PL2134685T3 - Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1 - Google Patents

Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1

Info

Publication number
PL2134685T3
PL2134685T3 PL08745934T PL08745934T PL2134685T3 PL 2134685 T3 PL2134685 T3 PL 2134685T3 PL 08745934 T PL08745934 T PL 08745934T PL 08745934 T PL08745934 T PL 08745934T PL 2134685 T3 PL2134685 T3 PL 2134685T3
Authority
PL
Poland
Prior art keywords
nonsubstituted
mcl
inhibitors
indole derivatives
indole
Prior art date
Application number
PL08745934T
Other languages
English (en)
Inventor
Milan Bruncko
Xiaohong Song
Hong Ding
Zhi-Fu Tao
Aaron R Kunzer
Steven W Elmore
Cheol-Min Park
David Madar
Xilu Wang
Andrew J Souers
Original Assignee
Abbvie 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 Abbvie Inc filed Critical Abbvie Inc
Publication of PL2134685T3 publication Critical patent/PL2134685T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/04Immunostimulants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/06Antianaemics
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
PL08745934T 2007-04-16 2008-04-16 Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1 PL2134685T3 (pl)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US91204907P 2007-04-16 2007-04-16
US94968307P 2007-07-13 2007-07-13
PCT/US2008/060427 WO2008130970A1 (en) 2007-04-16 2008-04-16 7-nonsubstituted indole mcl-1 inhibitors
EP08745934.3A EP2134685B1 (en) 2007-04-16 2008-04-16 7-nonsubstituted indole derivatives as mcl-1 inhibitors

Publications (1)

Publication Number Publication Date
PL2134685T3 true PL2134685T3 (pl) 2016-02-29

Family

ID=39683700

Family Applications (1)

Application Number Title Priority Date Filing Date
PL08745934T PL2134685T3 (pl) 2007-04-16 2008-04-16 Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1

Country Status (11)

