PE20240919A1 - Compuestos de tienopirrol - Google Patents

Compuestos de tienopirrol

Info

Publication number
PE20240919A1
PE20240919A1 PE2023002819A PE2023002819A PE20240919A1 PE 20240919 A1 PE20240919 A1 PE 20240919A1 PE 2023002819 A PE2023002819 A PE 2023002819A PE 2023002819 A PE2023002819 A PE 2023002819A PE 20240919 A1 PE20240919 A1 PE 20240919A1
Authority
PE
Peru
Prior art keywords
alkyl
fused bicyclic
membered fused
monocyclic
compounds
Prior art date
Application number
PE2023002819A
Other languages
English (en)
Inventor
Stephen E Ammann
Eda Y Canales
Weng K Chang
Henok H Kinfe
Scott E Lazerwith
Michael L Mitchell
Yasamin Moazami
Scott D Schroeder
Daniel G Shore
Christopher J Swank
Original Assignee
Gilead Sciences Inc
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 Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of PE20240919A1 publication Critical patent/PE20240919A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • 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
    • A61K31/47064-Aminoquinolines; 8-Aminoquinolines, e.g. chloroquine, primaquine
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Steroid Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

Referido a compuestos de tienopirrol de Formula I, o una sal farmaceuticamente aceptable de este, en donde R1 es heterociclilo biciclico fusionado de 8-10 miembros o heteroarilo biciclico fusionado de 8-10 miembros, en donde el heterociclilo biciclico fusionado de 8-10 miembros y el heteroarilo biciclico fusionado de 8-10 miembros estan cada uno sustituidos opcionalmente de manera independiente con grupos 1-4 Ra; R2 es H, alquilo C1-6, o cicloalquilo C3-7 monociclico, en donde el alquilo C1-6 y el cicloalquilo monociclico C3-7estan cada uno sustituidos opcionalmente de manera independiente con 1-4 grupos independientemente seleccionados del halogeno y alcoxi C1-6; R3 es H, halogeno, -CN, alquilo C1-6, cicloalquilo monociclico C 3-7 o heterociclilo monociclico de 4-7 miembros; Z es alquilo C1-6, alquenilo C2-6, -C(O)R13, -C(O)NR6R7 -S(O)2R6, entre otros. Estos compuestos inhiben la actividad del receptor 7 y/u 8 tipo toll. Tambien se refiere a una composicion farmaceutica que comprende dicho compuesto, metodos para prepararlos, y su uso para tratar una condicion inflamatoria, tales como enfermedad autoinmunitaria y/o condicion inflamatoria, que incluye el lupus eritematoso sistemico y lupus eritematoso cutaneo, entre otros.
PE2023002819A 2021-04-16 2022-04-15 Compuestos de tienopirrol PE20240919A1 (es)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US202163176109P 2021-04-16 2021-04-16
US202163216418P 2021-06-29 2021-06-29
US202263305610P 2022-02-01 2022-02-01
PCT/US2022/024984 WO2022221642A1 (en) 2021-04-16 2022-04-15 Thienopyrrole compounds

Publications (1)

Publication Number Publication Date
PE20240919A1 true PE20240919A1 (es) 2024-04-30

Family

ID=81580723

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2023002819A PE20240919A1 (es) 2021-04-16 2022-04-15 Compuestos de tienopirrol

Country Status (16)

Country Link
US (2) US11661431B2 (es)
EP (1) EP4323369A1 (es)
JP (1) JP2024513945A (es)
KR (1) KR20230171469A (es)
AU (1) AU2022257039A1 (es)
BR (1) BR112023021107A2 (es)
CA (1) CA3214808A1 (es)
CL (1) CL2023002998A1 (es)
CO (1) CO2023013397A2 (es)
CR (1) CR20230478A (es)
DO (1) DOP2023000219A (es)
IL (1) IL307203A (es)
MX (1) MX2023012110A (es)
PE (1) PE20240919A1 (es)
TW (1) TW202302598A (es)
WO (1) WO2022221642A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW202327574A (zh) * 2021-09-10 2023-07-16 美商基利科學股份有限公司 噻吩并吡咯化合物
WO2023247670A1 (en) * 2022-06-24 2023-12-28 F. Hoffmann-La Roche Ag New heterocyclic-carbonyl-cyclic compounds as magl inhibitors

