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Predicting antimicrobial activities of benzimidazole derivatives

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Abstract

A data set of 31 benzimidazole derivatives with antibacterial activities against gram-positive (e.g. Staphylococcus aureus, methicillin-resistant S. aureus (MRSA) and Bacillus subtilis) and gram-negative (e.g. Escherichai coli) bacteria as well as antifungal (e.g. Candida albicans) activity were used for quantitative structure–activity relationship (QSAR) study. Compounds were characterized by quantum chemical descriptors calculated at B3LYP/6-31G(d) level and molecular descriptors generated using Dragon software. The QSAR model was constructed using multiple linear regression method and sampled by leave-one-out cross-validation and the predictive performance can be deduced from the correlation coefficient (r), which was in the range of 0.4194–0.8485 while root mean square error (RMSE) was in the range of 0.039–0.3247. Particularly, QSAR model against S. aureus, MRSA (clinical isolates) and E. coli provided good predictive ability with r values of 0.8485, 0.8443 and 0.833, respectively, and RMSE values of 0.2662, 0.2488 and 0.039, respectively. The QSAR models demonstrated high potential for the rational design of novel benzimidazole derivatives with potent antimicrobial activities.

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References

  • Achar KC, Hosamani KM, Seetharamareddy HR (2010) In-vivo analgesic and anti-inflammatory activities of newly synthesized benzimidazole derivatives. Eur J Med Chem 45:2048–2054

    Article  CAS  PubMed  Google Scholar 

  • Becker K, Hu Y, Biller-Andorno N (2006) Infectious diseases–a global challenge. Int J Med Microbiol 296:179–185

    Article  PubMed  Google Scholar 

  • Chen JC, Qian L, Shen Y, Zheng KC (2008) A QSAR study and molecular design of benzothiazole derivatives as potent anticancer agents. Sci China Ser B-Chem 58:111–119

    Article  Google Scholar 

  • Chinedum IE (2005) Microbial resistance to antibiotics. Afr J Biotechnol 4:1606–1611

    CAS  Google Scholar 

  • de Melo EB (2010) Multivariate SAR/QSAR of 3-aryl-4-hydroxyquinolin-2(1H)-one derivatives as type I fatty acid synthase (FAS) inhibitors. Eur J Med Chem 45:5817–5826

    Article  PubMed  Google Scholar 

  • de Melo EB, Ferreira MM (2009) Multivariate QSAR study of 4,5-dihydroxypyrimidine carboxamides as HIV-1 integrase inhibitors. Eur J Med Chem 44:3577–3583

    Article  PubMed  Google Scholar 

  • Dennington II R, Keith T. Millam J. Eppinnett K, Hovell WL, Gilliland R (2003) GaussView,Version 3.09; Semichem, Inc., Shawnee Mission

  • Eicher T, Hauptmann S, Speicher A (2004) The chemistry of heterocycles: structure, reactions, syntheses, and applications. Wiley-VCH GmbH & Co. KGaA, Germany

    Google Scholar 

  • El-masry AH, Fahmy HH, Ali Abdelwahed SH (2000) Synthesis and antimicrobial activity of some new benzimidazole derivatives. Molecules 5:1429–1438

    Article  CAS  Google Scholar 

  • Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR, Scalmani G, Barone V, Mennucci B, Petersson GA, Nakatsuji H, Caricato M, Li X, Hratchian HP, Izmaylov AF, Bloino J, Zheng G, Sonnenberg JL, Hada M, Ehara M, Toyota K, Fukuda R, Hasegawa J, Ishida M, Nakajima T, Honda Y, Kitao O, Nakai H, Vreven T, Montgomery JA, Peralta JE, Ogliaro F, Bearpark M, Heyd JJ, Brothers E, Kudin KN, Staroverov VN, Kobayashi R, Normand J, Raghavachari K, Rendell A, Burant JC, Iyengar SS, Tomasi J, Cossi M, Rega N, Millam JM, Klene M, Knox JE, Cross JB, Bakken V, Adamo C, Jaramillo J, Gomperts R, Stratmann RE, Yazyev O, Austin AJ, Cammi R, Pomelli C, Ochterski JW, Martin RL, Morokuma K, Zakrzewski VG, Voth GA, Salvador P, Dannenberg JJ, Dapprich S, Daniels AD, Farkas Ö, Foresman JB, Ortiz JV, Cioslowski J, Fox DJ (2009) Gaussian 09, Revision A.1. Wallingford, Connecticut