Country Link
US (2) US7981888B2 (pl)
EP (1) EP2134685B1 (pl)
JP (2) JP5496876B2 (pl)
CN (1) CN101711235A (pl)
CA (2) CA2682354C (pl)
DK (1) DK2134685T3 (pl)
ES (1) ES2550753T3 (pl)
MX (1) MX2009011210A (pl)
PL (1) PL2134685T3 (pl)
PT (1) PT2134685E (pl)
WO (1) WO2008130970A1 (pl)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2682356C (en) 2007-04-16 2016-06-14 Abbott Laboratories 7-substituted indole mcl-1 inhibitors
CN102307862A (zh) * 2008-12-08 2012-01-04 贝林格尔.英格海姆国际有限公司 用于治疗癌症的化合物
NZ593537A (en) * 2008-12-19 2013-07-26 Genentech Inc Isoquinoline derivatives and methods of use
ES2462715T3 (es) 2008-12-19 2014-05-26 Genentech, Inc. Compuestos y métodos de uso
EP3138838A1 (en) 2010-01-29 2017-03-08 Dana-Farber Cancer Institute, Inc. Small molecules for the modulation of mcl-1 and methods of modulating cell death, cell division, cell differentiation and methods of treating disorders
EP2487159A1 (en) 2011-02-11 2012-08-15 MSD Oss B.V. RorgammaT inhibitors
EP2567698B1 (en) 2011-09-07 2014-02-12 Rheinische Friedrich-Wilhelms-Universität Bonn GPR 17 agonists and screening assay
US8940737B2 (en) 2011-10-14 2015-01-27 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
CA2868081C (en) 2012-03-20 2021-01-05 Loren D. Walensky Inhibition of mcl-1 and/or bfl-1/a1
WO2014026330A1 (en) * 2012-08-15 2014-02-20 Merck Sharp & Dohme Corp. 3-AMINOCYCLOALKYL COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF
WO2014026329A1 (en) 2012-08-15 2014-02-20 Merck Sharp & Dohme Corp. N-alkylated indole and indazole compounds as rorgammat inhibitors and uses thereof
WO2014026327A1 (en) 2012-08-15 2014-02-20 Merck Sharp & Dohme Corp. 4-heteroaryl substituted benzoic acid compounds as rorgammat inhibitors and uses thereof
US10093640B2 (en) 2012-09-21 2018-10-09 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
US10533010B2 (en) 2014-03-27 2020-01-14 Vanderbilt University Substituted indole Mcl-1 inhibitors
US9949965B2 (en) 2014-10-17 2018-04-24 Vanderbilt University Tricyclic indole Mcl-1 inhibitors and uses thereof
US20180291373A1 (en) 2014-10-29 2018-10-11 The Walter And Eliza Hall Institute Of Medical Research Use of therapeutic agents
JP2018510135A (ja) 2015-02-11 2018-04-12 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. RORγT阻害剤としての置換ピラゾール化合物及びその使用
WO2016200726A1 (en) 2015-06-08 2016-12-15 Texas Tech University System Inhibitors of mci-1 as drugs to overcome resistance to braf inhibitors and mek inhibitors
CA3002850A1 (en) 2015-10-27 2017-05-04 Merck Sharp & Dohme Corp. Substituted indazole compounds as rorgammat inhibitors and uses thereof
WO2017075178A1 (en) 2015-10-27 2017-05-04 Merck Sharp & Dohme Corp. SUBSTITUTED BICYCLIC PYRAZOLE COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF
CA3002853A1 (en) 2015-10-27 2017-05-04 Merck Sharp & Dohme Corp. Heteroaryl substituted benzoic acids as rorgammat inhibitors and uses thereof
EP3371173A4 (en) * 2015-11-02 2019-06-19 Carmel-Haifa University Economic Corporation Ltd. APOPTOSIS ASSOCIATED PROTEIN IN MIMETIC COMPOUNDS OF THE TGF-BETA SIGNALING PATH (ARTS), COMPOSITIONS, METHODS AND USES THEREOF IN INDUCING THE DIFFERENTIATION AND / OR APOPTOSIS OF PREMALIGNES AND MALIGNING CELLS FOR THE RECONSTRUCTION OF THEIR NORMAL PHENOTYPES
KR102396177B1 (ko) * 2016-03-04 2022-05-09 반더빌트유니버시티 치환된 인돌 mcl-1 억제제
PE20181803A1 (es) 2016-04-22 2018-11-19 Astrazeneca Ab Inhibidores de mcl-1 macrociclicos para tratar el cancer
EP3458459B1 (en) 2016-05-19 2022-04-27 Bayer Aktiengesellschaft Macrocyclic indole derivatives
WO2017198341A1 (en) 2016-05-19 2017-11-23 Bayer Aktiengesellschaft Macrocyclic indole derivatives
JP6910027B2 (ja) * 2017-03-29 2021-07-28 株式会社コーセー チロシナーゼ活性阻害剤、メラニン産生抑制剤及び美白剤
TW201841888A (zh) * 2017-04-30 2018-12-01 財團法人生物技術開發中心 一種抗癌幹性之藥物
US11447504B2 (en) 2017-11-17 2022-09-20 Bayer Aktiengesellschaft Macrocyclic chlorine substituted indole derivatives
CN111757884B (zh) 2017-11-17 2023-12-19 拜耳股份公司 取代的大环吲哚衍生物
US20210253598A1 (en) 2017-11-17 2021-08-19 Bayer Aktiengesellschaft Aryl annulated macrocyclic indole derivatives
US11478451B1 (en) 2017-11-17 2022-10-25 Bayer Aktiengesellschaft Macrocyclic chlorine substituted indole derivatives
WO2019096911A1 (en) 2017-11-17 2019-05-23 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
BR112021004805A2 (pt) * 2018-09-30 2021-06-01 Jiangsu Hengrui Medicine Co., Ltd. derivado macrocíclico de indol, método de preparação do mesmo e aplicação do mesmo na medicina
WO2020103864A1 (en) * 2018-11-22 2020-05-28 Ascentage Pharma (Suzhou) Co., Ltd. Macrocyclic indoles as mcl-1 inhibitors
WO2020236556A1 (en) 2019-05-17 2020-11-26 The Broad Institute, Inc. Methods of preparing macrocyclic indoles
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
WO2021099579A1 (en) 2019-11-21 2021-05-27 Janssen Pharmaceutica Nv Macrocyclic indole derivatives as mcl-1 inhibitors
JP2023502692A (ja) 2019-11-21 2023-01-25 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ルホニル誘導体
JPWO2021107125A1 (pl) 2019-11-29 2021-06-03
CN115335384B (zh) * 2020-03-30 2024-10-22 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
MX2022015005A (es) 2020-05-29 2023-01-04 Janssen Pharmaceutica Nv Derivados de 7-pirazol-5-il-indol macrociclicos como inhibidores de mcl-1.
EP4168412A1 (en) 2020-06-19 2023-04-26 JANSSEN Pharmaceutica NV N-linked macrocyclic 7-(pyrazol-5-yl)-indole derivatives as inhibitors of mcl-1
JP2024520801A (ja) 2021-06-11 2024-05-24 ギリアード サイエンシーズ, インコーポレイテッド Mcl-1阻害剤と抗がん剤との組み合わせ
TWI861509B (zh) 2021-06-11 2024-11-11 美商基利科學股份有限公司 Mcl-1抑制劑與抗體藥物接合物之組合

