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

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D497/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D497/22—Heterocyclic 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
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D515/00—Heterocyclic 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
    • C07D515/22—Heterocyclic 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)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Hematology (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)
  • 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)
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) MX386103B (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)
SM (1) SMT202000249T1 (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 (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11066416B2 (en) 2016-02-04 2021-07-20 The Johns Hopkins University Rapafucin derivative compounds and methods of use thereof
EP3411046B1 (en) 2016-02-04 2025-07-16 The Johns Hopkins University Rapaglutins, novel inhibitors of glut and use thereof
WO2017136717A1 (en) 2016-02-04 2017-08-10 The Johns Hopkins University Rapadocins, inhibitors of equilibrative nucleoside transporter 1 and uses thereof
SMT202000249T1 (it) 2016-04-22 2020-07-08 Astrazeneca Ab Inibitori di mcl1 macrociclici per il trattamento di cancro
US10981932B2 (en) 2016-05-19 2021-04-20 Bayer Aktiengesellschaft Macrocyclic indole derivatives
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
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
CR20200124A (es) 2017-08-15 2020-09-28 Abbvie Inc Inhibidores macrocíclicos de mcl-1 y métodos de uso
US20190055264A1 (en) * 2017-08-15 2019-02-21 Abbvie Inc. Macrocyclic MCL-1 inhibitors and methods of use
US11447504B2 (en) 2017-11-17 2022-09-20 Bayer Aktiengesellschaft Macrocyclic chlorine substituted indole derivatives
US11286263B2 (en) 2017-11-17 2022-03-29 The Broad Institute, Inc. Macrocyclic fluorine substituted indole derivatives
WO2019096905A1 (en) * 2017-11-17 2019-05-23 Bayer Aktiengesellschaft Macrocyclic chlorine substituted indole derivatives
US20210253598A1 (en) * 2017-11-17 2021-08-19 Bayer Aktiengesellschaft Aryl annulated macrocyclic indole derivatives
AR113886A1 (es) 2017-11-17 2020-06-24 Broad Inst Inc Derivados de indol macrocíclicos
TWI810220B (zh) * 2017-11-17 2023-08-01 德商拜耳廠股份有限公司 經取代之巨環吲哚衍生物
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
AU2019347963A1 (en) * 2018-09-30 2021-05-27 Jiangsu Hengrui Medicine Co., Ltd. Indole macrocyclic derivative, preparation method therefor 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
US12319703B2 (en) 2019-01-23 2025-06-03 Ascentage Pharma (Suzhou) Co., Ltd. Macrocyclic fused pyrazoles as Mcl-1 inhibitors
US20220144854A1 (en) * 2019-03-08 2022-05-12 Zeno Management, Inc. Macrocyclic compounds
CN113924300A (zh) 2019-04-11 2022-01-11 百时美施贵宝公司 用于达到治疗血浆浓度的增加效能的非晶形固体及经溶解调配物
CN113574058B (zh) * 2019-04-30 2024-04-16 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
AU2020273654B2 (en) 2019-05-10 2026-04-09 Janssen Biotech, Inc. Macrocyclic chelators and methods of use thereof
US12338250B2 (en) 2019-05-17 2025-06-24 The Broad Institute, Inc. Methods of preparing macrocyclic indoles
CA3138058A1 (en) 2019-05-20 2020-11-26 Matthew T. Burger Mcl-1 inhibitor antibody-drug conjugates and methods of use
JP7617861B2 (ja) * 2019-06-21 2025-01-20 ヤンセン ファーマシューティカ エヌ.ベー. Mcl-1の大環状阻害剤
BR112022000251A2 (pt) 2019-07-09 2022-05-17 Janssen Pharmaceutica Nv Derivados macrocíclicos de espirociclo como inibidores de mcl-1
US20220372014A1 (en) * 2019-10-01 2022-11-24 The Johns Hopkins University Neuroprotective compounds and methods of use thereof
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
WO2021092061A1 (en) * 2019-11-08 2021-05-14 Unity Biotechnology, Inc. Combination treatment for senescence-associated diseases
MX2022006179A (es) * 2019-11-21 2022-06-14 Janssen Pharmaceutica Nv Derivados macrociclicos de indol como inhibidores de mcl-1.
MX2022006180A (es) * 2019-11-21 2022-06-14 Janssen Pharmaceutica Nv Derivados macrociclicos de sulfonilo como inhibidores de mcl-1.
US20230192720A1 (en) * 2019-12-18 2023-06-22 Zeno Management, Inc. Macrocyclic compounds
EP4107161A1 (en) * 2020-02-21 2022-12-28 Janssen Pharmaceutica NV 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
KR20230017823A (ko) 2020-05-29 2023-02-06 얀센 파마슈티카 엔.브이. Mcl-1의 억제제로서의 마크로사이클릭 7-피라졸-5-일-인돌 유도체
AU2021291056A1 (en) 2020-06-19 2023-02-23 Janssen Pharmaceutica Nv N-linked macrocyclic 7-(pyrazol-5-yl)-indole derivatives as inhibitors of MCL-1
ES2994690T3 (en) * 2020-06-19 2025-01-30 Janssen Pharmaceutica Nv N-linked macrocyclic 4-(pyrazol-5-yl)-indole derivatives as inhibitors of mcl-1
BR112023000212A2 (pt) 2020-07-08 2023-01-31 Janssen Pharmaceutica Nv Éter macrocíclico contendo derivados de indol como inibidores de mcl-1
WO2022032284A1 (en) * 2020-08-07 2022-02-10 Zeno Management, Inc. Macrocyclic compounds
WO2022115451A1 (en) 2020-11-24 2022-06-02 Novartis Ag Mcl-1 inhibitor antibody-drug conjugates and methods of use
KR20230121807A (ko) 2020-12-17 2023-08-21 얀센 파마슈티카 엔.브이. Mcl-1의 억제제로서의 분지형 매크로사이클릭 4-(피라졸-5-일)-인돌유도체
AU2022220818A1 (en) 2021-02-12 2023-09-28 Janssen Pharmaceutica Nv Macrocyclic 1,3-bridged 6-chloro-7-pyrazol-4-yl-1h-indole-2-carboxylate and 6-chloro-7-pyrimidin-5-yl-1h-indole-2-carboxylate derivatives as mcl-1 inhibitors for the treatment of cancer
WO2022251247A1 (en) * 2021-05-28 2022-12-01 Zeno Management, Inc. Macrocyclic compounds
JP7673255B2 (ja) 2021-06-11 2025-05-08 ギリアード サイエンシーズ, インコーポレイテッド Mcl-1阻害剤と抗体薬物コンジュゲートとの組み合わせ
TWI910028B (zh) 2021-06-11 2025-12-21 美商基利科學股份有限公司 Mcl-1抑制劑與抗癌劑之組合
CN115490708B (zh) * 2021-06-18 2025-01-24 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
EP4413165A1 (en) 2021-10-06 2024-08-14 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for predicting and improving the efficacy of mcl-1 inhibitor therapy
PE20251072A1 (es) 2022-05-20 2025-04-10 Novartis Ag Conjugados de anticuerpo-farmaco de compuestos antineoplasicos y metodos de uso de los mismos
PY24103486A (es) 2023-11-22 2025-06-06 Servier Lab Conjugados de anticuerpo anti-cd74-fármaco y métodos de uso de los mismos
TW202540186A (zh) 2023-11-22 2025-10-16 瑞士商諾華公司 抗cd7抗體藥物結合物及其使用方法
WO2025126157A1 (en) 2023-12-15 2025-06-19 Advesya Anti-il-1rap binding domains and antibody-drug conjugates thereof

