Medicinal Chemistry Research, Journal Year: 2022, Volume and Issue: 31(6), P. 905 - 915
Published: April 19, 2022
Language: Английский
Medicinal Chemistry Research, Journal Year: 2022, Volume and Issue: 31(6), P. 905 - 915
Published: April 19, 2022
Language: Английский
Journal of Separation Science, Journal Year: 2023, Volume and Issue: 46(20)
Published: Aug. 17, 2023
Enantiomeric separation of furanocoumarins and dihydroflavones compounds were systematically studied in the normal-phase mode using four different polysaccharide-type chiral stationary phases, namely, Chiralpak IA, IC, IG, IK-3 by high-performance liquid chromatography. The effect alcohol modifiers content on enantiomeric was evaluated for dihydroflavones. All eight have achieved baseline with resolutions ranging between 1.52 23.11. For a better insight into enantiorecognition mechanisms, thermodynamic analysis carried out. mechanisms recognition been discussed. Among columns, IG exhibited most universal best enantioseparation ability toward when used n-hexane-isopropanol n-hexane-ethanol as mobile phase, respectively. steric hindrance, hydrogen bonding, π-π interaction played major roles IG. By comparing this work analyzed methods first time reported some active ingredients traditional Chinese medicine that never separated, which provided further phases.
Language: Английский
Citations
2Analytical Methods, Journal Year: 2023, Volume and Issue: 15(46), P. 6444 - 6450
Published: Jan. 1, 2023
A efficient method for simultaneous separation of the C-2 diastereomers naringin, neohesperidin, hesperidin and narirutin was developed, used determination each epimer them in traditional Chinese medicine Zhiqiao Zhishi.
Language: Английский
Citations
2Catalysts, Journal Year: 2022, Volume and Issue: 12(10), P. 1157 - 1157
Published: Oct. 1, 2022
Bacterial cytochrome P450 (CYP) enzymes are versatile biocatalysts that responsible for the biotransformation of diverse endogenous substances. CYP105A5 from Streptomyces sp. showed substrate flexibility with different flavonoids and was able to catalyze O-demethylation biochanin A, regioselective C3′-hydroxylation daidzein, genistein, naringenin, additional C8-hydroxylation daidzein using heterologous redox partners putidaredoxin reductase. By rational design substrate-binding pocket based on experimental data, homology modeling, molecular docking analysis, we enhanced product formation rate flavonoids. The double mutant L100A/I302A L100A/I408N exhibited greatly in vivo conversion rates flavonoid hydroxylation. Particularly, mutant’s kcat/Km values increased by 1.68-fold 2.57-fold, respectively, naringenin. Overall, our result might facilitate potential use future modification application whole-cell production valuable polyphenols.
Language: Английский
Citations
3Toxicology Letters, Journal Year: 2024, Volume and Issue: 401, P. 44 - 54
Published: Sept. 13, 2024
Language: Английский
Citations
0Medicinal Chemistry Research, Journal Year: 2022, Volume and Issue: 31(6), P. 905 - 915
Published: April 19, 2022
Language: Английский
Citations
2