[go: up one dir, main page]

PE20180044A1 - Compuestos novedosos - Google Patents

Compuestos novedosos

Info

Publication number
PE20180044A1
PE20180044A1 PE2017002302A PE2017002302A PE20180044A1 PE 20180044 A1 PE20180044 A1 PE 20180044A1 PE 2017002302 A PE2017002302 A PE 2017002302A PE 2017002302 A PE2017002302 A PE 2017002302A PE 20180044 A1 PE20180044 A1 PE 20180044A1
Authority
PE
Peru
Prior art keywords
alkyl
group
compounds
rip2 kinase
arylalkyl
Prior art date
Application number
PE2017002302A
Other languages
English (en)
Inventor
Linda N Casillas
John David Harling
Afjal Hussain Miah
Mark David Rackham
Ian Edward David Smith
Original Assignee
Glaxosmithkline Ip Dev Ltd
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 Glaxosmithkline Ip Dev Ltd filed Critical Glaxosmithkline Ip Dev Ltd
Publication of PE20180044A1 publication Critical patent/PE20180044A1/es

Links

Classifications

    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/14Heterocyclic 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
    • 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)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)
  • Peptides Or Proteins (AREA)

Abstract

Se refiere a un compuesto de Formula I, en la que X representa N o CH, R1 es H, -SO2 alquilo (C1-C4), o alquilo (C1-C4); R2 es SRa, -SORa, entre otros, en donde Ra es alquilo (C1-C6), halo alquilo (C1-C6) heterocicloalquilo, arilo o hereroarilo de 4-7 miembros, en donde dicho alquilo (C1-C6) esta sustituido opcionalmente por uno o dos grupos cada uno seleccionado independientemente del grupo que consiste en ciano, hidroxilo alcoxi, entre otros. Z es fenilo o arilalquil (C1-C4)-, en el que el grupo fenilo o el resto arilo del grupo arilalquil (C1-C4)- esta sustituido con R4, R5, R6, R7; R4 es H, halogeno, ciano, entre otros; Cada uno de R5, R6 y R7 esta seleccionado independientemente del grupo que consiste en H, hidroxilo, halogeno, entre otros. L es un grupo de enlace que comprende una longitud de 4-16 atomos en su longitud mas corta. Dichos compuestos modulan la actividad de la cinasa RIP2 incluyendo la degradacion de la misma que comprenden inhibidores de cinasa RIP2. Tambien se refiere a refiere a compuestos, composiciones, combinaciones y medicamentos que contienen dichos compuestos y a procedimientos para su preparacion. En donde pueden ser utiles para el tratamiento de enfermedades alergicas, autoinmunitarias; o estados inflamatorios, o cualquier estado mediado por la cinasa RIP2.
PE2017002302A 2015-04-22 2016-04-20 Compuestos novedosos PE20180044A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB1506872.9A GB201506872D0 (en) 2015-04-22 2015-04-22 Novel compounds

Publications (1)

Publication Number Publication Date
PE20180044A1 true PE20180044A1 (es) 2018-01-15

Family

ID=53299021

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2017002302A PE20180044A1 (es) 2015-04-22 2016-04-20 Compuestos novedosos

Country Status (21)

Country Link
US (2) US10435391B2 (es)
EP (1) EP3286169B1 (es)
JP (1) JP2018513867A (es)
KR (1) KR20170139096A (es)
CN (1) CN107709305B (es)
AU (1) AU2016252404B2 (es)
BR (1) BR112017022604A2 (es)
CA (1) CA2983414A1 (es)
CL (1) CL2017002650A1 (es)
CO (1) CO2017011851A2 (es)
CR (1) CR20170478A (es)
EA (1) EA033343B1 (es)
ES (1) ES2841548T3 (es)
GB (1) GB201506872D0 (es)
HK (1) HK1243410A1 (es)
IL (1) IL255067A0 (es)
MX (1) MX375674B (es)
PE (1) PE20180044A1 (es)
PH (1) PH12017501921A1 (es)
SG (1) SG11201708311UA (es)
WO (1) WO2016172134A2 (es)