Family Cites Families (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US4326525A (en) 1980-10-14 1982-04-27 Alza Corporation Osmotic device that improves delivery properties of agent in situ
US5364620A (en) 1983-12-22 1994-11-15 Elan Corporation, Plc Controlled absorption diltiazem formulation for once daily administration
US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
US4992445A (en) 1987-06-12 1991-02-12 American Cyanamid Co. Transdermal delivery of pharmaceuticals
US5001139A (en) 1987-06-12 1991-03-19 American Cyanamid Company Enchancers for the transdermal flux of nivadipine
US4902514A (en) 1988-07-21 1990-02-20 Alza Corporation Dosage form for administering nilvadipine for treating cardiovascular symptoms
GB9718833D0 (en) 1997-09-04 1997-11-12 Merck Sharp & Dohme Therapeutic agents
US6329412B1 (en) 1997-11-04 2001-12-11 Pfizer Inc Bisamidine compounds as antiproliferative agents
JP5390186B2 (ja) 2005-08-12 2014-01-15 ユナイテッド ステイツ ガバメント アズ レプリゼンティッド バイ ザ セクレタリー オブ ザ ユナイテッド ステイツ アーミー アンド ザ ユーエス アーミー メディカル リサーチ アンド マティリ 広い抗菌スペクトルを有する抗菌性化合物
AU2006279537A1 (en) 2005-08-15 2007-02-22 Irm Llc Compounds and compositions as TPO mimetics
EP1779848A1 (en) 2005-10-28 2007-05-02 Nikem Research S.R.L. V-ATPase inhibitors for the treatment of inflammatory and autoimmune diseases
WO2008008912A1 (en) * 2006-07-14 2008-01-17 Genelabs Technologies, Inc. Antiviral agents
DK2119703T3 (da) 2007-01-15 2013-01-14 Santen Pharmaceutical Co Ltd Nyt indolderivat med inhiberende virkning på I-B-kinase.
MX2009009792A (es) 2007-03-12 2009-09-23 Cytopia Res Pty Ltd Compuestos de fenil amino pirimidina y usos de los mismos.
WO2008152471A1 (en) 2007-06-12 2008-12-18 Coley Pharmaceutical Group, Inc. Quinazoline derivative useful as toll-like receptor antagonist
WO2010036905A1 (en) 2008-09-26 2010-04-01 Eisai R & D Management Co., Ltd. Benzoxazole compounds and methods of use
WO2011050245A1 (en) 2009-10-23 2011-04-28 Yangbo Feng Bicyclic heteroaryls as kinase inhibitors
AU2012262014B2 (en) 2011-06-01 2016-07-14 Janus Biotherapeutics, Inc. Novel immune system modulators
EP2713737B1 (en) 2011-06-01 2016-04-20 Janus Biotherapeutics, Inc. Novel immune system modulators
WO2013052263A2 (en) 2011-09-16 2013-04-11 Microbiotix, Inc. Antifungal compounds
WO2013052550A2 (en) 2011-10-04 2013-04-11 Janus Biotherapeutics, Inc. Novel imidazole quinoline-based immune system modulators
JO3407B1 (ar) 2012-05-31 2019-10-20 Eisai R&D Man Co Ltd مركبات رباعي هيدرو بيرازولو بيريميدين
KR101452579B1 (ko) 2012-08-17 2014-10-21 주식회사 두산 신규 화합물 및 이를 포함하는 유기 전계 발광 소자
SI3057964T1 (sl) 2013-10-14 2020-03-31 Eisai R&D Management Co., Ltd. Selektivno substituirane spojine kinolina
JP6483666B2 (ja) 2013-10-14 2019-03-13 エーザイ・アール・アンド・ディー・マネジメント株式会社 選択的に置換されたキノリン化合物
