RU2016115726A - Селективный ингибитор фосфатидилинозитол-3-киназы-гамма - Google Patents

Селективный ингибитор фосфатидилинозитол-3-киназы-гамма Download PDF

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RU2016115726A
RU2016115726A RU2016115726A RU2016115726A RU2016115726A RU 2016115726 A RU2016115726 A RU 2016115726A RU 2016115726 A RU2016115726 A RU 2016115726A RU 2016115726 A RU2016115726 A RU 2016115726A RU 2016115726 A RU2016115726 A RU 2016115726A
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disease
pi3k
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Майкл Джон БОЙД
Алекс АРОНОВ
Хардвин О'Доуд
Джереми ГРИН
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Вертекс Фармасьютикалз Инкорпорейтед
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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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    • A61K31/00Medicinal preparations containing organic active ingredients
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Epidemiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Claims (8)

1. Химическое соединение, имеющее следующую структурную формулу:
Figure 00000001
, или его фармацевтически приемлемая соль.
2. Фармацевтическая композиция, содержащая химическое соединение по п.1 и фармацевтически приемлемый носитель, адъювант или наполнитель.
3. Способ лечения или снижения тяжести заболевания или патологического состояния, выбранного из аутоиммунного заболевания или воспалительного заболевания, выбранного из астмы, атопического дерматита, ринита, аллергических заболеваний, хронической обструктивной болезни легких (ХОБЛ), септического шока, идиопатического легочного фиброза, инсульта, ожога, заболеваний суставов, ревматоидного артрита, системной красной волчанки, атеросклероза, острого панкреатита, псориаза, воспалительного заболевания кишечника, язвенного колита, болезни Крона и болезни Грейвcа, включающий в введение пациенту химического соединения или соли по п.1 или его фармацевтической композиции.
4. Способ по п.3, где указанное заболевание или патологическое состояние представляет собой ревматоидный артрит.
5. Способ ингибирования киназной активности PI3K-гамма в биологическом образце, включающий контактирование указанного биологического образца с соединением по п.1 или композицией, содержащей указанное соединение.
6. Способ селективного ингибирования изоформы PI3K-гамма по сравнению с, по меньшей мере, одной другой изоформой PI3K, включающий контактирование биологического образца с соединением по п.1 или композицией, содержащей указанное соединение или введение нуждающемуся в этом пациенту соединения по п.1 или композиции, содержащей указанное соединение.
7. Способ по п.6, в котором, по меньшей мере, одна другая изоформа PI3K выбрана из группы, состоящей из PI3K-альфа, PI3K-бета, PI3K-дельта и их комбинаций.
RU2016115726A 2013-09-25 2014-09-25 6,7-ДИГИДРО-5Н-ПИРРОЛО[3,4-b]ПИРИДИН-5-ОН, ПОЛЕЗНЫЙ В КАЧЕСТВЕ СЕЛЕКТИВНОГО ИНГИБИТОРА ФОСФАТИДИЛИНОЗИТОЛ-3-КИНАЗЫ-ГАММА RU2675814C2 (ru)

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US201361882473P 2013-09-25 2013-09-25
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PCT/US2014/057499 WO2015048318A1 (en) 2013-09-25 2014-09-25 A selective inhibitor of phosphatidylinositol 3-kinase-gamma

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US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
BR112016007467B1 (pt) 2013-10-04 2022-09-20 Infinity Pharmaceuticals, Inc Compostos heterocíclicos e usos dos mesmos
WO2015051241A1 (en) 2013-10-04 2015-04-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
CN106456628A (zh) 2014-03-19 2017-02-22 无限药品股份有限公司 用于治疗PI3K‑γ介导的障碍的杂环化合物
WO2016054491A1 (en) 2014-10-03 2016-04-07 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
JP6786529B2 (ja) * 2015-06-29 2020-11-18 バイオメッド バレー ディスカバリーズ,インコーポレイティド Lpt−723と免疫チェックポイント阻害剤との組み合わせおよび処置の方法
MX2018003058A (es) 2015-09-14 2018-08-01 Infinity Pharmaceuticals Inc Formas solidas de derivados de isoquinolinona, proceso de fabricacion, composiciones que las contienen y metodos de uso de las mismas.
WO2017153527A1 (en) * 2016-03-10 2017-09-14 Astrazeneca Ab Novel inhibitors of phosphatidylinositol 3-kinase gamma
US10759806B2 (en) 2016-03-17 2020-09-01 Infinity Pharmaceuticals, Inc. Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors
WO2017214269A1 (en) 2016-06-08 2017-12-14 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
WO2020210379A1 (en) 2019-04-10 2020-10-15 Hangzhou Zhengxiang Pharmaceuticals Co., Ltd. Phosphatidylinositol 3-kinase inhibitors

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AR071717A1 (es) * 2008-05-13 2010-07-07 Array Biopharma Inc Pirrolo[2,3-b]piridinas inhibidoras de quinasas chk1 y chk2,composiciones farmaceuticas que las contienen,proceso para prepararlas y uso de las mismas en el tratamiento y prevencion del cancer.
UY32582A (es) * 2009-04-28 2010-11-30 Amgen Inc Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero
JP5721187B2 (ja) * 2009-12-22 2015-05-20 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated ホスファチジルイノシトール3−キナーゼのイソインドリノンインヒビター

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EP3412668A2 (en) 2018-12-12
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SG11201602265PA (en) 2016-04-28
HK1223620A1 (zh) 2017-08-04
CN105722838B (zh) 2017-10-24
EP3049415B1 (en) 2018-07-04
UA117032C2 (uk) 2018-06-11
EP3412668B1 (en) 2020-02-05
JP2016531861A (ja) 2016-10-13
CN105722838A (zh) 2016-06-29
RU2675814C2 (ru) 2018-12-25
BR112016006388A2 (pt) 2017-08-01
RU2018142605A (ru) 2019-02-04
CA2925601C (en) 2022-11-01
ZA201702252B (en) 2019-06-26
CA2925601A1 (en) 2015-04-02
MX2016003823A (es) 2016-08-01
AU2014324873B2 (en) 2018-11-08
IL244742A0 (en) 2016-04-21
EP3049415A1 (en) 2016-08-03
US10301304B2 (en) 2019-05-28
EP3412668A3 (en) 2018-12-19
SG10201802061TA (en) 2018-05-30
WO2015048318A1 (en) 2015-04-02
US20160214980A1 (en) 2016-07-28
KR20160058950A (ko) 2016-05-25
RU2016115726A3 (ru) 2018-06-20
ES2785053T3 (es) 2020-10-05
JP6340416B2 (ja) 2018-06-06
AU2014324873A1 (en) 2016-04-21

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