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dc.date.accessioned | 2012-08-28T15:49:27Z | |
dc.date.available | 2012-08-28T15:49:27Z | |
dc.date.issued | 2012 | |
dc.identifier.uri | http://sedici.unlp.edu.ar/handle/10915/20230 | |
dc.description.abstract | The development of novel HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) offers the possibility of generating novel structures of increased potency. Based on the bioisosterism principle, two novel 2-(5-(naphthalen-1-yl)-1,2,3-thiadiazol-4-ylthio)-N-acetamides derivatives have been designed, synthesized and evaluated for their anti-HIV activities in MT-4 cells. The results indicate that these compounds show good activities against HIV-1. Especially, compound 9B (EC50 = 0.019 μM) was more effective than the reference drugs nevirapine and delavirdine. | en |
dc.format.extent | 751-755 | es |
dc.language | en | es |
dc.subject | Antiviral activity | en |
dc.subject | Agentes Antivirales | es |
dc.subject | Tiadiazoles | es |
dc.subject | HIV-1 | en |
dc.subject | Synthesis | en |
dc.subject | Thiadiazole | en |
dc.subject | Thioacetanilides | en |
dc.title | Synthesis and Anti-HIV Activity Evaluation of 2-(5-(Naphthalen-1-yl)-1,2,3-thiadiazol-4-ylthio)-N-acetamides Derivatives | en |
dc.type | Articulo | es |
sedici.identifier.uri | http://www.latamjpharm.org/resumenes/31/5/LAJOP_31_5_2_3.pdf | es |
sedici.identifier.issn | 0326-2383 | |
sedici.creator.person | Jiang, Xiaofei | es |
sedici.creator.person | Zhan, Peng | es |
sedici.creator.person | Liu, Xinyong | es |
sedici.creator.person | Clercq, Erik de | es |
sedici.subject.materias | Farmacia | es |
sedici.description.fulltext | false | es |
mods.originInfo.place | Colegio de Farmacéuticos de la Provincia de Buenos Aires | es |
sedici.subtype | Comunicacion | es |
sedici.description.peerReview | peer-review | es |
sedici.relation.journalTitle | Latin American Journal of Pharmacy | es |
sedici.relation.journalVolumeAndIssue | vol. 31, no. 5 | es |