EA201170595A1 - ПРОИЗВОДНОЕ ФЕНАНТРОИНДОЛИЗИДИНА И ИНГИБИТОР NFkB, СОДЕРЖАЩИЙ ЕГО В КАЧЕСТВЕ АКТИВНОГО ИНГРЕДИЕНТА - Google Patents

ПРОИЗВОДНОЕ ФЕНАНТРОИНДОЛИЗИДИНА И ИНГИБИТОР NFkB, СОДЕРЖАЩИЙ ЕГО В КАЧЕСТВЕ АКТИВНОГО ИНГРЕДИЕНТА

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Publication number
EA201170595A1
EA201170595A1 EA201170595A EA201170595A EA201170595A1 EA 201170595 A1 EA201170595 A1 EA 201170595A1 EA 201170595 A EA201170595 A EA 201170595A EA 201170595 A EA201170595 A EA 201170595A EA 201170595 A1 EA201170595 A1 EA 201170595A1
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Prior art keywords
group
hydrogen atom
formed together
lower alkyl
phenantroindolizidine
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EA201170595A
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English (en)
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EA023622B1 (ru
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Такаси Икеда
Сейго Савада
Такаси Яегаси
Такеси Мацузаки
Сусуке Хасимото
Риута Ямазаки
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Кабусики Кайся Якулт Хонса
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Publication of EA201170595A1 publication Critical patent/EA201170595A1/ru
Publication of EA023622B1 publication Critical patent/EA023622B1/ru

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    • 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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Abstract

Обеспечивают новое соединение, обладающее превосходным NFkB ингибирующим эффектом. В частности, раскрытое представляет собой соединение, представленное следующей формулой (1), или его соль, в которой Rпредставляет собой атом водорода, низшую алкильную группу или подобное; Rпредставляет собой атом водорода, низшую алкильную группу, атом галогена или подобное; Rпредставляет собой атом водорода, низшую алкильную группу, гидроксильную группу или атом галогена; Rпредставляет собой атом водорода или низшую алкилоксигруппу; Rпредставляет собой атом водорода, низшую алкилоксигруппу, атом галогена, гидроксильную группу, или метилендиоксигруппу, образованную вместе с R, или изопропилидендиоксигруппу, образованную вместе с R; Rпредставляет собой атом водорода, низшую алкилоксигруппу, или метилендиоксигруппу, образованную вместе с R, или изопропилидендиоксигруппу, образованную вместе с R; Rпредставляет собой атом водорода или низшую алкильную группу и Rпредставляет собой атом водорода, гидроксильную группу, аминогруппу, низшую алкилкарбонилоксигруппу или атом галогена.
EA201170595A 2008-10-23 2009-10-23 ПРОИЗВОДНОЕ ФЕНАНТРОИНДОЛИЗИДИНА И ИНГИБИТОР NFκB, СОДЕРЖАЩИЙ ЕГО В КАЧЕСТВЕ АКТИВНОГО ИНГРЕДИЕНТА EA023622B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2008273556 2008-10-23
PCT/JP2009/005593 WO2010047126A1 (ja) 2008-10-23 2009-10-23 フェナンスロインドリジジン誘導体及びこれを有効成分とするNFκB阻害剤

Publications (2)

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EA201170595A1 true EA201170595A1 (ru) 2011-12-30
EA023622B1 EA023622B1 (ru) 2016-06-30

Family

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EA201170595A EA023622B1 (ru) 2008-10-23 2009-10-23 ПРОИЗВОДНОЕ ФЕНАНТРОИНДОЛИЗИДИНА И ИНГИБИТОР NFκB, СОДЕРЖАЩИЙ ЕГО В КАЧЕСТВЕ АКТИВНОГО ИНГРЕДИЕНТА

Country Status (10)

Country Link
US (1) US8569327B2 (ru)
EP (1) EP2351753B1 (ru)
JP (1) JP5583589B2 (ru)
KR (1) KR101708512B1 (ru)
CN (1) CN102186850B (ru)
AU (1) AU2009307580B2 (ru)
CA (1) CA2740807C (ru)
EA (1) EA023622B1 (ru)
NZ (1) NZ592429A (ru)
WO (1) WO2010047126A1 (ru)

