TWI813957B - Mcl-1抑制劑 - Google Patents

Mcl-1抑制劑 Download PDF

Info

Publication number
TWI813957B
TWI813957B TW110107128A TW110107128A TWI813957B TW I813957 B TWI813957 B TW I813957B TW 110107128 A TW110107128 A TW 110107128A TW 110107128 A TW110107128 A TW 110107128A TW I813957 B TWI813957 B TW I813957B
Authority
TW
Taiwan
Prior art keywords
formula
mmol
pharmaceutically acceptable
lcms
esi
Prior art date
Application number
TW110107128A
Other languages
English (en)
Chinese (zh)
Other versions
TW202122403A (zh
Inventor
航 儲
尤安 A 桂烈羅
安娜 E 赫勒
太煥 黃
嵐 姜
達里爾 加登
小林徹也
約翰 E 諾斯
史考特 E 拉澤威斯
曉芬 李
大衛 W 林
強納森 W 梅得利
麥克 L 米契爾
戴文 那杜珊比
瑞確利 紐畢
尼爾 H 斯奎爾斯
曉薇 崔
錢德拉瑟卡 凡卡塔拉馬尼
威廉 J 瓦特金恩斯
楊紅
Original Assignee
美商基利科學股份有限公司
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 美商基利科學股份有限公司 filed Critical 美商基利科學股份有限公司
Publication of TW202122403A publication Critical patent/TW202122403A/zh
Application granted granted Critical
Publication of TWI813957B publication Critical patent/TWI813957B/zh

Links

Classifications

    • 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
    • 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
    • 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
    • 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

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)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
TW110107128A 2018-05-14 2019-05-14 Mcl-1抑制劑 TWI813957B (zh)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201862671306P 2018-05-14 2018-05-14
US62/671,306 2018-05-14
US201862749918P 2018-10-24 2018-10-24
US62/749,918 2018-10-24

Publications (2)

Publication Number Publication Date
TW202122403A TW202122403A (zh) 2021-06-16
TWI813957B true TWI813957B (zh) 2023-09-01

Family

ID=66770559

Family Applications (4)

Application Number Title Priority Date Filing Date
TW110107128A TWI813957B (zh) 2018-05-14 2019-05-14 Mcl-1抑制劑
TW108116508A TWI719478B (zh) 2018-05-14 2019-05-14 Mcl-1抑制劑
TW112131732A TWI844454B (zh) 2018-05-14 2019-05-14 Mcl-1抑制劑
TW113116186A TW202506687A (zh) 2018-05-14 2019-05-14 Mcl-1抑制劑

Family Applications After (3)

Application Number Title Priority Date Filing Date
TW108116508A TWI719478B (zh) 2018-05-14 2019-05-14 Mcl-1抑制劑
TW112131732A TWI844454B (zh) 2018-05-14 2019-05-14 Mcl-1抑制劑
TW113116186A TW202506687A (zh) 2018-05-14 2019-05-14 Mcl-1抑制劑

Country Status (30)