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102438072B1 (ko) 2012-01-12 2022-08-31 예일 유니버시티 E3 유비퀴틴 리가아제에 의한 표적 단백질 및 다른 폴리펩티드의 증진된 분해를 위한 화합물 및 방법
WO2015109391A1 (en) 2014-01-24 2015-07-30 Children's Hospital Of Eastern Ontario Research Institute Inc. Smc combination therapy for the treatment of cancer
US20180228907A1 (en) 2014-04-14 2018-08-16 Arvinas, Inc. Cereblon ligands and bifunctional compounds comprising the same
US10071164B2 (en) * 2014-08-11 2018-09-11 Yale University Estrogen-related receptor alpha based protac compounds and associated methods of use
US12312316B2 (en) 2015-01-20 2025-05-27 Arvinas Operations, Inc. Compounds and methods for the targeted degradation of androgen receptor
WO2016118666A1 (en) 2015-01-20 2016-07-28 Arvinas, Inc. Compounds and methods for the targeted degradation of the androgen receptor
JP7269731B2 (ja) 2015-03-18 2023-05-09 アルビナス・オペレーションズ・インコーポレイテッド 標的タンパク質の分解向上のための化合物および方法
GB201506872D0 (en) 2015-04-22 2015-06-03 Ge Oil & Gas Uk Ltd Novel compounds
EP3302482A4 (en) 2015-06-05 2018-12-19 Arvinas, Inc. Tank-binding kinase-1 protacs and associated methods of use
EP3337476A4 (en) 2015-08-19 2019-09-04 Arvinas, Inc. Compounds and methods for the targeted degradation of bromodomain-containing proteins
US10781205B2 (en) * 2016-04-20 2020-09-22 Glaxosmithkline Intellectual Property Development Limited Conjugates comprising RIPK2 inhibitors
WO2018053354A1 (en) 2016-09-15 2018-03-22 Arvinas, Inc. Indole derivatives as estrogen receptor degraders
PL3526202T3 (pl) 2016-10-11 2025-04-28 Arvinas Operations, Inc. Związki i sposoby do ukierunkowanej degradacji receptora androgenowego
KR20230127371A (ko) 2016-11-01 2023-08-31 아비나스 오퍼레이션스, 인코포레이티드 타우(Tau)-단백질 표적화 프로탁(PROTAC) 및 관련 사용 방법
CN114656452B (zh) 2016-12-01 2023-01-17 阿尔维纳斯运营股份有限公司 作为雌激素受体降解剂的四氢萘和四氢异喹啉衍生物
CN117510491A (zh) 2016-12-23 2024-02-06 阿尔维纳斯运营股份有限公司 用于迅速加速性纤维肉瘤多肽的靶向降解的化合物和方法
US11173211B2 (en) 2016-12-23 2021-11-16 Arvinas Operations, Inc. Compounds and methods for the targeted degradation of rapidly accelerated Fibrosarcoma polypeptides
EP3559006A4 (en) 2016-12-23 2021-03-03 Arvinas Operations, Inc. COMPOUNDS AND METHODS FOR TARGETED DEGRADATION OF F TAL LIVER KINASE POLYPEPTIDES
BR112019012682A2 (pt) 2016-12-23 2019-12-17 Arvinas Operations Inc moléculas quiméricas visando a proteólise de egfr e métodos associados de uso
US11191741B2 (en) 2016-12-24 2021-12-07 Arvinas Operations, Inc. Compounds and methods for the targeted degradation of enhancer of zeste homolog 2 polypeptide
JP7266526B6 (ja) 2017-01-26 2024-02-15 アルビナス・オペレーションズ・インコーポレイテッド エストロゲン受容体タンパク質分解性の調節因子およびその関連方法
CN115974840A (zh) 2017-01-31 2023-04-18 阿尔维纳斯运营股份有限公司 人小脑蛋白配体和包含其的双官能化合物
WO2019099926A1 (en) 2017-11-17 2019-05-23 Arvinas, Inc. Compounds and methods for the targeted degradation of interleukin-1 receptor-associated kinase 4 polypeptides
CN107987083A (zh) * 2017-11-24 2018-05-04 江苏亚盛医药开发有限公司 用于治疗和/或预防与肝炎病毒相关的疾病或病症的双二氮杂双环化合物
US11220515B2 (en) 2018-01-26 2022-01-11 Yale University Imide-based modulators of proteolysis and associated methods of use
KR20210006356A (ko) 2018-04-04 2021-01-18 아비나스 오퍼레이션스, 인코포레이티드 단백질분해 조절제 및 연관된 사용 방법
JP7515175B2 (ja) 2018-07-31 2024-07-12 ファイメクス株式会社 複素環化合物
JP7297053B2 (ja) 2018-08-20 2023-06-23 アルビナス・オペレーションズ・インコーポレイテッド 神経変性疾患を治療するためのe3ユビキチンリガーゼ結合活性を有するキメラ(protac)化合物を標的とし、アルファ-シヌクレインタンパク質を標的とするタンパク質分解
