ECSP11010830A - Derivados de heteroarilo como inhibidores de dgat1 - Google Patents

Derivados de heteroarilo como inhibidores de dgat1

Info

Publication number
ECSP11010830A
ECSP11010830A EC2011010830A ECSP11010830A ECSP11010830A EC SP11010830 A ECSP11010830 A EC SP11010830A EC 2011010830 A EC2011010830 A EC 2011010830A EC SP11010830 A ECSP11010830 A EC SP11010830A EC SP11010830 A ECSP11010830 A EC SP11010830A
Authority
EC
Ecuador
Prior art keywords
heteroarilo
derivatives
treatment
dgat1 inhibitors
disorders
Prior art date
Application number
EC2011010830A
Other languages
English (en)
Inventor
Cornelia Jutta Forster
Bin Wang
Katsumasa Nakajima
Young-Shin Kwak
Original Assignee
Novartis Ag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41136646&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ECSP11010830(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of ECSP11010830A publication Critical patent/ECSP11010830A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic 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
    • C07D277/32Heterocyclic 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
    • C07D277/38Nitrogen atoms
    • C07D277/44Acylated amino or imino radicals
    • C07D277/46Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/101,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
    • C07D249/14Nitrogen atoms
    • 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
    • A61K31/41Heterocyclic 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
    • A61K31/425Thiazoles
    • A61K31/4261,3-Thiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Diabetes (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Child & Adolescent Psychology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La invención se refiere a los compuestos de la fórmula (I), en donde A es un heteroarilo opcionalmente sustituido, útiles para el tratamiento de los trastornos mediados por acil-transferasa de acil-CoA-diacil-glicerol 1 (DGAT1), por ejemplo, trastornos metabólicos. La invención también proporciona métodos para el tratamiento de estos trastornos, y los compuestos y composiciones etc. para su tratamiento.
EC2011010830A 2008-07-15 2011-02-15 Derivados de heteroarilo como inhibidores de dgat1 ECSP11010830A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US8091308P 2008-07-15 2008-07-15

Publications (1)

Publication Number Publication Date
ECSP11010830A true ECSP11010830A (es) 2011-03-31

Family

ID=41136646

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2011010830A ECSP11010830A (es) 2008-07-15 2011-02-15 Derivados de heteroarilo como inhibidores de dgat1

Country Status (23)

