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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JP2015510515A (ja
JP6155285B2 (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) CN106046106A (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
SG11201505639SA (en) 2013-02-06 2015-08-28 Bristol Myers Squibb Co C-19 modified triterpenoids with hiv maturation inhibitory activity
SI3129392T1 (sl) * 2014-04-11 2020-11-30 VIIV Healthcare UK(No.4) Limited Triterpenoidi z inhibitorno aktivnostjo maturacije HIV-a, substituirani na položaju 3 z nearomatskim obročem, ki nosi haloalkilni substituent
WO2015195776A1 (en) 2014-06-19 2015-12-23 Bristol-Myers Squibb Company Betulinic acid derivatives with hiv maturation inhibitory activity
EP3218388A1 (en) 2014-11-14 2017-09-20 VIIV Healthcare UK (No.5) Limited C17-aryl substituted betulinic acid analogs
KR20170092580A (ko) * 2014-11-14 2017-08-11 비브 헬스케어 유케이 (넘버5) 리미티드 연장된 베툴린산 유사체
CN107250153A (zh) * 2014-11-14 2017-10-13 Viiv保健英国第五有限公司 氧代羽扇豆烯衍生物
RU2017134461A (ru) * 2015-04-14 2019-05-14 ВАЙВ ХЕЛТКЕР ЮКей (N4) ЛИМИТЕД Способы получения ингибитора созревания HIV
RU2018105352A (ru) 2015-07-28 2019-08-29 ГлаксоСмитКлайн Интеллекчуал Проперти (N2) Лимитед Производные бетулина для предупреждения или лечения ВИЧ-инфекций
WO2017017609A1 (en) 2015-07-28 2017-02-02 Glaxosmithkline Intellectual Property (No.2) Limited Betuin derivatives for preventing or treating hiv infections
RU2018112958A (ru) 2015-09-24 2019-10-28 ГлаксоСмитКлайн Интеллекчуал Проперти (N2) Лимитед Соединения с ингибирующей созревание ВИЧ активностью
WO2017125870A1 (en) * 2016-01-20 2017-07-27 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
WO2019055280A1 (en) 2017-09-13 2019-03-21 Emmyon, Inc. DIETHANOLAMINE SALTS AND URSOLIC ACID MORPHOLIN
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
SI3924361T1 (sl) 2019-02-11 2024-02-29 Hetero Labs Limited Novi derivati triterpena kot zaviralci virusa hiv
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
US5962527A (en) 1995-03-21 1999-10-05 The Board Of Trustees Of The University Of Illinois Method and composition for treating cancers
US5869535A (en) 1995-03-21 1999-02-09 The Board Of Trustees Of The University Of Illinois Method and composition for selectively inhibiting melanoma
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
US20050014730A1 (en) 2003-04-02 2005-01-20 Carlson Robert M. 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
EP1730163A4 (en) 2004-03-17 2009-12-30 Panacos Pharmaceuticals Inc Pharmaceutical salts of 3-O- (3,3-dimethylsuccinyl) betulinic acid
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
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US8802661B2 (en) 2010-06-04 2014-08-12 Bristol-Myers Squibb Company C-28 amides of modified C-3 betulinic acid derivatives as HIV maturation inhibitors
CN103038245B (zh) 2010-06-04 2015-03-25 百时美施贵宝公司 作为hiv成熟抑制剂的c-3经修饰的桦木酸衍生物
AP2013006706A0 (en) 2010-07-02 2013-02-28 Gilead Sciences Inc Napht-2-ylacetic acid derivatives to treat AIDS
PL2670764T3 (pl) * 2011-01-31 2016-02-29 Bristol Myers Squibb Co C-28 aminy zmodyfikowanych C-3 pochodnych kwasu betulinowego jako inhibitory dojrzewania HIV
KR101886467B1 (ko) * 2011-01-31 2018-08-07 비브 헬스케어 유케이 (넘버4) 리미티드 Hiv 성숙 억제 활성을 갖는 c-17 및 c-3 변형 트리테르페노이드
WO2013043778A1 (en) 2011-09-21 2013-03-28 Bristol-Myers Squibb Company Novel betulinic acid derivatives with antiviral activity
US8889854B2 (en) 2012-05-07 2014-11-18 Bristol-Myers Squibb Company C-17 bicyclic amines of triterpenoids with HIV maturation inhibitory activity
SG11201505639SA (en) * 2013-02-06 2015-08-28 Bristol Myers Squibb Co C-19 modified triterpenoids with hiv maturation inhibitory activity

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