[go: up one dir, main page]

CO2017013713A2 - Derivados de amidas policíclicas como inhibidores de cdk9 - Google Patents

Derivados de amidas policíclicas como inhibidores de cdk9

Info

Publication number
CO2017013713A2
CO2017013713A2 CONC2017/0013713A CO2017013713A CO2017013713A2 CO 2017013713 A2 CO2017013713 A2 CO 2017013713A2 CO 2017013713 A CO2017013713 A CO 2017013713A CO 2017013713 A2 CO2017013713 A2 CO 2017013713A2
Authority
CO
Colombia
Prior art keywords
cancer
amide derivatives
useful
treatment
cdk9 inhibitors
Prior art date
Application number
CONC2017/0013713A
Other languages
English (en)
Inventor
Kurt Gordon Pike
Bernard Christophe Barlaam
Janet Hawkins
Savi Christopher De
Melissa Marie 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 CO2017013713A2 publication Critical patent/CO2017013713A2/es

Links

Classifications

    • 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
    • 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
    • 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
    • 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
    • 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)
  • Polyesters Or Polycarbonates (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Detergent Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (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.
CONC2017/0013713A 2015-06-29 2017-12-28 Derivados de amidas policíclicas como inhibidores de cdk9 CO2017013713A2 (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 (1)

Publication Number Publication Date
CO2017013713A2 true CO2017013713A2 (es) 2018-03-28

Family

ID=56292699

Family Applications (1)

Application Number Title Priority Date Filing Date
CONC2017/0013713A CO2017013713A2 (es) 2015-06-29 2017-12-28 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) DK3313838T3 (es)
DO (2) DOP2017000295A (es)
EA (1) EA035383B1 (es)
ES (2) ES2902148T3 (es)
HR (2) HRP20211970T1 (es)
HU (2) HUE057343T2 (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) PL3539961T3 (es)
PT (2) PT3313838T (es)
RS (2) RS62781B1 (es)
SI (2) SI3313838T1 (es)
SM (2) SMT202200005T1 (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 (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2020003270A (es) 2017-09-25 2020-07-20 Astrazeneca Ab Combinacion de un inhibidor de btk y un inhibidor de cdk9 para tratar el 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
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
EP4028005A4 (en) * 2019-09-11 2023-09-20 Prelude Therapeutics, Incorporated Cdk inhibitors and their use as pharmaceuticals
US20230102081A1 (en) * 2019-12-09 2023-03-30 Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. Compound as cyclin-dependent kinase 9 inhibitor and use thereof
EP4140997A4 (en) * 2020-05-12 2023-09-06 Suzhou Alphama Biotechnology Co., Ltd. PYRIDINE ACETAMIDE DERIVATIVE AS CDK INHIBITOR, PREPARATION METHOD 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
CN116615248A (zh) * 2020-06-24 2023-08-18 阿斯利康(英国)有限公司 抗体-药物缀合物和cdk9抑制剂的组合
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
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
CN115381823B (zh) * 2021-05-24 2024-11-05 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
WO2023284775A1 (zh) * 2021-07-14 2023-01-19 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
MX2024007929A (es) * 2021-12-23 2024-09-10 Univ Leuven Kath Tetrahidropirazolopirimidinas y analogos relacionados para la inhibicion de yap/taz-tead.
JP2025528223A (ja) 2022-08-17 2025-08-26 コリア リサーチ インスティテュート オブ ケミカル テクノロジー Cdk2及び/又はcdk9の抑制又は分解用化合物及びこれらの医薬用途
AU2024258350A1 (en) * 2023-04-19 2025-10-30 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
WO2008129069A1 (en) 2007-04-24 2008-10-30 Ingenium Pharmaceuticals Gmbh Inhibitors of protein kinases
US8436007B2 (en) 2007-04-24 2013-05-07 Ingenium Pharmaceuticals Gmbh Inhibitors of protein kinases
US8507498B2 (en) 2007-04-24 2013-08-13 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
WO2008132138A1 (en) 2007-04-25 2008-11-06 Ingenium Pharmaceuticals Gmbh Derivatives of 4,6-disubstituted aminopyrimidines
NZ584454A (en) 2007-10-12 2011-09-30 Ingenium Pharmaceuticals Gmbh N-[6-phenyl-pyrimidin-4-yl]-amides and urea derivatives as inhibitors of protein kinases
EP2473502A1 (en) 2009-09-04 2012-07-11 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
NZ627520A (en) 2010-03-10 2015-10-30 Astrazeneca Ab 4-phenyl pyridine analogues as protein kinase inhibitors
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
JP2014506878A (ja) * 2011-01-28 2014-03-20 ノバルティス アーゲー Cdk9阻害剤としての置換ビ−ヘテロアリール化合物およびそれらの使用
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
US9314026B2 (en) 2011-10-06 2016-04-19 Bayer Intellectual Property Gmbh Heterocyclylpyri(mi)dinylpyrazole
EP2970200A1 (en) 2013-03-13 2016-01-20 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
UY35419A (es) 2013-03-14 2014-10-31 Abbvie Inc Inhibidores de cdk9 quinasa de pirrolo (2,3- b) piridina
CA2903538A1 (en) 2013-03-14 2014-10-02 Abbvie Inc. Pyrrolopyrimindine cdk9 kinase inhibitors

