日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Comparison of the CYP3A Selective Inhibitors CYP3cide, Clobetasol, and Azamulin for Their Potential to Distinguish CYP3A7 Activity in the Presence of CYP3A4/5

比较 CYP3A 选择性抑制剂 CYP3cide、氯倍他索和 Azamulin 在 CYP3A4/5 存在下区分 CYP3A7 活性的潜力

Hannah M Work, Sylvie E Kandel, Jed N Lampe

HCV Antiviral Drugs Have the Potential to Adversely Perturb the Fetal-Maternal Communication Axis through Inhibition of CYP3A7 DHEA-S Oxidation

HCV 抗病毒药物可能会通过抑制 CYP3A7 DHEA-S 氧化而对胎儿-母体沟通轴造成不利影响

Hannah M Work, John C Hackett, Jed N Lampe

Per- and polyfluoroalkyl substances (PFAS) inhibit cytochrome P450 CYP3A7 through direct coordination to the heme iron and water displacement

全氟和多氟烷基物质 (PFAS) 通过直接协调血红素铁和水置换来抑制细胞色素 P450 CYP3A7

Michaela Hvizdak, Sylvie E Kandel, Hannah M Work, Emily G Gracey, Rebecca L McCullough, Jed N Lampe

Pseudomonas aeruginosa cytochrome P450 CYP168A1 is a fatty acid hydroxylase that metabolizes arachidonic acid to the vasodilator 19-HETE

铜绿假单胞菌细胞色素 P450 CYP168A1 是一种脂肪酸羟化酶,可将花生四烯酸代谢为血管扩张剂 19-HETE

Brian C Tooker, Sylvie E Kandel, Hannah M Work, Jed N Lampe

Characterization of fluorescent probe substrates to develop an efficient high-throughput assay for neonatal hepatic CYP3A7 inhibition screening

表征荧光探针底物以开发用于新生儿肝脏 CYP3A7 抑制筛选的高效高通量检测方法

Hannah M Work, Sylvie E Kandel, Jed N Lampe