[1]
W.O. Foye, Principles of Medicinal Chemistry, 3rd edition, Bombay: Varghese Publishing House, (1989) p.240.
Google Scholar
[2]
S. Arora, and Saurabhvija, QSAR study on some newly synthesized pyrimido-benzimidazole derivatives as analgesic agents, Int. J. Pharm. Pharm. Sci. 3(5suppl), (2011) 457-461.
Google Scholar
[3]
USEPA (United States Environmental Protection Agency) T. E. S. T Tool, User's Guide for T.E.S.T, Version 4.1, A Program to Estimate Toxicity from Molecular Structure, Cincinnati, OH, USA, (2012).
Google Scholar
[4]
Accelrys Inc., TOPKAT software, Accelrys Inc., San Diego, CA, (2003).
Google Scholar
[5]
Talete, Dragon Version 5.4, (2006) (http://www.talete.mi.it/dragon_net.htm)
Google Scholar
[6]
User Manual ADMET, Version 5.5., Simulation Plus Inc, S.P.: Lancaster, CA, USA, (2011).
Google Scholar
[7]
F. Choplin, Comprehensive medicinal chemistry, Corwin Hansch, Vol 4, Elsevier Pergamon, Oxford, (2005) 33-57.
Google Scholar
[8]
C.W. Yap, Y. Xue, Z.R. Li, Y.Z. Chen, Application of support vector machines to in silico prediction of cytochrome P450 enzyme substrates and inhibitors, Curr. Topics Med. Chem. 6 (15) (2006) 1593-1607.
DOI: 10.2174/156802606778108942
Google Scholar
[9]
R.V. Guido, G. Oliva, A.D. Andricopulo, Virtual screening and its integration with modern drug design technologies, Curr. Med. Chem. 15 (1) (2008) 37-46.
DOI: 10.2174/092986708783330683
Google Scholar
[10]
A. Schwaighofer, T. Schroeter, S. Mika, G. Blanchard, How wrong can we get? A review of machine learning approaches and error bars, Comb. Chem. High Throughput Screen. 12 (5) (2009) 453-468.
DOI: 10.2174/138620709788489064
Google Scholar
[11]
L.G. Valerio Jr., In silico toxicology for the pharmaceutical sciences, Toxicol. Appl. Pharmacol. 241 (2009) 356-370.
Google Scholar
[12]
S.N. Talapatra, D. Misra, K. Banerjee, P. Banerjee, S. Swarnakar, QSAR modeling for acute toxicity prediction of fluroquinolone antibiotics by using software, Int. J. Adv. Res. 3 (6) (2015) 225-240.
Google Scholar
[13]
V. Kovalishyn, I. Kopernyk, S. Chumachenko, O. Shablykin, F. Kondratyuk, S. Pil'o, V. Prokopenko, V. Brovarets, L. Metelytsia, QSAR studies, design, synthesis and antimicrobial evaluation of azole derivatives, Comput. Biol. Bioinfor. 2(2) (2014) 25-32.
DOI: 10.2174/1570163813666161108125227
Google Scholar
[14]
P. Ruiz, G. Begluitti, T. Tincher, J. Wheeler, M. Mumtaz, Prediction of acute mammalian toxicity using QSAR methods: A case study of sulfur mustard and its breakdown products, Molecules 17 (2012) 8982-9001.
DOI: 10.3390/molecules17088982
Google Scholar
[15]
P. Banerjee, S.N. Talapatra, Assessment of medicinal tree diversity in the Chintamoni Kar Bird Sanctuary (CKBS), Kolkata, India and prediction of antimutagenic phytochemicals by using software, Int. J. Adv. Res. 3 (7) (2015) 225-243.
Google Scholar
[16]
S.N. Talapatra, A. Sarkar, Acute toxicity prediction of synthetic and natural preservatives in rat by using QSAR modeling software, Int. J. Adv. Res. 3 (7) (2015) 1424-1438.
Google Scholar
[17]
ChemIDplus, A Toxnet Database, U.S. National Library of Medicine, Available from: www.chem.sis.nlm.nih.gov/chemidplus.
Google Scholar
[18]
T.M. Martin, P. Harten, R. Venkatapathy, S. Das, D.M. Young, A hierarchical clustering methodology for the estimation of toxicity, Toxicol. Mech. Methods 18 (2008) 251-266.
DOI: 10.1080/15376510701857353
Google Scholar
[19]
M. Cleuvers, Mixture toxicity of the anti-inflammatory drugs diclofenac, ibuprofen, naproxen, and acetylsalicylic acid. Ecotoxicol. Environ. Saf. 59 (2004) 309-315.
DOI: 10.1016/s0147-6513(03)00141-6
Google Scholar
[20]
V.K. Gombar, D.V.S. Jain, Quantification of molecular shape and its correlation with physico-chemical properties, Indian J. Chem. 24A (1987) 554-555.
Google Scholar
[21]
V.K. Gombar, K. Enslein, Quantitative structure-activity relationship (QSAR) studies using electronic descriptors calculated from topological and molecular orbital (MO) methods, QSAR 9 (1990) 321-325.
DOI: 10.1002/qsar.19900090405
Google Scholar
[22]
L.H. Hall, B. Mohney, L.B. Kier, The electrotopological state: Structure information at the atomic level for molecular graphs, J. Chem. Inf. Comput. Sci. 31 (1991) 76-82.
DOI: 10.1021/ci00001a012
Google Scholar
[23]
S.J. Xu, Computer-assisted drug molecular design, Chemical Industry Press, Beijing, China (2004).
Google Scholar
[24]
Canadian Center for Occupational Health & Safety, What is an LD50 and LC50, (2012), Available from: http://www.ccohs.ca/oshanswers/chemicals/LD50.html#_1_6.
Google Scholar