ProTox: a web server for the in silico prediction of rodent oral toxicity

被引:472
作者
Drwal, Malgorzata N. [1 ]
Banerjee, Priyanka [1 ,2 ]
Dunkel, Mathias [1 ]
Wettig, Martin R. [1 ]
Preissner, Robert [1 ,3 ]
机构
[1] Charite, Inst Physiol, Struct Bioinformat Grp, D-13125 Berlin, Germany
[2] Humboldt Univ, Grad Sch Computat Syst Biol, D-10115 Berlin, Germany
[3] German Canc Consortium DKTK, D-69120 Heidelberg, Germany
关键词
COMPREHENSIVE DATABASE; DRUG; PHARMACOLOGY; SUPERTARGET;
D O I
10.1093/nar/gku401
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Animal trials are currently the major method for determining the possible toxic effects of drug candidates and cosmetics. In silico prediction methods represent an alternative approach and aim to rationalize the preclinical drug development, thus enabling the reduction of the associated time, costs and animal experiments. Here, we present ProTox, a web server for the prediction of rodent oral toxicity. The prediction method is based on the analysis of the similarity of compounds with known median lethal doses (LD50) and incorporates the identification of toxic fragments, therefore representing a novel approach in toxicity prediction. In addition, the web server includes an indication of possible toxicity targets which is based on an in-house collection of protein-ligand-based pharmacophore models ('toxicophores') for targets associated with adverse drug reactions. The ProTox web server is open to all users and can be accessed without registration at: http://tox.charite.de/tox. The only requirement for the prediction is the two-dimensional structure of the input compounds. All ProTox methods have been evaluated based on a diverse external validation set and displayed strong performance (sensitivity, specificity and precision of 76, 95 and 75%, respectively) and superiority over other toxicity prediction tools, indicating their possible applicability for other compound classes.
引用
收藏
页码:W53 / W58
页数:6
相关论文
共 29 条
[1]
FragmentStore-a comprehensive database of fragments linking metabolites, toxic molecules and drugs [J].
Ahmed, Jessica ;
Worth, Catherine L. ;
Thaben, Paul ;
Matzig, Christian ;
Blasse, Corinna ;
Dunkel, Mathias ;
Preissner, Robert .
NUCLEIC ACIDS RESEARCH, 2011, 39 :D1049-D1054
[2]
[Anonymous], 2011, Analysis of Existing Environmental Footprint Methodologies for Products and Organizations: Recommendations, Rationale, and Alignment, P1
[3]
Azzaoui K, 2007, CHEMMEDCHEM, V2, P874, DOI 10.1002/cmdc.200700036
[4]
Analysis of pharmacology data and the prediction of adverse drug reactions and off-target effects from chemical structure [J].
Bender, Andreas ;
Scheiber, Josef ;
Glick, Meir ;
Davies, John W. ;
Azzaoui, Kamal ;
Hamon, Jacques ;
Urban, Laszlo ;
Whitebread, Steven ;
Jenkins, Jeremy L. .
CHEMMEDCHEM, 2007, 2 (06) :861-873
[5]
The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[6]
DecoyFinder: an easy-to-use python']python GUI application for building target-specific decoy sets [J].
Cereto-Massague, Adria ;
Guasch, Laura ;
Valls, Cristina ;
Mulero, Miquel ;
Pujadas, Gerard ;
Garcia-Vallve, Santiago .
BIOINFORMATICS, 2012, 28 (12) :1661-1662
[7]
admetSAR: A Comprehensive Source and Free Tool for Assessment of Chemical ADMET Properties [J].
Cheng, Feixiong ;
Li, Weihua ;
Zhou, Yadi ;
Shen, Jie ;
Wu, Zengrui ;
Liu, Guixia ;
Lee, Philip W. ;
Tang, Yun .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2012, 52 (11) :3099-3105
[8]
SuperTarget and Matador:: resources for exploring drug-target relationships [J].
Guenther, Stefan ;
Kuhn, Michael ;
Dunkel, Mathias ;
Campillos, Monica ;
Senger, Christian ;
Petsalaki, Evangelia ;
Ahmed, Jessica ;
Urdiales, Eduardo Garcia ;
Gewiess, Andreas ;
Jensen, Lars Juhl ;
Schneider, Reinhard ;
Skoblo, Roman ;
Russell, Robert B. ;
Bourne, Philip E. ;
Bork, Peer ;
Preissner, Robert .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D919-D922
[9]
SuperTarget goes quantitative: update on drug-target interactions [J].
Hecker, Nikolai ;
Ahmed, Jessica ;
von Eichborn, Joachim ;
Dunkel, Mathias ;
Macha, Karel ;
Eckert, Andreas ;
Gilson, Michael K. ;
Bourne, Philip E. ;
Preissner, Robert .
NUCLEIC ACIDS RESEARCH, 2012, 40 (D1) :D1113-D1117
[10]
Performance Evaluation of 2D Fingerprint and 3D Shape Similarity Methods in Virtual Screening [J].
Hu, Guoping ;
Kuang, Guanglin ;
Xiao, Wen ;
Li, Weihua ;
Liu, Guixia ;
Tang, Yun .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2012, 52 (05) :1103-1113