HUE043440T2 - Policiklusos amidszármazékok mint CDK9 inhibitorok - Google Patents

Policiklusos amidszármazékok mint CDK9 inhibitorok

Info

Publication number
HUE043440T2
HUE043440T2 HUE16733459A HUE16733459A HUE043440T2 HU E043440 T2 HUE043440 T2 HU E043440T2 HU E16733459 A HUE16733459 A HU E16733459A HU E16733459 A HUE16733459 A HU E16733459A HU E043440 T2 HUE043440 T2 HU E043440T2
Authority
HU
Hungary
Prior art keywords
amide derivatives
cdk9 inhibitors
polycyclic amide
polycyclic
cdk9
Prior art date
Application number
HUE16733459A
Other languages
English (en)
Hungarian (hu)
Inventor
Kurt Pike
Bernard Barlaam
Janet Hawkins
Savi Christopher De
Melissa Vasbinder
Alexander Hird
Michelle Lamb
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 HUE043440T2 publication Critical patent/HUE043440T2/hu

Links

Classifications

    • 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
    • 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
    • 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)
  • 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)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Detergent Compositions (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
HUE16733459A 2015-06-29 2016-06-27 Policiklusos amidszármazékok mint CDK9 inhibitorok HUE043440T2 (hu)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562185852P 2015-06-29 2015-06-29

Publications (1)

Publication Number Publication Date
HUE043440T2 true HUE043440T2 (hu) 2019-08-28

Family

ID=56292699

Family Applications (2)

Application Number Title Priority Date Filing Date
HUE16733459A HUE043440T2 (hu) 2015-06-29 2016-06-27 Policiklusos amidszármazékok mint CDK9 inhibitorok
HUE19165726A HUE057343T2 (hu) 2015-06-29 2016-06-27 Policiklusos amidszármazékok mint CDK9 inhibitorok

Family Applications After (1)

Application Number Title Priority Date Filing Date
HUE19165726A HUE057343T2 (hu) 2015-06-29 2016-06-27 Policiklusos amidszármazékok mint CDK9 inhibitorok

Country Status (38)

Country Link
US (4) US9845331B2 (enExample)
EP (2) EP3539961B1 (enExample)
JP (1) JP6997627B2 (enExample)
KR (1) KR102663113B1 (enExample)
CN (1) CN107873028B (enExample)
AR (1) AR105179A1 (enExample)
AU (1) AU2016286200B2 (enExample)
BR (1) BR122019013677B1 (enExample)
CA (1) CA2989499C (enExample)
CL (1) CL2017003306A1 (enExample)
CO (1) CO2017013713A2 (enExample)
CR (2) CR20170596A (enExample)
CY (2) CY1122111T1 (enExample)
DK (2) DK3539961T3 (enExample)
DO (2) DOP2017000295A (enExample)
EA (1) EA035383B1 (enExample)
ES (2) ES2902148T3 (enExample)
HR (2) HRP20190748T1 (enExample)
HU (2) HUE043440T2 (enExample)
IL (1) IL256393B (enExample)
LT (2) LT3313838T (enExample)
ME (1) ME03404B (enExample)
MX (1) MX371034B (enExample)
MY (1) MY201673A (enExample)
NI (1) NI201700174A (enExample)
PE (1) PE20180530A1 (enExample)
PH (1) PH12017502334B1 (enExample)
PL (2) PL3313838T3 (enExample)
PT (2) PT3313838T (enExample)
RS (2) RS58712B1 (enExample)
SI (2) SI3313838T1 (enExample)
SM (2) SMT201900298T1 (enExample)
SV (1) SV2017005598A (enExample)
TN (1) TN2017000486A1 (enExample)
TR (1) TR201909286T4 (enExample)
TW (1) TWI723028B (enExample)
WO (1) WO2017001354A1 (enExample)
ZA (1) ZA201800563B (enExample)

