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PE20151654A1 - Inhibidores de cdc7 - Google Patents

Inhibidores de cdc7

Info

Publication number
PE20151654A1
PE20151654A1 PE2015001925A PE2015001925A PE20151654A1 PE 20151654 A1 PE20151654 A1 PE 20151654A1 PE 2015001925 A PE2015001925 A PE 2015001925A PE 2015001925 A PE2015001925 A PE 2015001925A PE 20151654 A1 PE20151654 A1 PE 20151654A1
Authority
PE
Peru
Prior art keywords
cdc7 inhibitors
cdc7
inhibitors
isoindolinone
cancer
Prior art date
Application number
PE2015001925A
Other languages
English (en)
Inventor
Robert Dean Dally
Timothy Andrew Woods
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of PE20151654A1 publication Critical patent/PE20151654A1/es

Links

Classifications

    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Epidemiology (AREA)

Abstract

La presente invencion se refiere a compuestos de 5 isoindolinona, o una sal del mismo farmaceuticamente aceptable, que inhiben CDC7 Y, por lo tanto pueden ser utiles en el tratamiento de cancer
PE2015001925A 2013-03-14 2014-03-07 Inhibidores de cdc7 PE20151654A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361782798P 2013-03-14 2013-03-14
US201361789108P 2013-03-15 2013-03-15

Publications (1)

Publication Number Publication Date
PE20151654A1 true PE20151654A1 (es) 2015-11-12

Family

ID=50382704

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2015001925A PE20151654A1 (es) 2013-03-14 2014-03-07 Inhibidores de cdc7

Country Status (37)

Country Link
US (1) US9156824B2 (es)
EP (1) EP2970221B1 (es)
JP (1) JP6064079B2 (es)
KR (1) KR101718645B1 (es)
CN (1) CN105008351B (es)
AP (1) AP2015008734A0 (es)
AU (1) AU2014228374B2 (es)
BR (1) BR112015020466B1 (es)
CA (1) CA2900773C (es)
CL (1) CL2015002530A1 (es)
CR (1) CR20150416A (es)
CY (1) CY1119199T1 (es)
DK (1) DK2970221T3 (es)
EA (1) EA027012B1 (es)
ES (1) ES2639793T3 (es)
GT (1) GT201500263A (es)
HK (1) HK1212696A1 (es)
HR (1) HRP20171151T1 (es)
HU (1) HUE033482T2 (es)
IL (1) IL240962B (es)
JO (1) JO3383B1 (es)
LT (1) LT2970221T (es)
ME (1) ME02805B (es)
MX (1) MX363438B (es)
MY (1) MY188145A (es)
NZ (1) NZ710392A (es)
PE (1) PE20151654A1 (es)
PH (1) PH12015502091A1 (es)
PL (1) PL2970221T3 (es)
PT (1) PT2970221T (es)
RS (1) RS56122B1 (es)
SG (1) SG11201507541PA (es)
SI (1) SI2970221T1 (es)
TN (1) TN2015000349A1 (es)
TW (1) TWI622396B (es)
UA (1) UA116125C2 (es)
WO (1) WO2014143601A1 (es)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT2906555T (pt) * 2012-10-15 2017-02-15 Pfizer Ireland Pharmaceuticals Processo para a preparação de voriconazol e análogos do mesmo
US9278950B2 (en) 2013-01-14 2016-03-08 Incyte Corporation Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors
RS60244B1 (sr) 2013-01-15 2020-06-30 Incyte Holdings Corp Jedinjenja tiazolkarboksamida i piridinkarboksamida korisna kao inhibitori pim kinaze
TWI599567B (zh) 2013-03-14 2017-09-21 健生藥品公司 P2x7調節劑
ES2654288T3 (es) 2013-03-14 2018-02-13 Janssen Pharmaceutica, N.V. Moduladores de P2X7
US10053463B2 (en) 2013-03-14 2018-08-21 Janssen Pharmaceutica Nv Substituted [1,2,4]triazolo[4,3-a]pyrazines as P2X7 modulators
JO3509B1 (ar) 2013-03-14 2020-07-05 Janssen Pharmaceutica Nv معدلات p2x7
TW201522307A (zh) 2013-03-14 2015-06-16 百靈佳殷格翰國際股份有限公司 經取代2-氮雜-雙環[2.2.1]庚烷-3-羧酸(苄基-氰基-甲基)-醯胺組織蛋白酶c抑制劑
AU2014308703A1 (en) 2013-08-23 2016-03-24 Incyte Corporation Furo- and thieno-pyridine carboxamide compounds useful as Pim kinase inhibitors
US9822124B2 (en) 2014-07-14 2017-11-21 Incyte Corporation Bicyclic heteroaromatic carboxamide compounds useful as Pim kinase inhibitors
US9580418B2 (en) 2014-07-14 2017-02-28 Incyte Corporation Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors
US10150766B2 (en) 2014-09-12 2018-12-11 Janssen Pharmaceutica Nv P2X7 modulators
HUE047208T2 (hu) 2014-09-12 2020-04-28 Boehringer Ingelheim Int A katepszin-C spirociklikus inhibitorai
US9540347B2 (en) 2015-05-29 2017-01-10 Incyte Corporation Pyridineamine compounds useful as Pim kinase inhibitors
TWI734699B (zh) 2015-09-09 2021-08-01 美商英塞特公司 Pim激酶抑制劑之鹽
US9920032B2 (en) 2015-10-02 2018-03-20 Incyte Corporation Heterocyclic compounds useful as pim kinase inhibitors
AU2017332839B2 (en) * 2016-09-22 2021-11-11 Cancer Research Technology Limited Preparation and uses of pyrimidinone derivatives
TW201924683A (zh) 2017-12-08 2019-07-01 美商英塞特公司 用於治療骨髓增生性贅瘤的低劑量組合療法
CN108383771A (zh) * 2018-01-08 2018-08-10 华东师范大学 手性3,3-二取代异吲哚啉-1-酮衍生物及其合成方法和应用
GB201807147D0 (en) 2018-05-01 2018-06-13 Oncologica Uk Ltd Therapeutic combination
NL2021185B1 (en) 2018-06-26 2020-01-06 Stichting Het Nederlands Kanker Inst Antoni Van Leeuwenhoek Ziekenhuis Combination Therapy and Use Thereof for Treating Cancer
AU2019349962A1 (en) 2018-09-28 2021-03-18 Janssen Pharmaceutica Nv Monoacylglycerol lipase modulators
KR20210069080A (ko) 2018-09-28 2021-06-10 얀센 파마슈티카 엔.브이. 모노아실글리세롤 리파아제 조절제
US20220220125A1 (en) * 2019-04-16 2022-07-14 Janssen Pharmaceutica Nv Fused isoindolin-1-one derivatives useful as grk2 inhibitors
US11839663B2 (en) 2019-09-30 2023-12-12 Janssen Pharmaceutica Nv Radiolabelled MGL pet ligands
MX2022011902A (es) 2020-03-26 2023-01-04 Janssen Pharmaceutica Nv Moduladores de la monoacilglicerol lipasa.

