MA41251A - Dérivés de thiéno[2,3-c]pyrrol-4-one comme inhibiteurs erk - Google Patents

Dérivés de thiéno[2,3-c]pyrrol-4-one comme inhibiteurs erk

Info

Publication number
MA41251A
MA41251A MA041251A MA41251A MA41251A MA 41251 A MA41251 A MA 41251A MA 041251 A MA041251 A MA 041251A MA 41251 A MA41251 A MA 41251A MA 41251 A MA41251 A MA 41251A
Authority
MA
Morocco
Prior art keywords
thiéno
pyrrol
derivatives
erk inhibitors
erk
Prior art date
Application number
MA041251A
Other languages
English (en)
Other versions
MA41251B1 (fr
Inventor
Guillermo S Cortez
Sajan Joseph
Johnathan Alexander Mclean
William T Mcmillen
Michael John Rodriguez
Gaiying Zhao
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of MA41251A publication Critical patent/MA41251A/fr
Publication of MA41251B1 publication Critical patent/MA41251B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic 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
    • C07D495/04—Ortho-condensed 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
    • A61K31/535—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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim 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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2863—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Endocrinology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
MA41251A 2014-12-22 2015-12-16 Dérivés de thiéno[2,3-c]pyrrol-4-one comme inhibiteurs erk MA41251B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462095185P 2014-12-22 2014-12-22
PCT/US2015/065940 WO2016106029A1 (fr) 2014-12-22 2015-12-16 Dérivés de thiéno[2,3-c]pyrrol-4-one utilisés en tant qu'inhibiteurs de erk
EP15823869.1A EP3237423B1 (fr) 2014-12-22 2015-12-16 Dérivés de thiéno[2,3-c]pyrrol-4-one comme inhibiteurs erk

Publications (2)

Publication Number Publication Date
MA41251A true MA41251A (fr) 2017-11-01
MA41251B1 MA41251B1 (fr) 2019-09-30

Family

ID=55135525

Family Applications (1)

Application Number Title Priority Date Filing Date
MA41251A MA41251B1 (fr) 2014-12-22 2015-12-16 Dérivés de thiéno[2,3-c]pyrrol-4-one comme inhibiteurs erk

Country Status (44)

