Human cytochrome P450 enzymes 5–51 as targets of drugs and natural and environmental compounds: Mechanisms, induction, and inhibition–toxic effects and …

SP Rendic, F Peter Guengerich - Drug metabolism reviews, 2018 - Taylor & Francis
Abstract Cytochrome P450 (P450, CYP) enzymes have long been of interest due to their
roles in the metabolism of drugs, pesticides, pro-carcinogens, and other xenobiotic …

Validation of an MD simulation approach for electrical field responsive micelles and their application in drug delivery

L Razavi, H Raissi, F Farzad - Scientific Reports, 2023 - nature.com
In the current work, a new type of micelle is designed that has active connectivity in respond
to exterior stimulus and the desired water solubility. Two end-ornamented homopolymers …

The tamoxifen metabolite norendoxifen is a potent and selective inhibitor of aromatase (CYP19) and a potential lead compound for novel therapeutic agents

WJ Lu, C Xu, Z Pei, AS Mayhoub, M Cushman… - Breast cancer research …, 2012 - Springer
To improve the treatment of breast cancer, there has been a need for alternative aromatase
inhibitors (AIs) that bring about adequate aromatase inhibition, while limiting side effects …

Comprehensive and automated linear interaction energy based binding-affinity prediction for multifarious cytochrome P450 aromatase inhibitors

M van Dijk, AM Ter Laak, JD Wichard… - Journal of Chemical …, 2017 - ACS Publications
Cytochrome P450 aromatase (CYP19A1) plays a key role in the development of estrogen
dependent breast cancer, and aromatase inhibitors have been at the front line of treatment …

In silico study for prediction of novel bioactivities of the endophytic fungal alkaloid, mycoleptodiscin B for human targets

US Deshapriya, DLS Dinuka, PB Ratnaweera… - Journal of Molecular …, 2021 - Elsevier
Mycoleptodiscin B is a natural product extracted from the endophytic fungus
Mycoleptodiscus sp. found in Sri Lanka and Panama with experimentally unexplored …

[引用][C] 芳香化酶的结构, 催化机制及其抑制剂研究进展

付静, 沈中华, 程飞雄, 刘桂霞, 李卫华, 唐赟 - 药学学报, 2012