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The Clinical Candidate VT-1161 Is a Highly Potent Inhibitor of Candida albicans CYP51 but Fails To Bind the Human Enzyme

机译：临床候选人VT-1161是白色念珠菌CYp51的高效抑制剂，但未能结合人体酶

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Hull, Claire;
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年度 2014
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1. The clinical candidate VT-1161 is a highly potent inhibitor of candida albicans CYP51 but fails to bind the human enzyme [J] . WarrilowA.G.S., HullC.M., ParkerJ.E., Antimicrobial agents and chemotherapy. . 2014,第12期

机译：临床候选药物VT-1161是白色念珠菌CYP51的高效抑制剂，但无法结合人酵素
2. The Investigational Drug VT-1129 Is a Highly Potent Inhibitor of Cryptococcus Species CYP51 but Only Weakly Inhibits the Human Enzyme [J] . Warrilow Andrew G. S., Parker Josie E., Price Claire L., Antimicrobial agents and chemotherapy. . 2016,第8期

机译：调查药物VT-1129是一种高效的碱性CYP51抑制剂，但只有弱抑制人酶
3. The Investigational Drug VT-1129 Is a Highly Potent Inhibitor of Cryptococcus Species CYP51 but Only Weakly Inhibits the Human Enzyme [J] . Warrilow Andrew G. S., Parker Josie E., Price Claire L., Antimicrobial agents and chemotherapy. . 2016,第8期

机译：研究用药物VT-1129是隐球菌CYP51的强抑制剂，但仅弱抑制人的酶
4. EAP1, A CANDIDA ALBICANS ADHESION RECEPTOR THAT BINDS HUMAN CELLS AND IS INVOLVED IN BIOFILM FORMATION [C] . Fang Li, Amy J. Karlsson, Sean P. Palecek Adhesion Society Annual Meeting; 20050213-16; Mobile,AL(US) . 2005

机译：EAP1，一种结合人细胞并参与生物膜形成的加拿大念珠菌粘附受体
5. Characterization of a Human Immunodeficiency Virus (HIV) Type I Integrase Inhibitor-Binding Pocket and Discovery of Novel Inhibitors Potent against Drug-Resistant Variants of HIV [D] . Crosby, David Charles 2010

机译：人类免疫缺陷病毒（HIV）I型整合酶抑制剂结合口袋的表征和新型抗HIV药物耐药变体的抑制剂的发现
6. The Clinical Candidate VT-1161 Is a Highly Potent Inhibitor of Candida albicans CYP51 but Fails To Bind the Human Enzyme [O] . A. G. S. Warrilow, C. M. Hull, J. E. Parker, 2014

机译：临床候选者VT-1161是白色念珠菌CYP51的高效抑制剂但未能结合人的酶
7. The Clinical Candidate VT-1161 Is a Highly Potent Inhibitor of Candida albicans CYP51 but Fails To Bind the Human Enzyme [O] . Kelly, Steven 2014

机译：临床候选人VT-1161是白色念珠菌CYp51的高效抑制剂，但未能结合人体酶

The Clinical Candidate VT-1161 Is a Highly Potent Inhibitor of Candida albicans CYP51 but Fails To Bind the Human Enzyme

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