MA40059A - Inhibiteurs de la phosphatidylinositol 3-kinase - Google Patents

Inhibiteurs de la phosphatidylinositol 3-kinase

Info

Publication number
MA40059A
MA40059A MA040059A MA40059A MA40059A MA 40059 A MA40059 A MA 40059A MA 040059 A MA040059 A MA 040059A MA 40059 A MA40059 A MA 40059A MA 40059 A MA40059 A MA 40059A
Authority
MA
Morocco
Prior art keywords
phosphatidylinositol
kinase inhibitors
tautomer
isomers
compounds
Prior art date
Application number
MA040059A
Other languages
English (en)
Inventor
Shaopei Cai
Zhimin Du
Musong Kim
Jennifer A Loyer-Drew
Devan Naduthambi
Leena Patel
Barton W Phillips
Gary Phillips
Kirk L Stevens
Jennifer Anne Treiberg
Veldhuizen Joshua Van
William J Watkins
Suet Chung Yeung
Original Assignee
Gilead Sciences Inc
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 Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of MA40059A publication Critical patent/MA40059A/fr

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    • 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
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
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    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
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    • 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
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    • 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
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D473/32Nitrogen atom
    • C07D473/34Nitrogen atom attached in position 6, e.g. adenine
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    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

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  • Diabetes (AREA)
  • Dermatology (AREA)
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  • Obesity (AREA)
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  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
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  • Oncology (AREA)
  • Cardiology (AREA)
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  • Transplantation (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pain & Pain Management (AREA)
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Abstract

La présente invention concerne les composés de formule (j), ou des sels, des isomères, un tautomère pharmaceutiquement acceptables, ou un mélange de ces derniers, n, w, a', b', r
MA040059A 2014-06-13 2015-06-10 Inhibiteurs de la phosphatidylinositol 3-kinase MA40059A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201462012172P 2014-06-13 2014-06-13

Publications (1)

Publication Number Publication Date
MA40059A true MA40059A (fr) 2015-12-17

Family

ID=53674245

Family Applications (1)

Application Number Title Priority Date Filing Date
MA040059A MA40059A (fr) 2014-06-13 2015-06-10 Inhibiteurs de la phosphatidylinositol 3-kinase

Country Status (18)

Country Link
US (1) US11021467B2 (fr)
EP (1) EP3154960A1 (fr)
JP (1) JP6455995B2 (fr)
KR (1) KR20170012560A (fr)
CN (1) CN106459005A (fr)
AR (1) AR100808A1 (fr)
AU (1) AU2015274696B2 (fr)
BR (1) BR112016028642A2 (fr)
CA (1) CA2952012A1 (fr)
EA (1) EA201692268A1 (fr)
HK (1) HK1231476A1 (fr)
IL (1) IL248897A0 (fr)
MA (1) MA40059A (fr)
MX (1) MX2016016530A (fr)
NZ (1) NZ726360A (fr)
SG (1) SG11201609877XA (fr)
TW (1) TW201625560A (fr)
WO (1) WO2015191726A1 (fr)

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Publication number Priority date Publication date Assignee Title
US6667300B2 (en) 2000-04-25 2003-12-23 Icos Corporation Inhibitors of human phosphatidylinositol 3-kinase delta
PL1761540T3 (pl) 2004-05-13 2017-06-30 Icos Corporation Chinazolinony jako inhibitory ludzkiej kinazy 3-fosfatydyloinozytolu delta
CA2952037A1 (fr) 2014-06-13 2015-12-17 Gilead Sciences, Inc. Inhibiteurs de phosphatidylinositol-3-kinase
US9499523B2 (en) 2014-06-13 2016-11-22 Gilead Sciences, Inc. Phosphatidylinositol 3-kinase inhibitors
CA2952025A1 (fr) 2014-06-13 2015-12-17 Gilead Sciences, Inc. Inhibiteur de la phosphatidylinositol 3-kinase
JP6455995B2 (ja) 2014-06-13 2019-01-23 ギリアード サイエンシーズ, インコーポレイテッド ホスファチジルイノシトール3−キナーゼ阻害剤
CA2952018A1 (fr) 2014-06-13 2015-12-17 Gilead Sciences, Inc. Derives de quinazolinone utilises comme inhibiteurs de la phosphatidylinositol 3-kinase
CN106459008A (zh) * 2014-06-24 2017-02-22 吉利德科学公司 磷脂酰肌醇3‑激酶抑制剂
PE20170640A1 (es) 2014-07-04 2017-05-26 Lupin Ltd Derivados de quinolizinona como inhibidores de pi3k
SG10202105371YA (en) 2014-12-26 2021-07-29 Univ Emory N4-hydroxycytidine and derivatives and anti-viral uses related thereto
TWI794171B (zh) 2016-05-11 2023-03-01 美商滬亞生物國際有限公司 Hdac抑制劑與pd-l1抑制劑之組合治療
TWI808055B (zh) 2016-05-11 2023-07-11 美商滬亞生物國際有限公司 Hdac 抑制劑與 pd-1 抑制劑之組合治療
FI3706762T3 (fi) 2017-12-07 2024-12-13 Univ Emory N4-hydroksisytidiini ja johdannaisia sekä niihin liittyviä virusten vastaisia käyttötapoja
CA3083040A1 (fr) 2018-01-20 2019-07-25 Sunshine Lake Pharma Co., Ltd. Composes d'aminopyrimidine substitues et procedes d'utilisation
CN110590681B (zh) * 2019-09-30 2021-06-01 中山大学 一种新型喹唑啉酮类化合物及其制备方法和应用
CN111440173B (zh) * 2020-03-27 2021-05-14 山东大学 一种pi3k抑制剂的制备方法

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