Country Link
US (3) US9469652B2 (fr)
EP (1) EP3237423B1 (fr)
JP (1) JP6445701B2 (fr)
KR (1) KR101917972B1 (fr)
CN (1) CN107108648B (fr)
AR (1) AR102977A1 (fr)
AU (1) AU2015369983C1 (fr)
BR (1) BR112017011130A2 (fr)
CA (1) CA2966559C (fr)
CL (1) CL2017001514A1 (fr)
CO (1) CO2017005217A2 (fr)
CR (1) CR20170182A (fr)
CY (1) CY1121831T1 (fr)
DK (1) DK3237423T3 (fr)
DO (1) DOP2017000122A (fr)
EA (1) EA031659B1 (fr)
EC (1) ECSP17038500A (fr)
ES (1) ES2738406T3 (fr)
GT (1) GT201700134A (fr)
HR (1) HRP20191268T1 (fr)
HU (1) HUE045933T2 (fr)
IL (1) IL252065B (fr)
JO (1) JO3596B1 (fr)
LT (1) LT3237423T (fr)
MA (1) MA41251B1 (fr)
MD (1) MD3237423T2 (fr)
ME (1) ME03490B (fr)
MX (1) MX371206B (fr)
MY (1) MY178426A (fr)
NZ (1) NZ731531A (fr)
PE (1) PE20171043A1 (fr)
PH (1) PH12017501155B1 (fr)
PL (1) PL3237423T3 (fr)
PT (1) PT3237423T (fr)
RS (1) RS59015B1 (fr)
SG (1) SG11201704521SA (fr)
SI (1) SI3237423T1 (fr)
SV (1) SV2017005443A (fr)
TN (1) TN2017000233A1 (fr)
TR (1) TR201909887T4 (fr)
TW (1) TWI704151B (fr)
UA (1) UA119686C2 (fr)
WO (1) WO2016106029A1 (fr)
ZA (1) ZA201702786B (fr)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SMT201800205T1 (it) 2013-10-03 2018-05-02 Kura Oncology Inc Inibitori di erk e metodi d'uso
TWI704151B (zh) * 2014-12-22 2020-09-11 美商美國禮來大藥廠 Erk抑制劑
WO2016106009A1 (fr) 2014-12-22 2016-06-30 Eli Lilly And Company Inhibiteurs d'erk
US10457669B2 (en) 2015-10-21 2019-10-29 Otsuka Pharmaceutical Co., Ltd. Benzolactam compounds as protein kinase inhibitors
US20200306254A1 (en) * 2016-06-29 2020-10-01 Eli Lilly And Company Combination of erk1/2 inhibitor compound with gemcitabine or with gemcitabine and nab-paclitaxel for use in treatment of pancreatic cancer
WO2018081204A1 (fr) * 2016-10-26 2018-05-03 Li George Y N-(5-((4-éthylpipérazine-1-yl)méthyl) pyridin-2-yl)-5-fluoro-4-(4-fluoro-1-isopropyl-2-méthyl-1h-benzo[d]imidazol-6-yl)pyrimidin-2-amine deutéré
GB201706327D0 (en) 2017-04-20 2017-06-07 Otsuka Pharma Co Ltd A pharmaceutical compound
CN111655690B (zh) 2017-11-24 2023-01-10 詹森药业有限公司 吡唑并吡啶酮化合物
AU2019253706A1 (en) * 2018-04-09 2020-11-26 G1 Therapeutics, Inc. Treatment of cancers having driving oncogenic mutations
AU2019272303B2 (en) * 2018-05-22 2024-11-07 Js Innomed Holdings Ltd. Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof
CA3124330A1 (fr) 2018-12-21 2020-06-25 Daiichi Sankyo Company, Limited Combinaison d'un conjugue anticorps-medicament et d'un inhibiteur de kinase
JP7367052B2 (ja) * 2019-03-27 2023-10-23 イーライ リリー アンド カンパニー Erk阻害剤としての5,6-ジヒドロ-4h-チエノ[2,3-c]ピロール-4-オン化合物の塩
WO2020192750A1 (fr) * 2019-03-28 2020-10-01 江苏恒瑞医药股份有限公司 Dérivé thiénohétérocyclique, son procédé de préparation et son utilisation médicale
MX2021011823A (es) * 2019-03-29 2021-10-22 Jiangsu Hengrui Medicine Co Derivado pirroloheterociclico, metodo de preparacion del mismo y su aplicacion en medicina.
JP7234418B2 (ja) * 2019-05-16 2023-03-07 イーライ リリー アンド カンパニー Brafv600e大腸癌の治療に使用するためのerk1/2阻害剤と、braf阻害剤およびegfr阻害剤との三重組み合わせ
CN112457326B (zh) * 2019-09-06 2022-02-15 上海凌达生物医药有限公司 一类芳香杂环并内酰胺类化合物、制备方法和用途
AU2020394767B2 (en) * 2019-12-06 2023-05-25 D3 Bio (Wuxi) Co., Ltd. Spiro compound serving as ERK inhibitor, and application thereof
CN110950876B (zh) * 2019-12-10 2021-08-17 上海凌达生物医药有限公司 一类呋喃并内酰胺类化合物、制备方法和用途
WO2021216777A1 (fr) * 2020-04-21 2021-10-28 The Trustees Of The Stevens Institute Of Technology Inhibiteurs d'erk pour thérapie anticancéreuse
KR20230079120A (ko) * 2020-09-29 2023-06-05 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 피롤로 헤테로고리계 유도체의 결정형 및 이의 제조 방법
CN114315837B (zh) * 2020-09-29 2023-06-16 江苏恒瑞医药股份有限公司 一种erk抑制剂的结晶形式及其制备方法
IL309711A (en) * 2021-06-28 2024-02-01 D3 Bio Wuxi Co Ltd THIAZOLE-LACTAM-SPIROHETEROCYCLIC COMPOUNDS AND THEIR USES
EP4353730A4 (fr) * 2021-06-28 2024-11-06 D3 Bio(Wuxi) Co., Ltd. Composé de thiazololactame à substitution diméthyle et son utilisation
CA3238655A1 (fr) * 2021-11-15 2023-05-19 Erasca, Inc. Inhibiteurs thiophenes de ulk1/2 et leur utilisation
