<?xml version="1.0" encoding="UTF-8"?>
<records>
<record>
<language>eng</language>
<publisher>Science and Education Publishing</publisher>
<journalTitle>American Journal of Biomedical Research</journalTitle>
<eissn>2328-3955</eissn>
<publicationDate>2013-11-15</publicationDate>
<volume>1</volume>
<issue>4</issue>
<startPage>120</startPage>
<endPage>131</endPage>
<doi>10.12691/ajbr-1-4-8</doi>
<publisherRecordId>AJBR2013148</publisherRecordId>
<documentType>article</documentType>
<title language="eng">Combined Support-Vector-Machine-Based Virtual Screening and Docking Method for the Discovery of IMP-1 Metallo-β-Lactamase Inhibitors Supplementary Data</title>
<authors>
<author>
<name>Jiao Chen</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Yifang Liu</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Mi Fang</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Hui Chen</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Xingzhen Lao</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Xiangdong Gao</name>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Heng Zheng</name>
<email>zhengh18@hotmail.com, (W. Yao)</email>
<affiliationId>1</affiliationId>
</author>
<author>
<name>Wenbing Yao</name>
<email>zhengh18@hotmail.com, (W. Yao)</email>
<affiliationId>1</affiliationId>
</author>

</authors>
<affiliationsList>
<affiliationName affiliationId="1">School of Life Science and Technology, China Pharmaceutical University, Nanjing, P.R. China</affiliationName>







</affiliationsList>
<abstract language="eng">Metallo-¦-lactamases can hydrolyze a broad range of ¦-lactam antibiotics and no effective inhibitors could be used in the clinic. Therefore, the discovery of metallo-¦-lactamase inhibitors has attracted much attention in recent years. In this study, a support vector machine (SVM) that separates compounds into positives and negatives, combined with docking method was employed for virtual screening of IMP-1 metallo-¦-lactamase inhibitors. Eight of the twenty five selected compounds were purchased for in vitro assays. Among them, four compounds show inhibitory potency against IMP-1. Two of them are found to have novel scaffolds, implying a good potential for further optimization.</abstract>
<fullTextUrl format="pdf">http://pubs.sciepub.com/ajbr/1/4/8/ajbr-1-4-8.pdf</fullTextUrl>
<keywords language="eng">IMP-1 metallo-¦-lactamase inhibitorssupport vector machinedockingvirtual screeningin vitro assays</keywords>
</record>
</records>