Country Link
US (5) US10703733B2 (enExample)
EP (2) EP4029868A1 (enExample)
JP (3) JP6899975B2 (enExample)
KR (4) KR102732008B1 (enExample)
CN (2) CN112118845B (enExample)
AU (3) AU2019269391B2 (enExample)
BR (1) BR112020021648A2 (enExample)
CA (1) CA3099152C (enExample)
CL (1) CL2020002919A1 (enExample)
CO (1) CO2020014009A2 (enExample)
CR (1) CR20200544A (enExample)
CY (1) CY1125065T1 (enExample)
DK (1) DK3793565T3 (enExample)
ES (1) ES2907923T3 (enExample)
HR (1) HRP20220215T1 (enExample)
HU (1) HUE057852T2 (enExample)
IL (2) IL291430B2 (enExample)
LT (1) LT3793565T (enExample)
MX (1) MX2020012137A (enExample)
MY (1) MY198871A (enExample)
PE (1) PE20210004A1 (enExample)
PH (1) PH12020551881A1 (enExample)
PL (1) PL3793565T3 (enExample)
PT (1) PT3793565T (enExample)
SG (1) SG11202010964VA (enExample)
SI (1) SI3793565T1 (enExample)
TW (4) TWI813957B (enExample)
UA (1) UA125163C2 (enExample)
WO (1) WO2019222112A1 (enExample)
ZA (1) ZA202007007B (enExample)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102732008B1 (ko) 2018-05-14 2024-11-20 길리애드 사이언시즈, 인코포레이티드 Mcl-1 억제제
EP3643711A1 (en) 2018-10-24 2020-04-29 Bayer Animal Health GmbH New anthelmintic compounds
ES2987630T3 (es) 2019-07-09 2024-11-15 Janssen Pharmaceutica Nv Derivados de espirociclos macrocíclicos como inhibidores de MCL-1
US11795223B2 (en) 2019-10-18 2023-10-24 Forty Seven, Inc. Combination therapies for treating myelodysplastic syndromes and acute myeloid leukemia
MX2022005123A (es) 2019-10-31 2022-05-30 Forty Seven Inc Tratamiento basado en anti-cd47 y anti-cd20 para cancer hematologico.
TWI778443B (zh) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1抑制劑
US11325891B2 (en) 2019-11-26 2022-05-10 Gilead Sciences, Inc. Processes and intermediates for preparing MCL1 inhibitors
MX2022007930A (es) 2019-12-24 2022-08-08 Carna Biosciences Inc Compuestos moduladores de diacilglicerol quinasa.
US20230212191A1 (en) * 2020-04-16 2023-07-06 Prelude Therapeutics, Incorporated Spiro-sulfonimidamide derivatives as inhibitors of myeloid cell leukemia-1 (mcl-1) protein
US20230219906A1 (en) 2020-06-10 2023-07-13 Janssen Pharmaceutica Nv Macrocyclic-2-amino-3-fluoro-but-3-enamides as inhibitors of mcl-1
CN116457334A (zh) * 2020-11-19 2023-07-18 吉利德科学公司 用于制备大环mcl1抑制剂的方法和中间体
ES3026771T3 (en) 2020-12-17 2025-06-12 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
AU2022267722A1 (en) 2021-04-26 2023-12-14 Janssen Pharmaceutica Nv Macrocyclic 2-allyltetrahydrofurans as inhibitors of mcl-1
US20220389394A1 (en) 2021-05-18 2022-12-08 Gilead Sciences, Inc. METHODS OF USING FLT3L-Fc FUSION PROTEINS
WO2022261310A1 (en) 2021-06-11 2022-12-15 Gilead Sciences, Inc. Combination mcl-1 inhibitors with anti-body drug conjugates
CN117651554A (zh) * 2021-06-11 2024-03-05 吉利德科学公司 Mcl-1抑制剂与抗癌剂的组合
WO2022271684A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
KR20240005901A (ko) 2021-06-23 2024-01-12 길리애드 사이언시즈, 인코포레이티드 디아실글리세롤 키나제 조절 화합물
JP7686086B2 (ja) 2021-06-23 2025-05-30 ギリアード サイエンシーズ, インコーポレイテッド ジアシルグリエルコール(diacylglyercol)キナーゼ調節化合物
WO2022271659A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
MX2024005928A (es) 2021-11-16 2024-06-04 Janssen Pharmaceutica Nv 2-amino-but-3-enamidas macrociclicas como inhibidores de mcl-1.
JP2025509662A (ja) 2022-03-24 2025-04-11 ギリアード サイエンシーズ, インコーポレイテッド Trop-2発現がんを治療するための併用療法
TWI876305B (zh) 2022-04-05 2025-03-11 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
US12162896B2 (en) * 2022-05-04 2024-12-10 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