WO2023137297A2 (fr) * 2022-01-11 2023-07-20 Suvalent Therapeutics, Inc. Inhibiteurs de 5,6-dihydro-4h-thieno[2,3-c]pyrrole sumo et leurs utilisations
WO2024216249A1 (fr) * 2023-04-14 2024-10-17 Prelude Therapeutics Incorporated Inhibiteurs de cdk et leur utilisation en tant que produits pharmaceutiques
CN121712509A (zh) 2023-05-04 2026-03-20 锐新医药公司 用于ras相关疾病或病症的组合疗法
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
IL327306A (en) 2023-10-12 2026-05-01 Revolution Medicines Inc Macrocyclic RAS inhibitors
WO2025171296A1 (fr) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Inhibiteurs de ras
WO2025240847A1 (fr) 2024-05-17 2025-11-20 Revolution Medicines, Inc. Inhibiteurs de ras
WO2025255438A1 (fr) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Procédés de traitement d'une maladie ou d'un trouble lié à la protéine ras
WO2025265060A1 (fr) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Compositions thérapeutiques et procédés de gestion d'effets liés au traitement
WO2026006747A1 (fr) 2024-06-28 2026-01-02 Revolution Medicines, Inc. Inhibiteurs de ras
WO2026015796A1 (fr) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Méthodes de traitement d'une maladie ou d'un trouble lié à ras
WO2026015790A1 (fr) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Méthodes de traitement d'une maladie ou d'un trouble lié à ras
WO2026015825A1 (fr) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Utilisation d'un inhibiteur de ras pour traiter le cancer du pancréas
WO2026015801A1 (fr) 2024-07-12 2026-01-15 Revolution Medicines, Inc. Méthodes de traitement d'une maladie ou d'un trouble liés à ras
WO2026050446A1 (fr) 2024-08-29 2026-03-05 Revolution Medicines, Inc. Inhibiteurs de ras
WO2026072904A2 (fr) 2024-09-26 2026-04-02 Revolution Medicines, Inc. Compositions et méthodes de traitement du cancer du poumon
WO2026090116A2 (fr) 2024-10-21 2026-04-30 Revolution Medicines, Inc. Inhibiteurs de ras
WO2026090245A1 (fr) 2024-10-22 2026-04-30 Revolution Medicines, Inc. Utilisation d'inhibiteurs ras pour traiter un cancer
US20260108528A1 (en) 2024-10-22 2026-04-23 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4023048A1 (de) * 1990-07-20 1992-01-23 Basf Ag Dicarbonsaeureimide, verfahren zu ihrer herstellung und ihre verwendung als herbizide
US7473691B2 (en) * 2000-09-15 2009-01-06 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
ES2266258T3 (es) * 2000-09-15 2007-03-01 Vertex Pharmaceuticals Incorporated Compuestos de pirazol utiles como inhibidores de proteina cinasas.
US7498414B2 (en) 2002-03-04 2009-03-03 Imclone Systems Incorporated Human antibodies specific to KDR and uses thereof
US7259161B2 (en) * 2002-11-04 2007-08-21 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of JAK and other protein kinases
UA80571C2 (en) 2002-11-22 2007-10-10 Lilly Co Eli Quinolinyl-pyrrolopyrazoles
EP1948647A1 (fr) * 2005-11-03 2008-07-30 SGX Pharmaceuticals, Inc. Modulateurs de kinase de type pyrimidinylthiophène
CA2734486A1 (fr) 2008-08-20 2010-02-25 Southern Research Institute Derives de pyridine et pyrimidine substituees et leur utilisation dans le traitement d'infections virales
EP2346860B1 (fr) * 2008-10-08 2012-09-19 Bristol-Myers Squibb Company Antagonistes de récepteur d'hormone concentrant la mélanine 1 de type pyrrolone
PA8852901A1 (es) * 2008-12-22 2010-07-27 Lilly Co Eli Inhibidores de proteina cinasa
WO2012030990A1 (fr) * 2010-09-01 2012-03-08 Gilead Connecticut, Inc. Pyridazinones, leur procédé de fabrication et leur procédé d'utilisation
AR087107A1 (es) 2011-07-27 2014-02-12 Lilly Co Eli Compuesto inhibidor de la señalizacion de la trayectoria notch
HRP20180591T1 (hr) * 2012-03-01 2018-05-18 Array Biopharma, Inc. Inhibitori kinaze serina ili treonina
AR090151A1 (es) 2012-03-07 2014-10-22 Lilly Co Eli Compuestos inhibidores de raf
BR112015006363A2 (pt) * 2012-09-28 2017-08-08 Boehringer Ingelheim Int combinações farmacêuticas compreendendo ligantes angiopoietina-2/dll4 duplos e agentes anti-vegf-r
WO2016106009A1 (fr) * 2014-12-22 2016-06-30 Eli Lilly And Company Inhibiteurs d'erk
TWI704151B (zh) * 2014-12-22 2020-09-11 美商美國禮來大藥廠 Erk抑制劑

