PL3793565T3 - Inhibitory MCL-1 - Google Patents

Inhibitory MCL-1

Info

Publication number
PL3793565T3
PL3793565T3 PL19728793T PL19728793T PL3793565T3 PL 3793565 T3 PL3793565 T3 PL 3793565T3 PL 19728793 T PL19728793 T PL 19728793T PL 19728793 T PL19728793 T PL 19728793T PL 3793565 T3 PL3793565 T3 PL 3793565T3
Authority
PL
Poland
Prior art keywords
mcl
inhibitors
Prior art date
Application number
PL19728793T
Other languages
English (en)
Polish (pl)
Inventor
Hang CHU
Juan A. Guerrero
Anna E. Hurtley
Tae H. Hwang
Lan Jiang
Darryl Kato
Tetsuya Kobayashi
John E. Knox
Scott E. Lazerwith
Xiaofen Li
David W. Lin
Jonathan W. Medley
Michael L. Mitchell
Devan Naduthambi
Zachary NEWBY
Neil H. Squires
Vickie H. Tsui
Chandrasekar Venkataramani
William J. Watkins
Hong Yang
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 PL3793565T3 publication Critical patent/PL3793565T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic 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
    • C07D513/02Heterocyclic 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
    • C07D513/08Bridged systems
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D267/00Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D267/02Seven-membered rings
    • C07D267/08Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D267/00Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D267/02Seven-membered rings
    • C07D267/08Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D267/12Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D267/16Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
    • C07D267/20[b, f]-condensed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C381/00Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
    • C07C381/10Compounds containing sulfur atoms doubly-bound to nitrogen atoms
    • 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
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic 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
    • C07D498/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic 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
    • C07D513/02Heterocyclic 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
    • C07D513/10Spiro-condensed systems
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
PL19728793T 2018-05-14 2019-05-13 Inhibitory MCL-1 PL3793565T3 (pl)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201862671306P 2018-05-14 2018-05-14
US201862749918P 2018-10-24 2018-10-24
PCT/US2019/032053 WO2019222112A1 (en) 2018-05-14 2019-05-13 Mcl-1 inhibitors
EP19728793.1A EP3793565B1 (en) 2018-05-14 2019-05-13 Mcl-1 inhibitors

Publications (1)

Publication Number Publication Date
PL3793565T3 true PL3793565T3 (pl) 2022-05-02

Family

ID=66770559

Family Applications (1)

Application Number Title Priority Date Filing Date
PL19728793T PL3793565T3 (pl) 2018-05-14 2019-05-13 Inhibitory MCL-1

Country Status (29)

