C. Schaeffer

发表

The site of antiviral action of 3-nitrosobenzamide on the infectivity process of human immunodeficiency virus in human lymphocytes.

W. Rice, M. Fesen, J. Mcdougal, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Inhibition of the replication of native and 3′‐azido‐2′,3′‐dideoxy‐thymidine (AZT)‐resistant simian immunodeficiency virus (SIV) by 3‐nitrosobenzamide

E. Kun, W. Rice, R. Chuang, 1993, FEBS letters.

Induction of endonuclease-mediated apoptosis in tumor cells by C-nitroso-substituted ligands of poly(ADP-ribose) polymerase.

C. Hillyer, W. Rice, K. Buki, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Evaluation of selected chemotypes in coupled cellular and molecular target-based screens identifies novel HIV-1 zinc finger inhibitors.

D. Covell, D. Zaharevitz, A. Wallqvist, 1996, Journal of medicinal chemistry.

Inhibitors of HIV Nucleocapsid Protein Zinc Fingers as Candidates for the Treatment of AIDS

L. Arthur, J. Domagala, J. Supko, 1995, Science.

Inhibition of HIV-1 infectivity by zinc-ejecting aromatic C-nitroso compounds

M. Summers, L. Arthur, J. Bess, 1993, Nature.

Inhibition of multiple phases of human immunodeficiency virus type 1 replication by a dithiane compound that attacks the conserved zinc fingers of retroviral nucleocapsid proteins

R. Schultz, D. Clanton, W. Rice, 1997, Antimicrobial agents and chemotherapy.

Inhibition of Acute-, Latent-, and Chronic-Phase Human Immunodeficiency Virus Type 1 (HIV-1) Replication by a Bistriazoloacridone Analog That Selectively Inhibits HIV-1 Transcription

C. Michejda, W. Rice, R. Buckheit, 1998, Antimicrobial Agents and Chemotherapy.

Extension of the polyanionic cosalane pharmacophore as a strategy for increasing anti-HIV potency.

E. De Clercq, C. Pannecouque, D. Schols, 1999, Journal of medicinal chemistry.

Human immunodeficiency virus type-1 (HIV-1) replication is unaffected by human secretory leukocyte protease inhibitor.

D. Clanton, W. Rice, R. Buckheit, 1996, Antiviral research.

New alkenyldiarylmethanes with enhanced potencies as anti-HIV agents which act as non-nucleoside reverse transcriptase inhibitors.

W. Rice, M. Cushman, R. Buckheit, 1998, Journal of medicinal chemistry.

Synthesis of a cosalane analog with an extended polyanionic pharmacophore conferring enhanced potency as an anti-HIV agent.

W. Rice, M. Cushman, M Cushman, 1998, Bioorganic & medicinal chemistry letters.

Reverse Transcription of Human Immunodeficiency Virus Type 1 is Blocked by Retroviral Zinc Finger Inhibitors

L. Graham, M. Bu, Jason Turpin, 1997 .

Inhibitors of human immunodeficiency virus type 1 zinc fingers prevent normal processing of gag precursors and result in the release of noninfectious virus particles

E. Sausville, G. Yu, W. Rice, 1996, Journal of virology.

All-atom models for the non-nucleoside binding site of HIV-1 reverse transcriptase complexed with inhibitors: a 3D QSAR approach.

N. Pattabiraman, D. Zaharevitz, G. Kellogg, 1996, Journal of medicinal chemistry.