RU2440991C2 - Хиназолины, полезные в качестве модуляторов ионных каналов - Google Patents

Хиназолины, полезные в качестве модуляторов ионных каналов Download PDF

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Publication number
RU2440991C2
RU2440991C2 RU2007111897/04A RU2007111897A RU2440991C2 RU 2440991 C2 RU2440991 C2 RU 2440991C2 RU 2007111897/04 A RU2007111897/04 A RU 2007111897/04A RU 2007111897 A RU2007111897 A RU 2007111897A RU 2440991 C2 RU2440991 C2 RU 2440991C2
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Russia
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compound
independently
ring
halogen
membered saturated
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RU2007111897/04A
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Russian (ru)
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RU2007111897A (ru
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Дин М. УИЛСОН (US)
Дин М. УИЛСОН
Андреас П. ТЕРМИН (US)
Андреас П. ТЕРМИН
Хесус Э. ГОНСАЛЕС III (US)
Хесус Э. ГОНСАЛЕС III
Лев Т.Д. ФЭННИНГ (US)
Лев Т.Д. ФЭННИНГ
Тимоти Д. НЬЮБЕРТ (US)
Тимоти Д. НЬЮБЕРТ
Пол КРЕНИЦКИ (US)
Пол КРЕНИЦКИ
Прамод ДЖОШИ (US)
Прамод ДЖОШИ
Деннис Дж. ХАРЛИ (US)
Деннис Дж. ХАРЛИ
Урви ШЕТ (US)
Урви Шет
Джошуа С. БОДЖЕР (US)
Джошуа С. БОДЖЕР
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Вертекс Фармасьютикалз Инкорпорейтед
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    • C07ORGANIC CHEMISTRY
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    • 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
    • C07D401/02Heterocyclic 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 two hetero rings
    • C07D401/04Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
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    • 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
    • A61K31/498Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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    • C07D239/72Quinazolines; Hydrogenated quinazolines
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    • C07D401/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
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  • Animal Behavior & Ethology (AREA)
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  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Diabetes (AREA)
  • Orthopedic Medicine & Surgery (AREA)
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  • Heart & Thoracic Surgery (AREA)
  • Anesthesiology (AREA)
  • Psychology (AREA)
  • Dermatology (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Compounds Of Unknown Constitution (AREA)
RU2007111897/04A 2004-09-02 2005-08-31 Хиназолины, полезные в качестве модуляторов ионных каналов RU2440991C2 (ru)

Applications Claiming Priority (11)

Application Number Priority Date Filing Date Title
US60703604P 2004-09-02 2004-09-02
US60703304P 2004-09-02 2004-09-02
US60724504P 2004-09-02 2004-09-02
US60715004P 2004-09-02 2004-09-02
US60703704P 2004-09-02 2004-09-02
US60/607,150 2004-09-02
US60/607,033 2004-09-02
US60/607,036 2004-09-02
US60/607,037 2004-09-02
US60/607,245 2004-09-02
PCT/US2005/031146 WO2006028904A1 (en) 2004-09-02 2005-08-31 Quinazolines useful as modulators of ion channels

Publications (2)

Publication Number Publication Date
RU2007111897A RU2007111897A (ru) 2008-10-10
RU2440991C2 true RU2440991C2 (ru) 2012-01-27

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RU2007111897/04A RU2440991C2 (ru) 2004-09-02 2005-08-31 Хиназолины, полезные в качестве модуляторов ионных каналов

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EP (1) EP1784393B1 (enExample)
JP (1) JP5014994B2 (enExample)
KR (1) KR20070057914A (enExample)
CN (1) CN101068794B (enExample)
AT (1) ATE435214T1 (enExample)
AU (1) AU2005282761B2 (enExample)
BR (1) BRPI0514893A (enExample)
CA (1) CA2578739A1 (enExample)
DE (1) DE602005015231D1 (enExample)
ES (1) ES2327945T4 (enExample)
IL (1) IL181700A0 (enExample)
MA (1) MA28909B1 (enExample)
MX (1) MX2007002582A (enExample)
NO (1) NO20071742L (enExample)
NZ (1) NZ589252A (enExample)
RU (1) RU2440991C2 (enExample)
WO (1) WO2006028904A1 (enExample)
ZA (1) ZA200702375B (enExample)