Country Link
US (4) US10703733B2 (US07981874-20110719-C00313.png)
EP (2) EP3793565B1 (US07981874-20110719-C00313.png)
JP (3) JP6899975B2 (US07981874-20110719-C00313.png)
KR (3) KR102666717B1 (US07981874-20110719-C00313.png)
CN (2) CN117304130A (US07981874-20110719-C00313.png)
AU (3) AU2019269391B2 (US07981874-20110719-C00313.png)
BR (1) BR112020021648A2 (US07981874-20110719-C00313.png)
CA (1) CA3099152C (US07981874-20110719-C00313.png)
CL (1) CL2020002919A1 (US07981874-20110719-C00313.png)
CO (1) CO2020014009A2 (US07981874-20110719-C00313.png)
CR (1) CR20200544A (US07981874-20110719-C00313.png)
CY (1) CY1125065T1 (US07981874-20110719-C00313.png)
DK (1) DK3793565T3 (US07981874-20110719-C00313.png)
ES (1) ES2907923T3 (US07981874-20110719-C00313.png)
HR (1) HRP20220215T1 (US07981874-20110719-C00313.png)
HU (1) HUE057852T2 (US07981874-20110719-C00313.png)
IL (2) IL291430B2 (US07981874-20110719-C00313.png)
LT (1) LT3793565T (US07981874-20110719-C00313.png)
MX (1) MX2020012137A (US07981874-20110719-C00313.png)
PE (1) PE20210004A1 (US07981874-20110719-C00313.png)
PH (1) PH12020551881A1 (US07981874-20110719-C00313.png)
PL (1) PL3793565T3 (US07981874-20110719-C00313.png)
PT (1) PT3793565T (US07981874-20110719-C00313.png)
SG (1) SG11202010964VA (US07981874-20110719-C00313.png)
SI (1) SI3793565T1 (US07981874-20110719-C00313.png)
TW (2) TWI719478B (US07981874-20110719-C00313.png)
UA (1) UA125163C2 (US07981874-20110719-C00313.png)
WO (1) WO2019222112A1 (US07981874-20110719-C00313.png)
ZA (1) ZA202007007B (US07981874-20110719-C00313.png)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3099152C (en) 2018-05-14 2023-10-24 Gilead Sciences, Inc. Mcl-1 inhibitors
JP2022540825A (ja) 2019-07-09 2022-09-20 ヤンセン ファーマシューティカ エヌ.ベー. Mcl-1阻害剤としての大環状スピロ環誘導体
US11795223B2 (en) 2019-10-18 2023-10-24 Forty Seven, Inc. Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia
AU2020374947A1 (en) 2019-10-31 2022-03-31 Forty Seven, Inc. Anti-CD47 and anti-CD20 based treatment of blood cancer
TWI778443B (zh) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1抑制劑
JP7441947B2 (ja) 2019-11-26 2024-03-01 ギリアード サイエンシーズ, インコーポレイテッド Mcl1阻害剤を調製するためのプロセス及び中間体
MX2022007930A (es) 2019-12-24 2022-08-08 Carna Biosciences Inc Compuestos moduladores de diacilglicerol quinasa.
WO2021211922A1 (en) * 2020-04-16 2021-10-21 Prelude Therapeutics, Incorporated Spiro-sulfonimidamide derivatives as inhibitors of myeloid cell leukemia-1 (mcl-1) protein
EP4165050A1 (en) 2020-06-10 2023-04-19 JANSSEN Pharmaceutica NV Macrocyclic 2-amino-3-fluoro-but-3-enamides as inhibitors of mcl-1
AU2021381769B2 (en) * 2020-11-19 2024-05-30 Gilead Sciences, Inc. Processes and intermediates for preparing macrocyclic mcl1 inhibitors
EP4263558A1 (en) 2020-12-17 2023-10-25 JANSSEN Pharmaceutica NV Macrocyclic branched 3-fluoro-but-3-enamides as inhibitors of mcl-1
TW202302145A (zh) 2021-04-14 2023-01-16 美商基利科學股份有限公司 CD47/SIRPα結合及NEDD8活化酶E1調節次單元之共抑制以用於治療癌症
WO2022229102A1 (en) 2021-04-26 2022-11-03 Janssen Pharmaceutica Nv Macrocyclic 2-allyltetrahydrofurans as inhibitors of mcl-1
WO2022245671A1 (en) 2021-05-18 2022-11-24 Gilead Sciences, Inc. Methods of using flt3l-fc fusion proteins
EP4351657A1 (en) * 2021-06-11 2024-04-17 Gilead Sciences, Inc. Combination mcl-1 inhibitors with anti-body drug conjugates
WO2022261301A1 (en) 2021-06-11 2022-12-15 Gilead Sciences, Inc. Combination mcl-1 inhibitors with anti-cancer agents
IL309378A (en) 2021-06-23 2024-02-01 Gilead Sciences Inc DIACYLGLYERCOL KINASE MODULATING COMPOUNDS
WO2022271684A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
US11926628B2 (en) 2021-06-23 2024-03-12 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
KR20240023628A (ko) 2021-06-23 2024-02-22 길리애드 사이언시즈, 인코포레이티드 디아실글리세롤 키나제 조절 화합물
CA3237011A1 (en) 2021-11-16 2023-05-25 Soufyan JERHAOUI Macrocyclic 2-amino-but-3-enamides as inhibitors of mcl-1
WO2023183817A1 (en) 2022-03-24 2023-09-28 Gilead Sciences, Inc. Combination therapy for treating trop-2 expressing cancers
TW202345901A (zh) 2022-04-05 2023-12-01 美商基利科學股份有限公司 用於治療結腸直腸癌之組合療法
US20230357274A1 (en) * 2022-05-04 2023-11-09 Gilead Sciences, Inc. Salts and polymorphs of certain mcl-1 inhibitors
WO2024064668A1 (en) 2022-09-21 2024-03-28 Gilead Sciences, Inc. FOCAL IONIZING RADIATION AND CD47/SIRPα DISRUPTION ANTICANCER COMBINATION THERAPY