Also Published As

Publication number Publication date
CY1122111T1 (el) 2020-11-25
LT3539961T (lt) 2021-12-27
ME03404B (me) 2020-01-20
BR112017027394A2 (pt) 2018-11-06
TWI723028B (zh) 2021-04-01
ZA201800563B (en) 2022-08-31
US9845331B2 (en) 2017-12-19
DOP2017000295A (es) 2017-12-31
EP3313838B1 (en) 2019-04-03
KR20180021830A (ko) 2018-03-05
US20160376287A1 (en) 2016-12-29
AU2016286200B2 (en) 2018-10-04
SV2017005598A (es) 2018-02-23
JP6997627B2 (ja) 2022-01-17
TR201909286T4 (tr) 2019-07-22
SMT202200005T1 (it) 2022-03-21
TW201718573A (zh) 2017-06-01
US20210171541A1 (en) 2021-06-10
CR20170596A (es) 2018-07-04
PT3539961T (pt) 2021-12-20
EP3539961A1 (en) 2019-09-18
CY1125066T1 (el) 2023-03-24
MX371034B (es) 2020-01-13
HRP20211970T1 (hr) 2022-03-18
DK3313838T3 (da) 2019-06-11
PH12017502334B1 (en) 2023-05-26
PT3313838T (pt) 2019-06-24
ES2728356T3 (es) 2019-10-23
PL3539961T3 (pl) 2022-02-14
JP2018522869A (ja) 2018-08-16
MY201673A (en) 2024-03-12
SI3539961T1 (sl) 2022-02-28
SI3313838T1 (sl) 2019-06-28
CN107873028A (zh) 2018-04-03
RS62781B1 (sr) 2022-01-31
SMT201900298T1 (it) 2019-07-11
ES2902148T3 (es) 2022-03-25
TN2017000486A1 (en) 2019-04-12
WO2017001354A1 (en) 2017-01-05
PL3313838T3 (pl) 2019-08-30
US10717746B2 (en) 2020-07-21
RS58712B1 (sr) 2019-06-28
CA2989499C (en) 2023-10-31
PE20180530A1 (es) 2018-03-19
US20220340592A1 (en) 2022-10-27
HUE057343T2 (hu) 2022-05-28
NI201700174A (es) 2018-10-19
HRP20190748T1 (hr) 2019-06-14
HUE043440T2 (hu) 2019-08-28
CA2989499A1 (en) 2017-01-05
AR105179A1 (es) 2017-09-13
EP3539961B1 (en) 2021-10-06
MX2017016244A (es) 2018-04-20
US20180093998A1 (en) 2018-04-05
LT3313838T (lt) 2019-06-10
PH12017502334A1 (en) 2018-06-25
EA201890094A1 (ru) 2018-07-31
CR20210297A (es) 2021-09-29
DK3539961T3 (da) 2022-01-03
EA035383B1 (ru) 2020-06-04
EP3313838A1 (en) 2018-05-02
IL256393B (en) 2021-12-01
CN107873028B (zh) 2021-02-02
AU2016286200A1 (en) 2018-02-08
KR102663113B1 (ko) 2024-05-02
CL2017003306A1 (es) 2018-06-29
BR122019013677B1 (pt) 2024-01-02
IL256393A (en) 2018-02-28
US11352369B2 (en) 2022-06-07
DOP2018000207A (es) 2018-10-15

Similar Documents

Publication Publication Date Title
CO2017013713A2 (es) Derivados de amidas policíclicas como inhibidores de cdk9
AR123996A2 (es) Compuestos tricíclicos novedosos como agentes antineoplásicos
CY1123938T1 (el) Συνδυασμος αντισωματος αντι-cd20 και εκλεκτικου αναστολεα κινασης p13
CL2018003316A1 (es) Compuestos para la inhibición de k-ras y para el tratamiento del cáncer. (divisional solicitud 201702786)
CL2018001591A1 (es) Compuestos útiles como inhibidores de cinasa.-
CL2019000542A1 (es) Compuestos de tetraciclina y métodos de uso de los mismos.
ECSP17072987A (es) Compuestos nucleósidos 5’-sustituidos
NI201800042A (es) Nuevos derivados de pirrolo[2,3-d]pirimidina como inhibidores duales de dyrk1/clk1
NI201700071A (es) Anticuerpos anti-cd38 para el tratamiento de la leucemia mieloide aguda
MX2017005553A (es) Terapia de combinacion para cancer.
JO3433B1 (ar) حلقة كاربوكسامايد ذات أربع أعضاء للاستخدام كمبيدات النيماتودا
NZ716392A (en) Fused tricyclic urea compounds as raf kinase and/or raf kinase dimer inhibitors
MX2016001963A (es) Metodo de seleccion.
MD3395820T2 (ro) Compuși antitumorali
MX373121B (es) Composiciones y metodos para el tratamiento de leucemia.
CL2017001511A1 (es) Derivados de piperidina como inhibidores de hdac1/2.
CL2017001336A1 (es) Nuevos aminoácidos ester fosforamidatos 2' y/o 5', 3' deoxiadenosina derivativos como compuestos anticancerígenos
CL2016001368A1 (es) Inhibidores de cinasa serina/treonina
PH12019500070A1 (en) Uses of indolinone compounds
BR112019003130A2 (pt) agonista de ppargama para tratamento de cânceres de sangue
MX385940B (es) Nuevos antiestrógenos heterocíclicos.
IL282853A (en) Feeding unit for a gemstone machine
AR109273A1 (es) Usos de compuestos de indolina
EA201992557A1 (ru) Противоопухолевые соединения