AP2008004459A0 - Composition and sythesis of new reagents for inhibition of HIV replication - Google Patents
Composition and sythesis of new reagents for inhibition of HIV replicationInfo
- Publication number
- AP2008004459A0 AP2008004459A0 AP2008004459A AP2008004459A AP2008004459A0 AP 2008004459 A0 AP2008004459 A0 AP 2008004459A0 AP 2008004459 A AP2008004459 A AP 2008004459A AP 2008004459 A AP2008004459 A AP 2008004459A AP 2008004459 A0 AP2008004459 A0 AP 2008004459A0
- Authority
- AP
- ARIPO
- Prior art keywords
- sythesis
- inhibition
- composition
- hiv replication
- new reagents
- Prior art date
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- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/62—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
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- C07D209/04—Indoles; Hydrogenated indoles
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- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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PCT/US2006/039228 WO2007044565A2 (fr) | 2005-10-06 | 2006-10-06 | Composition et synthese de nouveaux reactifs pour inhiber la replication du vih |
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CN101743008A (zh) * | 2007-05-23 | 2010-06-16 | 西佳技术公司 | 用于治疗或预防登革热感染的抗病毒药 |
DK2025750T3 (da) * | 2007-08-13 | 2012-02-20 | Nexigen Gmbh | Targets og forbindelser til terapeutisk intervention af HIV-infektion |
GB0813403D0 (en) | 2008-07-22 | 2008-08-27 | Lectus Therapeutics Ltd | Potassium ion channel modulators & uses thereof |
CA2735593C (fr) | 2008-09-03 | 2017-08-15 | Repligen Corporation | Compositions comprenant des derives d'acide 6-aminohexanoique utilisees comme inhibiteurs de hdac |
WO2010073011A2 (fr) | 2008-12-23 | 2010-07-01 | Betagenon Ab | Composés utiles comme médicaments |
US9452980B2 (en) * | 2009-12-22 | 2016-09-27 | Hoffmann-La Roche Inc. | Substituted benzamides |
EP2580191A2 (fr) * | 2010-06-10 | 2013-04-17 | The U.S.A. as represented by the Secretary, Department of Health and Human Services | Compositions de précurseur de thioéther en tant qu'agents anti-vih et anti-rétroviraux |
EP2580190A4 (fr) * | 2010-06-11 | 2014-04-16 | Goeran Wadell | Nouveaux composés antiviraux |
KR20110137941A (ko) * | 2010-06-18 | 2011-12-26 | (주) 에빅스젠 | 신규한 티오우레아 또는 우레아 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 aids 예방 또는 치료용 약학 조성물 |
US8921381B2 (en) | 2010-10-04 | 2014-12-30 | Baruch S. Blumberg Institute | Inhibitors of secretion of hepatitis B virus antigens |
CN102603585B (zh) * | 2011-01-20 | 2015-04-15 | 四川大学 | N-苯基-2-巯基苯甲酰胺衍生物及其制备方法和用途 |
US10059723B2 (en) | 2011-02-28 | 2018-08-28 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
EP3524324A1 (fr) | 2011-02-28 | 2019-08-14 | BioMarin Pharmaceutical Inc. | Inhibiteurs de l'histone désacétylase |
US8957066B2 (en) | 2011-02-28 | 2015-02-17 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
US9555106B2 (en) * | 2011-09-30 | 2017-01-31 | Kineta, Inc. | Anti-viral compounds |
CN103183625B (zh) | 2011-12-28 | 2015-07-08 | 四川大学 | 抗hiv的化合物及其制备方法和用途 |
CN103665043B (zh) | 2012-08-30 | 2017-11-10 | 江苏豪森药业集团有限公司 | 一种替诺福韦前药及其在医药上的应用 |
KR101241370B1 (ko) * | 2012-09-28 | 2013-04-10 | (주) 에빅스젠 | 신규한 티오우레아 또는 우레아 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 aids 예방 또는 치료용 약학 조성물 |
EP2924021B1 (fr) * | 2012-11-26 | 2019-08-28 | Sichuan University | Composé anti-vih et procédé de préparation et utilisation correspondants |
EP2935284A4 (fr) * | 2012-12-21 | 2016-04-27 | Abbvie Inc | Modulateurs hétérocycliques des récepteurs nucléaires aux hormones |
KR20150132345A (ko) | 2013-03-15 | 2015-11-25 | 바이오마린 파머수티컬 인크. | Hdac 저해제 |
TW201512171A (zh) | 2013-04-19 | 2015-04-01 | Pfizer Ltd | 化學化合物 |