Family Cites Families (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6319494B1 (en) 1990-12-14 2001-11-20 Cell Genesys, Inc. Chimeric chains for receptor-associated signal transduction pathways
IL104570A0 (en) 1992-03-18 1993-05-13 Yeda Res & Dev Chimeric genes and cells transformed therewith
US7446190B2 (en) 2002-05-28 2008-11-04 Sloan-Kettering Institute For Cancer Research Nucleic acids encoding chimeric T cell receptors
US7405295B2 (en) 2003-06-04 2008-07-29 Cgi Pharmaceuticals, Inc. Certain imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of Bruton's tyrosine kinase by such compounds
LT2612862T (lt) 2004-05-13 2017-01-25 Icos Corporation Chinazolinonai kaip žmogaus fosfatidilinozitol-3-kinazės delta inhibitoriai
US20090142345A1 (en) 2005-03-15 2009-06-04 Takeda Pharmaceutical Company Limited Prophylactic/therapeutic agent for cancer
KR101339628B1 (ko) 2005-05-09 2013-12-09 메다렉스, 인코포레이티드 예정 사멸 인자 1(pd-1)에 대한 인간 모노클로날 항체, 및 항-pd-1 항체를 단독 사용하거나 기타 면역 요법제와 병용한 암 치료 방법
KR101888321B1 (ko) 2005-07-01 2018-08-13 이. 알. 스퀴부 앤드 선즈, 엘.엘.씨. 예정 사멸 리간드 1 (피디-엘1)에 대한 인간 모노클로날 항체
EP3023422A1 (en) 2007-03-12 2016-05-25 YM BioSciences Australia Pty Ltd Phenyl amino pyrimidine compounds and uses thereof
SI2182981T1 (sl) 2007-08-02 2013-05-31 Gilead Biologics, Inc. Postopki in sestavki za zdravljenje in diagnozo fibroze
US8450460B2 (en) 2008-07-21 2013-05-28 Apogenix Gmbh Single-chain TNFSF fusion polypeptides
WO2010019702A2 (en) 2008-08-12 2010-02-18 Oncomed Pharmaceuticals, Inc. Ddr1-binding agents and methods of use thereof
US8450321B2 (en) 2008-12-08 2013-05-28 Gilead Connecticut, Inc. 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor
TWI625121B (zh) 2009-07-13 2018-06-01 基利科學股份有限公司 調節細胞凋亡信號之激酶的抑制劑
CN105622757A (zh) 2010-02-04 2016-06-01 吉联亚生物科技有限公司 结合赖氨酰氧化酶样2(loxl2)的抗体和其使用方法
WO2011146862A1 (en) 2010-05-21 2011-11-24 Bellicum Pharmaceuticals, Inc. Methods for inducing selective apoptosis
PE20131376A1 (es) 2010-08-27 2013-11-25 Gilead Biologics Inc Anticuerpos para metaloproteinasa-9 de matriz
CN107699585A (zh) 2010-12-09 2018-02-16 宾夕法尼亚大学董事会 嵌合抗原受体‑修饰的t细胞治疗癌症的用途
TWI567061B (zh) 2011-07-01 2017-01-21 吉李德科學股份有限公司 用於治療成癮之化合物
JP6101205B2 (ja) 2011-08-23 2017-03-22 中外製薬株式会社 抗腫瘍活性を有する新規な抗ddr1抗体
GB201115529D0 (en) 2011-09-08 2011-10-26 Imp Innovations Ltd Antibodies, uses and methods
