MA32341B1 - Dérivés de 3h- [1, 2, 3] triazolo [4, 5, d] pyrimidine, leur utilisation comme inhibiteurs de la kinase mtor et de la kinase pi3, et leurs synthèses - Google Patents

Dérivés de 3h- [1, 2, 3] triazolo [4, 5, d] pyrimidine, leur utilisation comme inhibiteurs de la kinase mtor et de la kinase pi3, et leurs synthèses

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Publication number
MA32341B1
MA32341B1 MA33020A MA33020A MA32341B1 MA 32341 B1 MA32341 B1 MA 32341B1 MA 33020 A MA33020 A MA 33020A MA 33020 A MA33020 A MA 33020A MA 32341 B1 MA32341 B1 MA 32341B1
Authority
MA
Morocco
Prior art keywords
kinase
triazolo
pyrimidine
syntheses
inhibitors
Prior art date
Application number
MA33020A
Other languages
Arabic (ar)
English (en)
Inventor
Christoph Martin Dehnhardt
Aranapakam Mudumbai Venkatesan
Santos Efren Guillermo Delos
Zecheng Chen
Santos Osvaldo Dos
Natasja Brooijmans
Arie Zask
Jeroen Cunera Verheijen
Semiramis Ayral-Kaloustian
Original Assignee
Wyeth Llc
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 Wyeth Llc filed Critical Wyeth Llc
Publication of MA32341B1 publication Critical patent/MA32341B1/fr

Links

Classifications

    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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

Abstract

La présente invention concerne des composés de 3h-[1,2,3]triazolo[4,5-d]pyrimidine de formule 1 ou un sel pharmaceutiquement acceptable de ceux-ci, dont les variables constituantes sont telles que définies ici. L'invention concerne également des compositions comprenant lesdits composés, ainsi que des procédés de fabrication et d'utilisation de ces composés.
MA33020A 2008-01-15 2010-07-15 Dérivés de 3h- [1, 2, 3] triazolo [4, 5, d] pyrimidine, leur utilisation comme inhibiteurs de la kinase mtor et de la kinase pi3, et leurs synthèses MA32341B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US2108408P 2008-01-15 2008-01-15
US3468008P 2008-03-07 2008-03-07
PCT/US2009/030939 WO2009091788A1 (fr) 2008-01-15 2009-01-14 Composés de 3h-[1,2,3]triazolo[4,5-d]pyrimidine, utilisations de ceux-ci en tant qu'inhibiteurs de la mtor kinase et de la pi3 kinase, et synthèses de ceux-ci

Publications (1)

Publication Number Publication Date
MA32341B1 true MA32341B1 (fr) 2011-06-01

Family

ID=40377318

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33020A MA32341B1 (fr) 2008-01-15 2010-07-15 Dérivés de 3h- [1, 2, 3] triazolo [4, 5, d] pyrimidine, leur utilisation comme inhibiteurs de la kinase mtor et de la kinase pi3, et leurs synthèses

Country Status (21)

Country Link
US (1) US20090181963A1 (fr)
EP (1) EP2252296A1 (fr)
JP (1) JP2011510010A (fr)
KR (1) KR20100113567A (fr)
CN (1) CN102014914A (fr)
AP (1) AP2010005346A0 (fr)
AU (1) AU2009205501A1 (fr)
BR (1) BRPI0906519A2 (fr)
CA (1) CA2712267A1 (fr)
CO (1) CO6321259A2 (fr)
CR (1) CR11568A (fr)
DO (1) DOP2010000217A (fr)
EA (1) EA201001017A1 (fr)
EC (1) ECSP10010346A (fr)
IL (1) IL206820A0 (fr)
MA (1) MA32341B1 (fr)
MX (1) MX2010007746A (fr)
NI (1) NI201000119A (fr)
SV (1) SV2010003621A (fr)
WO (1) WO2009091788A1 (fr)
ZA (2) ZA201004603B (fr)

