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MX2017016244A - Derivados de amidas policiclicas como inhibidores de cdk9. - Google Patents

Derivados de amidas policiclicas como inhibidores de cdk9.

Info

Publication number
MX2017016244A
MX2017016244A MX2017016244A MX2017016244A MX2017016244A MX 2017016244 A MX2017016244 A MX 2017016244A MX 2017016244 A MX2017016244 A MX 2017016244A MX 2017016244 A MX2017016244 A MX 2017016244A MX 2017016244 A MX2017016244 A MX 2017016244A
Authority
MX
Mexico
Prior art keywords
cancer
cdk9
derivatives
amidas
political
Prior art date
Application number
MX2017016244A
Other languages
English (en)
Other versions
MX371034B (es
Inventor
Christophe Barlaam Bernard
Gordon Pike Kurt
Hawkins Janet
De Savi Christopher
Marie Vasbinder Melissa
Hird Alexander
Lamb Michelle
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 MX2017016244A publication Critical patent/MX2017016244A/es
Publication of MX371034B publication Critical patent/MX371034B/es

Links

Classifications

    • 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
    • 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
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Detergent Compositions (AREA)

Abstract

Se provee una serie de derivados novedosos de piridina o pirimidina que inhiben CDK9 y pueden se útiles para el tratamiento de enfermedades hiperproliferativas. En particular, los compuestos son útiles en el tratamiento de enfermedades proliferativas como por ejemplo cáncer, incluyendo trastornos hematológicos malignos, como por ejemplo leucemia mieloide aguda, mieloma múltiple, leucemia linfocítica crónica, linfoma difuso de células B grandes, linfoma de Burkitt, linfoma folicular y tumores sólidos como por ejemplo cáncer de mama, cáncer de pulmón, neuroblastoma y cáncer de colon.
MX2017016244A 2015-06-29 2016-06-27 Derivados de amidas policíclicas como inhibidores de cdk9. MX371034B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562185852P 2015-06-29 2015-06-29
PCT/EP2016/064899 WO2017001354A1 (en) 2015-06-29 2016-06-27 Polycyclic amide derivatives as cdk9 inhibitors

Publications (2)

Publication Number Publication Date
MX2017016244A true MX2017016244A (es) 2018-04-20
MX371034B MX371034B (es) 2020-01-13

Family

ID=56292699

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017016244A MX371034B (es) 2015-06-29 2016-06-27 Derivados de amidas policíclicas como inhibidores de cdk9.

Country Status (38)