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE0400970D0 (sv) * 2004-04-14 2004-04-14 Astrazeneca Ab Nicotinic acetylcholine receptor ligands
TW200639163A (en) * 2005-02-04 2006-11-16 Genentech Inc RAF inhibitor compounds and methods
US7576082B2 (en) * 2005-06-24 2009-08-18 Hoffman-La Roche Inc. Oxindole derivatives
EP2073806B1 (en) * 2006-10-12 2012-02-15 Xenon Pharmaceuticals Inc. Use of spiro-oxindole compounds as therapeutic agents
US8648069B2 (en) * 2007-06-08 2014-02-11 Abbvie Inc. 5-substituted indazoles as kinase inhibitors
WO2008154241A1 (en) * 2007-06-08 2008-12-18 Abbott Laboratories 5-heteroaryl substituted indazoles as kinase inhibitors

Also Published As

Publication number Publication date
PH12015502091B1 (en) 2016-01-18
GT201500263A (es) 2016-03-02
HUE033482T2 (en) 2017-12-28
SG11201507541PA (en) 2015-10-29
ES2639793T3 (es) 2017-10-30
CR20150416A (es) 2015-09-16
MY188145A (en) 2021-11-23
BR112015020466A2 (pt) 2017-07-18
AP2015008734A0 (en) 2015-09-30
RS56122B1 (sr) 2017-10-31
AU2014228374B2 (en) 2016-09-01
EA201591509A1 (ru) 2015-12-30
SI2970221T1 (sl) 2017-08-31
CA2900773C (en) 2018-04-17
BR112015020466B1 (pt) 2022-07-26
BR112015020466A8 (pt) 2019-11-12
CN105008351A (zh) 2015-10-28
JO3383B1 (ar) 2019-03-13
NZ710392A (en) 2020-05-29
CN105008351B (zh) 2017-03-15
US20140275121A1 (en) 2014-09-18
EP2970221A1 (en) 2016-01-20
TWI622396B (zh) 2018-05-01
HK1212696A1 (zh) 2016-06-17
MX2015012583A (es) 2016-01-20
WO2014143601A1 (en) 2014-09-18
ME02805B (me) 2018-01-20
PL2970221T3 (pl) 2017-11-30
LT2970221T (lt) 2017-09-11
CL2015002530A1 (es) 2016-03-28
PH12015502091A1 (en) 2016-01-18
MX363438B (es) 2019-03-22
EA027012B1 (ru) 2017-06-30
US9156824B2 (en) 2015-10-13
CY1119199T1 (el) 2018-02-14
IL240962A0 (en) 2015-11-30
TW201521726A (zh) 2015-06-16
HRP20171151T1 (hr) 2017-10-06
AU2014228374A1 (en) 2015-08-06
IL240962B (en) 2020-04-30
KR101718645B1 (ko) 2017-03-21
JP2016512498A (ja) 2016-04-28
DK2970221T3 (en) 2017-07-31
CA2900773A1 (en) 2014-09-18
UA116125C2 (uk) 2018-02-12
KR20150119101A (ko) 2015-10-23
PT2970221T (pt) 2017-09-22
EP2970221B1 (en) 2017-06-28
JP6064079B2 (ja) 2017-01-18
TN2015000349A1 (en) 2017-01-03

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