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- W2083144463 abstract "Aromatase is an enzyme that plays a critical role in the development of estrogen receptor positive breast cancer. As aromatase catalyzes the aromatization of androstenedione to estrone, a naturally occurring estrogen, it is a promising drug target for therapeutic management. The undesirable effects found in aromatase inhibitors (AIs) that are in clinical use necessitate the discovery of novel AIs with higher selectivity, less toxicity and improving potency. In this study, we elucidate the binding mode of all three generations of AI drugs to the crystal structure of aromatase by means of molecular docking. It was demonstrated that the docking protocol could reliably reproduce the interaction of aromatase with its substrate with an RMSD of 1.350 Å. The docking study revealed that polar (D309, T310, S478 and M374), aromatic (F134, F221 and W224) and non-polar (A306, A307, V370, L372 and L477) residues were important for interacting with the AIs. The insights gained from the study herein have great potential for the design of novel AIs." @default.
- W2083144463 created "2016-06-24" @default.
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- W2083144463 date "2011-04-28" @default.
- W2083144463 modified "2023-09-30" @default.
- W2083144463 title "Molecular Docking of Aromatase Inhibitors" @default.
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- W2083144463 doi "https://doi.org/10.3390/molecules16053597" @default.
- W2083144463 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6263336" @default.
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