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016033486A1 (en) * 2014-08-29 2016-03-03 Amgen Inc. Tetrahydronaphthalene derivatives that inhibit mcl-1 protein
WO2017147410A1 (en) * 2016-02-25 2017-08-31 Amgen Inc. Compounds that inhibit mcl-1 protein

Family Cites Families (60)

* 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
WO2005014599A1 (en) 2003-06-04 2005-02-17 Cellular Genomics, Inc. Imidazo[1,2-a]pyrazin-8-ylamines and method of inhibition of bruton’s tyrosine kinase by such compounds
WO2005113556A1 (en) 2004-05-13 2005-12-01 Icos Corporation Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta
US20090142345A1 (en) 2005-03-15 2009-06-04 Takeda Pharmaceutical Company Limited Prophylactic/therapeutic agent for cancer
CN109485727A (zh) 2005-05-09 2019-03-19 小野药品工业株式会社 程序性死亡-1(pd-1)的人单克隆抗体及使用抗pd-1抗体来治疗癌症的方法
KR101411165B1 (ko) 2005-07-01 2014-06-25 메다렉스, 엘.엘.시. 예정 사멸 리간드 1 (피디-엘1)에 대한 인간 모노클로날항체
HUE029188T2 (en) 2007-03-12 2017-03-28 Ym Biosciences Australia Pty Phenylamino-pyrimidine compounds and their use
CN110372795A (zh) 2007-08-02 2019-10-25 吉利德生物制剂公司 Lox和loxl2抑制剂及其应用
PL2310509T3 (pl) 2008-07-21 2015-08-31 Apogenix Ag Jednołańcuchowe cząsteczki TNFSF
US8652843B2 (en) 2008-08-12 2014-02-18 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
RU2015108348A (ru) 2010-02-04 2015-07-20 Джилид Байолоджикс, Инк. Антитела, связывающиеся с лизилоксидазоподобным ферментом-2 (loxl2), и способы их применения
US9089520B2 (en) 2010-05-21 2015-07-28 Baylor College Of Medicine Methods for inducing selective apoptosis
AU2011293125B2 (en) 2010-08-27 2015-02-05 Gilead Sciences, Inc. Antibodies to matrix metalloproteinase 9
PH12013501201A1 (en) 2010-12-09 2013-07-29 Univ Pennsylvania Use of chimeric antigen receptor-modified t cells to treat cancer
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
US9550835B2 (en) 2011-08-23 2017-01-24 Chugai Seiyaku Kabushiki Kaisha Anti-DDR1 antibody having anti-tumor activity
GB201115529D0 (en) 2011-09-08 2011-10-26 Imp Innovations Ltd Antibodies, uses and methods
CA2850763A1 (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
UY35044A (es) 2012-09-24 2014-04-30 Gilead Sciences Inc ANTICUERPOS ANTI-dDr1
US9029384B2 (en) 2012-12-21 2015-05-12 Gilead Calistoga, LLC. Phosphatidylinositol 3-kinase inhibitors
AU2013364068B2 (en) 2012-12-21 2016-10-20 Gilead Calistoga Llc Substituted pyrimidine aminoalkyl-quinazolones as 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
TWI644909B (zh) 2013-06-14 2018-12-21 基利科學股份有限公司 磷脂酸肌醇3-激酶抑制劑
MX2016001304A (es) 2013-07-30 2016-04-07 Gilead Connecticut Inc Polimorfo de inhibidores de syk.
US9290505B2 (en) 2013-12-23 2016-03-22 Gilead Sciences, Inc. Substituted imidazo[1,2-a]pyrazines as Syk inhibitors
TWI735853B (zh) 2013-12-23 2021-08-11 美商克洛諾斯生技有限公司 脾酪胺酸激酶抑制劑
CA2943815C (en) * 2014-03-27 2023-04-04 Vanderbilt University Substituted indole mcl-1 inhibitors
SG11201608393TA (en) 2014-04-10 2016-11-29 Seattle Children S Hospital Dba Seattle Children S Res Inst Transgene genetic tags and methods of use
