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Identification and quantitative analysis of bioactive components from Potentilla kleiniana Wight et Arn with anti HIV-1 proteases activity.
Zhou, Yong Qiang; Li, Su Mei; Wei, Xin; Yang, Xin; Xiao, Jun Wei; Pan, Bo Wen; Xie, Shou Xia; Zhou, Ying; Yang, Jian; Wei, Ying.
  • Zhou YQ; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang, China.
  • Li SM; Department of Pharmacology, Shenzhen People's Hospital (The Second Clinical Medical College, Jinan University, The First Affiliated Hospital, Southern University of Science and Technology), Shenzhen, China.
  • Wei X; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang, China.
  • Yang X; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang, China.
  • Xiao JW; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang, China.
  • Pan BW; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang, China.
  • Xie SX; Department of Pharmacology, Shenzhen People's Hospital (The Second Clinical Medical College, Jinan University, The First Affiliated Hospital, Southern University of Science and Technology), Shenzhen, China.
  • Zhou Y; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang, China.
  • Yang J; College of Pharmacy and Nutrition, University of Saskatchewan, Saskatoon, Canada.
  • Wei Y; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang, China.
Nat Prod Res ; : 1-4, 2022 Dec 30.
Article in English | MEDLINE | ID: covidwho-20245396
ABSTRACT
Potentilla kleiniana Wight et Arn(PK, 'Wu Pi Feng' in Chinese) was recorded as Miao ethnic medicine for treatment of fever, cough, ulcer, and erysipelas for thousands years. This study aimed to evaluate the antiviral activity of four PK extracts and seven compounds by using HIV-1 protease (HIV-1 PR). In addition, Ultra-High Performance Liquid Chromatography and High Resolution Mass Spectrometry (UPLC-HRMS) was employed to identify the bioactive components. The toxicity assessment of the extracts was done before antiviral screening using a highly specific human aspartyl protease, renin protease by fluorimetric method. As a result, seven compounds and four extracts of PK inhibited HIV-1 PR with IC50 range from 0.009 to 0.36 mg/mL, and did not appreciably inhibit the general human protease renin. This study first demonstrated that four PK extracts, ellagic acid and ursolic acid potent inhibit HIV-1 protease, could be used as an efficacious drug candidate to treat SARS-CoV-2 infection.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Language: English Journal: Nat Prod Res Year: 2022 Document Type: Article Affiliation country: 14786419.2022.2162513

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Language: English Journal: Nat Prod Res Year: 2022 Document Type: Article Affiliation country: 14786419.2022.2162513