Stereoselectivity of In Vivo Processes and Bioactivity of Farrerol Enantiomers

Farrerol, a bioactive compound found in Folium Rhododendri daurici, demonstrates various biological and pharmacological effects. Nevertheless, the stereoselectivity of in vivo processes and bioactivity between its enantiomers have not been thoroughly investigated. This study aimed to explore the ste...

Full description

Saved in:
Bibliographic Details
Main Authors: Lirong Chen, Tang Yan, Dongting Huang, Wei Xu, Yongjing Liu, Xiaoying Wang, Hua Li
Format: Article
Language:English
Published: MDPI AG 2025-05-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/30/9/2038
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849312727548297216
author Lirong Chen
Tang Yan
Dongting Huang
Wei Xu
Yongjing Liu
Xiaoying Wang
Hua Li
author_facet Lirong Chen
Tang Yan
Dongting Huang
Wei Xu
Yongjing Liu
Xiaoying Wang
Hua Li
author_sort Lirong Chen
collection DOAJ
description Farrerol, a bioactive compound found in Folium Rhododendri daurici, demonstrates various biological and pharmacological effects. Nevertheless, the stereoselectivity of in vivo processes and bioactivity between its enantiomers have not been thoroughly investigated. This study aimed to explore the stereoselectivity and pharmacological activity variations in farrerol enantiomers, focusing on stereoselective pharmacokinetics, tissue distribution, in vitro metabolism using liver microsomes, in vivo intestinal absorption, molecular simulations of binding affinity with antiproliferative target, and cell viability assessed through the CCK-8 assay. The findings indicated that the pharmacokinetic characteristics of farrerol in rats’ plasma, liver, and kidney tissues displayed enantioselectivity after intragastric administration. Then, no chiral transformation between farrerol enantiomers was observed in the rat plasma when (+)-farrerol and (−)-farrerol were orally administered. Additionally, there are notable stereoselective differences in the inhibition of CYP 1A2, CYP 2C9, CYP 2C19, and CYP 3A4/5 enzymes by (+)-farrerol and (−)-farrerol (<i>p</i> < 0.01). These differences may contribute to the stereoselectivity observed in the hepatic metabolism of the two enantiomers of farrerol. In addition, there were selective differences in the binding of farrerol enantiomers to anti-proliferative targets, including UCHL3, STAT3β, PTP1B, and GSK3β. Farrerol enantiomers exhibited similar growth inhibitory effects in HT-29 cell. Overall, our work will provide a solid theoretical basis and experimental reference for the further development and utilization of farrerol enantiomers.
format Article
id doaj-art-a0e684ddbf604332a3846b46d630ffa2
institution Kabale University
issn 1420-3049
language English
publishDate 2025-05-01
publisher MDPI AG
record_format Article
series Molecules
spelling doaj-art-a0e684ddbf604332a3846b46d630ffa22025-08-20T03:52:57ZengMDPI AGMolecules1420-30492025-05-01309203810.3390/molecules30092038Stereoselectivity of In Vivo Processes and Bioactivity of Farrerol EnantiomersLirong Chen0Tang Yan1Dongting Huang2Wei Xu3Yongjing Liu4Xiaoying Wang5Hua Li6Institute of Structural Pharmacology & TCM Chemical Biology, College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaInstitute of Structural Pharmacology & TCM Chemical Biology, College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaInstitute of Structural Pharmacology & TCM Chemical Biology, College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaInstitute of Structural Pharmacology & TCM Chemical Biology, College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaInstitute of Structural Pharmacology & TCM Chemical Biology, College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaInstitute of Structural Pharmacology & TCM Chemical Biology, College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaInstitute of Structural Pharmacology & TCM Chemical Biology, College of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, ChinaFarrerol, a bioactive compound found in Folium Rhododendri daurici, demonstrates various biological and pharmacological effects. Nevertheless, the stereoselectivity of in vivo processes and bioactivity between its enantiomers have not been thoroughly investigated. This study aimed to explore the stereoselectivity and pharmacological activity variations in farrerol enantiomers, focusing on stereoselective pharmacokinetics, tissue distribution, in vitro metabolism using liver microsomes, in vivo intestinal absorption, molecular simulations of binding affinity with antiproliferative target, and cell viability assessed through the CCK-8 assay. The findings indicated that the pharmacokinetic characteristics of farrerol in rats’ plasma, liver, and kidney tissues displayed enantioselectivity after intragastric administration. Then, no chiral transformation between farrerol enantiomers was observed in the rat plasma when (+)-farrerol and (−)-farrerol were orally administered. Additionally, there are notable stereoselective differences in the inhibition of CYP 1A2, CYP 2C9, CYP 2C19, and CYP 3A4/5 enzymes by (+)-farrerol and (−)-farrerol (<i>p</i> < 0.01). These differences may contribute to the stereoselectivity observed in the hepatic metabolism of the two enantiomers of farrerol. In addition, there were selective differences in the binding of farrerol enantiomers to anti-proliferative targets, including UCHL3, STAT3β, PTP1B, and GSK3β. Farrerol enantiomers exhibited similar growth inhibitory effects in HT-29 cell. Overall, our work will provide a solid theoretical basis and experimental reference for the further development and utilization of farrerol enantiomers.https://www.mdpi.com/1420-3049/30/9/2038farrerol enantiomersstereoselectivein vivo processesantiproliferative targetHT-29 cell
spellingShingle Lirong Chen
Tang Yan
Dongting Huang
Wei Xu
Yongjing Liu
Xiaoying Wang
Hua Li
Stereoselectivity of In Vivo Processes and Bioactivity of Farrerol Enantiomers
Molecules
farrerol enantiomers
stereoselective
in vivo processes
antiproliferative target
HT-29 cell
title Stereoselectivity of In Vivo Processes and Bioactivity of Farrerol Enantiomers
title_full Stereoselectivity of In Vivo Processes and Bioactivity of Farrerol Enantiomers
title_fullStr Stereoselectivity of In Vivo Processes and Bioactivity of Farrerol Enantiomers
title_full_unstemmed Stereoselectivity of In Vivo Processes and Bioactivity of Farrerol Enantiomers
title_short Stereoselectivity of In Vivo Processes and Bioactivity of Farrerol Enantiomers
title_sort stereoselectivity of in vivo processes and bioactivity of farrerol enantiomers
topic farrerol enantiomers
stereoselective
in vivo processes
antiproliferative target
HT-29 cell
url https://www.mdpi.com/1420-3049/30/9/2038
work_keys_str_mv AT lirongchen stereoselectivityofinvivoprocessesandbioactivityoffarrerolenantiomers
AT tangyan stereoselectivityofinvivoprocessesandbioactivityoffarrerolenantiomers
AT dongtinghuang stereoselectivityofinvivoprocessesandbioactivityoffarrerolenantiomers
AT weixu stereoselectivityofinvivoprocessesandbioactivityoffarrerolenantiomers
AT yongjingliu stereoselectivityofinvivoprocessesandbioactivityoffarrerolenantiomers
AT xiaoyingwang stereoselectivityofinvivoprocessesandbioactivityoffarrerolenantiomers
AT huali stereoselectivityofinvivoprocessesandbioactivityoffarrerolenantiomers