The metabolic stability of madecassoside in liver microsomes is good.
羟基积雪草苷在大鼠肝微粒体中的代谢稳定性很高。
Objective:To study activity of cytochrome P450 for human liver microsomes.
目的：为测定人肝细胞微粒体细胞色素P450氧化酶的活性。
They are synthesized from glycerol phosphate and fatty acyl CoAs, usually in the microsomes.
其合成多在微生物中进行，原料为磷酸甘油和脂肪酰辅酶a。
The metabolism of hainanensine derivative HH07A has been studied in vitro with rat microsomes.
用大鼠肝微粒体体外代谢法对HH07A进行了代谢转化研究。
Thus, a simple, economical, accurate and reliable method to separate and purify microsomes was established.
从而为滑面内质网及粗面内质网的分离和纯化建立了一种简单、经济、准确、可靠的方法。
At the end of perfusion, microsomes were prepared and analyzed for P450 activities and other metabolic markers.
灌注结束后，制备微粒体并进行P 450活性以及其他代谢指标的分析。
OBJECTIVE To establish a HPLC/MS method to determine microsomes activity in vitro using nifedipine as a probe drug.
目的建立以硝苯地平为探针药物测定大鼠和犬肝微粒体活性的HPLC/MS。
In conclusion, levofloxacin significantly inhibited metabolism of metoprolol in the cytochrome P450 of rat hepatic microsomes.
结论：左氧氟沙星可抑制大鼠肝微粒体细胞色素P 45 0系统对美托洛尔的代谢。
AIM: To study the bioequivalence and pharmacokinetics of doxycycline enteric-coated microsomes capsules and doxycycline tablets.
目的：研究多西环素肠溶微粒胶囊和多西环素片的人体生物等效性与药动学。
ConclusionThe metabolism of DBDCT in rat liver microsomes was faster, suggesting that the liver first-pass effect of the drug may be stronger.
结论DBDCT在大鼠肝微粒体中代谢较快，提示该药可能肝首过效应较强。
The in vitro biotransformation of 6 methoxy butyl phthalide (MBP) by phenobarbital induced rat liver microsomes was investigated by GC/MS and GC/MS with TMS derivatization.
报道了用GC／MS方法及衍生化技术研究6甲氧基正丁苯酞（MBP）在大鼠肝微粒体中的代谢转化结果。
The in vitro biotransformation of 6 methoxy butyl phthalide (MBP) by phenobarbital induced rat liver microsomes was investigated by GC/MS and GC/MS with TMS derivatization.
报道了用GC／MS方法及衍生化技术研究6甲氧基正丁苯酞（MBP）在大鼠肝微粒体中的代谢转化结果。
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