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
EP3694506B1 (en) 2017-10-09 2023-08-02 Merck Sharp & Dohme LLC Novel 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
TWI810397B (zh) 2018-11-14 2023-08-01 瑞典商阿斯特捷利康公司 治療癌症之方法
WO2020259556A1 (zh) * 2019-06-27 2020-12-30 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
US11673893B2 (en) 2019-09-11 2023-06-13 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
US20230219961A1 (en) 2020-05-12 2023-07-13 Suzhou Alphama Biotechnology Co., Ltd. Pyridine acetamide derivative serving as CDK inhibitor, and preparation method therefor and use thereof
CN113149996B (zh) * 2020-05-12 2022-12-20 苏州阿尔脉生物科技有限公司 一种作为cdk9抑制剂的多环酰胺类衍生物、其制备方法及用途
EP4171654A1 (en) 2020-06-24 2023-05-03 AstraZeneca UK Limited Combination of antibody-drug conjugate and cdk9 inhibitor
CN115843296B (zh) 2020-08-07 2024-03-08 南京迈晟科技有限责任公司 Cdk9抑制剂及其用途
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
WO2022247796A1 (zh) * 2021-05-24 2022-12-01 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
IL313630A (en) * 2021-12-23 2024-08-01 Springworks Therapeutics Inc Tetrahydropyrazolopyrimidines and related analogs inhibit YAP/TAZ-TEAD
WO2024039210A1 (ko) 2022-08-17 2024-02-22 한국화학연구원 Cdk2 및/또는 cdk9의 억제 또는 분해용 화합물 및 이들의 의약 용도
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
WO2024220876A1 (en) * 2023-04-19 2024-10-24 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
ES2539518T3 (es) 2007-04-24 2015-07-01 Astrazeneca Ab Inhibidores de proteínas quinasas
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
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
KR20100090772A (ko) 2007-10-12 2010-08-17 인게니움 파르마코이티칼스 게엠베하 단백질 키나제 억제제
AU2010291212A1 (en) 2009-09-04 2012-02-23 Novartis Ag Heteroaryl compounds as kinase inhibitors
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
EA201201274A1 (ru) 2010-03-10 2013-04-30 Инджениум Фармасьютиклз Гмбх Ингибиторы протеинкиназ
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
WO2012101063A1 (en) * 2011-01-28 2012-08-02 Novartis Ag N-acyl pyridine biaryl compounds and their uses
WO2012101062A1 (en) * 2011-01-28 2012-08-02 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
PL2763993T3 (pl) 2011-10-06 2017-09-29 Bayer Intellectual Property Gmbh Heterocyklilopiry(mi)dynylopirazol
CA2901334A1 (en) * 2013-03-13 2014-10-02 Abbvie Inc. Pyridine cdk9 kinase inhibitors
JP2016512559A (ja) 2013-03-13 2016-04-28 アッヴィ・インコーポレイテッド Cdk9キナーゼ阻害薬
TW201444836A (zh) 2013-03-14 2014-12-01 Abbvie Inc 吡咯并[2,3-b]吡啶cdk9激酶抑制劑
WO2014160028A1 (en) 2013-03-14 2014-10-02 Abbvie Inc. Pyrrolopyrimindine cdk9 kinase inhibitors

