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Inhibition by components of Glycyrrhiza uralensis of 3CLpro and HCoV-OC43 proliferation.
Kim, Jang Hoon; Park, Yea-In; Hur, Mok; Park, Woo Tae; Moon, Youn-Ho; Huh, Yun-Chan; Kim, Tae Il; Kang, Min Hye; Kang, Jong Seong; Cho, Chong Woon; Park, Junsoo.
Afiliación
  • Kim JH; Department of Herbal Crop Research, National Institute of Horticultural & Herbal Science, RDA, Eumsung, Republic of Korea.
  • Park YI; Division of Biological Science and Technology, Yonsei University, Wonju, Republic of Korea.
  • Hur M; Department of Herbal Crop Research, National Institute of Horticultural & Herbal Science, RDA, Eumsung, Republic of Korea.
  • Park WT; Department of Herbal Crop Research, National Institute of Horticultural & Herbal Science, RDA, Eumsung, Republic of Korea.
  • Moon YH; Department of Herbal Crop Research, National Institute of Horticultural & Herbal Science, RDA, Eumsung, Republic of Korea.
  • Huh YC; Department of Herbal Crop Research, National Institute of Horticultural & Herbal Science, RDA, Eumsung, Republic of Korea.
  • Kim TI; Department of Herbal Crop Research, National Institute of Horticultural & Herbal Science, RDA, Eumsung, Republic of Korea.
  • Kang MH; Department of Herbal Crop Research, National Institute of Horticultural & Herbal Science, RDA, Eumsung, Republic of Korea.
  • Kang JS; College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.
  • Cho CW; College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.
  • Park J; Division of Biological Science and Technology, Yonsei University, Wonju, Republic of Korea.
J Enzyme Inhib Med Chem ; 38(1): 2242704, 2023 Dec.
Article en En | MEDLINE | ID: mdl-37537881
ABSTRACT
Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). 3CLpro is a key enzyme in coronavirus proliferation and a treatment target for COVID-19. In vitro and in silico, compounds 1-3 from Glycyrrhiza uralensis had inhibitory activity and binding affinity for 3CLpro. These compounds decreased HCoV-OC43 cytotoxicity in RD cells. Moreover, they inhibited viral growth by reducing the amounts of the necessary proteins (M, N, and RDRP). Therefore, compounds 1-3 are inhibitors of 3CLpro and HCoV-OC43 proliferation.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Coronavirus Humano OC43 / Glycyrrhiza uralensis / Proteasas 3C de Coronavirus Idioma: En Revista: J Enzyme Inhib Med Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Coronavirus Humano OC43 / Glycyrrhiza uralensis / Proteasas 3C de Coronavirus Idioma: En Revista: J Enzyme Inhib Med Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2023 Tipo del documento: Article