TWI805109B (zh) 2014-08-28 2023-06-11 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
CN106715419A (zh) 2014-09-26 2017-05-24 吉利德科学公司 用作tank‑结合激酶抑制剂化合物的氨基三嗪衍生物
EP3227323B1 (en) 2014-12-03 2020-08-05 Juno Therapeutics, Inc. Methods and compositions for adoptive cell therapy
CA2966234A1 (en) 2014-12-15 2016-06-23 Bellicum Pharmaceuticals, Inc. Methods for controlled elimination of therapeutic cells
WO2016186967A1 (en) 2015-05-15 2016-11-24 Gilead Sciences, Inc. Benzimidazole and imadazopyridine carboximidamide compounds having activity as inhibitors of indoleamine 2,3-dioxygenase
WO2016196388A1 (en) 2015-05-29 2016-12-08 Juno Therapeutics, Inc. Composition and methods for regulating inhibitory interactions in genetically engineered cells
MX2018003353A (es) 2015-09-17 2018-09-17 Novartis Ag Terapias con celulas cart con una eficacia mejorada.
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
EP3668878B1 (en) 2017-08-18 2025-05-21 Amgen Inc. Compounds that inhibit mcl-1 protein
US11279712B2 (en) 2017-08-29 2022-03-22 Amgen Inc. Macrocyclic compounds that inhibit MCL-1 protein
CA3079081A1 (en) 2017-10-19 2019-04-25 Michael D. Bartberger Benzimidazole derivatives and their uses
MA54985A (fr) 2018-03-05 2021-12-29 Amgen Inc Pharmacophores d'acide alpha-hydroxy phénylacétique ou antagonistes de la protéine bio-isostère mcl-1
EP3794009A1 (en) 2018-05-14 2021-03-24 Reata Pharmaceuticals, Inc. Biaryl amides with modified sugar groups for treatment of diseases associated with heat shock protein pathway
KR102732008B1 (ko) 2018-05-14 2024-11-20 길리애드 사이언시즈, 인코포레이티드 Mcl-1 억제제
SG11202011228TA (en) 2018-05-15 2020-12-30 Lundbeck La Jolla Research Center Inc Magl inhibitors
SG11202100158WA (en) 2018-07-24 2021-02-25 Epizyme Inc Pyridin-2-one compounds useful as smarca2 antagonists
JP2022506973A (ja) 2018-11-09 2022-01-17 プレリュード セラピューティクス,インコーポレイティド 骨髄性細胞白血病-1(mcl-1)タンパク質の阻害剤としてのスピロ-スルホンアミド誘導体
WO2020147802A1 (en) 2019-01-18 2020-07-23 Ascentage Pharma (Suzhou) Co., Ltd. Macrocyclic spiroethers as mcl-1 inhibitors
TWI778443B (zh) 2019-11-12 2022-09-21 美商基利科學股份有限公司 Mcl1抑制劑
US11325891B2 (en) 2019-11-26 2022-05-10 Gilead Sciences, Inc. Processes and intermediates for preparing MCL1 inhibitors
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
CA3181214A1 (en) 2020-05-06 2021-11-11 Amgen Inc. Synthesis of vinylic protected alcohol intermediates
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
US20230219906A1 (en) 2020-06-10 2023-07-13 Janssen Pharmaceutica Nv Macrocyclic-2-amino-3-fluoro-but-3-enamides as inhibitors of mcl-1
EP4178677A1 (en) 2020-07-08 2023-05-17 JANSSEN Pharmaceutica NV Macrocyclic ether containing indole derivatives as inhibitors of mcl-1
CN116457334A (zh) 2020-11-19 2023-07-18 吉利德科学公司 用于制备大环mcl1抑制剂的方法和中间体

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016033486A1 (en) * 2014-08-29 2016-03-03 Amgen Inc. Tetrahydronaphthalene derivatives that inhibit mcl-1 protein
WO2017147410A1 (en) * 2016-02-25 2017-08-31 Amgen Inc. Compounds that inhibit mcl-1 protein

