CL2018002410A1 - Inhibidores de mcl-1 y métodos de uso de los mismos - Google Patents

Inhibidores de mcl-1 y métodos de uso de los mismos

Info

Publication number
CL2018002410A1
CL2018002410A1 CL2018002410A CL2018002410A CL2018002410A1 CL 2018002410 A1 CL2018002410 A1 CL 2018002410A1 CL 2018002410 A CL2018002410 A CL 2018002410A CL 2018002410 A CL2018002410 A CL 2018002410A CL 2018002410 A1 CL2018002410 A1 CL 2018002410A1
Authority
CL
Chile
Prior art keywords
methods
mcl
inhibitors
tridecaeno
pentaazaheptaciclo
Prior art date
Application number
CL2018002410A
Other languages
English (en)
Inventor
Alexander Hird
Matthew Alan Belmonte
Wenzhan Yang
John Paul Secrist
Daniel William Robbins
Steven Lee Kazmirski
Dedong Wu
Bo Peng
Jeffrey Johannes
Michelle Laurae Lamb
Qing Ye
Xiaolan Zheng
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of CL2018002410A1 publication Critical patent/CL2018002410A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D497/00Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D497/22Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms in which the condensed system contains four 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D515/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D515/22Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen, oxygen, 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 four or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

SE DA A CONOCER UN COMPUESTO QUE ES ÁCIDO 17-CLORO-5,13,14,22-TETRAMETIL-28-OXA-2,9-DITIA-5,6,12,13,22 PENTAAZAHEPTACICLO [27.7.1.14,7.011,15.016,21.020,24.030,35] OCTATRIAC ONTA-1(37),4(38),6,11,14,16,18,20,23,29,31,33,35-TRIDECAENO-23-CARBOXÍLICO (FÓRMULA I), Y ENANTIÓMEROS Y SALES FARMACÉUTICAMENTE ACEPTABLES DEL MISMO. TAMBIÉN SE DAN A CONOCER COMPOSICIONES FARMACÉUTICAS DE ÁCIDO 17-CLORO-5,13,14,22-TETRAMETIL-28-OXA-2,9-DITIA-5,6,12,13,22 PENTAAZAHEPTACICLO [27.7.1.14,7.011,15.016,21.020,24.030,35] OCTATRIACONTA 1(37),4(38) ,6,11 ,14 ,16 ,18 ,20 ,23,29,31,33,35 -TRIDECAENO-23-CARBOXÍLICO, Y ENANTIÓMEROS Y SALES FARMACÉUTICAMENTE ACEPTABLES DEL MISMO, Y MÉTODOS DE TRATAMIENTO DEL CÁNCER CON TALES COMPUESTOS Y COMPOSICIONES.
CL2018002410A 2016-04-22 2018-08-23 Inhibidores de mcl-1 y métodos de uso de los mismos CL2018002410A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662326156P 2016-04-22 2016-04-22

Publications (1)

Publication Number Publication Date
CL2018002410A1 true CL2018002410A1 (es) 2018-12-07

Family

ID=58664658

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2018002410A CL2018002410A1 (es) 2016-04-22 2018-08-23 Inhibidores de mcl-1 y métodos de uso de los mismos

Country Status (37)