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2705599T3 (es) * 2007-04-16 2019-03-26 Abbvie Inc Indoles sustituidos en la posición 7 como inhibidores de mcl-1
US7981888B2 (en) 2007-04-16 2011-07-19 Abbott Laboratories 1-oxyalkyl-2-carboxyl-7-nonsubstituted indole derivatives
DK2379580T3 (da) * 2008-12-22 2014-01-20 Cubist Pharm Inc Hidtil ukendte antibakterielle midler til behandling af gram-positive infektioner
US8674115B2 (en) * 2009-12-23 2014-03-18 Ironwood Pharmaceuticals, Inc. CRTH2 modulators
JP5997763B2 (ja) * 2011-05-19 2016-09-28 フンダシオン セントロ ナシオナル デ インベスティガシオネス オンコロヒカス カルロス ザ サードFundacion Centro Nacional de Investigaciones Oncologicas Carlos III タンパク質キナーゼ阻害剤としての大環状化合物
WO2014047427A2 (en) 2012-09-21 2014-03-27 Vanderbilt University Substituted benzofuran, benzothiophene and indole mcl-1 inhibitors
CA2922341C (en) 2013-08-28 2022-06-07 Vanderbilt University Substituted indole mcl-1 inhibitors
ES2654242T3 (es) * 2014-02-12 2018-02-12 Viiv Healthcare (No.5) Limited Macrociclos de benzotiazol como inhibidores de la réplica del virus de la inmunodeficiencia humana
JP6757312B2 (ja) 2014-03-27 2020-09-16 ヴァンダービルト ユニバーシティー 置換インドールmcl−1阻害剤
CR20160471A (es) * 2014-04-11 2016-12-21 Bayer Pharma AG Compuestos novedosos macrocíclicos
US9949965B2 (en) 2014-10-17 2018-04-24 Vanderbilt University Tricyclic indole Mcl-1 inhibitors and uses thereof
SMT202000249T1 (it) 2016-04-22 2020-07-08 Astrazeneca Ab Inibitori di mcl1 macrociclici per il trattamento di cancro

