生物信息学
生物化学
微粒体
酶
细胞色素P450
药物代谢
谷胱甘肽
胞浆
同工酶
葡萄糖醛酸转移酶
化学
生物
药理学
基因
作者
Shalenie P. den Braver-Sewradj,Michiel W. den Braver,Marc van Dijk,Yongjie Zhang,Stefan J. Dekker,Lukas S. Wijaya,Nico Vermeulen,Lysiane Richert,Jan N. M. Commandeur,J. Chris Vos
标识
DOI:10.2174/1389200219666180108160046
摘要
While hepatic NQO1 activity was highly variable, NQO2 activity was more conserved. In addition, we found that of the hepatic GST isoforms, the variation in GSTM3 levels, which is poorly studied, was highest. The majority of significant correlations were found amongst CYP and UGT enzyme activities. The dataset presented provides the absolute quantification of the largest number of hepatic DME activities so far and constitute an essential resource for in silico toxicokinetic and metabolic modelling studies.
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