Country Link
US (4) US9840518B2 (es)
EP (1) EP3445767B1 (es)
JP (1) JP6894449B2 (es)
KR (1) KR102388208B1 (es)
CN (1) CN109071566B (es)
AR (1) AR108301A1 (es)
AU (1) AU2017252222B2 (es)
BR (1) BR112018070677B1 (es)
CA (1) CA3020378A1 (es)
CL (1) CL2018002410A1 (es)
CO (1) CO2018008759A2 (es)
CR (1) CR20180499A (es)
CY (1) CY1123186T1 (es)
DK (1) DK3445767T3 (es)
DO (1) DOP2018000222A (es)
EA (1) EA036551B1 (es)
ES (1) ES2791319T3 (es)
HR (1) HRP20200673T1 (es)
HU (1) HUE049591T2 (es)
IL (1) IL262237B (es)
LT (1) LT3445767T (es)
MA (1) MA44721B1 (es)
ME (1) ME03729B (es)
MX (1) MX2018012711A (es)
NI (1) NI201800093A (es)
PE (1) PE20181803A1 (es)
PH (1) PH12018502227A1 (es)
PL (1) PL3445767T3 (es)
PT (1) PT3445767T (es)
RS (1) RS60257B1 (es)
SG (1) SG11201805838UA (es)
SI (1) SI3445767T1 (es)
SV (1) SV2018005742A (es)
TN (1) TN2018000319A1 (es)
TW (1) TWI742074B (es)
WO (1) WO2017182625A1 (es)
ZA (1) ZA201807766B (es)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3782636B1 (en) 2016-02-04 2024-05-15 The Johns Hopkins University Rapadocins, inhibitors of equilibrative nucleoside transporter 1 and uses thereof
US11708391B2 (en) 2016-02-04 2023-07-25 The Johns Hopkins University Rapaglutins, novel inhibitors of GLUT and use thereof
US11066416B2 (en) 2016-02-04 2021-07-20 The Johns Hopkins University Rapafucin derivative compounds and methods of use thereof
CO2018008759A2 (es) 2016-04-22 2018-09-20 Astrazeneca Ab Inhibidores de mcl-1 y métodos de uso de los mismos
EP3458459B1 (en) 2016-05-19 2022-04-27 Bayer Aktiengesellschaft Macrocyclic indole derivatives
TW201904976A (zh) * 2017-03-31 2019-02-01 瑞典商阿斯特捷利康公司 Mcl-1抑制劑及其使用方法
TWI781996B (zh) 2017-03-31 2022-11-01 瑞典商阿斯特捷利康公司 合成mcl-1抑制劑之方法
BR112020003180A2 (pt) 2017-08-15 2020-09-15 AbbVie Deutschland GmbH & Co. KG inibidores macrocíclicos de mcl-1 e métodos de uso
WO2019035899A1 (en) * 2017-08-15 2019-02-21 Abbvie Inc. MACROCYCLIC MCL-1 INHIBITORS AND METHODS OF USE
EP3710450A1 (en) * 2017-11-17 2020-09-23 Bayer Aktiengesellschaft Macrocyclic chlorine substituted indole derivatives
US11401278B2 (en) 2017-11-17 2022-08-02 The Broad Institute, Inc. Macrocyclic indole derivatives
EP3710449B1 (en) * 2017-11-17 2022-07-06 The Broad Institute, Inc. Macrocyclic fluorine substituted indole derivatives as mcl-1 inhibitors, for use in the treatment of cancer
JP7234250B2 (ja) * 2017-11-17 2023-03-07 バイエル アクチェンゲゼルシャフト 置換大環状インドール誘導体
UY37972A (es) * 2017-11-17 2019-06-28 Bayer Pharma AG Derivados de indol macrocíclicos sustituidos con cloro
US20210253598A1 (en) * 2017-11-17 2021-08-19 Bayer Aktiengesellschaft Aryl annulated macrocyclic indole derivatives
TW202014184A (zh) * 2018-04-30 2020-04-16 瑞典商阿斯特捷利康公司 用於治療癌症之組合
US20220041623A1 (en) 2018-09-30 2022-02-10 Jiangsu Hengrui Medicine Co., Ltd. Indole macrocyclic derivative, preparation method thereof and application thereof in medicine
TW202344250A (zh) 2018-11-14 2023-11-16 瑞典商阿斯特捷利康公司 治療癌症之方法
CN111205309B (zh) * 2018-11-21 2023-04-07 江苏恒瑞医药股份有限公司 吲哚类大环衍生物、其制备方法及其在医药上的应用
TWI749404B (zh) * 2018-11-22 2021-12-11 大陸商蘇州亞盛藥業有限公司 作為mcl-1抑制劑的大環吲哚
US20220396587A1 (en) * 2019-01-23 2022-12-15 Ascentage Pharma (Suzhou) Co., Ltd. Macrocyclic fused pyrrazoles as mcl-1 inhibitors
SG11202109367WA (en) * 2019-03-08 2021-09-29 Zeno Management Inc Macrocyclic compounds
TW202106693A (zh) * 2019-04-30 2021-02-16 大陸商江蘇恆瑞醫藥股份有限公司 吲哚類大環衍生物、其製備方法及其在醫藥上的應用
