scispace - formally typeset
B

Billy Lin

Researcher at National Institutes of Health

Publications -  7
Citations -  274

Billy Lin is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Hepatitis C virus & Hepatitis C. The author has an hindex of 6, co-authored 7 publications receiving 225 citations. Previous affiliations of Billy Lin include University of California, Los Angeles.

Papers
More filters
Journal ArticleDOI

Repurposing of the antihistamine chlorcyclizine and related compounds for treatment of hepatitis C virus infection

TL;DR: Chlorcyclizine HCl (CCZ), an over-the-counter drug for allergy symptoms, is identified and characterized as an anti-HCV drug in vitro and in vivo, and represents a promising candidate for drug repurposing and further development as an effective and accessible agent for treatment of HCV infection.
Journal ArticleDOI

Discovery, Optimization, and Characterization of Novel Chlorcyclizine Derivatives for the Treatment of Hepatitis C Virus Infection

TL;DR: Struct–activity relationship (SAR) efforts that resulted in the optimization of novel chlorcyclizine derivatives as anti-HCV agents can serve as lead preclinical candidates for the treatment of hepatitis C virus infection and as probes to study hepatitis Cirus pathogenesis and host–virus interaction.
Journal ArticleDOI

High-Throughput Screening, Discovery, and Optimization To Develop a Benzofuran Class of Hepatitis C Virus Inhibitors.

TL;DR: The optimization of the benzofuran scaffold led to the identification of several exemplars with potent inhibition of HCV, low cytotoxicity, and excellent selectivity, and the design and synthesis of a 45-compound library to comprehensively explore the anti-HCV activity.
Journal ArticleDOI

Evaluation of antiviral drug synergy in an infectious HCV system.

TL;DR: The results show that in vitro combination studies of anti-HCV DAAs in the HCVcc system may provide useful guidance for drug combination designs in clinical studies and demonstrate that these DAA classes in combination with host-targeting agents or entry inhibitors may improve HCV treatment response.