WO2020043122A1 (zh) * 2018-08-28 2020-03-05 南京明德新药研发有限公司 作为rip2激酶抑制剂的喹唑啉类衍生物
US11547759B2 (en) 2019-01-30 2023-01-10 Montelino Therapeutics, Inc. Bi-functional compounds and methods for targeted ubiquitination of androgen receptor
US11098025B2 (en) 2019-01-30 2021-08-24 Montelino Therapeutics, Inc. Bi-functional compounds and methods for targeted ubiquitination of androgen receptor
EP3941607A1 (en) 2019-03-21 2022-01-26 Codiak BioSciences, Inc. Process for preparing extracellular vesicles
SG11202109587TA (en) 2019-03-21 2021-10-28 Codiak Biosciences Inc Extracellular vesicle conjugates and uses thereof
EP3999182A1 (en) 2019-07-17 2022-05-25 Arvinas Operations, Inc. Tau-protein targeting compounds and associated methods of use
JP2021024787A (ja) 2019-07-31 2021-02-22 ファイメクス株式会社 複素環化合物
WO2021020585A1 (ja) 2019-07-31 2021-02-04 ファイメクス株式会社 複素環化合物
WO2021041348A1 (en) 2019-08-26 2021-03-04 Arvinas Operations, Inc. Methods of treating breast cancer with tetrahydronaphthalene derivatives as estrogen receptor degraders
CN115397821B (zh) 2019-10-17 2024-09-03 阿尔维纳斯运营股份有限公司 含有与bcl6靶向部分连接的e3泛素连接酶结合部分的双官能分子
MX2022007678A (es) 2019-12-19 2022-09-19 Arvinas Operations Inc Compuestos y metodos para la degradacion dirigida del receptor de androgenos.
MX2022014071A (es) 2020-05-09 2023-01-30 Arvinas Operations Inc Metodos para fabricar un compuesto bifuncional, formas ultrapuras del compuesto bifuncional y formas de dosificacion que comprenden el mismo.
WO2021237100A1 (en) 2020-05-21 2021-11-25 Codiak Biosciences, Inc. Methods of targeting extracellular vesicles to lung
US12180193B2 (en) 2020-08-28 2024-12-31 Arvinas Operations, Inc. Accelerating fibrosarcoma protein degrading compounds and associated methods of use
US12162859B2 (en) 2020-09-14 2024-12-10 Arvinas Operations, Inc. Crystalline and amorphous forms of a compound for the targeted degradation of estrogen receptor
US20240025863A1 (en) * 2020-09-16 2024-01-25 Biotheryx, Inc. Sos1 protein degraders, pharmaceutical compositions thereof, and their therapeutic applications
WO2022066928A2 (en) 2020-09-23 2022-03-31 Codiak Biosciences, Inc. Process for preparing extracellular vesicles
WO2022197862A1 (en) * 2021-03-17 2022-09-22 Biotheryx, Inc. Sos1 protein degraders, pharmaceutical compositions thereof, and their therapeutic applications
AU2022259683A1 (en) 2021-04-16 2023-10-19 Arvinas Operations, Inc. Modulators of bcl6 proteolysis and associated methods of use
US11981672B2 (en) 2021-09-13 2024-05-14 Montelino Therapeutics Inc. Bi-functional compounds and methods for targeted ubiquitination of androgen receptor
US12419962B2 (en) 2022-03-16 2025-09-23 Biotheryx, Inc. Quinazolines, pharmaceutical compositions, and therapeutic applications
CA3246569A1 (en) 2022-03-24 2023-09-28 Glaxosmithkline Ip Dev Ltd 2,4-DIOXOTETRAHYDROPYRIMIDINYL DERIVATIVES USED AS DEGRONS IN PROTACS
TW202432544A (zh) 2022-09-07 2024-08-16 美商亞文納營運公司 快速加速纖維肉瘤降解化合物及相關使用方法
CN115869308B (zh) * 2022-12-30 2024-03-26 中山大学肿瘤防治中心(中山大学附属肿瘤医院、中山大学肿瘤研究所) 一种小分子化合物在制备抗结直肠癌药物中的应用
AU2024212035A1 (en) 2023-01-26 2025-08-14 Arvinas Operations, Inc. Cereblon-based kras degrading protacs ans uses related thereto
WO2024240858A1 (en) 2023-05-23 2024-11-28 Valerio Therapeutics Protac molecules directed against dna damage repair system and uses thereof
WO2025092821A1 (zh) * 2023-11-01 2025-05-08 成都赜灵生物医药科技有限公司 喹唑啉衍生物类ripk2抑制剂及其用途

