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Tracy L. Hartman

Researcher at Southern Research Institute

Publications -  37
Citations -  1019

Tracy L. Hartman is an academic researcher from Southern Research Institute. The author has contributed to research in topics: Nucleoside Reverse Transcriptase Inhibitor & Virus. The author has an hindex of 18, co-authored 36 publications receiving 945 citations. Previous affiliations of Tracy L. Hartman include Rega Institute for Medical Research & Purdue University.

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Antiviral Activity of Hop Constituents Against a Series of DNA and RNA Viruses

TL;DR: In summary, iso-alpha-acids and xanthohumol were shown to have a low-to-moderate antiviral activity against several viruses and might serve as interesting lead compounds from which more active anti-HCV, anti-Rhino and anti-herpesvirus antiviral agents could be synthesized.
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Benzamide-based thiolcarbamates: a new class of HIV-1 NCp7 inhibitors.

TL;DR: A new class of NCp7 inhibitors is reported that possess good antiviral activity with low cellular toxicity and are effective against HIV-1 nucleocapsid protein.
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Carrageenan/MIV-150 (PC-815), a combination microbicide.

TL;DR: Theoretically, PC-815 is likely to be a more efficacious microbicide than Carraguard in blocking HIV-1 and HIV-2 infections in vitro as compared with Carraguar alone.
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Synthesis and anti-HIV activity of new alkenyldiarylmethane (ADAM) non-nucleoside reverse transcriptase inhibitors (NNRTIs) incorporating benzoxazolone and benzisoxazole rings.

TL;DR: The most potent compound identified was (E)-5-[1-(3,7-dimethyl-2-oxo-2,3-dihydro-benzoxazol-5-yl)-5-methoxycarbonyl-pent-1-enyl]-2- methoxy-3-methylbenzoic acid methyl ester (7), which inhibited the cytopathic effect of HIV-1 in cell culture.
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Synthesis and anti-HIV activity of new metabolically stable alkenyldiarylmethane non-nucleoside reverse transcriptase inhibitors incorporating N-methoxy imidoyl halide and 1,2,4-oxadiazole systems.

TL;DR: The design and synthesis of a new class of ADAMs with N-methoxy imidoyl halide and 1,2,4-oxadiazole systems were attempted and the resulting new ADAM 6 displayed enhanced metabolic stability in rat plasma along with the ability to inhibit HIV-1 reverse transcriptase and the cytopathic effect of HIV- 1RF and HIV-2IIIB at submicromolar concentrations.