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Bevirimat (research code MPC-4326) is an anti-HIV drug derived from a betulinic acid-like compound, first isolated from Syzygium claviflorum, a Chinese herb. It is believed to inhibit HIV by a novel mechanism, so-called maturation inhibition. It is not currently U.S. Food and Drug Administration (FDA) … See more
According to the only currently available study, "the mean terminal elimination half-life of bevirimat ranged from 56.3 to 69.5 hours, and the mean clearance ranged from 173.9… See more
It has been found that bevirimat does not inhibit the cytochrome P450 system or interact with the human P-glycoprotein. Unformulated bevirimat is not well absorbed from the … See more
In vitro studies have shown that presence of a number of single nucleotide polymorphisms in the CA/SP1 cleavage site have resulted … See more
In December 2007, some results of the Phase IIb trial were released. Thomson Financial News reported that, "some patients respond 'very well' to the drug, while another… See more
Like protease inhibitors, bevirimat and other maturation inhibitors interfere with protease processing of newly translated HIV polyprotein precursor, called gag. Gag is an essential … See more
Preclinical studies have not presented any sign that bevirimat might be associated with any specific safety concerns that would limit its clinical use. In vitro preclinical… See more
Wikipedia text under CC-BY-SA license Bevirimat - an overview | ScienceDirect Topics
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Bevirimat | C36H56O6 | CID 457928 - PubChem
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MicroED for the study of protein–ligand interactions and the
New Phosphorus Analogs of Bevirimat: Synthesis, Evaluation of …
The prototype HIV-1 maturation inhibitor, bevirimat, binds to the …
Bevirimat (PA-457) | HIV Inhibitor | MedChemExpress
The prototype HIV-1 maturation inhibitor, bevirimat, binds to the …