Country Link
US (4) US9845331B2 (es)
EP (2) EP3313838B1 (es)
JP (1) JP6997627B2 (es)
KR (1) KR102663113B1 (es)
CN (1) CN107873028B (es)
AR (1) AR105179A1 (es)
AU (1) AU2016286200B2 (es)
BR (1) BR122019013677B1 (es)
CA (1) CA2989499C (es)
CL (1) CL2017003306A1 (es)
CO (1) CO2017013713A2 (es)
CR (2) CR20210297A (es)
CY (2) CY1122111T1 (es)
DK (2) DK3539961T3 (es)
DO (2) DOP2017000295A (es)
EA (1) EA035383B1 (es)
ES (2) ES2728356T3 (es)
HR (2) HRP20190748T1 (es)
HU (2) HUE043440T2 (es)
IL (1) IL256393B (es)
LT (2) LT3539961T (es)
ME (1) ME03404B (es)
MX (1) MX371034B (es)
MY (1) MY201673A (es)
NI (1) NI201700174A (es)
PE (1) PE20180530A1 (es)
PH (1) PH12017502334B1 (es)
PL (2) PL3313838T3 (es)
PT (2) PT3313838T (es)
RS (2) RS58712B1 (es)
SI (2) SI3539961T1 (es)
SM (2) SMT201900298T1 (es)
SV (1) SV2017005598A (es)
TN (1) TN2017000486A1 (es)
TR (1) TR201909286T4 (es)
TW (1) TWI723028B (es)
WO (1) WO2017001354A1 (es)
ZA (1) ZA201800563B (es)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3075952A1 (en) 2017-09-25 2019-03-28 Astrazeneca Ab Combination of a btk inhibitor and an inhibitor of cdk9 to treat cancer
US11319295B2 (en) 2017-10-09 2022-05-03 Merck Sharp & Dohme Corp. Substituted phenyloxetane and phenyltetrahydrofuran compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
CN108129288B (zh) * 2017-12-27 2021-01-22 上海毕得医药科技股份有限公司 一种反式-3-羟基环丁基甲酸的合成方法
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
CN114008046B (zh) * 2019-06-27 2023-08-18 南京明德新药研发有限公司 作为cdk9抑制剂的氮杂吲哚连吡唑类化合物
CA3153531A1 (en) 2019-09-11 2021-03-18 Prelude Therapeutics Incorporated Cdk inhibitors and their use as pharmaceuticals
CN114787142B (zh) * 2019-12-09 2024-08-02 石药集团中奇制药技术(石家庄)有限公司 作为周期蛋白依赖性激酶9抑制剂的化合物及其应用
WO2021227906A1 (zh) * 2020-05-12 2021-11-18 苏州阿尔脉生物科技有限公司 一种作为cdk抑制剂的吡啶乙酰胺类衍生物、其制备方法及用途
EP4141004A4 (en) * 2020-05-12 2023-08-23 Suzhou Alphama Biotechnology Co., Ltd. POLYCYCLIC AMIDE DERIVATIVE SERVING AS A CDK9 INHIBITOR, METHOD FOR PREPARING IT AND ITS USE
JP7794766B2 (ja) * 2020-06-24 2026-01-06 アストラゼネカ ユーケー リミテッド 抗体-薬物複合物及びcdk9阻害剤の組み合わせ
JP7537002B2 (ja) 2020-08-07 2024-08-20 南京薬石科技股▲フン▼有限公司 Cdk9阻害剤およびその使用
TWI809330B (zh) * 2020-11-20 2023-07-21 大陸商勁方醫藥科技(上海)有限公司 Cdk9抑制劑的多晶型物及其製法和用途
WO2022247785A1 (zh) * 2021-05-24 2022-12-01 石药集团中奇制药技术(石家庄)有限公司 一种周期蛋白依赖性激酶9抑制剂的用途
CN115381824B (zh) * 2021-05-24 2024-11-05 石药集团中奇制药技术(石家庄)有限公司 周期蛋白依赖性激酶9抑制剂的用途
CN117813289A (zh) * 2021-07-14 2024-04-02 上海海雁医药科技有限公司 吡唑衍生物及其中间体和制备方法
CN115703738B (zh) * 2021-08-16 2024-06-21 中国科学院上海药物研究所 含2-芳杂环取代的脲类化合物、其制备方法和用途
CN118613257A (zh) * 2021-12-23 2024-09-06 鲁汶大学 用于抑制yap/taz-tead的四氢吡唑并嘧啶及相关类似物
AU2023326499A1 (en) 2022-08-17 2025-03-27 Korea Research Institute Of Bioscience And Biotechnology Compounds for inhibiting or decomposing cdk2 and/or cdk9, and medicinal uses thereof
CN117659022A (zh) * 2022-09-06 2024-03-08 苏州阿尔脉生物科技有限公司 脲基取代吡啶类化合物、包含其的药物组合物及其医药用途
US20240360075A1 (en) * 2023-04-19 2024-10-31 Alcon Inc. N-substituted c6 cyclyl carboxamide compounds and uses thereof
WO2025076115A1 (en) * 2023-10-02 2025-04-10 Prelude Therapeutics Incorporated Cdk inhibitors and their use as pharmaceuticals

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008133192A1 (ja) 2007-04-19 2008-11-06 Takeda Pharmaceutical Company Limited 縮合イミダゾール化合物およびその用途
EP2137166B1 (en) 2007-04-24 2012-05-30 Ingenium Pharmaceuticals GmbH 4, 6-disubstituted aminopyrimidine derivatives as inhibitors of protein kinases
WO2008129071A1 (en) 2007-04-24 2008-10-30 Ingenium Pharmaceuticals Gmbh Inhibitors of protein kinases
ES2539518T3 (es) 2007-04-24 2015-07-01 Astrazeneca Ab Inhibidores de proteínas quinasas
WO2008129069A1 (en) 2007-04-24 2008-10-30 Ingenium Pharmaceuticals Gmbh Inhibitors of protein kinases
WO2008132138A1 (en) 2007-04-25 2008-11-06 Ingenium Pharmaceuticals Gmbh Derivatives of 4,6-disubstituted aminopyrimidines
BRPI0818543A2 (pt) 2007-10-12 2018-10-23 Ingenium Pharmaceuticals Gmbh inibidores de proteína cinase
KR20120049940A (ko) 2009-09-04 2012-05-17 노파르티스 아게 키나제 억제제로서의 헤테로아릴 화합물
US20110113038A1 (en) 2009-11-12 2011-05-12 International Business Machines Corporation Search term security
GB201002911D0 (en) 2010-02-19 2010-04-07 Medical Res Council Compound
KR20130016244A (ko) 2010-03-10 2013-02-14 인게니움 파르마코이티칼스 게엠베하 단백질 키나아제의 억제제
AR081810A1 (es) 2010-04-07 2012-10-24 Bayer Cropscience Ag Piridinilpirazoles biciclicos
WO2012066065A1 (en) 2010-11-17 2012-05-24 Novartis Ag Phenyl-heteroaryl amine compounds and their uses
EP2668162A1 (en) * 2011-01-28 2013-12-04 Novartis AG Substituted bi-heteroaryl compounds as cdk9 inhibitors and their uses
WO2012101064A1 (en) * 2011-01-28 2012-08-02 Novartis Ag N-acyl pyrimidine biaryl compounds as protein kinase inhibitors
WO2012101063A1 (en) 2011-01-28 2012-08-02 Novartis Ag N-acyl pyridine biaryl compounds and their uses
KR20140072177A (ko) 2011-10-06 2014-06-12 바이엘 인텔렉쳐 프로퍼티 게엠베하 헤테로사이클릴피리(미)디닐피라졸
MX2015012432A (es) * 2013-03-13 2016-02-05 Abbvie Inc Inhibidores piridinicos de la cinasa cdk9.
BR112015023013A2 (pt) 2013-03-13 2017-07-18 Abbvie Inc inibidores de quinase cdk9
BR112015023078A2 (pt) 2013-03-14 2017-07-18 Abbvie Inc inibidores de pirrolopirimindina cdk9 quinase
TW201446763A (zh) 2013-03-14 2014-12-16 Abbvie Inc 吡咯并[2,3-b]吡啶cdk9激酶抑制劑