Country Link
US (1) US8703761B2 (es)
EP (4) EP2559455A1 (es)
JP (1) JP5401544B2 (es)
KR (1) KR20110028661A (es)
CN (1) CN102119047B (es)
AR (1) AR072559A1 (es)
AU (1) AU2009272826A1 (es)
BR (1) BRPI0916216A2 (es)
CA (1) CA2731097A1 (es)
CL (1) CL2011000087A1 (es)
CO (1) CO6341581A2 (es)
CR (1) CR20110013A (es)
EA (1) EA201100189A1 (es)
EC (1) ECSP11010830A (es)
IL (1) IL210292A0 (es)
MA (1) MA32558B1 (es)
MX (1) MX2011000628A (es)
NZ (1) NZ590285A (es)
PE (1) PE20110105A1 (es)
SV (1) SV2011003809A (es)
TW (1) TW201006832A (es)
UY (1) UY31986A (es)
WO (1) WO2010007046A2 (es)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR066169A1 (es) * 2007-09-28 2009-07-29 Novartis Ag Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat
WO2010011821A2 (en) * 2008-07-24 2010-01-28 Theravance, Inc. Dual-acting antihypertensive agents
CA2752739A1 (en) * 2009-02-17 2010-08-26 Msd K.K. 1,4-benzodiazepin-2-on derivatives
JP6099753B2 (ja) * 2012-10-03 2017-03-22 アドビナス セラピューティクス リミテッド スピロ環化合物、その組成物及びその医薬応用
LT3319959T (lt) 2015-07-06 2021-12-27 Alkermes, Inc. Histono deacetilazės hetero-halogeno inhibitoriai
WO2017007755A1 (en) 2015-07-06 2017-01-12 Rodin Therapeutics, Inc. Heterobicyclic n-aminophenyl-amides as inhibitors of histone deacetylase
WO2017087885A1 (en) 2015-11-19 2017-05-26 Dana-Farber Cancer Institute, Inc. Methods of identifying compounds that interfere with erg-driven misguidance of baf complexes in tmprss2-erg driven prostate cancers
TWI691486B (zh) 2016-01-29 2020-04-21 日商東麗股份有限公司 環狀胺衍生物及其醫藥用途
US10793567B2 (en) 2017-01-11 2020-10-06 Rodin Therapeutics, Inc. Bicyclic inhibitors of histone deacetylase
CN110913859A (zh) 2017-07-27 2020-03-24 东丽株式会社 圆形脱毛症的治疗剂或预防剂
EA039417B1 (ru) 2017-08-07 2022-01-25 Родин Терапеутикс, Инк. Бициклические ингибиторы гистондеацетилазы
CN112153984A (zh) * 2018-01-30 2020-12-29 福宏治疗公司 化合物及其用途
TWI805699B (zh) 2018-03-01 2023-06-21 日商日本煙草產業股份有限公司 甲基內醯胺環化合物及其用途
MX2020010433A (es) 2018-04-04 2020-10-28 Japan Tobacco Inc Compuestos de pirazol sustituidos con heteroarilo y uso farmaceutico de los mismos.
WO2020036869A1 (en) 2018-08-16 2020-02-20 Emd Millipore Corporation Closed bioprocessing device
WO2020081588A1 (en) 2018-10-17 2020-04-23 Dana-Farber Cancer Institute, Inc. Swi/snf family chromatin remodeling complexes and uses thereof
EP3886854A4 (en) 2018-11-30 2022-07-06 Nuvation Bio Inc. Pyrrole and pyrazole compounds and methods of use thereof
WO2020160100A1 (en) 2019-01-29 2020-08-06 Foghorn Therapeutics Inc. Compounds and uses thereof
US12384776B2 (en) 2019-01-29 2025-08-12 Foghorn Therapeutics Inc. Compounds and uses thereof
IL285177B2 (en) * 2019-01-29 2025-09-01 Foghorn Therapeutics Inc Compounds and their use
JP7561195B2 (ja) 2020-01-29 2024-10-03 フォグホーン セラピューティクス インコーポレイテッド 化合物及びその使用
CA3166404A1 (en) * 2020-01-29 2021-08-05 Matthew Netherton A bifunctional molecule comprising an active compound,a linker and a degradation moiety, and its use to treat disorders associated with baf complex function
CA3166455A1 (en) * 2020-01-29 2021-08-05 Neville John ANTHONY Heterocyclic compounds useful for modulating baf complexes
US12383555B2 (en) 2020-05-20 2025-08-12 Foghorn Therapeutics Inc. Methods of treating cancers
CA3196233A1 (en) 2020-10-22 2022-04-28 Josep Bassaganya-Riera Lancl ligands
WO2023111996A1 (en) 2021-12-17 2023-06-22 Reglagene Holding, Inc. Compositions and methods of making and using small molecules in the treatment of cancer
TWD226927S (zh) 2022-09-21 2023-08-11 精誠軟體服務股份有限公司 電腦程式之具變化外觀之圖形化使用者介面
TWD226926S (zh) 2022-09-21 2023-08-11 精誠軟體服務股份有限公司 電腦程式之具變化外觀之圖形化使用者介面
KR20250176573A (ko) 2023-02-28 2025-12-19 레글라진, 아이엔씨. 건강 상태의 치료를 위한 소분자 제조 및 사용을 위한 조성물 및 방법
KR20240140019A (ko) * 2023-03-15 2024-09-24 현대약품 주식회사 신규한 화합물, 및 이를 포함하는 약학적 조성물
WO2026054614A1 (ko) * 2024-09-09 2026-03-12 현대약품 주식회사 신규한 화합물, 및 이를 포함하는 약학적 조성물

