I Nitta

Specific anti-HIV-1 "acyclonucleosides" which cannot be phosphorylated: synthesis of some deoxy analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine.

R T Walker, R. T. Walker, M. Baba, 1991, Journal of medicinal chemistry.

Synthesis and antiviral activity of deoxy analogs of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT) as potent and selective anti-HIV-1 agents.

R T Walker, R. T. Walker, S Shigeta, 1992, Journal of medicinal chemistry.

Structure-activity relationships of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine analogues: effect of substitutions at the C-6 phenyl ring and at the C-5 position on anti-HIV-1 activity.

R T Walker, R. T. Walker, S Shigeta, 1992, Journal of medicinal chemistry.

Synthesis and anti-HIV activity of 2-, 3-, and 4-substituted analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT).

R T Walker, R. T. Walker, S Shigeta, 1991, Journal of medicinal chemistry.

A new class of HIV-1-specific 6-substituted acyclouridine derivatives: synthesis and anti-HIV-1 activity of 5- or 6-substituted analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT).

S Shigeta, H. Hayakawa, M. Baba, 1991, Journal of medicinal chemistry.