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AU2008343813B2 (en) 2007-12-19 2012-04-12 Amgen Inc. Inhibitors of PI3 kinase
JP2011515462A (ja) * 2008-03-27 2011-05-19 アウククランド ウニセルビセス リミテッド 置換されたピリミジン、及びトリアジン、並びに癌療法におけるこれらの使用
TWI378933B (en) 2008-10-14 2012-12-11 Daiichi Sankyo Co Ltd Morpholinopurine derivatives
TW201038567A (en) * 2009-03-27 2010-11-01 Pathway Therapeutics Ltd Pyrimidinyl and 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy
US20100331305A1 (en) * 2009-06-24 2010-12-30 Genentech, Inc. Oxo-heterocycle fused pyrimidine compounds, compositions and methods of use
CA2767008C (fr) * 2009-07-07 2018-01-30 Pathway Therapeutics, Inc. Pyrimidinyl et 1,3,5-triazinyl benzimidazoles et leur utilisation dans le traitement du cancer
CA2788678C (fr) 2010-02-03 2019-02-26 Signal Pharmaceuticals, Llc Identification d'une mutation lkb1 comme biomarqueur de prediction de sensibilite a des inhibiteurs de kinase tor
MY170236A (en) 2010-10-06 2019-07-11 Glaxosmithkline Llc Benzimidazole derivatives as pi3 kinase inhibitors
TWI572599B (zh) 2011-03-28 2017-03-01 Mei製藥公司 (α-經取代之芳烷胺基及雜芳烷胺基)嘧啶基及1,3,5-三基苯并咪唑,其醫藥組合物及其在治療增生性疾病之用途
CN107375289A (zh) * 2011-11-01 2017-11-24 埃克塞利希斯股份有限公司 用于治疗淋巴组织增生性恶性肿瘤的作为磷脂酰肌醇3‑激酶抑制剂的化合物
US9499561B2 (en) 2012-04-10 2016-11-22 Shanghai Yingli Pharmaceutical Co., Ltd. Fused pyrimidine compound, and preparation method, intermediate, composition, and uses thereof
KR20160027219A (ko) 2012-05-23 2016-03-09 에프. 호프만-라 로슈 아게 내배엽 및 간세포를 수득하고 사용하는 조성물 및 방법
AU2013203714B2 (en) 2012-10-18 2015-12-03 Signal Pharmaceuticals, Llc Inhibition of phosphorylation of PRAS40, GSK3-beta or P70S6K1 as a marker for TOR kinase inhibitory activity
WO2014172436A1 (fr) 2013-04-17 2014-10-23 Signal Pharmaceuticals, Llc Polythérapie comprenant un inhibiteur de kinase tor et un composé de quinazolinone substitué en 5 pour le traitement du cancer
CA2909579A1 (fr) 2013-04-17 2014-10-23 Signal Pharmaceuticals, Llc Therapie combinee comprenant un inhibiteur de la kinase tor et du n-(3-(5-fluoro-2-(4-(2-methoxyethoxy)phenylamino)pyrimidin-4-ylamino)phenyl)acrylamide pour le traitement d'un cancer
US9505764B2 (en) 2013-04-17 2016-11-29 Signal Pharmaceuticals, Llc Treatment of cancer with dihydropyrazino-pyrazines
CA2908742C (fr) 2013-04-17 2021-06-01 Signal Pharmaceuticals, Llc Polytherapie comprenant un inhibiteur de la kinase tor et un analogue de la cytidine pour le traitement du cancer
CN105377299B (zh) 2013-04-17 2018-06-12 西格诺药品有限公司 用于治疗前列腺癌的包含二氢吡嗪并-吡嗪化合物和雄激素受体拮抗剂的组合疗法
US9630966B2 (en) 2013-04-17 2017-04-25 Signal Pharmaceuticals, Llc Treatment of cancer with dihydropyrazino-pyrazines
CA2909629C (fr) 2013-04-17 2022-12-13 Signal Pharmaceuticals, Llc Formulations pharmaceutiques, procedes, formes solides et methodes d'utilisation associes a la 1-ethyl-7-(2-methyl-6-(1h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one
NZ629486A (en) 2013-05-29 2017-11-24 Signal Pharm Llc Pharmaceutical compositions of 7-(6-(2-hydroxypropan-2-yl)pyridin-3-yl)-1-((trans)-4-methoxycyclohexyl)-3,4-dihydropyrazino [2,3-b]pyrazin-2(1h)-one, a solid form thereof and methods of their use
EP3053926B1 (fr) 2013-09-30 2018-08-08 Shanghai Yingli Pharmaceutical Co. Ltd. Composé de pyrimidine condensée, intermédiaire, procédé de préparation s'y rapportant et composition et application correspondantes
US9512129B2 (en) 2014-04-16 2016-12-06 Signal Pharmaceuticals, Llc Solid forms comprising 1-ethyl-7-(2-methyl-6-(1H-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one and a coformer
NZ714742A (en) 2014-04-16 2017-04-28 Signal Pharm Llc Solid forms of 1-ethyl-7-(2-methyl-6-(1h-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1h)-one, compositions thereof and methods of their use
KR20170002623A (ko) 2014-05-14 2017-01-06 화이자 인코포레이티드 피라졸로피리딘 및 피라졸로피리미딘
WO2017087818A1 (fr) * 2015-11-19 2017-05-26 The Regents Of The University Of Michigan Double inhibiteur de kinase p38/src et leur utilisation comme agents thérapeutiques
US11304953B2 (en) 2017-05-23 2022-04-19 Mei Pharma, Inc. Combination therapy
TWI787284B (zh) 2017-06-22 2022-12-21 美商西建公司 以b型肝炎病毒感染表徵之肝細胞癌之治療
US12054488B2 (en) * 2018-09-27 2024-08-06 Suzhou Raymon Pharmaceuticals Company, Ltd. Pyrazolopyrimidine compound and preparation method therefor and use thereof in preparation of anti-cancer drug
CN113549080B (zh) * 2021-08-27 2023-05-16 中国医学科学院放射医学研究所 一类1,2,3-三氮唑并嘧啶类化合物、其制备方法和用途
KR20240015978A (ko) 2022-07-28 2024-02-06 박수산 다층 수력 발전시스템
GB202415232D0 (en) 2024-10-16 2024-11-27 Nacamed As Composition

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Publication number Priority date Publication date Assignee Title
KR100774855B1 (ko) * 2000-04-27 2007-11-08 아스텔라스세이야쿠 가부시키가이샤 축합 헤테로아릴 유도체

Also Published As

Publication number Publication date
DOP2010000217A (es) 2010-07-31
KR20100113567A (ko) 2010-10-21
NI201000119A (es) 2011-05-04
CN102014914A (zh) 2011-04-13
EA201001017A1 (ru) 2011-02-28
ZA201004603B (en) 2011-03-30
EP2252296A1 (fr) 2010-11-24
ECSP10010346A (es) 2010-08-31
AU2009205501A1 (en) 2009-07-23
ZA201005793B (en) 2011-04-28
BRPI0906519A2 (pt) 2015-07-14
SV2010003621A (es) 2011-07-05
WO2009091788A1 (fr) 2009-07-23
US20090181963A1 (en) 2009-07-16
IL206820A0 (en) 2010-12-30
CR11568A (es) 2010-08-11
AP2010005346A0 (en) 2010-08-31
JP2011510010A (ja) 2011-03-31
CO6321259A2 (es) 2011-09-20
CA2712267A1 (fr) 2009-07-23
MX2010007746A (es) 2010-08-18

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