JP2015510515A5 - - Google Patents

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Publication number
JP2015510515A5
JP2015510515A5 JP2014557739A JP2014557739A JP2015510515A5 JP 2015510515 A5 JP2015510515 A5 JP 2015510515A5 JP 2014557739 A JP2014557739 A JP 2014557739A JP 2014557739 A JP2014557739 A JP 2014557739A JP 2015510515 A5 JP2015510515 A5 JP 2015510515A5
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JP
Japan
Prior art keywords
alkyl
group
substituted
cycloalkyl
coor
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Application number
JP2014557739A
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English (en)
Japanese (ja)
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JP6155285B2 (ja
JP2015510515A (ja
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Priority claimed from US13/760,726 external-priority patent/US8906889B2/en
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Publication of JP2015510515A publication Critical patent/JP2015510515A/ja
Publication of JP2015510515A5 publication Critical patent/JP2015510515A5/ja
Application granted granted Critical
Publication of JP6155285B2 publication Critical patent/JP6155285B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2014557739A 2012-02-15 2013-02-13 Hiv成熟阻害活性のあるc−3シクロアルケニルトリテルペノイド Expired - Fee Related JP6155285B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201261599040P 2012-02-15 2012-02-15
US61/599,040 2012-02-15
US13/760,726 2013-02-06
US13/760,726 US8906889B2 (en) 2012-02-15 2013-02-06 C-3 cycloalkenyl triterpenoids with HIV maturation inhibitory activity
PCT/US2013/025897 WO2013123019A1 (en) 2012-02-15 2013-02-13 C-3 cycloalkenyl triterpenoids with hiv maturation inhibitory activity

Publications (3)

Publication Number Publication Date
JP2015510515A JP2015510515A (ja) 2015-04-09
JP2015510515A5 true JP2015510515A5 (https=) 2016-03-17
JP6155285B2 JP6155285B2 (ja) 2017-06-28

Family

ID=48946098

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014557739A Expired - Fee Related JP6155285B2 (ja) 2012-02-15 2013-02-13 Hiv成熟阻害活性のあるc−3シクロアルケニルトリテルペノイド

Country Status (26)

Country Link
US (1) US8906889B2 (https=)
EP (1) EP2814834B1 (https=)
JP (1) JP6155285B2 (https=)
KR (1) KR20140123584A (https=)
CN (2) CN104220451B (https=)
AR (1) AR089996A1 (https=)
AU (1) AU2013221725B2 (https=)
BR (1) BR112014019672A8 (https=)
CA (1) CA2864656A1 (https=)
CL (1) CL2014002141A1 (https=)
CO (1) CO7061077A2 (https=)
EA (1) EA024361B1 (https=)
ES (1) ES2656984T3 (https=)
HK (1) HK1204608A1 (https=)
IL (1) IL234077A (https=)
MX (1) MX2014009235A (https=)
MY (1) MY166793A (https=)
NZ (1) NZ631408A (https=)
PE (1) PE20142315A1 (https=)
PH (1) PH12014501816A1 (https=)
PT (1) PT2814834T (https=)
SG (1) SG11201404748XA (https=)
TW (1) TW201336863A (https=)
UY (1) UY34627A (https=)
WO (1) WO2013123019A1 (https=)
ZA (1) ZA201406724B (https=)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8889854B2 (en) 2012-05-07 2014-11-18 Bristol-Myers Squibb Company C-17 bicyclic amines of triterpenoids with HIV maturation inhibitory activity
JP6186010B2 (ja) 2013-02-06 2017-08-23 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Hiv成熟阻害活性を有するc−19修飾トリテルペノイド類
UY36070A (es) 2014-04-11 2015-10-30 Bristol Myers Squibb Company Una Corporación Del Estado De Delaware Triterpenoides con actividad inhibidora de la maduración de hiv
WO2015195776A1 (en) 2014-06-19 2015-12-23 Bristol-Myers Squibb Company Betulinic acid derivatives with hiv maturation inhibitory activity
AU2015346314B2 (en) * 2014-11-14 2018-04-12 VIIV Healthcare UK (No.5) Limited Extended betulinic acid analogs
US9969767B2 (en) 2014-11-14 2018-05-15 VIIV Healthcare UK (No.5) Limited Oxolupene derivatives
CN107250152A (zh) 2014-11-14 2017-10-13 Viiv保健英国第五有限公司 C17‑芳基取代的桦木酸类似物
EP3283467A1 (en) * 2015-04-14 2018-02-21 VIIV Healthcare UK(No.4) Limited Methods of producing an hiv maturation inhibitor
US20180194799A1 (en) 2015-07-28 2018-07-12 Glaxosmithkline Intellectual Property (No.2) Limited Betuin derivatives for preventing or treating hiv infections
WO2017017609A1 (en) 2015-07-28 2017-02-02 Glaxosmithkline Intellectual Property (No.2) Limited Betuin derivatives for preventing or treating hiv infections
KR20180054826A (ko) 2015-09-24 2018-05-24 글락소스미스클라인 인털렉츄얼 프로퍼티 (넘버 2) 리미티드 Hiv 성숙 억제 활성을 갖는 화합물
EP3405474A1 (en) * 2016-01-20 2018-11-28 Glaxosmithkline Intellectual Property (No. 2) Limited Amine derivatives of lupanes with hiv maturation inhibitory activity
AR107512A1 (es) 2016-02-04 2018-05-09 VIIV HEALTHCARE UK Nº 5 LTD Triterpenoides modificados en c-3 y c-17 como inhibidores del vih-1
CN106905264B (zh) * 2017-04-12 2019-06-07 连云港杰瑞药业有限公司 一种合成阿扎拉韦中间体的方法
IL273078B2 (en) 2017-09-13 2025-06-01 Emmyon Inc Ursolic acid morpholine and diethanolamine salts
ES2970042T3 (es) 2018-04-24 2024-05-24 Viiv Healthcare Uk No 5 Ltd Compuestos con actividad inhibidora de la maduración del VIH
CN109705189B (zh) * 2018-12-29 2020-06-05 中国医学科学院药用植物研究所 具有式i所示结构的三萜衍生物及其制备方法和应用
AU2020222299C1 (en) 2019-02-11 2024-05-16 Hetero Labs Limited Novel triterpene derivatives as HIV inhibitors
WO2020229398A1 (de) 2019-05-14 2020-11-19 Bayer Aktiengesellschaft (1-alkenyl)-substituierte pyrazole und triazole als schädlingsbekämpfungsmittel

