7MBO
FACTOR XIA (PICHIA PASTORIS; C500S [C122S]) IN COMPLEX WITH THE INHIBITOR Milvexian (BMS-986177), IUPAC NAME:(6R,10S)-10-{4-[5-chloro-2-(4-chloro-1H-1,2,3-triazol-1-yl)phenyl]-6- oxopyrimidin-1(6H)-yl}-1-(difluoromethyl)-6-methyl-1,4,7,8,9,10-hexahydro-15,11- (metheno)pyrazolo[4,3-b][1,7]diazacyclotetradecin-5(6H)-one
7MBO の概要
| エントリーDOI | 10.2210/pdb7mbo/pdb |
| 分子名称 | Coagulation factor XIa light chain, 2-acetamido-2-deoxy-beta-D-glucopyranose, Milvexian, ... (4 entities in total) |
| 機能のキーワード | hydrolase, serine protease, coagulation factor, syntethic inhibitor, blood, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
| 由来する生物種 | Homo sapiens (Human) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 27704.15 |
| 構造登録者 | |
| 主引用文献 | Dilger, A.K.,Pabbisetty, K.B.,Corte, J.R.,De Lucca, I.,Fang, T.,Yang, W.,Pinto, D.J.P.,Wang, Y.,Zhu, Y.,Mathur, A.,Li, J.,Hou, X.,Smith, D.,Sun, D.,Zhang, H.,Krishnananthan, S.,Wu, D.R.,Myers Jr., J.E.,Sheriff, S.,Rossi, K.A.,Chacko, S.,Zheng, J.J.,Galella, M.A.,Ziemba, T.,Dierks, E.A.,Bozarth, J.M.,Wu, Y.,Crain, E.,Wong, P.C.,Luettgen, J.M.,Wexler, R.R.,Ewing, W.R. Discovery of Milvexian, a High-Affinity, Orally Bioavailable Inhibitor of Factor XIa in Clinical Studies for Antithrombotic Therapy. J.Med.Chem., 65:1770-1785, 2022 Cited by PubMed Abstract: Factor XIa (FXIa) is an enzyme in the coagulation cascade thought to amplify thrombin generation but has a limited role in hemostasis. From preclinical models and human genetics, an inhibitor of FXIa has the potential to be an antithrombotic agent with superior efficacy and safety. Reversible and irreversible inhibitors of FXIa have demonstrated excellent antithrombotic efficacy without increased bleeding time in animal models (Weitz, J. I., Chan, N. C. 2019, 39 (1), 7-12). Herein, we report the discovery of a novel series of macrocyclic FXIa inhibitors containing a pyrazole P2' moiety. Optimization of the series for (pharmacokinetic) PK properties, free fraction, and solubility resulted in the identification of (, , FXIa = 0.11 nM) as a clinical candidate for the prevention and treatment of thromboembolic disorders, suitable for oral administration. PubMed: 34494428DOI: 10.1021/acs.jmedchem.1c00613 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (0.924 Å) |
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