US20170275287A1 (en) 2014-08-22 2017-09-28 Janus Biotherapeutics, Inc. Novel n2, n4, n7, 6-tetrasubstituted pteridine-2,4,7-triamine and 2, 4, 6, 7-tetrasubstituted pteridine compounds and methods of synthesis and use thereof
CN112707893B (zh) 2015-03-30 2023-10-31 特殊治疗有限公司 作为usp30抑制剂的1-氰基吡咯烷化合物
US20180312493A1 (en) 2015-11-04 2018-11-01 Simon Fraser University Antibiotic Compounds, Pharmaceutical Formulations Thereof And Methods And Uses Therefor
EP3889145B1 (en) 2015-12-17 2024-02-21 Merck Patent GmbH 8-cyano-5-piperidino-quinolines as tlr7/8 antagonists and their uses for treating immune disorders
RS62322B1 (sr) 2016-04-15 2021-10-29 Cancer Research Tech Ltd Heterociklična jedinjenja kao inhibitori ret kinaze
CA3021947A1 (en) 2016-04-26 2017-11-02 Sumitomo Dainippon Pharma Co., Ltd. Substituted purine derivative
US10071079B2 (en) 2016-06-29 2018-09-11 Bristol-Myers Squibb Company [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds
EA038972B1 (ru) 2016-07-30 2021-11-16 Бристол-Маерс Сквибб Компани Диметоксифенилзамещенные соединения индола в качестве ингибиторов tlr7, tlr8 или tlr9
MX2019001096A (es) 2016-08-08 2019-07-04 Merck Patent Gmbh Antagonistas del receptor 7/8 tipo toll (tlr7/8) y uso de los mismos.
AU2017323584C1 (en) 2016-09-09 2020-09-17 Novartis Ag Compounds and compositions as inhibitors of endosomal toll-like receptors
KR102519535B1 (ko) 2016-09-09 2023-04-06 브리스톨-마이어스 스큅 컴퍼니 피리딜 치환된 인돌 화합물
EP3655401B1 (en) 2017-07-18 2023-09-06 Merck Patent GmbH Tlr7/8 antagonists and uses thereof
KR20200036913A (ko) 2017-08-04 2020-04-07 브리스톨-마이어스 스큅 컴퍼니 [1,2,4]트리아졸로[4,3-a]피리디닐 치환된 인돌 화합물
CN110997656B (zh) 2017-08-04 2023-04-14 百时美施贵宝公司 用作tlr7/8/9抑制剂的取代的吲哚化合物
JP2021035910A (ja) 2017-11-01 2021-03-04 大日本住友製薬株式会社 置換プリン化合物
EP3707140B1 (en) 2017-11-08 2021-10-13 Council of Scientific and Industrial Research Purine based compounds as toll-like receptor 9 antagonists
KR20200086709A (ko) 2017-11-14 2020-07-17 브리스톨-마이어스 스큅 컴퍼니 치환된 인돌 화합물
BR112020011668A2 (pt) 2017-12-15 2020-11-17 Bristol-Myers Squibb Company compostos de éter de indol substituído
JP7289301B2 (ja) 2017-12-18 2023-06-09 ブリストル-マイヤーズ スクイブ カンパニー 4-アザインドール化合物
CA3086172A1 (en) 2017-12-19 2019-06-27 Merck Patent Gmbh Tlr7/8 antagonists and uses thereof
KR20200101402A (ko) 2017-12-19 2020-08-27 브리스톨-마이어스 스큅 컴퍼니 Tlr 억제제로서 유용한 치환된 인돌 화합물
CA3085761A1 (en) 2017-12-19 2019-06-27 Bristol-Myers Squibb Company Triazole n-linked carbamoylcyclohexyl acids as lpa antagonists
CA3085346A1 (en) 2017-12-19 2019-06-27 Bristol-Myers Squibb Company Amide substituted indole compounds useful as tlr inhibitors
BR112020011984A2 (pt) 2017-12-20 2020-11-17 Bristol-Myers Squibb Company compostos de amino indol úteis como inibidores de tlr
ES2904773T3 (es) 2017-12-20 2022-04-06 Bristol Myers Squibb Co Compuestos de diazaindol
CA3085942A1 (en) 2017-12-20 2019-06-27 Bristol-Myers Squibb Company Aryl and heteroaryl substituted indole compounds