Also Published As

Publication number Publication date
PH12017502334B1 (en) 2023-05-26
CN107873028B (zh) 2021-02-02
LT3313838T (lt) 2019-06-10
AU2016286200B2 (en) 2018-10-04
BR122019013677B1 (pt) 2024-01-02
JP6997627B2 (ja) 2022-01-17
EP3539961B1 (en) 2021-10-06
IL256393A (en) 2018-02-28
CA2989499C (en) 2023-10-31
HRP20190748T1 (hr) 2019-06-14
SI3313838T1 (sl) 2019-06-28
EA201890094A1 (ru) 2018-07-31
MY201673A (en) 2024-03-12
US20160376287A1 (en) 2016-12-29
TR201909286T4 (tr) 2019-07-22
PH12017502334A1 (en) 2018-06-25
RS62781B1 (sr) 2022-01-31
RS58712B1 (sr) 2019-06-28
TN2017000486A1 (en) 2019-04-12
CO2017013713A2 (es) 2018-03-28
BR112017027394A2 (pt) 2018-11-06
PL3313838T3 (pl) 2019-08-30
KR20180021830A (ko) 2018-03-05
CR20210297A (es) 2021-09-29
DK3539961T3 (da) 2022-01-03
DOP2018000207A (es) 2018-10-15
CR20170596A (es) 2018-07-04
EA035383B1 (ru) 2020-06-04
EP3313838B1 (en) 2019-04-03
HUE057343T2 (hu) 2022-05-28
HRP20211970T1 (hr) 2022-03-18
EP3313838A1 (en) 2018-05-02
IL256393B (en) 2021-12-01
PL3539961T3 (pl) 2022-02-14
NI201700174A (es) 2018-10-19
US11352369B2 (en) 2022-06-07
SV2017005598A (es) 2018-02-23
CN107873028A (zh) 2018-04-03
JP2018522869A (ja) 2018-08-16
EP3539961A1 (en) 2019-09-18
TWI723028B (zh) 2021-04-01
US10717746B2 (en) 2020-07-21
CY1125066T1 (el) 2023-03-24
SI3539961T1 (sl) 2022-02-28
MX371034B (es) 2020-01-13
SMT201900298T1 (it) 2019-07-11
DK3313838T3 (da) 2019-06-11
CY1122111T1 (el) 2020-11-25
CA2989499A1 (en) 2017-01-05
US20210171541A1 (en) 2021-06-10
AR105179A1 (es) 2017-09-13
CL2017003306A1 (es) 2018-06-29
AU2016286200A1 (en) 2018-02-08
TW201718573A (zh) 2017-06-01
WO2017001354A1 (en) 2017-01-05
DOP2017000295A (es) 2017-12-31
ZA201800563B (en) 2022-08-31
US9845331B2 (en) 2017-12-19
KR102663113B1 (ko) 2024-05-02
ES2728356T3 (es) 2019-10-23
ME03404B (me) 2020-01-20
LT3539961T (lt) 2021-12-27
US20180093998A1 (en) 2018-04-05
PE20180530A1 (es) 2018-03-19
ES2902148T3 (es) 2022-03-25
SMT202200005T1 (it) 2022-03-21
US20220340592A1 (en) 2022-10-27
MX2017016244A (es) 2018-04-20
PT3539961T (pt) 2021-12-20
PT3313838T (pt) 2019-06-24

Similar Documents

Publication Publication Date Title
CY2024003I2 (el) Ενωσεις χρησιμες ως αναστολεις κινασης
HUE043440T2 (hu) Policiklusos amidszármazékok mint CDK9 inhibitorok
IL263586A (en) Inhibitors of the menin-mll interaction
HUE057801T2 (hu) Aminotriazolopiridinek mint kináz inhibitorok
DK3497103T3 (da) Pyridopyrimdinon-cdk2/4/6-inhibitorer
LT3436461T (lt) Pirolotriazino junginiai kaip tam inhibitoriai
HUE053564T2 (hu) Heterociklusos amidok kinázinhibitorként
DK3319956T3 (da) Substituerede oxopyridinderivater
LT3303334T (lt) Tirozinkinazės inhibitoriai
HUE046273T2 (hu) Ciklopropilaminok mint LSD1 inhibitorok
HUE045725T2 (hu) Ciklopropilaminok mint LSD1 inhibitorok
MA53944A (fr) Inhibiteurs de la glycosidase
DK3442972T3 (da) Bromdomænehæmmere
CU20160125A7 (es) Inhibidores de diacilglicerol aciltransferasa 2
HUE058292T2 (hu) Aminoimidazopiridazinok mint kináz inhibitorok
HUE049502T2 (hu) Policiklusos vegyületek mint bruton-tirozin-kináz inhibitorok
HUE047684T2 (hu) Új szubsztituált cianoindolin származékok mint NIK inhibitorok
DK3544981T3 (da) Benzodiazoliumforbindelser som enac-inhibitorer
DK3114120T3 (da) Tetrazolon-substituerede dihydropyridinon-mgat2-hæmmere
HUE046994T2 (hu) Pirido-oxazinon származékok TNAP inhibitorokként
HUE045220T2 (hu) Imidazopiridazin-származékok mint PI3Kbéta inhibitorok
DK3481826T3 (da) Tyrosinkinaseinhibitorer
HUE042119T2 (hu) Aminoészter-származékok
HUE054912T2 (hu) Pirazolil-amino-benzimidazol-származékok mint JAK inhibitorok
EP3525786A4 (en) KDM5 INHIBITORS