TW202100184A (zh) 2019-05-20 2021-01-01 瑞士商諾華公司 Mcl-1抑制劑抗體-藥物結合物及使用方法
MX2021015770A (es) * 2019-06-21 2022-04-12 Janssen Pharmaceutica Nv Inhibidores macrociclicos de mcl-1.
MX2022000390A (es) 2019-07-09 2022-02-10 Janssen Pharmaceutica Nv Derivados macrociclicos espirociclicos como inhibidores de mcl-1.
US20220372014A1 (en) * 2019-10-01 2022-11-24 The Johns Hopkins University Neuroprotective compounds and methods of use thereof
WO2021092061A1 (en) * 2019-11-08 2021-05-14 Unity Biotechnology, Inc. Combination treatment for senescence-associated diseases
WO2021092053A1 (en) * 2019-11-08 2021-05-14 Unity Biotechnology, Inc. Mcl-1 inhibitor macrocycle compounds for use in clinical management of conditions caused or mediated by senescent cells and for treating cancer
MX2022006179A (es) 2019-11-21 2022-06-14 Janssen Pharmaceutica Nv Derivados macrociclicos de indol como inhibidores de mcl-1.
EP4061820A1 (en) 2019-11-21 2022-09-28 Janssen Pharmaceutica NV Macrocyclic sulfonyl derivatives as mcl-1 inhibitors
CN115052880A (zh) * 2019-12-18 2022-09-13 芝诺管理公司 大环化合物
CA3168355A1 (en) 2020-02-21 2021-08-26 Frederik Jan Rita Rombouts Macrocyclic indole derivatives as inhibitors of mcl-1
WO2021197295A1 (zh) * 2020-03-30 2021-10-07 江苏恒瑞医药股份有限公司 一种吲哚类大环衍生物的结晶形式及其制备方法
EP4157852A1 (en) * 2020-05-29 2023-04-05 JANSSEN Pharmaceutica NV Macrocyclic 7-pyrazol-5-yl-indole derivatives as inhibitors of mcl-1
JP2023530985A (ja) 2020-06-19 2023-07-20 ヤンセン ファーマシューティカ エヌ.ベー. Mcl-1の阻害剤としてのn結合大環状7-(ピラゾール-5-イル)-インドール誘導体
BR112022025631A2 (pt) 2020-06-19 2023-01-17 Janssen Pharmaceutica Nv Derivados de 4-(pirazol-5-il)-indol macrocíclico n-ligados como inibidores de mcl-1
US20230250109A1 (en) 2020-07-08 2023-08-10 Janssen Pharmaceutica Nv Macrocyclic ether containing indole derivatives as inhibitors of mcl-1
WO2022032284A1 (en) * 2020-08-07 2022-02-10 Zeno Management, Inc. Macrocyclic compounds
AU2021385349A1 (en) 2020-11-24 2023-06-22 Les Laboratoires Servier Mcl-1 inhibitor antibody-drug conjugates and methods of use
EP4008324A1 (en) 2020-12-07 2022-06-08 Cellestia Biotech AG Combinations comprising an inhibitor of an anti-apoptotic protein, such as bcl-2, bcl-xl, bclw or mcl-1, and a notch signaling pathway inhibitor for treating cancer
AU2021403616A1 (en) 2020-12-17 2023-08-03 Janssen Pharmaceutica Nv Branched macrocyclic 4-(pyrazol-5-yl)-indole derivatives as inhibitors of mcl-1
MX2023009475A (es) 2021-02-12 2023-08-22 Janssen Pharmaceutica Nv Derivados macrociclicos 1,3-con puente 6-cloro-7-pirazol-4-il-1h-i ndol-2-carboxilato y 6-cloro-7-pirimidina-5-il-1h-indol-2-carboxil ato como inhibidores de mcl-1 para el tratamiento del cancer.
WO2022251247A1 (en) * 2021-05-28 2022-12-01 Zeno Management, Inc. Macrocyclic compounds
KR20240019283A (ko) 2021-06-11 2024-02-14 길리애드 사이언시즈, 인코포레이티드 Mcl-1 저해제와 항암제의 병용
US11931424B2 (en) 2021-06-11 2024-03-19 Gilead Sciences, Inc. Combination MCL-1 inhibitors with anti-body drug conjugates
CN115490708A (zh) * 2021-06-18 2022-12-20 苏州亚盛药业有限公司 磺酰胺类大环衍生物及其制备方法和用途
WO2023057484A1 (en) 2021-10-06 2023-04-13 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for predicting and improving the efficacy of mcl-1 inhibitor therapy
WO2023225359A1 (en) 2022-05-20 2023-11-23 Novartis Ag Antibody-drug conjugates of antineoplastic compounds and methods of use thereof