Also Published As

Publication number Publication date
CA2989499A1 (en) 2017-01-05
ES2728356T3 (es) 2019-10-23
PH12017502334B1 (en) 2023-05-26
CR20210297A (es) 2021-09-29
US20160376287A1 (en) 2016-12-29
CO2017013713A2 (es) 2018-03-28
ES2902148T3 (es) 2022-03-25
HRP20211970T1 (hr) 2022-03-18
ME03404B (me) 2020-01-20
MX371034B (es) 2020-01-13
EP3539961B1 (en) 2021-10-06
AR105179A1 (es) 2017-09-13
US9845331B2 (en) 2017-12-19
EA035383B1 (ru) 2020-06-04
PT3539961T (pt) 2021-12-20
CA2989499C (en) 2023-10-31
EP3539961A1 (en) 2019-09-18
US20220340592A1 (en) 2022-10-27
EP3313838B1 (en) 2019-04-03
US10717746B2 (en) 2020-07-21
TR201909286T4 (tr) 2019-07-22
BR122019013677B1 (pt) 2024-01-02
US20180093998A1 (en) 2018-04-05
AU2016286200A1 (en) 2018-02-08
DK3539961T3 (da) 2022-01-03
CY1122111T1 (el) 2020-11-25
PE20180530A1 (es) 2018-03-19
JP6997627B2 (ja) 2022-01-17
US20210171541A1 (en) 2021-06-10
WO2017001354A1 (en) 2017-01-05
HRP20190748T1 (hr) 2019-06-14
HUE043440T2 (hu) 2019-08-28
EP3313838A1 (en) 2018-05-02
IL256393B (en) 2021-12-01
SV2017005598A (es) 2018-02-23
NI201700174A (es) 2018-10-19
SI3313838T1 (sl) 2019-06-28
AU2016286200B2 (en) 2018-10-04
DOP2018000207A (es) 2018-10-15
JP2018522869A (ja) 2018-08-16
PT3313838T (pt) 2019-06-24
CL2017003306A1 (es) 2018-06-29
DOP2017000295A (es) 2017-12-31
MY201673A (en) 2024-03-12
ZA201800563B (en) 2022-08-31
IL256393A (en) 2018-02-28
KR20180021830A (ko) 2018-03-05
RS62781B1 (sr) 2022-01-31
HUE057343T2 (hu) 2022-05-28
PL3313838T3 (pl) 2019-08-30
CN107873028A (zh) 2018-04-03
US11352369B2 (en) 2022-06-07
TWI723028B (zh) 2021-04-01
LT3539961T (lt) 2021-12-27
KR102663113B1 (ko) 2024-05-02
PH12017502334A1 (en) 2018-06-25
TW201718573A (zh) 2017-06-01
CY1125066T1 (el) 2023-03-24
BR112017027394A2 (pt) 2018-11-06
PL3539961T3 (pl) 2022-02-14
RS58712B1 (sr) 2019-06-28
TN2017000486A1 (en) 2019-04-12
CN107873028B (zh) 2021-02-02
EA201890094A1 (ru) 2018-07-31
SMT201900298T1 (it) 2019-07-11
SMT202200005T1 (it) 2022-03-21
CR20170596A (es) 2018-07-04
SI3539961T1 (sl) 2022-02-28
LT3313838T (lt) 2019-06-10
DK3313838T3 (da) 2019-06-11

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