WO2013052699A2 (en) 2011-10-04 2013-04-11 Gilead Calistoga Llc Novel quinoxaline inhibitors of pi3k
UY34573A (es) 2012-01-27 2013-06-28 Gilead Sciences Inc Inhibidor de la quinasa que regula la señal de la apoptosis
WO2013116562A1 (en) 2012-02-03 2013-08-08 Gilead Calistoga Llc Compositions and methods of treating a disease with (s)-4 amino-6-((1-(5-chloro-4-oxo-3-phenyl-3,4-dihydroquinazolin-2-yl)ethyl)amino)pyrimidine-5-carbonitrile
WO2014047624A1 (en) 2012-09-24 2014-03-27 Gilead Sciences, Inc. Anti-ddr1 antibodies
CA2895782C (en) 2012-12-21 2017-08-22 Gilead Calistoga Llc Substituted pyrimidine aminoalkyl-quinazolones as phosphatidylinositol 3-kinase inhibitors
NZ708870A (en) 2012-12-21 2016-09-30 Gilead Calistoga Llc Isoquinolinone or quinazolinone phosphatidylinositol 3-kinase inhibitors
TWI527811B (zh) 2013-05-09 2016-04-01 吉李德科學股份有限公司 作爲溴結構域抑制劑的苯並咪唑衍生物
JP6030783B2 (ja) 2013-06-14 2016-11-24 ギリアード サイエンシーズ, インコーポレイテッド ホスファチジルイノシトール3−キナーゼ阻害剤
US9657023B2 (en) 2013-07-30 2017-05-23 Gilead Connecticut, Inc. Polymorph of Syk inhibitors
US9290505B2 (en) 2013-12-23 2016-03-22 Gilead Sciences, Inc. Substituted imidazo[1,2-a]pyrazines as Syk inhibitors
UY35898A (es) 2013-12-23 2015-07-31 Gilead Sciences Inc ?compuestos inhibidores de syk y composiciones que los comprenden?.
AU2015235944B2 (en) * 2014-03-27 2020-06-25 Vanderbilt University Substituted indole Mcl-1 inhibitors
JP6765968B2 (ja) 2014-04-10 2020-10-07 シアトル チルドレンズ ホスピタル, ディービーエー シアトル チルドレンズ リサーチ インスティテュート 薬物制御による導入遺伝子の発現
TWI751102B (zh) 2014-08-28 2022-01-01 美商奇諾治療有限公司 對cd19具專一性之抗體及嵌合抗原受體
JO3474B1 (ar) 2014-08-29 2020-07-05 Amgen Inc مشتقات تيتراهيدرونافثالين التي تثبط بروتين mcl-1
AU2015320675B2 (en) 2014-09-26 2018-10-18 Gilead Sciences, Inc. Aminotriazine derivatives useful as tank-binding kinase inhibitor compounds
MX2017007138A (es) 2014-12-03 2017-08-28 Juno Therapeutics Inc Metodos y composiciones para terapia celular adoptiva.
JP6821568B2 (ja) 2014-12-15 2021-01-27 ベリカム ファーマシューティカルズ, インコーポレイテッド 治療用細胞のコントロールされた排除方法
NZ736709A (en) 2015-05-15 2019-05-31 Gilead Sciences Inc Benzimidazole and imidazopyridine carboximidamide compounds having activity as inhibitors of indoleamine 2,3-dioxygenase
EP3303586A1 (en) 2015-05-29 2018-04-11 Juno Therapeutics, Inc. Composition and methods for regulating inhibitory interactions in genetically engineered cells