CN104418764B (zh) * | 2013-09-11 | 2017-02-01 | 上海伊明化学科技有限公司 | 一种二氢燕麦酰基邻氨基苯甲酸d合成方法 |
WO2016179505A1 (fr) * | 2015-05-06 | 2016-11-10 | University Of Maryland, College Park | Composés pour traiter des infections parasitaires |
SG11201807516UA (en) | 2016-03-17 | 2018-09-27 | Hoffmann La Roche | 5-ethyl-4-methyl-pyrazole-3-carboxamide derivative having activity as agonist of taar |
WO2018085348A1 (fr) * | 2016-11-03 | 2018-05-11 | Actavalon, Inc. | Quinoléines substituées et procédés pour traiter le cancer |
ES2922932T3 (es) * | 2016-12-29 | 2022-09-21 | Enyo Pharma | Derivados de tiofeno como agentes antivirales |
CA3108484A1 (fr) * | 2017-08-04 | 2019-02-07 | Anthony Stewart Campbell | Inhibiteurs de la formation d'amyloides induite par voie microbienne |
WO2019133666A1 (fr) * | 2017-12-28 | 2019-07-04 | Southern Research Institute | Composés de triazolophtalazine, utilisation en tant qu'inhibiteurs du virus de l'immunodéficience humaine de la dégradation dépendante du vif du vih de l'apobec3 |
CN111333663A (zh) * | 2018-12-19 | 2020-06-26 | 天津医科大学 | 一类环烷基并噻吩并嘧啶酮化合物及其制法和用途 |
CN111548313A (zh) * | 2019-02-11 | 2020-08-18 | 绍兴从零医药科技有限公司 | 预防和治疗慢性疼痛药物的胍类化合物 |
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GB1184251A (en) * | 1966-04-15 | 1970-03-11 | American Cyanamid Co | Oxazepines and Thiazepines |
DE2126149A1 (en) * | 1971-05-26 | 1972-12-07 | Farbenfabriken Bayer Ag, 5090 Leverkusen | Halo-salicylanilide derivs - with acaricidal and fungicidal activity |
US4356325A (en) * | 1980-11-28 | 1982-10-26 | Gulf Research & Development Company | Process for preparation of acetylene terminated sulfones, oligomers and precursors therefor |
KR20010074779A (ko) * | 1998-07-28 | 2001-08-09 | 스튜어트 알. 수터, 스티븐 베네티아너, 피터 존 기딩스 | 치환된 아닐리드 화합물 및 제조방법 |
GB9817548D0 (en) * | 1998-08-12 | 1998-10-07 | Novartis Ag | Organic compounds |
KR100658489B1 (ko) * | 1998-11-10 | 2006-12-18 | 얀센 파마슈티카 엔.브이. | Hiv 복제를 억제하는 피리미딘 |
AU2871900A (en) * | 1999-02-04 | 2000-08-25 | Millennium Pharmaceuticals, Inc. | G-protein coupled heptahelical receptor binding compounds and methods of use thereof |
US20050049242A1 (en) * | 2000-12-21 | 2005-03-03 | W. Edward Robinson | Novel HIV integrase inhibitors and HIV therapy based on drug combinations including integrase inhibitors |
US7105522B2 (en) * | 2001-03-15 | 2006-09-12 | Janssen Pharmaceutica, N.V. | HIV inhibiting pyrazinone derivatives |
JP2006521316A (ja) * | 2003-03-24 | 2006-09-21 | ビーエーエスエフ アクチェンゲゼルシャフト | トリフルオロメチルチオフェンカルボキシアニリドおよび殺菌剤としてのその使用 |
US20050123906A1 (en) * | 2003-11-06 | 2005-06-09 | Rana Tariq M. | Protein modulation |
-
2006
- 2006-10-06 KR KR1020087010911A patent/KR20080059634A/ko not_active Application Discontinuation
- 2006-10-06 WO PCT/US2006/039228 patent/WO2007044565A2/fr active Application Filing
- 2006-10-06 CN CNA2006800462146A patent/CN101355939A/zh active Pending
- 2006-10-06 EA EA200801025A patent/EA200801025A1/ru unknown
- 2006-10-06 EP EP06825592A patent/EP1945208A4/fr not_active Withdrawn
- 2006-10-06 AP AP2008004459A patent/AP2008004459A0/xx unknown
- 2006-10-06 CA CA002628863A patent/CA2628863A1/fr not_active Abandoned
- 2006-10-06 US US11/544,068 patent/US7754773B2/en active Active
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2008
- 2008-05-06 ZA ZA2008/03862A patent/ZA200803862B/en unknown
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EP1945208A4 (fr) | 2011-08-03 |
US20070099919A1 (en) | 2007-05-03 |
ZA200803862B (en) | 2014-10-29 |
US7754773B2 (en) | 2010-07-13 |
WO2007044565A2 (fr) | 2007-04-19 |
EA200801025A1 (ru) | 2008-12-30 |
CA2628863A1 (fr) | 2007-04-19 |
KR20080059634A (ko) | 2008-06-30 |
CN101355939A (zh) | 2009-01-28 |
EP1945208A2 (fr) | 2008-07-23 |
WO2007044565A3 (fr) | 2007-06-07 |
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