Also Published As

Publication number Publication date
US9526733B1 (en) 2016-12-27
TR201909887T4 (tr) 2019-07-22
ES2738406T3 (es) 2020-01-22
CR20170182A (es) 2017-06-21
MA41251B1 (fr) 2019-09-30
MD3237423T2 (ro) 2019-11-30
GT201700134A (es) 2018-11-23
DK3237423T3 (da) 2019-07-22
ME03490B (fr) 2020-01-20
ECSP17038500A (es) 2017-12-01
CY1121831T1 (el) 2020-07-31
DOP2017000122A (es) 2017-06-15
IL252065B (en) 2020-08-31
LT3237423T (lt) 2019-08-26
SI3237423T1 (sl) 2019-08-30
KR101917972B1 (ko) 2018-11-12
CN107108648A (zh) 2017-08-29
RS59015B1 (sr) 2019-08-30
SV2017005443A (es) 2018-08-27
MX2017008242A (es) 2017-10-06
JO3596B1 (ar) 2020-07-05
AU2015369983B2 (en) 2018-08-23
CO2017005217A2 (es) 2017-09-20
HUE045933T2 (hu) 2020-01-28
MY178426A (en) 2020-10-13
HRP20191268T1 (hr) 2019-11-01
ZA201702786B (en) 2019-02-27
CL2017001514A1 (es) 2018-02-09
PT3237423T (pt) 2019-08-21
TN2017000233A1 (en) 2018-10-19
CA2966559C (fr) 2019-06-18
PH12017501155B1 (en) 2022-03-25
EA201791133A1 (ru) 2017-10-31
SG11201704521SA (en) 2017-07-28
EP3237423B1 (fr) 2019-06-05
MX371206B (es) 2020-01-22
PE20171043A1 (es) 2017-07-19
JP6445701B2 (ja) 2018-12-26
NZ731531A (en) 2018-12-21
JP2017538768A (ja) 2017-12-28
AU2015369983C1 (en) 2019-02-21
EP3237423A1 (fr) 2017-11-01
PL3237423T3 (pl) 2020-01-31
CA2966559A1 (fr) 2016-06-30
USRE48635E1 (en) 2021-07-13
US9469652B2 (en) 2016-10-18
AR102977A1 (es) 2017-04-05
US20160375030A1 (en) 2016-12-29
WO2016106029A1 (fr) 2016-06-30
PH12017501155A1 (en) 2017-11-27
KR20170083145A (ko) 2017-07-17
UA119686C2 (uk) 2019-07-25
CN107108648B (zh) 2019-07-12
EA031659B1 (ru) 2019-02-28
IL252065A0 (en) 2017-07-31
TWI704151B (zh) 2020-09-11
TW201632530A (zh) 2016-09-16
AU2015369983A1 (en) 2017-05-25
BR112017011130A2 (pt) 2017-12-26
US20160176896A1 (en) 2016-06-23

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