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4541882B2 (ja) * 2002-07-02 2010-09-08 ノバルティス アーゲー Smacタンパク質のアポトーシスタンパク質阻害物質(iap)との結合に対するペプチド阻害剤
BRPI0513310A (pt) * 2004-07-12 2008-05-06 Idun Pharmaceuticals Inc análogos de tetrapeptìdeo
EA017797B1 (ru) 2007-04-13 2013-03-29 Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган Бициклические диазомиметики smac, способы их получения, их применения, содержащие их фармацевтические композиции и набор, содержащий указанные композиции
CA2683392A1 (en) 2007-04-30 2008-11-06 Genentech, Inc. Inhibitors of iap
WO2009136290A1 (en) * 2008-05-05 2009-11-12 Aegera Therapeutics, Inc. Functionalized pyrrolidines and use thereof as iap inhibitors
ES2643233T3 (es) 2009-10-23 2017-11-21 The Regents Of The University Of Michigan Miméticos de SMAC bicíclicos diazo bivalentes y los usos de los mismos
EP2566477B1 (en) * 2010-05-07 2015-09-02 GlaxoSmithKline Intellectual Property Development Limited Amino-quinolines as kinase inhibitors
UY33549A (es) 2010-08-10 2012-01-31 Glaxo Group Ltd Quinolil aminas como agentes inhibidores de las quinasas
CA2829131C (en) * 2011-03-04 2018-11-20 Glaxosmithkline Intellectual Property (No.2) Limited Amino-quinolines as kinase inhibitors
TWI547494B (zh) * 2011-08-18 2016-09-01 葛蘭素史克智慧財產發展有限公司 作為激酶抑制劑之胺基喹唑啉類
KR102438072B1 (ko) * 2012-01-12 2022-08-31 예일 유니버시티 E3 유비퀴틴 리가아제에 의한 표적 단백질 및 다른 폴리펩티드의 증진된 분해를 위한 화합물 및 방법
CN104718209A (zh) 2012-08-23 2015-06-17 密执安大学评议会 Iap蛋白的二价抑制剂和使用其的治疗方法
AR092529A1 (es) * 2012-09-13 2015-04-22 Glaxosmithkline Llc Compuesto de aminoquinazolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento
TW201425307A (zh) * 2012-09-13 2014-07-01 Glaxosmithkline Llc 作為激酶抑制劑之胺基-喹啉類
WO2014047024A1 (en) 2012-09-18 2014-03-27 Bristol-Myers Squibb Company Iap antagonists
EP2903998B1 (en) 2012-10-02 2017-03-15 Bristol-Myers Squibb Company Iap antagonists
CN104854100B (zh) 2012-12-11 2017-05-24 霍夫曼-拉罗奇有限公司 二聚化合物
RU2662810C2 (ru) 2013-02-21 2018-07-31 Глэксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед Хиназолины в качестве ингибиторов киназы
AU2015247817C1 (en) 2014-04-14 2022-02-10 Arvinas Operations, Inc. Imide-based modulators of proteolysis and associated methods of use
AU2015261812B2 (en) 2014-05-23 2019-11-21 F. Hoffmann-La Roche Ag 5-chloro-2-difluoromethoxyphenyl pyrazolopyrimidine compounds which are JAK inhibitors
EP3189054B1 (en) 2014-09-05 2019-07-24 Merck Patent GmbH (1-fluoro-cyclohex-1-yl)-ethyl substituted diaza- and triaza-tricyclic compounds as indole-amine-2,3-dioxygenase (ido) antagonists for the treatment of cancer
GB201506872D0 (en) 2015-04-22 2015-06-03 Ge Oil & Gas Uk Ltd Novel compounds
TW201642860A (zh) 2015-04-22 2016-12-16 塞爾基因定量細胞研究公司 布羅莫結構域抑制劑
DK3286181T3 (da) 2015-04-22 2021-04-06 Rigel Pharmaceuticals Inc Pyrazolforbindelser og fremgangsmåde til fremstilling og anvendelse af forbindelserne
GB201506871D0 (en) * 2015-04-22 2015-06-03 Glaxosmithkline Ip Dev Ltd Novel compounds
GB201516243D0 (en) 2015-09-14 2015-10-28 Glaxosmithkline Ip Dev Ltd Novel compounds
US10781205B2 (en) * 2016-04-20 2020-09-22 Glaxosmithkline Intellectual Property Development Limited Conjugates comprising RIPK2 inhibitors