SG10202110257UA (en) 2015-09-17 2021-10-28 Novartis Ag Car t cell therapies with enhanced efficacy
WO2017147410A1 (en) * 2016-02-25 2017-08-31 Amgen Inc. Compounds that inhibit mcl-1 protein
JP6453507B2 (ja) 2017-03-30 2019-01-16 アムジエン・インコーポレーテツド Mcl−1タンパク質を阻害する化合物
WO2019036575A1 (en) 2017-08-18 2019-02-21 Amgen Inc. MCL-1 PROTEIN INHIBITING COMPOUNDS
WO2019046150A1 (en) 2017-08-29 2019-03-07 Amgen Inc. MACROCYCLIC COMPOUNDS FOR INHIBITING MCL-1 PROTEIN
CN111417394B (zh) 2017-10-19 2023-11-07 帝人制药株式会社 苯并咪唑衍生物及其用途
EP3762393B1 (en) 2018-03-05 2023-01-11 Amgen Inc. Alpha-hydroxy phenylacetic acid pharmacophore or bioisostere mcl-1 protein antagonists
IL278698B2 (en) 2018-05-14 2024-06-01 Reata Pharmaceuticals Inc Bi-aryl amides with sugar groups that are adapted to the treatment of diseases related to the heat stroke protein pathway
CA3099152C (en) 2018-05-14 2023-10-24 Gilead Sciences, Inc. Mcl-1 inhibitors
EA202092586A1 (ru) 2018-05-15 2021-03-10 Лундбекк Ла-Хойя Рисерч Сентер, Инк. Ингибиторы magl
BR112021001263A2 (pt) 2018-07-24 2021-04-27 Epizyme, Inc. compostos, seus usos, método para tratar câncer e método para modular uma atividade de smarca2
BR112021008796A2 (pt) 2018-11-09 2021-08-03 Prelude Therapeutics, Incorporated derivados de espiro-sulfonamida como inibidores de proteína de leucemia-1 de células mieloides (mcl-1)
CN112867722B (zh) 2019-01-18 2022-09-23 苏州亚盛药业有限公司 作为mcl-1抑制剂的大螺环醚(macrocyclic spiroethers)
TWI778443B (zh) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1抑制劑
JP7441947B2 (ja) 2019-11-26 2024-03-01 ギリアード サイエンシーズ, インコーポレイテッド Mcl1阻害剤を調製するためのプロセス及び中間体
JP2021161114A (ja) 2020-03-31 2021-10-11 アムジエン・インコーポレーテツド Mcl−1化合物のメチル化
BR112022022400A2 (pt) 2020-05-06 2022-12-13 Amgen Inc Síntese de intermediários de álcool vinílico protegidos
TWI827924B (zh) 2020-05-06 2024-01-01 美商安進公司 大環Mcl-1抑制劑中間體的閉環合成
EP4165050A1 (en) 2020-06-10 2023-04-19 JANSSEN Pharmaceutica NV Macrocyclic 2-amino-3-fluoro-but-3-enamides as inhibitors of mcl-1
MX2023000438A (es) 2020-07-08 2023-02-09 Janssen Pharmaceutica Nv Eter macrociclico que contiene derivados de indol como inhibidores de mcl-1.
AU2021381769B2 (en) 2020-11-19 2024-05-30 Gilead Sciences, Inc. Processes and intermediates for preparing macrocyclic mcl1 inhibitors