Also Published As

Publication number Publication date
EP3445767B1 (en) 2020-02-19
HUE049591T2 (hu) 2020-09-28
US11472816B2 (en) 2022-10-18
US10196404B2 (en) 2019-02-05
ES2791319T3 (es) 2020-11-03
JP6894449B2 (ja) 2021-06-30
WO2017182625A1 (en) 2017-10-26
US9840518B2 (en) 2017-12-12
US20180155362A1 (en) 2018-06-07
NI201800093A (es) 2019-03-14
DK3445767T3 (da) 2020-05-18
US10889594B2 (en) 2021-01-12
EP3445767A1 (en) 2019-02-27
US20190185485A1 (en) 2019-06-20
CN109071566A (zh) 2018-12-21
MX2018012711A (es) 2019-05-30
MA44721B1 (fr) 2020-05-29
CN109071566B (zh) 2021-08-31
CR20180499A (es) 2019-01-25
EA036551B1 (ru) 2020-11-23
PE20181803A1 (es) 2018-11-19
SI3445767T1 (sl) 2020-07-31
PT3445767T (pt) 2020-05-13
CA3020378A1 (en) 2017-10-26
KR102388208B1 (ko) 2022-04-18
MA44721A (fr) 2019-02-27
LT3445767T (lt) 2020-05-25
AU2017252222B2 (en) 2019-11-07
CY1123186T1 (el) 2021-10-29
KR20180135030A (ko) 2018-12-19
NZ748173A (en) 2025-05-02
PH12018502227A1 (en) 2019-07-29
IL262237B (en) 2021-08-31
DOP2018000222A (es) 2018-10-31
SG11201805838UA (en) 2018-11-29
SMT202000249T1 (it) 2020-07-08
AR108301A1 (es) 2018-08-08
JP2019514863A (ja) 2019-06-06
IL262237A (en) 2018-11-29
BR112018070677B1 (pt) 2024-02-06
US20170305926A1 (en) 2017-10-26
EA201892300A1 (ru) 2019-05-31
MX386103B (es) 2025-03-18
PL3445767T3 (pl) 2020-07-13
SV2018005742A (es) 2019-03-25
AU2017252222A1 (en) 2018-11-29
RS60257B1 (sr) 2020-06-30
TWI742074B (zh) 2021-10-11
ZA201807766B (en) 2021-09-29
TW201803879A (zh) 2018-02-01
ME03729B (me) 2021-01-20
BR112018070677A2 (pt) 2019-02-05
CO2018008759A2 (es) 2018-09-20
TN2018000319A1 (en) 2020-01-16
US20210230184A1 (en) 2021-07-29
HRP20200673T1 (hr) 2020-07-10

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