Also Published As

Publication number Publication date
CY1125065T1 (el) 2023-06-09
AU2019269391B2 (en) 2021-02-25
JP2025109849A (ja) 2025-07-25
JP2021515030A (ja) 2021-06-17
KR102666717B1 (ko) 2024-05-20
US20230312490A1 (en) 2023-10-05
KR20240074001A (ko) 2024-05-27
CN112118845A (zh) 2020-12-22
CN112118845B (zh) 2023-06-13
ES2907923T3 (es) 2022-04-27
JP7240431B2 (ja) 2023-03-15
JP6899975B2 (ja) 2021-07-07
IL291430B2 (en) 2024-04-01
WO2019222112A8 (en) 2020-11-12
PL3793565T3 (pl) 2022-05-02
CN117304130A (zh) 2023-12-29
TWI844454B (zh) 2024-06-01
KR20210006981A (ko) 2021-01-19
ZA202007007B (en) 2023-11-29
BR112020021648A2 (pt) 2021-01-26
US12162844B2 (en) 2024-12-10
US10988451B2 (en) 2021-04-27
TW202506687A (zh) 2025-02-16
EP4029868A1 (en) 2022-07-20
CA3099152A1 (en) 2019-11-21
IL278336B (en) 2022-04-01
US11643400B2 (en) 2023-05-09
KR20230107889A (ko) 2023-07-18
KR20240165483A (ko) 2024-11-22
US20250154116A1 (en) 2025-05-15
KR102551319B1 (ko) 2023-07-05
CO2020014009A2 (es) 2020-11-30
PT3793565T (pt) 2022-04-13
IL291430A (en) 2022-05-01
JP2023060145A (ja) 2023-04-27
AU2019269391A1 (en) 2020-11-19
MX2020012137A (es) 2021-01-29
US10703733B2 (en) 2020-07-07
US20200331870A1 (en) 2020-10-22
NZ769257A (en) 2024-05-31
CR20200544A (es) 2021-02-11
CL2020002919A1 (es) 2021-04-16
US20190352271A1 (en) 2019-11-21
AU2023270332B2 (en) 2025-10-02
TW202010740A (zh) 2020-03-16
MY198871A (en) 2023-10-02
TW202417457A (zh) 2024-05-01
HUE057852T2 (hu) 2022-06-28
IL291430B1 (en) 2023-12-01
JP2021098728A (ja) 2021-07-01
AU2021203373B2 (en) 2023-09-14
HRP20220215T1 (hr) 2022-04-29
SI3793565T1 (sl) 2022-04-29
AU2021203373A1 (en) 2021-06-24
AU2023270332A1 (en) 2023-12-14
EP3793565B1 (en) 2022-01-05
LT3793565T (lt) 2022-02-25
UA125163C2 (uk) 2022-01-19
TW202122403A (zh) 2021-06-16
WO2019222112A1 (en) 2019-11-21
PE20210004A1 (es) 2021-01-05
US20220340535A1 (en) 2022-10-27
EP3793565A1 (en) 2021-03-24
TWI719478B (zh) 2021-02-21
DK3793565T3 (en) 2022-03-07
PH12020551881A1 (en) 2021-05-31
KR102732008B1 (ko) 2024-11-20
SG11202010964VA (en) 2020-12-30
CA3099152C (en) 2023-10-24

Similar Documents

Publication Publication Date Title
TWI813957B (zh) Mcl-1抑制劑
JP7792036B2 (ja) Mcl-1阻害剤
HK40078700A (en) Mcl-1 inhibitors
HK40048157A (en) Mcl-1 inhibitors
HK40048157B (en) Mcl-1 inhibitors
HK40038496B (en) Mcl-1 inhibitors
EA043742B1 (ru) Ингибиторы mcl-1
HK40038496A (en) Mcl-1 inhibitors