[1]
WHO HIV report, 2017.
[2]
Jain, V.; Gupta, D.; Pareek, A.; Ratan, Y. Novel second generation HIV integrase inhibitor-DOLUTEGRAVIR: An emerging weapon against HIV. Lett. Drug Des. Discov., 2017, 14(3), 354-371.
[3]
Alexandrova, L.; Zicari, S.; Matyugina, E.; Khandazhinskaya, A.; Smirnova, T.; Andreevskaya, S.; Chernousova, L.; Vanpouille, C.; Kochetkov, S.; Margolis, L. Dual-targeted anti-TB/anti-HIV heterodimers. Antiviral Res., 2017, 145, 175-183.
[4]
Pawlowski, A.; Jansson, M.; Skold, M.; Rottenberg, M.E.; Kallenius, G. Tuberculosis and HIV co-infection. PLoS Pathog., 2012, 8(2), e1002464.
[5]
Patil, S.M.; Asgaonkar, K.D.; Chitre, T.S.; Kinikar, A.; Kharat, C.; Bhoirekar, V.; Athavale, M.; Katkar, M. Comparative study of various non-nucleoside reverse transcriptase inhibitors on different reverse transcriptase enzyme. Indian J. Pharma. Edu. Res, 2017, 51(4S), S722-S728.
[6]
Pawar, V.; Lokwani, D.; Bhandari, S.; Mitra, D.; Bothara, K.; Madgulkar, A. Design of potential reverse transcriptase inhibitor containing Isatin nucleus using molecular modeling studies. Bioorg. Med. Chem., 2010, 18, 3198-3211.
[7]
Huang, B.; Lin, C.; Chen, W.; Liu, T.; Yu, M.; Fu, L.; Sun, Y.; Liu, H.; De Clercq, E.; Pannecouque, C.; Balzarini, J.; Zhan, P.; Liu, X. Fused heterocycles bearing bridgehead nitrogen as potent HIV-1 NNRTIs. Part 4: Design, synthesis and biological evaluation of novel imidazo[1,2-a] pyrazines. Eur. J. Med. Chem., 2015, 93(26), 330-337.
[8]
Viira, B.; García-Sosa, A.T.; Maran, U. Chemical structure and correlation analysis of HIV-1 NNRT and NRT inhibitors and database-curated, published inhibition constants with chemical structure in diverse datasets. J. Mol. Graph. Model., 2017, 76, 205-223.
[9]
Suryawanshi, R.; Jadhav, S.; Makwana, N.; Desai, D.; Chaturbhuj, D.; Sonawani, A.; Idicula-Thomas, S.; Murugesan, V.; Katti, S.B.; Tripathy, S.; Paranjape, R.; Kulkarni, S. Evaluation of 4-thiazolidinone derivatives as potential reverse transcriptase inhibitors against HIV-1 drug resistant strains. Bioorg. Chem., 2017, 71, 211-218.
[10]
Tripathi, A.C.; Gupta, S.J.; Fatima, G.N.; Sonara, P.K.; Verma, A.; Saraf, S.K. 4-Thiazolidinones: The advances continue. Eur. J. Med. Chem., 2014, 72(24), 52-77.
[11]
Rawal, R.K.; Solomon, V.R.; Prabhakar, Y.S.; Katti, S.B.; De Clercq, E. Synthesis and QSAR studies on thiazolidinones as anti-HIV agents. Comb. Chem. High Throughput Screen., 2005, 8(5), 439-443.
[12]
Shaveta; Sahil, M.S.; Singh, P. Hybrid molecules: The privileged scaffolds for various pharmaceuticals. Eur. J. Med. Chem., 2016, 124, 500-536.
[13]
Chander, S.; Penta, A.; Singh, R.P.; Jha, P.N.; Zheng, Y.; Wang, P.; Murugesan, S. Rational design, synthesis, anti-HIV-1 RT and anti-microbial activity of novel 2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)-N-phenylpropanamide derivatives. Anti-Inf. Agts, 2016, 14(1), 63-73.
[14]
Tiwari, S.V.; Nikalje, A.P.G.; Lokwani, D.K.; Sarkate, A.P.; Jamir, K. Synthesis, biological evaluation, molecular docking study and acute oral toxicity study of coupled imidazole-pyrimidine derivatives. Lett. Drug Des. Discov., 2018, 15(5), 475-487.
[15]
Meng, X. Zhang. H.; Mezei, M.; Cui, M. Molecular docking: A powerful approach for structure-based drug discovery. Curr. Comp. Aided Drug Design, 2011, 7(2), 146-157.
[16]
Khan, I.H.; Patel, N.B.; Patel, V.N. Synthesis, in silico molecular docking and pharmacokinetic studies, in vitro antimycobacterial and antimicrobial studies of new imidozolones clubbed with thiazolidinedione. Curr. Comp. Aided Drug Design, 2018, 14(4), 269-283.
[17]
Dubey, K.D.; Tiwari, R.K.; Ojha, P. Recent advances in protein-ligand interactions: molecular dynamics simulations and binding free energy. Curr. Comp. Aided Drug Design., 2013, 9(4), 518-531.
[18]
Chitre, T.S.; Asgaonkar, K.D.; Miniyar, P.B.; Dharme, A.B.; Arkile, M.A.; Yeware, A.; Khedkar, V.M.; Jha, P.C.; Sarkar, D. Synthesis and docking studies of pyrazine–thiazolidinone hybrid scaffold targeting dormant tuberculosis. Bioorg. Med. Chem. Lett., 2016, 26, 2224-2228.
[19]
V-Life Sciences Technologies Pvt. Ltd. manual.
[20]
Noolvi, M.N.; Patel, H.M. A comparative QSAR analysis and molecular docking studies of quinazoline derivatives as tyrosine kinase (EGFR) inhibitors: A rational approach to anticancer drug design. J. Saudi Chem. Soc., 2013, 17, 361-379.
[21]
Menghani, S.; Kerzare, D.; Rarokar, N.; Khedekar, P. Molecular docking, synthesis and evaluation of antianxiety and anticonvulsant potential of some novel 3-(substituted benzylidene)- 5-phenyl-7-nitro-1, 3-dihydro-1H, 3H-1,4-Benzodiazepine-2-one. Am. J. Pharm. Tech. Res, 2016, 6(6), 185-199.
[22]
Sankpal, S.; Choudhari, P.; Kumbhar, S.; Phalle, S.; Deshmukh, M. One pot synthesis and docking study of some tetrahydrobenzo[b]pyran derivatives as extended spectrum class lactamase inhibitors for urinary tract infection. Thai. J. Pharm. Sci., 2016, 40(3), 190-193.
[23]
Motiejunas, D.; Wade, R.C. Computer-Assisted drug design. Compreh. Medi. Chemi., 2007, 4, 193-213.