Family Cites Families (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1526938A (en) * 1974-12-19 1978-10-04 Shell Int Research Derivatives of n-phenyl-n-aroylalanine and herbicidal compositions containing them
CA1160234A (en) * 1980-10-30 1984-01-10 Masahiko Nagakura Thiadiazole derivatives and process for preparing same
CA2342471C (en) 1995-06-06 2002-10-29 Judith L. Treadway Heterocyclecarbonylmethyl amine intermediates
US5952294A (en) 1996-07-31 1999-09-14 University Of Pittsburgh Of The Commonwealth System Of Higher Education Peptidyl prodrugs and methods of making and using the same
FR2763337B1 (fr) * 1997-05-13 1999-08-20 Sanofi Sa Nouveaux derives du triazole, un procede pour leur preparation et compositions pharmaceutiques les contenant
AU6229699A (en) * 1998-10-26 2000-05-15 Sumitomo Pharmaceuticals Company, Limited Beta-amyloid formation inhibitors
WO2000044731A1 (en) * 1999-01-27 2000-08-03 G.D. Searle & Co. Novel hydroxyamidino carboxylate derivatives useful as nitric oxide synthase inhibitors
AU2001253090A1 (en) * 2000-04-03 2001-10-15 Bristol-Myers Squibb Pharma Company Cyclic lactams as inhibitors of abeta protein production
AU2002226330A1 (en) * 2000-10-26 2002-05-06 Sanofi-Synthelabo Triazole derivatives and pharmaceutical compositions comprising them
CA2448737C (en) * 2001-07-20 2010-06-01 Boehringer Ingelheim (Canada) Ltd. Viral polymerase inhibitors
EP2335700A1 (en) 2001-07-25 2011-06-22 Boehringer Ingelheim (Canada) Ltd. Hepatitis C virus polymerase inhibitors with a heterobicylic structure
TW200303742A (en) 2001-11-21 2003-09-16 Novartis Ag Organic compounds
US7030141B2 (en) * 2001-11-29 2006-04-18 Christopher Franklin Bigge Inhibitors of factor Xa and other serine proteases involved in the coagulation cascade
JP4164645B2 (ja) 2002-08-09 2008-10-15 株式会社大塚製薬工場 Dgat阻害剤
CA2501803A1 (en) 2002-10-09 2004-04-22 Pfizer Products Inc. Thiazole compounds for the treatment of neurodegenerative disorders
EP1551809A1 (en) * 2002-10-09 2005-07-13 Pfizer Products Inc. Pyrazole compounds for treatment of neurodegenerative disorders
EP1618090A1 (en) * 2003-04-11 2006-01-25 Novo Nordisk A/S 11ß-HYDROXYSTEROID DEHYDROGENASE TYPE 1 ACTIVE COMPOUNDS
KR100909918B1 (ko) 2003-05-20 2009-07-29 노파르티스 아게 과산화소체 증식체-활성화 수용체의 리간드로서의 n-아실질소 헤테로환
JP2005206492A (ja) * 2004-01-21 2005-08-04 Sankyo Co Ltd スルホンアミド化合物
TW200604168A (en) * 2004-04-02 2006-02-01 Vertex Pharma Azaindoles useful as inhibitors of rock and other protein kinases
US7402704B2 (en) 2004-04-14 2008-07-22 Amgen Inc. Arylsulfones and uses related thereto
JP2006089485A (ja) 2004-08-24 2006-04-06 Santen Pharmaceut Co Ltd ジヒドロオロテートデヒドロゲナーゼ阻害活性を有する新規複素環アミド誘導体
WO2006033434A1 (ja) 2004-09-24 2006-03-30 Midori Anzen Co., Ltd. 靴底及び靴
DE102004047840A1 (de) * 2004-09-29 2006-03-30 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue substituierte Thiophencarbonsäureamide, deren Herstellung und deren Verwendung als Arzneimittel
FR2876692B1 (fr) * 2004-10-19 2007-02-23 Sanofi Aventis Sa Derives de 2-amido-4-phenylthiazole, leur preparation et leur application en therapeutique
TWI360539B (en) * 2004-10-28 2012-03-21 Shionogi & Co 3-carbamoyl-2-pyridone derivatives
WO2006082952A1 (ja) 2005-02-01 2006-08-10 Takeda Pharmaceutical Company Limited アミド化合物
CN101171231A (zh) 2005-05-10 2008-04-30 霍夫曼-拉罗奇有限公司 二酰基甘油酰基转移酶抑制剂
WO2006127550A1 (en) * 2005-05-23 2006-11-30 Merck & Co., Inc. Proline bis-amide orexin receptor antagonists
AR055203A1 (es) * 2005-08-31 2007-08-08 Otsuka Pharma Co Ltd Derivados de benzotiofeno con propiedades antipsicoticas
EP1963313B1 (en) * 2005-11-28 2012-11-14 Madrigal Pharmaceuticals, Inc. Inhibitors of diacylglycerol acyltransferase (dgat)
EP2007716A1 (en) 2006-04-13 2008-12-31 Glaxo Group Limited Aryl and heteroaryl sulphonamides as growth hormone secretagogue receptor agonists
JP2009544616A (ja) 2006-07-21 2009-12-17 武田薬品工業株式会社 アミド化合物
TW200827340A (en) 2006-11-10 2008-07-01 Astrazeneca Ab Chemical compounds
JP2008133218A (ja) 2006-11-28 2008-06-12 Hokko Chem Ind Co Ltd フェノキシ酪酸アミド誘導体および除草剤
JP5496918B2 (ja) * 2008-02-21 2014-05-21 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Cb2受容体を調節するアミン化合物及びエーテル化合物