Also Published As

Publication number Publication date
EP3286169A2 (en) 2018-02-28
HK1243410A1 (zh) 2018-07-13
CO2017011851A2 (es) 2018-02-09
EP3286169A4 (en) 2018-11-21
WO2016172134A2 (en) 2016-10-27
CL2017002650A1 (es) 2018-03-16
EA033343B1 (ru) 2019-09-30
AU2016252404A1 (en) 2017-12-07
CA2983414A1 (en) 2016-10-27
EP3286169B1 (en) 2020-10-07
SG11201708311UA (en) 2017-11-29
GB201506872D0 (en) 2015-06-03
PH12017501921A1 (en) 2018-03-19
US20190382381A1 (en) 2019-12-19
CN107709305B (zh) 2020-09-29
US20180134688A1 (en) 2018-05-17
MX2017013556A (es) 2018-08-01
JP2018513867A (ja) 2018-05-31
IL255067A0 (en) 2017-12-31
US10435391B2 (en) 2019-10-08
CR20170478A (es) 2018-01-22
ES2841548T3 (es) 2021-07-08
CN107709305A (zh) 2018-02-16
AU2016252404B2 (en) 2018-07-26
EA201792047A1 (ru) 2018-04-30
WO2016172134A3 (en) 2016-12-01
KR20170139096A (ko) 2017-12-18
BR112017022604A2 (pt) 2018-07-17
MX375674B (es) 2025-03-06

Similar Documents

Publication Publication Date Title
PE20180044A1 (es) Compuestos novedosos
CU20170073A7 (es) Compuestos de indazol sustituidos y compuestos intermediarios para la preparación de los mismos
PE20190656A1 (es) Compuestos de tiazolo-piridina sustituida como inhibidores de malt1
PE20181298A1 (es) Inhibidores de bromodominio bivalentes y usos de los mismos
MX2023007581A (es) Analogos de rapamicina unidos a c26 como inhibidores de mtor.
AR072063A1 (es) Mimeticos de glucocorticoides metodos para su fabricacion, composiciones farmaceuticas y usos de los mismos
CU24643B1 (es) Compuestos de 1,2,4-oxadiazol como inhibidores de las vías de señalización de cd47
AR086829A1 (es) Compuestos heterociclicos fusionados como moduladores del canal ionico
PE20181093A1 (es) Compuestos heterociclicos y usos de los mismos
AR107032A1 (es) Inhibidores bicíclicos de pad4
MX2015012815A (es) Derivados de 1-acil-4-amino-1,2,3,4-tetrahidroquinolina 2,3-disustituidos y su uso como inhibidores de bromodominio.
PE20180024A1 (es) Triazolopirazinonas como inhibidores de pde1
PE20180462A1 (es) Moduladores cot y metodos de uso de los mismos
AR101179A1 (es) Combinaciones anti-pd-l1 para tratar tumores
PE20160875A1 (es) Compuestos de biaril-amida como inhibidores de cinasa
AR103265A1 (es) Compuestos de azolina sustituidos con un sistema de anillos condensado
ECSP088926A (es) Compuestos de piridil amida sustituidos como moduladores del receptor h3 de la histamina
DOP2015000270A (es) Potenciador de inhibidores del homólogo de zeste
PE20140192A1 (es) Derivados de bencimidazol como inhibidores de cinasa pi3
PE20220567A1 (es) Nuevos derivados piperidinilo, un proceso para su preparacion y composiciones farmaceuticas que los contienen
AR074021A1 (es) Compuestos heterociclicos fusionados como moduladores del canal ionico
PE20180121A1 (es) Imidazopirazinonas como inhibidores de pde1
PE20160934A1 (es) (aza) piridopirazolopirimidinonas e indazolopirimidinonas como inhibidores de fibrinolisis
AR071652A1 (es) Derivados 2- fenil-piridina substituidos
MX2017015739A (es) Moduladores de ror gamma (ror?).