  • Isarankura-Na-Ayudhya C, Nantasenamat C, Buraparuangsang P, Piacham T, Ye L, Bülow L, Prachayasittikul V (2008) Computational insights on sulfonamide imprinted polymers. Molecules 13:3077–3091

    Article  CAS  PubMed  Google Scholar 

  • Kalidhar U, Kaur A (2011) An Overview on some benzimidazole and sulfonamide derivatives with anti-microbial activity. Res J Pharm Biol Chem Sci 2:1116–1135

    CAS  Google Scholar 

  • Karelson M, Lobanov VS, Katritzky AR (1996) Quantum-chemical descriptors in QSAR/QSPR studies. Chem Rev 96:1027–1044

    Article  CAS  PubMed  Google Scholar 

  • Kuş C, Sözüdönmez F, Can-Eke B, Coban T (2010) Antioxidant and antifungal properties of benzimidazole derivatives. Z Naturforsch C 65:537–542

    PubMed  Google Scholar 

  • Low Y, Uehara T, Minowa Y, Yamada H, Ohno Y, Urushidani T, Sedykh A, Muratov E, Kuz’min V, Fourches D, Zhu H, Rusyn I, Tropsha A (2011) Predicting drug-induced hepatotoxicity using QSAR and toxicogenomics approaches. Chem Res Toxicol 24:1251–1262

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Nantasenamat C, Naenna T, Isarankura Na-Ayudhya C, Prachayasittikul V (2005) Quantitative prediction of imprinting factor of molecularly imprinted polymers by artificial neural network. J Comput Aided Mol Des 19:509–524

    Article  CAS  PubMed  Google Scholar 

  • Nantasenamat C, Tantimongcolwat T, Naenna T, Isarankura Na-Ayudhya C, Prachayasittikul (2006) Prediciton of selectivity index of pentachlorophenol-imprinted polymers. EXCLI J 5:150–163

    Google Scholar 

  • Nantasenamat C, Isarankura-Na-Ayudhya C, Naenna T, Prachayasittikul V (2007a) Quantitative structure-imprinting factor relationship of molecularly imprinted polymers. Biosens Bioelectron 22:3309–3317

    Article  CAS  PubMed  Google Scholar 

  • Nantasenamat C, Isarankura-Na-Ayudhya C, Tansila N, Naenna T, Prachayasittikul V (2007b) Prediction of GFP spectral properties using artificial neural network. J Comput Chem 28:1275–1289

    Article  CAS  PubMed  Google Scholar 

  • Nantasenamat C, Isarankura-Na-Ayudhya C, Naenna T, Prachayasittikul V (2008a) Prediction of bond dissociation enthalpy of antioxidant phenols by support vector machine. J Mol Graph Model 27:188–196

    Article  CAS  PubMed  Google Scholar 

  • Nantasenamat C, Piacham T, Tantimongcolwat T, Naenna T, Isarankura-Na-Ayudhya C, Prachayasittikul V (2008b) QSAR model of the quorum-quenching N-acyl-homoserine lactone lactonase activity. J Biol Syst 16:279–293

    Article  CAS  Google Scholar 

  • Nantasenamat C, Isarankura-Na-Ayudhya C, Naenna T, Prachayasittikul V (2009) A practical overview of quantitative structure-activity relationship. EXCLI J 8:74–88

    Google Scholar 

  • Nantasenamat C, Isarankura-Na-Ayudhya C, Prachayasittikul V (2010) Advances in computational methods to predict the biological activity of compounds. Exp Opin Drug Discov 5:633–654

    Article  CAS  Google Scholar 

  • Nantasenamat C, Srungboonmee K, Jamsak S, Tansila N, Isarankura-Na-Ayudhya C, Prachayasittikul V (2013) Quantitative structure-property relationship study of spectral properties of green fluorescent protein with support vector machine. Chemometr Intell Lab Syst 120:42–52

    Article  CAS  Google Scholar 

  • Novotarskyi S, Sushko I, Körner R, Pandey AK, Tetko IV (2011) A comparison of different QSAR approaches to modeling CYP450 1A2 inhibition. J Chem Inf Model 51:1271–1280

    Article  CAS  PubMed  Google Scholar 

  • Nowaczyk A, Kulig K (2012) QSAR studies on a number of pyrrolidin-2-one antiarrhythmic arylpiperazinyls. Med Chem Res 21:373–381