Also Published As

Publication number Publication date
IL210292A0 (en) 2011-03-31
MA32558B1 (fr) 2011-08-01
US20100022513A1 (en) 2010-01-28
TW201006832A (en) 2010-02-16
WO2010007046A3 (en) 2010-07-22
AU2009272826A1 (en) 2010-01-21
CN102119047A (zh) 2011-07-06
EA201100189A1 (ru) 2011-08-30
CN102119047B (zh) 2014-09-24
SV2011003809A (es) 2011-07-05
CL2011000087A1 (es) 2011-07-01
EP2380631A1 (en) 2011-10-26
JP5401544B2 (ja) 2014-01-29
MX2011000628A (es) 2011-02-25
CR20110013A (es) 2011-02-11
PE20110105A1 (es) 2011-02-25
EP2548618A3 (en) 2013-02-27
CO6341581A2 (es) 2011-11-21
EP2349484A2 (en) 2011-08-03
UY31986A (es) 2010-02-26
JP2011528016A (ja) 2011-11-10
NZ590285A (en) 2012-10-26
EP2559455A1 (en) 2013-02-20
EP2548618A2 (en) 2013-01-23
KR20110028661A (ko) 2011-03-21
CA2731097A1 (en) 2010-01-21
AR072559A1 (es) 2010-09-08
WO2010007046A2 (en) 2010-01-21
BRPI0916216A2 (pt) 2018-03-13
US8703761B2 (en) 2014-04-22

Similar Documents

Publication Publication Date Title
ECSP11010830A (es) Derivados de heteroarilo como inhibidores de dgat1
CR20110028A (es) Derivados de pirimidina como inhibidores de cinasa
CO6321282A2 (es) Derivados de piperidinilindol como inhibidores de aldosterona sintasa
EA201100447A1 (ru) Органические соединения
NI201000198A (es) Compuestos triazina como inhibidores mtor y quinasa p13.
SV2010003598A (es) Derivados de tiazol usados como inhibidores de pi 3-cinasa
BR112015004111A2 (pt) novos derivados bicíclicos
PA8848201A1 (es) Aminotetrahidropiranos como inhibidores de dipeptidil peptidasa-iv para el tratamiento o prevención de diabetes
ECSP11011411A (es) Derivados de prolina como inhibidores de catepsina
BR122019015876B8 (pt) compostos derivados de 1,2,5-oxadiazóis, composição, bem como seus usos
EA201200741A1 (ru) Способ получения этексилата дабигатрана
CR20120641A (es) Compuestos macrocìclicos como inhibidores de quinasa trk
MX2012012527A (es) Compuestos quimicos.
MA32508B1 (fr) Composes organiques
CR11803A (es) Pirrolopiridinas como inhibidores de cinasa
CO6362015A2 (es) Derivados de acido 1-amino-2ciclobutiletilboronico
UY39338A (es) Derivados de piperidinona como inhibidores mdm2, composiciones farmacéuticas que los contienen y sus usos
CO7111275A2 (es) Inhibidores de dgat1 de éter cíclico de cabeza de puente
EA200900945A1 (ru) Новый способ синтеза агомелатина
EA200900924A1 (ru) Циклизованные производные как ингибиторы eg-5
EA200900946A1 (ru) Новый способ синтеза агомелатина
MX394835B (es) Metodos para la preparacion de compuestos heterociclicos de 1,3-benzodioxol.
DOP2012000260A (es) Uso de nuevos inhibidores de pan–cdk para tratar tumores
CR11860A (es) Derivados de dibenzotiazepina y sus usos - 424
EA200900943A1 (ru) Новый способ синтеза агомелатина