Concept of Viral Inhibitors via NTCP.

Kento Fukano, Senko Tsukuda, Koichi Watashi, Takaji Wakita

Journal: Seminars in liver disease 2019;39(1):78-85

PMID: 30809790

Abstract

Identification of sodium taurocholate cotransporting polypeptide (NTCP) as an entry receptor for hepatitis B and D viruses (HBV and HDV) has not only promoted our understanding of the mechanism underlying the viral entry process, but also provided cell culture models supporting viral infection. These models have greatly facilitated cell-based chemical screening for the discovery of entry inhibitors, and mode of action studies using such inhibitors have shown the advantages of NTCP as a drug target. Furthermore, in vitro chemical screening by application of high-throughput affinity-based technologies that target NTCP has identified a variety of unique small molecules that interfere with viral entry. This review summarizes this hot topic in the development of HBV/HDV entry inhibitors, with special focus on the use of NTCP as a drug target.

Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Address: Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.; Department of Analytical Biochemistry, Meiji Pharmaceutical University, Kiyose, Japan.; Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.; Liver Cancer Prevention Research Unit, RIKEN Center for Integrative Medical Sciences (IMS), Wako, Japan.; Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.; Department of Applied Biological Science, Tokyo University of Science, Noda, Japan.; JST CREST, Saitama, Japan.; Department of Virology II, National Institute of Infectious Diseases, Tokyo, Japan.
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