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Ozkay Y, Tunalı Y, Karaca H, Işıkdağ I (2011) Antimicrobial activity of a new series of benzimidazole derivatives. Arch Pharm Res 34:1427–1435

    Article  PubMed  Google Scholar 

  • Parr RG, Pearson RG (1983) Absolute hardness: companion parameter to absolute electronegativity. J Am Chem Soc 105:7512–7516

    Article  CAS  Google Scholar 

  • Parr RG, Donnelly RA, Levy M, Palke WE (1978) Electronegativity: the density functional viewpoint. J Chem Phys 68:3801–3807

    Article  CAS  Google Scholar 

  • Parr RG, Szentpaly Lv, Liu S (1999) Electrophilicity index. J Am Chem Soc 121:1922–1924

    Article  CAS  Google Scholar 

  • Pasquale G, Romanelli GP, Autino JC, García J, Ortiz EV, Duchowicz PR (2012) Quantitative structure-activity relationships of mosquito larvicidal chalcone derivatives. J Agric Food Chem 60:692–697

    Article  CAS  PubMed  Google Scholar 

  • Patel JR, Prajapati LM (2012) Predictive QSAR modeling on tetrahydropyrimidine-2-one derivatives as HIV-1 protease enzyme inhibitors. Med Chem Res. doi:10.1007/s00044-012-0275-8

  • Patil A, Ganguly S, Surana S (2008) A systematic review of benzimidazole derivatives as an antiulcer agent. Rasayan J Chem 3:447–460

    Google Scholar 

  • Piacham T, Isarankura-Na-Ayudhya C, Nantasenamat C, Yainoy S, Ye L, Bülow L, Prachayasittikul V (2006) Metalloantibiotic Mn(II)-bacitracin complex mimicking manganese superoxide dismutase. Biochem Biophys Res Commun 341:925–930

    Article  CAS  PubMed  Google Scholar 

  • Piacham T, Nantasenamat C, Suksrichavalit T, Puttipanyalears C, Pissawong T, Maneewas S, Isarankura-Na-Ayudhya C, Prachayasittikul V (2009) Synthesis and theoretical study of molecularly imprinted nanospheres for recognition of tocopherols. Molecules 14:2985–3002

    Article  CAS  PubMed  Google Scholar 

  • Plata K, Rosato AE, Wegrzyn G (2009) Staphylococcus aureus as an infectious agent: overview of biochemistry and molecular genetics of its pathogenicity. Acta Biochim Pol 56:597–612

    CAS  PubMed  Google Scholar 

  • Podunavac-Kuzmanovic SO, Cvetkovic DD (2011) QSAR modeling of antibacterial activity of some benzimidazole derivatives. Chem Ind Chem Eng Q 17:33–38

    Article  CAS  Google Scholar 

  • Prachayasittikul V, Isarankura-Na-Ayudhya C, Tantimongcolwat T, Nantasenamat C, Galla HJ (2007) EDTA-induced membrane fluidization and destabilization: biophysical studies on artificial lipid membranes. Acta Biochim Biophys Sin 39:901–913

    Article  PubMed  Google Scholar 

  • Prachayasittikul S, Wongsawatkul O, Worachartcheewan A, Nantasenamat C, Ruchirawat S, Prachayasittikul V (2010) Elucidating the structure-activity relationships of the vasorelaxation and antioxidation properties of thionicotinic acid derivatives. Molecules 15:198–214

    Article  CAS  PubMed  Google Scholar 

  • Refaat HM (2010) Synthesis and anticancer activity of some novel 2-substituted benzimidazole derivatives. Eur J Med Chem 45:2949–2956

    Article  CAS  PubMed  Google Scholar 

  • Saghaie L, Sakhi H, Hassan Sabzyan H, Shahlaei M, Shamshirian D (2012) Stepwise MLR and PCR QSAR study of the pharmaceutical activities of antimalarial 3-hydroxypyridinone agents using B3LYP/6-311++G** descriptors. Med Chem Res. doi:10.1007/s00044-012-0152-5

  • Sharma MC, Kohli DV, Sahu NK, Sharma S, Chaturvedi SC (2009) 2D-QSAR studies of some 1,3,4-thidiazole-2yl azetidine 2-one as antimicrobial activity. Dig J Nanomater Bios 4:339–347

