Fluvastatin
From Proteopedia
Jump to navigationJump to search
| ||||||||||||
Pharmacokinetics
For References, See References |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
References
Better Known as: Lescol
Mechanism of ActionFluvastatin is an inhibitor of HMG-CoA Reductase (HMGR), a highly regulated enzyme responsible for the committed step in cholesterol synthesis.[1] Fluvastatin, like most of the statins, binds HMGR via a number of polar interactions with the "cis loop" of HMGR, particularly residues Ser 684, Asp 690, Lys 691, Lys 692, and hydrogen bond interactions between Glu 559 and Asp 767 with the O5-hydroxyl of the statins. Van der Waals interactions between Leu 562, Val 683, Leu 853, Ala 856, and Leu 857 of HMGR and hydrophobic ring structures of Fluvastatin contribute to binding as well.[2] These interactions help Fluvastatin outcompete HMG-CoA, the substrate of HMGR, in binding to HMGR.[3]
| ||||||||||||
For References, See References |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
This page was last modified 12:39, 10 January 2024.