos inhibidores de la cinasa de union a tank.
MA39749A (fr) Dérivés de pipéridine-dione
MX2016009794A (es) Derivado de sulfonamida heterociclico y medicina que comprende el mismo.
JO3318B1 (ar) مثبطات bace
MX2017016619A (es) Derivados de pirimidina como inhibidores de tirosina cinasa de bruton (btk) y usos de los mismos.
PH12018500903A1 (en) Pyranodipyridine compound
EA201591915A1 (ru) Соединения феноксиэтил дигидро-1h-изохинолина
MX2015008829A (es) Momelotinib deuterado.
NZ730816A (en) Quinoline carboxamides for use in the treatment of multiple myeloma
MX2017006110A (es) Carboxamidas de quinolina para usarse en el tratamiento de leucemia.
MX2016013439A (es) Formas solidas de un compuesto farmaceuticamente activo.
MX2017005140A (es) Procedimiento para la preparacion de benzotrihaluro sustituido.
MX2015012610A (es) Pacritinib deuterizado.
EA201791596A1 (ru) Пиразоловые соединения
MX2018002193A (es) Metodo de uso de quinoxalinilo-piperazinamida.
MX2017005669A (es) Derivados de hidroxido de bencilo, preparacion de los mismos y uso terapeutico de los mismos.
TWD167156S (zh) 鞋墊