MA32009B1 - Nouveaux derives de pyrazolo [3,4-d]pyrimidine en tant qu'agents anticancereux - Google Patents

Nouveaux derives de pyrazolo [3,4-d]pyrimidine en tant qu'agents anticancereux

Info

Publication number
MA32009B1
MA32009B1 MA33007A MA33007A MA32009B1 MA 32009 B1 MA32009 B1 MA 32009B1 MA 33007 A MA33007 A MA 33007A MA 33007 A MA33007 A MA 33007A MA 32009 B1 MA32009 B1 MA 32009B1
Authority
MA
Morocco
Prior art keywords
pyrazolo
pyrimidine
anticancer agents
novel derivatives
human
Prior art date
Application number
MA33007A
Other languages
Arabic (ar)
English (en)
Inventor
Durga Prasad Konakanchi
Subba Rao Pula
Lakshmi Ananthaneni
Ramakrishna Pilli
Reddy Muddasani Pulla
Kali Satya Bhujanga Rao Adibhatla
Chowdary Nannapaneni Venkaiah
Original Assignee
Natco Pharma 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 Natco Pharma Ltd filed Critical Natco Pharma Ltd
Publication of MA32009B1 publication Critical patent/MA32009B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Landscapes

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

Abstract

La présente invention concerne des dérivés substitutes de pyrazolo [3,4-d] pyrimidine de formule (i), ou leurs sels pharmaceutiquement acceptables, qui possèdent une activité anti-proliférante telle qu'une activité anticancéreuse et sont donc utiles dans des procédés de traitement de l'organisme humain ou animal. L'invention concerne également des procédés de fabrication de dérivés substitués de pyrazolo [3,4-d] pyrimidine, des compositions pharmaceutiques contenant le composé et son utilisation dans la fabrication de médicaments pour la production d'un effet anti-proliférant dans un animal à sang chaud tel qu'un humain.
MA33007A 2008-01-11 2010-07-09 Nouveaux derives de pyrazolo [3,4-d]pyrimidine en tant qu'agents anticancereux MA32009B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IN109CH2008 2008-01-11
PCT/IN2009/000037 WO2009098715A2 (fr) 2008-01-11 2009-01-12 Nouveaux dérivés de pyrazolo [3, 4 -d] pyrimidine en tant qu’agents anticancéreux

Publications (1)

Publication Number Publication Date
MA32009B1 true MA32009B1 (fr) 2011-01-03

Family

ID=40933862

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33007A MA32009B1 (fr) 2008-01-11 2010-07-09 Nouveaux derives de pyrazolo [3,4-d]pyrimidine en tant qu'agents anticancereux

Country Status (18)

Country Link
US (1) US8349847B2 (fr)
EP (1) EP2247596A2 (fr)
JP (1) JP2011509290A (fr)
KR (1) KR20100116607A (fr)
CN (1) CN101965350A (fr)
AP (1) AP2010005347A0 (fr)
AU (1) AU2009211004C1 (fr)
BR (1) BRPI0906475A2 (fr)
CA (1) CA2711777A1 (fr)
CO (1) CO6382174A2 (fr)
EA (1) EA201070841A1 (fr)
GE (1) GEP20135780B (fr)
IL (1) IL206811A0 (fr)
MA (1) MA32009B1 (fr)
MX (1) MX2010007523A (fr)
NZ (1) NZ586642A (fr)
WO (1) WO2009098715A2 (fr)
ZA (1) ZA201004823B (fr)

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US8680108B2 (en) * 2009-12-18 2014-03-25 Incyte Corporation Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors
US8759359B2 (en) * 2009-12-18 2014-06-24 Incyte Corporation Substituted heteroaryl fused derivatives as PI3K inhibitors
EP2558463A1 (fr) 2010-04-14 2013-02-20 Incyte Corporation Dérivés condensés en tant qu'inhibiteurs de i3
WO2011163195A1 (fr) 2010-06-21 2011-12-29 Incyte Corporation Dérivés condensés de pyrrole en tant qu'inhibiteurs de pi3k
AR084366A1 (es) 2010-12-20 2013-05-08 Incyte Corp N-(1-(fenil sustituido)etil)-9h-purin-6-aminas como inhibidores de pi3k
US9108984B2 (en) 2011-03-14 2015-08-18 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
WO2012135009A1 (fr) 2011-03-25 2012-10-04 Incyte Corporation Dérivés de pyrimidine-4,6-diamine en tant qu'inhibiteurs de pi3k
BR122019020716B1 (pt) 2011-09-02 2021-02-17 Incyte Holdings Corporation heterociclilaminas como inibidores de pi3k e composição farmacêutica que as compreende
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
CN102746307B (zh) * 2012-07-09 2013-07-31 四川大学 1-n-苄基别嘌醇衍生物及其制备方法和用途
CN102746309B (zh) * 2012-07-09 2013-06-05 四川大学 1-N-乙基-4-N-2′-取代酰基肼-1H-吡唑[3,4-d]嘧啶类衍生物及其制备方法和用途
CN103965202B (zh) * 2014-05-21 2016-01-20 邹宏丽 二环稠合杂环化合物、其制备方法及用途
US10077277B2 (en) 2014-06-11 2018-09-18 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
MD3262046T2 (ro) 2015-02-27 2021-03-31 Incyte Corp Săruri de inhibitori ai PI3K și procedee pentru prepararea lor
US9732097B2 (en) 2015-05-11 2017-08-15 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
WO2016183063A1 (fr) 2015-05-11 2016-11-17 Incyte Corporation Formes cristallines d'un inhibiteur de pi3k
CN106008527B (zh) * 2016-06-29 2018-05-15 四川大学华西医院 吡唑并[3,4-d]嘧啶衍生物
CN107698596A (zh) * 2017-11-15 2018-02-16 双鹤药业（商丘）有限责任公司 一种别嘌醇的合成方法
CN115304607B (zh) * 2022-07-06 2023-06-27 华南农业大学 吡唑并嘧啶衍生物的制备方法

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Also Published As

Publication number Publication date
CO6382174A2 (es) 2012-02-15
WO2009098715A2 (fr) 2009-08-13
US8349847B2 (en) 2013-01-08
JP2011509290A (ja) 2011-03-24
EP2247596A2 (fr) 2010-11-10
AP2010005347A0 (en) 2010-08-31
NZ586642A (en) 2012-04-27
CA2711777A1 (fr) 2009-08-13
WO2009098715A4 (fr) 2009-12-10
US20100298351A1 (en) 2010-11-25
MX2010007523A (es) 2010-08-18
AU2009211004C1 (en) 2013-08-01
ZA201004823B (en) 2011-09-28
IL206811A0 (en) 2010-12-30
WO2009098715A3 (fr) 2009-10-15
AU2009211004A1 (en) 2009-08-13
AU2009211004A2 (en) 2011-01-27
AU2009211004B2 (en) 2011-09-01
EA201070841A1 (ru) 2011-02-28
CN101965350A (zh) 2011-02-02
GEP20135780B (en) 2013-03-11
KR20100116607A (ko) 2010-11-01
BRPI0906475A2 (pt) 2015-07-14

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