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RU2836663C1 (ru) * 2020-08-12 2025-03-18 Дженентек, Инк. Синтез соединений хиназолина

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AU2006329202A1 (en) * 2005-12-21 2007-06-28 Painceptor Pharma Corporation Compositions and methods for modulating gated ion channels
WO2007146284A2 (en) 2006-06-12 2007-12-21 Vertex Pharmaceuticals Incorporated Thienopyrimidines useful as modulators of ion channels
AU2007328336B2 (en) 2006-12-01 2014-04-17 President And Fellows Of Harvard College Compounds and methods for enzyme-mediated tumor imaging and therapy
WO2008147864A2 (en) * 2007-05-22 2008-12-04 Xenon Pharmaceuticals Inc. Methods of using piperazine compounds in treating sodium channel-mediated diseases or conditions
WO2008157500A1 (en) * 2007-06-17 2008-12-24 Kalypsys, Inc. Aminoquinazoline cannabinoid receptor modulators for treatment of disease
WO2012046132A1 (en) 2010-10-05 2012-04-12 Purdue Pharma L.P. Quinazoline compounds as sodium channel blockers
WO2012068096A2 (en) 2010-11-15 2012-05-24 Exelixis, Inc. Benzoxazepines as inhibitors of pi3k/mtor and methods of their use and manufacture
EP2670722B1 (en) 2011-01-31 2016-10-12 Council of Scientific & Industrial Research Chiral 1-(4-methylphenylmethyl)-5-oxo-{n-[(3-t-butoxycarbonyl-aminomethyl)]-piperidin-1-yl}-pyrrolidine-2-carboxamides as inhibitors of collagen induced platelet activation and adhesion
HRP20161412T1 (hr) 2011-06-27 2016-12-02 Newron Pharmaceuticals S.P.A. Fluorirani derivati arilalkilaminokarboksamida
PL3438096T3 (pl) * 2016-04-01 2021-05-17 Impact Therapeutics, Inc Sposób wytwarzania 1-(arylometylo)chinazolino-2,4(1H,3H)-dionu
CN111094233B (zh) 2017-08-09 2024-03-15 戴纳立制药公司 化合物、组合物及方法
PT3676297T (pt) 2017-09-01 2023-08-29 Denali Therapeutics Inc Compostos, composições e métodos
US20210130308A1 (en) * 2018-03-23 2021-05-06 Denali Therapeutics Inc. Modulators of eukaryotic initiation factor 2
JPWO2020017569A1 (ja) * 2018-07-17 2021-12-02 日本ケミファ株式会社 T型カルシウムチャネル阻害剤
CA3129609A1 (en) 2019-02-13 2020-08-20 Denali Therapeutics Inc. Eukaryotic initiation factor 2b modulators
MA54959A (fr) 2019-02-13 2021-12-22 Denali Therapeutics Inc Composés, compositions et procédés
BR112022006692A2 (pt) * 2019-10-10 2022-07-12 Esteve Pharmaceuticals Sa Composto de fórmula geral (i); processo para a preparação de compostos de fórmula (i); uso dos compostos de fórmula iia, iib, iii, iv, v, vi, vii, viia, viii, ix, xii, xiii, xiv, xv, xvi, xvii, xviii ou xix; e composição farmacêutica
PH12022551379A1 (en) 2019-12-06 2023-05-03 Vertex Pharma Substituted tetrahydrofurans as modulators of sodium channels
DK4347031T3 (da) 2021-06-04 2025-12-01 Vertex Pharma N-(hydroxyalkyl-(hetero)aryl)-tetrahydrofuran-carboxamider som modulatorer af natriumkanaler
CN119757730A (zh) * 2024-12-24 2025-04-04 浙江省海洋水产研究所 一种河豚毒素的胶体金检测卡

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RU2198879C2 (ru) * 1996-09-25 2003-02-20 Зенека Лимитед Производные хиназолина, способы их получения, содержащие их фармацевтические композиции, способ достижения антиангиогенного и/или эффекта снижения проницаемости кровеносных сосудов у теплокровного животного
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