CR10784A - Nuevos derivados de aminopirimidina como inhibidores de plki - Google Patents

Nuevos derivados de aminopirimidina como inhibidores de plki

Info

Publication number
CR10784A
CR10784A CR10784A CR10784A CR10784A CR 10784 A CR10784 A CR 10784A CR 10784 A CR10784 A CR 10784A CR 10784 A CR10784 A CR 10784A CR 10784 A CR10784 A CR 10784A
Authority
CR
Costa Rica
Prior art keywords
aminopirimidine
plki
inhibitors
new derivatives
lower alkyl
Prior art date
Application number
CR10784A
Other languages
English (en)
Inventor
Hashiyata Takashi
Kawamura Mikako
Mtsuya Morihiro
Satoh Yoshiyuki
Original Assignee
Banyu Pharma Co Ltd
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 Banyu Pharma Co Ltd filed Critical Banyu Pharma Co Ltd
Publication of CR10784A publication Critical patent/CR10784A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

La presente invencion se refiere a un compuesto representado por la Formula [I]: o una sal farmaceuticamente aceptable o ester del mismo, donde cada uno de R1 y R2, que pueden ser iguales o diferentes, es un atomo de hidrogeno, un atomo de halogeno, un grupo alquilo inferior que puede estar sustituido, o un grupo ciclopropilo; cada uno de R3 y R4, que pueden ser iguales o diferentes es un atomo de hidrogeno, un grupo alquilo inferior sustituido con NRaRb.
CR10784A 2006-12-28 2009-05-08 Nuevos derivados de aminopirimidina como inhibidores de plki CR10784A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2006356575 2006-12-28
JP2007265783 2007-10-11

Publications (1)

Publication Number Publication Date
CR10784A true CR10784A (es) 2009-09-16

Family

ID=39588592

Family Applications (1)

Application Number Title Priority Date Filing Date
CR10784A CR10784A (es) 2006-12-28 2009-05-08 Nuevos derivados de aminopirimidina como inhibidores de plki

Country Status (24)

Country Link
US (1) US7977336B2 (es)
EP (2) EP2116543A4 (es)
JP (1) JPWO2008081914A1 (es)
KR (1) KR101481388B1 (es)
CN (1) CN101573361B (es)
AR (1) AR064619A1 (es)
AU (1) AU2007340530B2 (es)
BR (1) BRPI0718966B8 (es)
CA (1) CA2668738A1 (es)
CL (1) CL2007003758A1 (es)
CO (1) CO6190523A2 (es)
CR (1) CR10784A (es)
EC (1) ECSP099324A (es)
GT (1) GT200900124A (es)
IL (1) IL198675A0 (es)
MA (1) MA31109B1 (es)
MX (1) MX2009004920A (es)
NO (1) NO20092770L (es)
NZ (1) NZ577273A (es)
PE (1) PE20081845A1 (es)
RU (1) RU2458062C2 (es)
SV (1) SV2009003258A (es)
TW (1) TW200835485A (es)
WO (2) WO2008081910A1 (es)

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EP2463289A1 (en) 2010-11-26 2012-06-13 Almirall, S.A. Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors
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WO2014001314A1 (en) 2012-06-26 2014-01-03 Janssen Pharmaceutica Nv Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders
AU2013289284B2 (en) 2012-07-09 2017-03-30 Janssen Pharmaceutica Nv Inhibitors of phosphodiesterase 10 enzyme
US9921222B2 (en) 2012-07-31 2018-03-20 Crown Bioscience, Inc. (Taicang) Histological markers for identifying non-small cell lung carcinoma patients for treatment with an anti-EGFR drug
WO2014046617A1 (en) * 2012-09-19 2014-03-27 Agency For Science, Technology And Research Compositions and methods for treating cancer
EP3194367B1 (en) 2014-09-17 2021-08-18 Boehringer Ingelheim International GmbH Tetrahydroisoquinoline derivatives and pharmaceutical compositions useful for the treatment of obesity and diabetes
US20230190717A1 (en) * 2017-04-10 2023-06-22 City Of Hope P38 gamma inhibitors and method of use thereof
CN114269742B (zh) * 2019-07-10 2024-07-16 常州千红生化制药股份有限公司 作为治疗剂的4-(咪唑并[1,2-a]吡啶-3-基)-N-(吡啶基)嘧啶-2-胺的衍生物
EP4003992A1 (en) * 2019-07-24 2022-06-01 Merck Patent GmbH 4-(imidazo[1,2-a]pyridin-3-yl) -pyrimidine derivatives
CN112592318B (zh) * 2020-12-12 2022-05-03 贵州医科大学 2-(4-甲氨酰基)苯胺基-4-氨基嘧啶衍生物及应用
WO2024071401A1 (ja) 2022-09-29 2024-04-04 公益財団法人がん研究会 Ｐｌｋ１キナーゼ活性化による染色体制御破綻が誘導するがん細胞増殖抑制を創薬概念とする医薬のスクリーニング方法
CN119318874B (zh) * 2024-12-18 2025-04-15 淄博凯美可工贸有限公司 一种节能型复合脱硫剂的制备方法

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Also Published As

Publication number Publication date
CN101573361A (zh) 2009-11-04
AU2007340530B2 (en) 2012-09-13
RU2458062C2 (ru) 2012-08-10
EP2116543A1 (en) 2009-11-11
EP2114942A4 (en) 2010-09-08
SV2009003258A (es) 2010-08-23
CO6190523A2 (es) 2010-08-19
RU2009128966A (ru) 2011-02-10
BRPI0718966A2 (pt) 2014-01-07
BRPI0718966B8 (pt) 2021-05-25
KR20090092822A (ko) 2009-09-01
AR064619A1 (es) 2009-04-15
CN101573361B (zh) 2012-05-30
EP2114942A1 (en) 2009-11-11
EP2114942B1 (en) 2012-10-31
WO2008081914A1 (ja) 2008-07-10
PE20081845A1 (es) 2008-12-27
NO20092770L (no) 2009-09-25
AU2007340530A1 (en) 2008-07-10
BRPI0718966B1 (pt) 2020-11-17
US20080305081A1 (en) 2008-12-11
MX2009004920A (es) 2009-05-21
GT200900124A (es) 2010-11-03
MA31109B1 (fr) 2010-01-04
CL2007003758A1 (es) 2008-07-04
WO2008081910A1 (en) 2008-07-10
EP2116543A4 (en) 2010-09-08
IL198675A0 (en) 2010-02-17
TW200835485A (en) 2008-09-01
CA2668738A1 (en) 2008-07-10
KR101481388B1 (ko) 2015-01-12
NZ577273A (en) 2011-03-31
ECSP099324A (es) 2009-06-30
JPWO2008081914A1 (ja) 2010-04-30
US7977336B2 (en) 2011-07-12

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