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3632805A (en) 1967-12-08 1972-01-04 Sumitomo Chemical Co Process for producing 1-aminoalkyl-benzodiazepine derivatives
FR2187318B1 (pl) 1972-06-08 1975-06-20 Delalande Sa
US4994477A (en) * 1988-03-24 1991-02-19 Abbott Laboratories Heterocyclic renin inhibitors
KR100482268B1 (ko) * 1996-08-01 2005-04-14 메르클레 게엠베하 세포질 포스포리파제 a2의 저해제로서의 아실피롤디카르복실산
GB9716657D0 (en) * 1997-08-07 1997-10-15 Zeneca Ltd Chemical compounds
DE69929720T2 (de) 1998-11-27 2006-09-21 Mitsubishi Chemical Corp. Verfahren zur Herstellung von Maleinsäureanhydrid
GB9902452D0 (en) * 1999-02-05 1999-03-24 Zeneca Ltd Chemical compounds
GB9902455D0 (en) * 1999-02-05 1999-03-24 Zeneca Ltd Chemical compounds
GB0000626D0 (en) * 2000-01-13 2000-03-01 Zeneca Ltd Chemical compounds
US6787651B2 (en) * 2000-10-10 2004-09-07 Smithkline Beecham Corporation Substituted indoles, pharmaceutical compounds containing such indoles and their use as PPAR-γ binding agents
DE10153346A1 (de) * 2001-10-29 2004-04-22 Grünenthal GmbH Substituierte Indole
JP2005516908A (ja) * 2001-11-30 2005-06-09 ザ バーナム インスティチュート 癌細胞におけるアポトーシスの誘導
EP1513522A2 (en) * 2002-01-18 2005-03-16 Sri International Methods of treating conditions associated with an edg receptor
AU2003239150A1 (en) * 2002-04-23 2003-11-10 Aventis Pharmaceuticals Inc. 3-substituted amino-1h-indole-2-carboxylic acid and 3-substituted amino-benzo
JP4695588B2 (ja) 2003-02-26 2011-06-08 スージェン, インク. プロテインキナーゼ阻害剤としてのアミノヘテロアリール化合物
WO2004092346A2 (en) * 2003-04-15 2004-10-28 The Regents Of The University Of California Small molecule inhibition of a pdz-domain interaction
SE0302035D0 (sv) * 2003-07-09 2003-07-09 Biolipox Ab New compound
US7268159B2 (en) * 2003-09-25 2007-09-11 Wyeth Substituted indoles
ITMI20040874A1 (it) * 2004-04-30 2004-07-30 Ist Naz Stud Cura Dei Tumori Derivati indolici ed azaindolici con azione antitumorale
KR20070029809A (ko) * 2004-06-18 2007-03-14 바이올리폭스 에이비 염증치료에 유용한 인돌
DE602005014233D1 (de) * 2004-06-18 2009-06-10 Biolipox Ab Zur behandlung von entzündungen geeignete indole
BRPI0512252A (pt) * 2004-06-18 2008-02-19 Biolipox Ab composto ou um sal farmaceuticamente aceitável do mesmo, formulação farmacêutica, uso de um composto, método de tratamento de uma doença, produto combinado, e, processo para a preparação de um composto
WO2006041961A1 (en) * 2004-10-05 2006-04-20 GOVERNMENT OF THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, DEPARTMENT OF HEALTHAND HUMAN SERVICES Arylthioindole tubulin polymerization inhibitors and methods of treating or preventing cancer using same
FR2878849B1 (fr) * 2004-12-06 2008-09-12 Aventis Pharma Sa Indoles substitues, compositions les contenant, procede de fabrication et utilisation
JP2008527030A (ja) * 2005-01-19 2008-07-24 バイオリポックス エービー 炎症の治療に有用なインドール類
CA2593155A1 (en) * 2005-01-19 2006-07-27 Biolipox Ab Indoles useful in the treatment of inflammation
US7750004B2 (en) * 2005-07-07 2010-07-06 Abbott Laboratories Apoptosis promoters
CL2007002516A1 (es) * 2006-08-31 2008-05-16 Smithkline Beecham Corp Compuestos derivados de indol indano; composicion farmaceutica; y su uso para tratar hiperglicemia, diabetes tipo 2, tolerancia deteriorada a la glucosa, resistencia a la insulina, sindrome x, dislipidemia.
CA2682356C (en) 2007-04-16 2016-06-14 Abbott Laboratories 7-substituted indole mcl-1 inhibitors
NZ593537A (en) 2008-12-19 2013-07-26 Genentech Inc Isoquinoline derivatives and methods of use
ES2462715T3 (es) 2008-12-19 2014-05-26 Genentech, Inc. Compuestos y métodos de uso

Also Published As

Publication number Publication date
EP2134685B1 (en) 2015-09-02
CA2682354A1 (en) 2008-10-30
ES2550753T3 (es) 2015-11-12
CN101711235A (zh) 2010-05-19
US20110263599A1 (en) 2011-10-27
DK2134685T3 (en) 2015-12-07
PT2134685E (pt) 2015-11-25
US7981888B2 (en) 2011-07-19
EP2134685A1 (en) 2009-12-23
CA2951295A1 (en) 2008-10-30
CA2951295C (en) 2020-04-28
JP2010524955A (ja) 2010-07-22
MX2009011210A (es) 2009-10-30
US8853209B2 (en) 2014-10-07
US20090124616A1 (en) 2009-05-14
JP2014129396A (ja) 2014-07-10
JP5895011B2 (ja) 2016-03-30
JP5496876B2 (ja) 2014-05-21
CA2682354C (en) 2016-12-13
WO2008130970A1 (en) 2008-10-30

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