WO2019123294A2 (en) 2017-12-22 2019-06-27 Novartis Ag Novel uses of pyrazolo piperidine derivatives
WO2019220390A1 (en) 2018-05-18 2019-11-21 Novartis Ag Crystalline forms of a tlr7/tlr8 inhibitor
MX2021000093A (es) 2018-07-31 2021-03-25 Merck Patent Gmbh Antagonistas del receptor de tipo toll 7/8 (tlr7/8) y usos de los mismos.
WO2020086505A1 (en) 2018-10-24 2020-04-30 Bristol-Myers Squibb Company Substituted indole dimer compounds
JP2022505707A (ja) 2018-10-24 2022-01-14 ブリストル-マイヤーズ スクイブ カンパニー 置換インドールおよびインダゾール化合物
US20220213099A1 (en) 2019-05-07 2022-07-07 Bristol-Myers Squibb Company Prodrug compounds
KR20220006571A (ko) 2019-05-09 2022-01-17 브리스톨-마이어스 스큅 컴퍼니 치환된 벤즈이미다졸론 화합물
US20220241410A1 (en) 2019-05-23 2022-08-04 The University Of Montana Vaccine adjuvants based on tlr receptor ligands
EP4041730A1 (en) * 2019-10-01 2022-08-17 Bristol-Myers Squibb Company Substituted bicyclic heteroaryl compounds
ES2965164T3 (es) 2019-10-04 2024-04-11 Bristol Myers Squibb Co Compuestos de carbazol sustituidos
JP2023501956A (ja) 2019-11-01 2023-01-20 ブリストル-マイヤーズ スクイブ カンパニー 置換ピラゾール化合物
JP2023526304A (ja) 2020-05-14 2023-06-21 メルク ヘルスケア コマンディトゲゼルシャフト アウフ アクティーン コロナウイルス感染症治療のためのtlr7/8拮抗薬
MX2022015760A (es) 2020-06-11 2023-01-19 Bristol Myers Squibb Co Inhibidor del receptor tipo toll 7 (tlr7) en combinacion con prednisolona o hidroxicloroquina para el tratamiento del lupus eritematoso cutaneo.
US20230310409A1 (en) 2020-06-22 2023-10-05 Bristol-Myers Squibb Company Treating rheumatoid arthritis
WO2022022489A1 (zh) 2020-07-27 2022-02-03 江苏恒瑞医药股份有限公司 吲哚稠环类衍生物、其制备方法及其在医药上的应用
CN114075219B (zh) 2020-08-14 2023-11-14 江苏恒瑞医药股份有限公司 喹啉稠环类衍生物、其制备方法及其在医药上的应用
CN114075212B (zh) 2020-08-14 2023-05-12 江苏恒瑞医药股份有限公司 稠合三环类衍生物、其制备方法及其在医药上的应用
EP4200015A1 (en) 2020-08-19 2023-06-28 Bristol-Myers Squibb Company Substituted heteroaryl compounds useful as inhibitors of tlr9
MX2023006193A (es) 2020-11-26 2023-06-09 Jiangsu Hengrui Pharmaceuticals Co Ltd Compuesto triciclico fusionado, metodo de preparacion y aplicacion del mismo en medicina.
WO2022140325A1 (en) 2020-12-22 2022-06-30 Gilead Sciences, Inc. 6-substituted indole compounds
EP4267559A1 (en) 2020-12-22 2023-11-01 Gilead Sciences, Inc. Substituted indole compounds

Also Published As

Publication number Publication date
CR20230478A (es) 2023-11-30
AU2022257039A1 (en) 2023-10-05
KR20230171469A (ko) 2023-12-20
TW202302598A (zh) 2023-01-16
US11661431B2 (en) 2023-05-30
WO2022221642A1 (en) 2022-10-20
EP4323369A1 (en) 2024-02-21
CL2023002998A1 (es) 2024-04-26
MX2023012110A (es) 2023-10-24
CA3214808A1 (en) 2022-10-20
CO2023013397A2 (es) 2023-10-30
JP2024513945A (ja) 2024-03-27
BR112023021107A2 (pt) 2023-12-12
US20230365594A1 (en) 2023-11-16
US20220389034A1 (en) 2022-12-08
DOP2023000219A (es) 2023-11-15
IL307203A (en) 2023-11-01

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