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2134685B1 (en) 2007-04-16 2015-09-02 AbbVie Inc. 7-nonsubstituted indole derivatives as mcl-1 inhibitors
US8445679B2 (en) * 2007-04-16 2013-05-21 Abbvie Inc. 7-substituted indole MCL-1 inhibitors
PT2379580E (pt) * 2008-12-22 2014-01-20 Cubist Pharm Inc Novos agentes antibacterianos para o tratamento de infecções por bactérias gram positivas
JP5731538B2 (ja) * 2009-12-23 2015-06-10 アイアンウッド ファーマシューティカルズ インコーポレイテッド Crth2モジュレーター
MX349366B (es) * 2011-05-19 2017-07-26 Centro Nac De Investigaciones Oncologicas (Cnio) Compuestos novedosos.
US10093640B2 (en) 2012-09-21 2018-10-09 Vanderbilt University Substituted benzofuran, benzothiophene and indole MCL-1 inhibitors
EP3038618B1 (en) 2013-08-28 2020-10-14 Vanderbilt University Substituted indole mcl-1 inhibitors
EP3105236B1 (en) * 2014-02-12 2017-10-18 ViiV Healthcare UK (No.5) Limited Benzothiazole macrocycles as inhibitors of human immunodeficiency virus replication
CN106456602B (zh) 2014-03-27 2020-11-24 范德比尔特大学 取代的吲哚mcl-1抑制剂
AU2015243585B2 (en) * 2014-04-11 2019-08-01 Bayer Pharma Aktiengesellschaft Novel macrocyclic compounds
US9949965B2 (en) 2014-10-17 2018-04-24 Vanderbilt University Tricyclic indole Mcl-1 inhibitors and uses thereof
CO2018008759A2 (es) 2016-04-22 2018-09-20 Astrazeneca Ab Inhibidores de mcl-1 y métodos de uso de los mismos