Also Published As

Publication number Publication date
US11643400B2 (en) 2023-05-09
CA3099152A1 (en) 2019-11-21
EP3793565A1 (en) 2021-03-24
AU2021203373B2 (en) 2023-09-14
JP6899975B2 (ja) 2021-07-07
KR20240074001A (ko) 2024-05-27
US20230312490A1 (en) 2023-10-05
IL278336B (en) 2022-04-01
US20190352271A1 (en) 2019-11-21
CL2020002919A1 (es) 2021-04-16
ZA202007007B (en) 2023-11-29
PT3793565T (pt) 2022-04-13
EP4029868A1 (en) 2022-07-20
CA3099152C (en) 2023-10-24
HUE057852T2 (hu) 2022-06-28
SG11202010964VA (en) 2020-12-30
AU2019269391B2 (en) 2021-02-25
DK3793565T3 (en) 2022-03-07
TW202122403A (zh) 2021-06-16
CN117304130A (zh) 2023-12-29
HRP20220215T1 (hr) 2022-04-29
US10703733B2 (en) 2020-07-07
AU2019269391A1 (en) 2020-11-19
IL291430B1 (en) 2023-12-01
EP3793565B1 (en) 2022-01-05
KR102666717B1 (ko) 2024-05-20
JP7240431B2 (ja) 2023-03-15
JP2023060145A (ja) 2023-04-27
US20220340535A1 (en) 2022-10-27
MX2020012137A (es) 2021-01-29
US10988451B2 (en) 2021-04-27
CR20200544A (es) 2021-02-11
CO2020014009A2 (es) 2020-11-30
WO2019222112A1 (en) 2019-11-21
IL291430B2 (en) 2024-04-01
US20200331870A1 (en) 2020-10-22
JP2021515030A (ja) 2021-06-17
CN112118845A (zh) 2020-12-22
TWI813957B (zh) 2023-09-01
KR20230107889A (ko) 2023-07-18
AU2023270332A1 (en) 2023-12-14
PH12020551881A1 (en) 2021-05-31
KR20210006981A (ko) 2021-01-19
AU2021203373A1 (en) 2021-06-24
TWI719478B (zh) 2021-02-21
PE20210004A1 (es) 2021-01-05
ES2907923T3 (es) 2022-04-27
CY1125065T1 (el) 2023-06-09
SI3793565T1 (sl) 2022-04-29
LT3793565T (lt) 2022-02-25
BR112020021648A2 (pt) 2021-01-26
KR102551319B1 (ko) 2023-07-05
UA125163C2 (uk) 2022-01-19
IL291430A (en) 2022-05-01
JP2021098728A (ja) 2021-07-01
WO2019222112A8 (en) 2020-11-12
CN112118845B (zh) 2023-06-13
TW202010740A (zh) 2020-03-16

Similar Documents

Publication Publication Date Title
IL291430A (en) mcl–1 inhibitors
IL283639A (en) kif18a inhibitors
IL277006A (en) CD73 inhibitors
IL269196A (en) New inhibitors
IL304348A (en) cd73 inhibitors
GB201807014D0 (en) Factor xlla inhibitors
SG11202010347XA (en) Stat3 inhibitors
ZA201907136B (en) Ip6k inhibitors
GB201819126D0 (en) Inhibitor compounds
IL276013A (en) pi4kiiibeta inhibitors
IL281514A (en) O-glycoprotein-2-acetamido-2-deoxy-3-D-glucopyranosidase inhibitors
IL274550A (en) Dopamine-B-hydroxylase inhibitors
GB201819839D0 (en) MAP4K4 inhibitors
GB201812462D0 (en) Inhibitors
GB201804439D0 (en) Dopamin-b-hydroxylase inhibitors
GB201809939D0 (en) Eastase inhibitor
GB201908044D0 (en) Dopamine-B-Hydroxylase inhibitors
GB201905476D0 (en) MAPA4K4 Inhibitors
GB201819136D0 (en) Inhibitor compounds
GB201813252D0 (en) MAP4K4 inhibitors
GB201721465D0 (en) Inhibitors
GB201720189D0 (en) Dopamine-B-hydroxylase inhibitors
GB201806131D0 (en) Inhibitor compounds
GB201806130D0 (en) Inhibitor compounds
GB201705968D0 (en) Inhibitor compounds