Discovery of a synthetic dual inhibitor of HIV and HCV infection based on a tetrabutoxy-calix[4]arene scaffold.

Abstract:

:A potential anti-HIV and HCV drug candidate is highly desirable as coinfection has become a worldwide public health challenge. A potent compound based on a tetrabutoxy-calix[4]arene scaffold that possesses dual inhibition for both HIV and HCV is described. Structural activity relationship studies demonstrate the effects of lower-rim alkylation in maintaining cone conformation and upper-rim interacting head groups on the calix[4]arene play key roles for its potent dual antiviral activities.

journal_name

Bioorg Med Chem Lett

authors

Tsou LK,Dutschman GE,Gullen EA,Telpoukhovskaia M,Cheng YC,Hamilton AD

doi

10.1016/j.bmcl.2010.02.043

subject

Has Abstract

pub_date

2010-04-01 00:00:00

pages

2137-9

issue

7

eissn

0960-894X

issn

1464-3405

pii

S0960-894X(10)00243-X

journal_volume

20

pub_type

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