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HIV protease inhibitors as anti-AIDS drugs

Viral envdoppe pnMdn. gpliMI. bixKfing to CD4 rcccptcMrs on helper T-cdb [Pg.153]

Viril mRNA produced under die ccmtrol of regulatory gene products TAT.REV.NEFeto [Pg.153]

Transput to cell membrane Specific cleavi polypqidde precursOTS to generue fimcdonal and structural viral proteins Glycosyhoion mi trimming [Pg.153]

Almost simultaneously, protein and medicinal chemists began to characterise HIV protease by structural studies and inhibitor synthesis, respectively [59,60]. In the aspartate protease family, gene duplication gives rise to two structurally similar domains each having a conserved sequence. Asp- [Pg.154]

Compound Inhibitor of HIV Protease, ICj inM) Antiviral activity IC5o(/rM) TC, (/iM) Reference [Pg.158]


See other pages where HIV protease inhibitors as anti-AIDS drugs is mentioned: [Pg.152]   


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AIDS drugs

Anti-AIDS drugs

Anti-HIV

Anti-HIV drugs

HIV drugs

HIV inhibitors

HIV-1 protease

HIV/AIDS

Inhibitors as Drugs

Protease A

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