    Google Scholar 

  • Suksrichavalit T, Prachayasittikul S, Piacham T, Isarankura-Na-Ayudhya C, Nantasenamat C, Prachayasittikul V (2008) Copper complexes of nicotinic-aromatic carboxylic acids as superoxide dismutase mimetics. Molecules 13:3040–3056

    Article  CAS  PubMed  Google Scholar 

  • Suksrichavalit T, Prachayasittikul S, Nantasenamat C, Isarankura-Na-Ayudhya C, Prachayasittikul V (2009) Copper complexes of pyridine derivatives with superoxide scavenging and antimicrobial activities. Eur J Med Chem 44:3259–3265

    Article  CAS  PubMed  Google Scholar 

  • Thanikaivelan P, Subramanian V, Raghava Rao J, Unni Nair B (2000) Application of quantum chemical descriptor in quantitative structure activity and structure property relationship. Chem Phys Lett 323:59–70

    Article  CAS  Google Scholar 

  • Thippakorn C, Suksrichavalit T, Nantasenamat C, Tantimongcolwat T, Isarankura-Na-Ayudhya C, Naenna T, Prachayasittikul V (2009) Modeling the LPS neutralization activity of anti-endotoxins. Molecules 14:1869–1888

    Article  CAS  PubMed  Google Scholar 

  • Tuncbilek M, Kiper T, Altanlar N (2009) Synthesis and in vitro antimicrobial activity of some novel substituted benzimidazole derivatives having potent activity against MRSA. Eur J Med Chem 44:1024–1033

    Article  CAS  PubMed  Google Scholar 

  • Vasanthanathan P, Taboureau O, Oostenbrink C, Vermeulen NP, Olsen L, Jørgensen FS (2009) Classification of cytochrome P450 1A2 inhibitors and noninhibitors by machine learning techniques. Drug Metab Dispos 37:658–664

    Article  CAS  PubMed  Google Scholar 

  • Walia R, Hedaitullah Md, Naaz SF, Iqbal K, Lamba HS (2011) Benzimidazole derivatives-an overview. IJRPC 1:565–574

    CAS  Google Scholar 

  • Whitley DC, Ford MG, Livingstone DJ (2000) Unsupervised forward selection: a method for eliminating redundant variables. J Chem Inf Comput Sci 40:1160–1168

    Article  CAS  PubMed  Google Scholar 

  • Witten IH, Frank E, Hall MA (2011) Data mining: practical machine learning tools and techniques, 3rd edn. Morgan Kaufmann, San Francisco

    Google Scholar 

  • Worachartcheewan A, Nantasenamat C, Naenna T, Isarankura-Na-Ayudhya C, Prachayasittikul V (2009) Modeling the activity of furin inhibitors using artificial neural network. Eur J Med Chem 44:1664–1673

    Article  CAS  PubMed  Google Scholar 

  • Worachartcheewan A, Prachayasittikul S, Pingaew R, Nantasenamat C, Tantimongcolwat T, Ruchirawat S, Prachayasittikul V (2011a) Antioxidant, cytotoxicity, and QSAR study of 1-adamantylthio derivatives of 3-picoline and phenylpyridines. Med Chem Res 21:3514–3522

    Article  Google Scholar 

  • Worachartcheewan A, Nantasenamat C, Isarankura-Na-Ayudhya C, Prachayasittikul S, Prachayasittikul V (2011b) Predicting the free radical scavenging activity of curcumin derivatives. Chemometr Intell Lab Syst 109:207–216

    Article  CAS  Google Scholar 

  • Zetola N, Francis JS, Nuermberger EL, Bishai WR (2005) Community-acquired meticillin-resistant Staphylococcus aureus: an emerging threat. Lancet Infect Dis 5:275–286

    Article  PubMed  Google Scholar 

  • Zhang L, Zhu H, Oprea TI, Golbraikh A, Tropsha A (2008) QSAR modeling of the blood-brain barrier permeability for diverse organic compounds. Pharm Res 25:1902–1914

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This research project is supported by Office of the Higher Education Commission and Mahidol University under the National Research Universities Initiative.

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Correspondence to Chanin Nantasenamat or Virapong Prachayasittikul.

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Worachartcheewan, A., Nantasenamat, C., Isarankura-Na-Ayudhya, C. et al. Predicting antimicrobial activities of benzimidazole derivatives. Med Chem Res 22, 5418–5430 (2013). https://doi.org/10.1007/s00044-013-0539-y

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