骨化三醇受体
分子力学
碎片分子轨道
化学
对接(动物)
分子模型
分子动力学
从头算
分子轨道
立体化学
计算化学
受体
生物化学
分子
有机化学
医学
护理部
作者
Shunya Nakamura,Ryosuke Saito,Shohei Yamamoto,Yuta Terauchi,Atsushi Kittaka,Midori Takimoto‐Kamimura,Noriyuki Kurita
标识
DOI:10.1016/j.bpc.2020.106540
摘要
The specific binding of active vitamin-D to the vitamin-D receptor (VDR) is closely related to the onset of immunological diseases. To inhibit the binding, various compounds have been developed as potent inhibitors against VDR. Among them, a compound NS-54c, which was developed based on the first VDR antagonist TEI-9647 (25-dehydro-1α-hydroxyvitamin D3-26,23-lactone), was revealed to posse almost 1000-fold improved antagonistic activity over the original TEI-9647. However, the reason for this significant improvement has not been elucidated. In the present study, we investigated the specific interactions between VDR and these inhibitors, using molecular simulations based on molecular docking, molecular mechanics and ab initio fragment molecular orbital calculations. Based on the results simulated, we furthermore proposed novel inhibitors and investigated their binding properties to VDR. The results elucidate that the replacement of propyl group at the 24th site of NS-54c by a phenethyl group can enhance the binding affinity of the inhibitor to VDR. This finding provides useful information for developing novel potent inhibitors against VDR.
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