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* Cited by examiner, † Cited by third party
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CN103446211B (zh) * 2013-09-24 2016-02-10 兰州理工大学 一种牛心朴子总生物碱及其制备方法和应用
CN104557909B (zh) * 2013-10-09 2019-01-01 中国医学科学院药物研究所 3-酰氧基取代右旋去氧娃儿藤宁衍生物、其制法和药物组合物与用途
KR101693035B1 (ko) 2015-01-14 2017-01-06 충북대학교 산학협력단 1,2,3,4-테트라하이드로퀴놀린-2-카르복실산 n-(치환)페닐아미드 유도체 및 이의 용도
CN105924380B (zh) * 2015-02-27 2019-03-05 顺天乡大学校产学协力团 菲类化合物或其衍生物、以及含有该菲类化合物或其衍生物的治疗结核病用药物组合物
WO2016161538A1 (zh) * 2015-04-09 2016-10-13 中国医学科学院药物研究所 3-酰氧基取代右旋去氧娃儿藤宁衍生物、其制法和药物组合物与用途
JP6363765B1 (ja) * 2017-05-02 2018-07-25 スンチョンヒャン ユニバーシティ インダストリー アカデミー コーポレーション ファウンデーション 新規な化合物及びそれを含む結核の治療用薬学組成物
CN110294752B (zh) * 2018-03-21 2022-01-11 中国医学科学院药物研究所 光学纯(s)-3-新戊酰氧基-6,7-二甲氧基菲并吲哚里西啶的制备
CN110283170B (zh) * 2019-07-17 2020-11-06 清华大学 一种化合物制备及其在抑制多种肿瘤细胞生长中的应用
TWI811724B (zh) 2020-07-08 2023-08-11 財團法人國家衛生研究院 正股核糖核酸病毒之抑制劑
KR102249543B1 (ko) 2020-08-26 2021-05-11 한국화학연구원 페난트로인돌리지딘 및 페난트로퀴놀리지딘 알칼로이드 유도체, 이의 광학이성질체, 또는 이의 약학적으로 허용가능한 염을 유효성분으로 포함하는 코로나바이러스감염증-19 치료용 조성물

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JPH08319238A (ja) * 1995-05-24 1996-12-03 Asahi Chem Ind Co Ltd リン酸化酵素阻害剤
JPH11322602A (ja) * 1998-05-13 1999-11-24 Kazuo Umezawa 転写因子NFκB活性化阻害剤
WO2001023384A1 (fr) 1999-09-27 2001-04-05 Japan As Represented By Director General Of Agency Of National Cancer Center Agents antitumoraux
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AU2003217373B2 (en) 2002-02-15 2009-04-30 University Of Tennessee Research Foundation Novel tyloindicines and related processes, pharmaceutical compositions and methods
EP1604990A1 (en) 2004-06-11 2005-12-14 National Health Research Institutes Phenanthroindolizidine alkaloids
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Also Published As

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KR20110079661A (ko) 2011-07-07
WO2010047126A1 (ja) 2010-04-29
CN102186850A (zh) 2011-09-14
EA023622B1 (ru) 2016-06-30
EP2351753B1 (en) 2015-02-11
US8569327B2 (en) 2013-10-29
US20110201637A1 (en) 2011-08-18
JP5583589B2 (ja) 2014-09-03
CA2740807A1 (en) 2010-04-29
AU2009307580B2 (en) 2015-04-23
NZ592429A (en) 2012-10-26
EP2351753A1 (en) 2011-08-03
AU2009307580A1 (en) 2010-04-29
CN102186850B (zh) 2014-10-29
CA2740807C (en) 2016-12-20
EP2351753A4 (en) 2012-05-30
KR101708512B1 (ko) 2017-02-20
JPWO2010047126A1 (ja) 2012-03-22

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