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US5413999A (en) 1991-11-08 1995-05-09 Merck & Co., Inc. HIV protease inhibitors useful for the treatment of AIDS
US5869535A (en) 1995-03-21 1999-02-09 The Board Of Trustees Of The University Of Illinois Method and composition for selectively inhibiting melanoma
US5962527A (en) 1995-03-21 1999-10-05 The Board Of Trustees Of The University Of Illinois Method and composition for treating cancers
US5679828A (en) 1995-06-05 1997-10-21 Biotech Research Labs, Inc. Betulinic acid and dihydrobetulinic acid derivatives and uses therefor
US20040110785A1 (en) 2001-02-02 2004-06-10 Tao Wang Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
US7365221B2 (en) 2002-09-26 2008-04-29 Panacos Pharmaceuticals, Inc. Monoacylated betulin and dihydrobetulin derivatives, preparation thereof and use thereof
WO2004089357A2 (en) 2003-04-02 2004-10-21 Regents Of The University Of Minnesota Anti-fungal formulation of triterpene and essential oil
US7745625B2 (en) 2004-03-15 2010-06-29 Bristol-Myers Squibb Company Prodrugs of piperazine and substituted piperidine antiviral agents
BRPI0508854A (pt) 2004-03-17 2007-08-28 Panacos Pharmaceuticals Inc sais farmacêuticos de ácido-3-o-(3',3'-dimetilsuccinil) betulìnico
TW200628161A (en) 2004-11-12 2006-08-16 Panacos Pharmaceuticals Inc Novel betulin derivatives, preparation thereof and use thereof
WO2008127364A2 (en) 2006-10-13 2008-10-23 Myriad Genetics, Inc. Antiviral compounds and use thereof
WO2008115281A2 (en) 2006-10-16 2008-09-25 Myriad Genetics, Inc. Compounds for treating viral infections
WO2009020732A1 (en) 2007-08-03 2009-02-12 Advanced Life Sciences, Inc. Lupane-type triterpenoids modified at 30-position and analogues thereof
CA2711424A1 (en) * 2008-01-03 2009-07-09 Virochem Pharma Inc. Novel lupane derivatives
CA2714049A1 (en) 2008-02-14 2009-08-20 Virochem Pharma Inc. Novel 17.beta. lupane derivatives
US9067966B2 (en) 2009-07-14 2015-06-30 Hetero Research Foundation, Hetero Drugs Ltd. Lupeol-type triterpene derivatives as antivirals
KR101445012B1 (ko) 2009-12-17 2014-09-26 머크 샤프 앤드 돔 코포레이션 Syk 억제제로서의 아미노피리미딘
RS54239B1 (sr) 2010-06-04 2015-12-31 Bristol-Myers Squibb Company C-28 amidi modifikovanih derivata c-3 betulinske kiseline kao inhibitori sazrevanja hiv-a
US8754068B2 (en) 2010-06-04 2014-06-17 Bristol-Myers Squibb Company Modified C-3 betulinic acid derivatives as HIV maturation inhibitors
MX2012015097A (es) 2010-07-02 2013-05-28 Gilead Sciences Inc Derivados de acido naft-2-ilacetico para tratar sida.
US8846647B2 (en) * 2011-01-31 2014-09-30 Bristol-Myers Squibb Company C-17 and C-3 modified triterpenoids with HIV maturation inhibitory activity
HUE026371T2 (en) * 2011-01-31 2016-05-30 Bristol Myers Squibb Co C-28 amines from modified C-3 betulinic acid derivatives as anti-HIV matrices
MX2014002936A (es) 2011-09-21 2014-04-25 Bristol Myers Squibb Co Nuevos derivados de acido betulinico con actividad antiviral.
US8889854B2 (en) 2012-05-07 2014-11-18 Bristol-Myers Squibb Company C-17 bicyclic amines of triterpenoids with HIV maturation inhibitory activity
JP6186010B2 (ja) * 2013-02-06 2017-08-23 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company Hiv成熟阻害活性を有するc−19修飾トリテルペノイド類

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