نتایج جستجو برای: hiv fusion inhibitors

تعداد نتایج: 504964  

Some new diazo incorporated coumarin compounds were designed and synthesized to evaluate their anti-HIV activity. Overall, compounds were active against HIV at 100 μM. Additionally, no cytotoxic effect was observed at this concentration. The compound with 4-chlorobenzyl group indicated the best anti-HIV activity (52%). Docking studies using the later crystallographic data available for PFV inte...

In an attempt to identify potential new agents that are active against HIV-1, a series of novel pyridopyrimidine-5-carbohydrazide derivatives featuring a substituted benzylidene fragment were designed and synthesized based on the general pharmacophore of HIV-1 integrase inhibitors. The cytotoxicity profiles of these compounds showed no significant toxicity to human cells and they exhibited anti...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Paolo Ingallinella Elisabetta Bianchi Neal A Ladwa Ying-Jie Wang Renee Hrin Maria Veneziano Fabio Bonelli Thomas J Ketas John P Moore Michael D Miller Antonello Pessi

Peptides derived from the heptad repeat 2 (HR2) region of the HIV fusogenic protein gp41 are potent inhibitors of viral infection, and one of them, enfuvirtide, is used for the treatment of therapy-experienced AIDS patients. The mechanism of action of these peptides is binding to a critical intermediate along the virus-cell fusion pathway, and accordingly, increasing the affinity for the interm...

2012
Chien-Hsing Chang Jorma Hinkula Meiyu Loo Tina Falkeborn Rongxiu Li Thomas M. Cardillo Edmund A. Rossi David M. Goldenberg Britta Wahren

We constructed novel HIV-1 fusion inhibitors that may overcome the current limitations of enfuvirtide, the first such therapeutic in this class. The three prototypes generated by the Dock-and-Lock (DNL) technology to comprise four copies of enfuvirtide tethered site-specifically to the Fc end of different humanized monoclonal antibodies potently neutralize primary isolates (both R5-tropic and X...

Journal: :The Journal of antimicrobial chemotherapy 2012
Maria José Buzon Itziar Erkizia Christian Pou Gerard Minuesa Maria Carmen Puertas Anna Esteve Alfredo Castello Jose Ramón Santos Julia G Prado Nuria Izquierdo-Useros Theresa Pattery Margriet Van Houtte Luis Carrasco Bonaventura Clotet Lidia Ruiz Javier Martinez-Picado

OBJECTIVES HIV-1 genotyping is widely accepted as a diagnostic tool to optimize therapy changes in patients whose antiretroviral regimen is failing. Phenotyping can substantially complement the information obtained from genotyping, especially in the presence of complex mutational patterns. However, drug susceptibility tests are laborious and require biosafety facilities. We describe the molecul...

2013
Kristin Eissmann Sebastian Mueller Heinrich Sticht Susan Jung Peng Zou Shibo Jiang Andrea Gross Jutta Eichler Bernhard Fleckenstein Heide Reil

A strategy for antiviral drug discovery is the elucidation and imitation of viral interference mechanisms. HIV-1 patients benefit from a coinfection with GB Virus C (GBV-C), since HIV-positive individuals with long-term GBV-C viraemia show better survival rates than HIV-1 patients without persisting GBV-C. A direct influence of GBV-C on HIV-1 replication has been shown in coinfection experiment...

Journal: :journal of sciences islamic republic of iran 0

a few analogues of atevirdine or 1-[(5-methoxyindol-2-yl) carbonyl]-4-[3- (ethylamino)-2-pyridyl] piperazine – an anti-hiv belonging to non-nucleoside reverse transcriptase inhibitors were synthesized and evaluated for anti-hiv activity. replacement of indolyl moiety with 2-alkylthio-1-benzyl-5-imidazolyl substituent afforded 1-[2-(alkylthio-1-benzyl-5-imidazolyl) carbonyl]-4-[3-(isopropylamino...

2009
Kosuke Miyauchi Michael M. Kozlov Gregory B. Melikyan

The HIV envelope (Env) glycoprotein mediates membrane fusion through sequential interactions with CD4 and coreceptors, followed by the refolding of the transmembrane gp41 subunit into the stable 6-helix bundle (6HB) conformation. Synthetic peptides derived from the gp41 C-terminal heptad repeat domain (C-peptides) potently inhibit fusion by binding to the gp41 pre-bundle intermediates and block...

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