Also Published As

Publication number Publication date
HRP20200673T1 (hr) 2020-07-10
IL262237B (en) 2021-08-31
PT3445767T (pt) 2020-05-13
PE20181803A1 (es) 2018-11-19
SI3445767T1 (sl) 2020-07-31
KR20180135030A (ko) 2018-12-19
US20170305926A1 (en) 2017-10-26
NI201800093A (es) 2019-03-14
CY1123186T1 (el) 2021-10-29
AU2017252222A1 (en) 2018-11-29
TW201803879A (zh) 2018-02-01
ME03729B (me) 2021-01-20
SV2018005742A (es) 2019-03-25
CO2018008759A2 (es) 2018-09-20
PL3445767T3 (pl) 2020-07-13
US20190185485A1 (en) 2019-06-20
TWI742074B (zh) 2021-10-11
CR20180499A (es) 2019-01-25
AR108301A1 (es) 2018-08-08
WO2017182625A1 (en) 2017-10-26
US10889594B2 (en) 2021-01-12
RS60257B1 (sr) 2020-06-30
EA036551B1 (ru) 2020-11-23
JP6894449B2 (ja) 2021-06-30
CA3020378A1 (en) 2017-10-26
MA44721B1 (fr) 2020-05-29
ES2791319T3 (es) 2020-11-03
CN109071566B (zh) 2021-08-31
US11472816B2 (en) 2022-10-18
US10196404B2 (en) 2019-02-05
DK3445767T3 (da) 2020-05-18
CN109071566A (zh) 2018-12-21
DOP2018000222A (es) 2018-10-31
BR112018070677B1 (pt) 2024-02-06
JP2019514863A (ja) 2019-06-06
PH12018502227A1 (en) 2019-07-29
EA201892300A1 (ru) 2019-05-31
US20210230184A1 (en) 2021-07-29
SG11201805838UA (en) 2018-11-29
BR112018070677A2 (pt) 2019-02-05
US20180155362A1 (en) 2018-06-07
EP3445767A1 (en) 2019-02-27
US9840518B2 (en) 2017-12-12
IL262237A (en) 2018-11-29
KR102388208B1 (ko) 2022-04-18
AU2017252222B2 (en) 2019-11-07
ZA201807766B (en) 2021-09-29
MA44721A (fr) 2019-02-27
LT3445767T (lt) 2020-05-25
MX2018012711A (es) 2019-05-30
TN2018000319A1 (en) 2020-01-16
EP3445767B1 (en) 2020-02-19
HUE049591T2 (hu) 2020-09-28

Similar Documents

Publication Publication Date Title
CL2018002410A1 (es) Inhibidores de mcl-1 y métodos de uso de los mismos
CL2019001077A1 (es) Derivados de 6,7,8,9-tetrahidro-3h-pirazolo[4,3-f] isoquinolina útiles en el tratamiento del cáncer.
NI201700020A (es) Compuestos de aminopirimidinilo como inhibidores de jak
NI201900070A (es) Compuestos heterocíclicos como inmunomoduladores
CO2019007129A2 (es) Modulador del regulador de conductancia transmembrana de fibrosis quística, composiciones farmacéuticas, métodos de tratamiento y proceso para producir el modulador
CO2019000386A2 (es) Compuestos heterocíclicos como inmunomoduladores
CO2018008916A2 (es) Compuestos de benzopirazol y análogos de estos
CO2018004857A2 (es) Derivados de dihidroimidazopirazinona usados en el tratamiento del cáncer
CL2020001218A1 (es) Compuestos útiles para inhibir a cdk7.
AR093244A1 (es) Compuestos de benceno sustituidos utilizables en el tratamiento de trastornos mediados por ezh2
AR102981A1 (es) Inhibidores de la necrosis celular y métodos de preparación de los mismos
BR112018070123A2 (pt) oxiesterós e métodos de uso dos mesmos
MX2021009806A (es) Ésteres de ácidos grasos de cadena media de beta-hidroxibutirato y butanodiol y composiciones y métodos para usar los mismos.
UY36875A (es) Composiciones inhibidoras de bromodominios para el tratamiento de diversas enfermedades
EA201691600A1 (ru) Дигидропиридиноновые ингибиторы mgat2 для применения в лечении метаболических нарушений
DOP2016000254A (es) Formulaciones farmeceuticas de inhibidor de la quinasa pan-raf, procedimientos para su preparacion, y metodos de uso.
AR101414A1 (es) Derivados de pirrolidinona como inhibidores de metap-2
SV2016005313A (es) Derivados de carboxamida
CL2021002309A1 (es) Compuestos útiles en la terapia del vih
UY36123A (es) Derivados de carboxamida
CO2021007172A2 (es) Sales cristalinas de un inhibidor de calicreína plasmática
TR201819805T4 (tr) Flavaglin türevleri̇.
AR105400A1 (es) Inhibidores de jak1
CO2021008962A2 (es) Derivados activos de éster de testosterona, composiciones y usos de los mismos
AR113817A1 (es) Compuestos útiles para inhibir a cdk7