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P. Vijay, T. Kalpana, M.M. Sonali, R. Mohan, and C.S. Ramaa Synthesis and primary cytotoxicity evaluation of new 5-benzylidene-2,4-thiazolidinedione derivatives Eur. J. Med. Chem. 45 2010 4539 4544
Synthesis of some novel 5-substituted arylidine 2,4-thiazolidinediones as bioactive agents
A. Garg, P. Chawla, D. Panjvani, and S.A. Saraf Synthesis of some novel 5-substituted arylidine 2,4-thiazolidinediones as bioactive agents Int. J. Pharm. Sci. Nanotechnol. 4 2011 1373 1378
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A. Galli, E. Ceni, T. Mello, S. Polvani, M. Tarocchi, F. Buccoliero, F. Lisi, L. Cioni, B. Ottanelli, V. Foresta, G. Mastrobuoni, G. Moneti, G. Pieraccini, C. Surrenti, and S. Milani Thiazolidinediones inhibit hepatocarcinogensis in hepatitis B virus-transgenic mice by peroxisome proliferator-activated receptor γ-independent regulation of nucleophosmin Hepatology 52 2010 493 505
Rapid discovery and structure activity profiling of novel inhibitors of human immunodeficiency virus type 1 protease enabled by the copper(I) catalyzed synthesis of 1,2,3,-triazoles and their further functionalization
M. Whiting, J.C. Tripp, Y.C. Lin, W. Lindstrom, A.J. Olson, J.H. Elder, K.B. Sharpless, and V.V. Fokin Rapid discovery and structure activity profiling of novel inhibitors of human immunodeficiency virus type 1 protease enabled by the copper(I) catalyzed synthesis of 1,2,3,-triazoles and their further functionalization J. Med. Chem. 49 2006 7697 7710
A copper(I)-catalyzed 1,2,3-triazole azide-alkyne click compound is a potent inhibitor of a multidrug-resistant HIV-1 protease variant
M.J. Giffin, H. Heaslet, A. Brik, Y.C. Lin, G. Cauvi, C.H. Wong, D.E. McRee, J.H. Elder, C.D. Stout, and B.E. Torbett A copper(I)-catalyzed 1,2,3-triazole azide-alkyne click compound is a potent inhibitor of a multidrug-resistant HIV-1 protease variant J. Med. Chem. 51 2008 6263 6270
Synthesis and antimicrobial activities of some new 1,2,3-triazole derivatives
H. Bektas, N. Karaali, D. Sahin, A. Demirbas, S.A. Karaoglu, and N. Demirbas Synthesis and antimicrobial activities of some new 1,2,3-triazole derivatives Molecules 15 2010 2427 2438
Design, synthesis, antiviral and cytostatic evaluation of novel isoxazolidine nucleotide analogues with a 1,2,3-triazole linker
G.P. Dorota, B. Jan, and E.G. Iwona Design, synthesis, antiviral and cytostatic evaluation of novel isoxazolidine nucleotide analogues with a 1,2,3-triazole linker Eur. J. Med. Chem. 47 2012 501 509
The synthesis and insecticidal activity of a series of 2-aryl-1,2,3-triazoles
I.K. Boddy, G.G. Briggs, R.P. Harrison, T.H. Jones, M.J. O'Mahony, I.D. Marlow, B.G. Roberts, R.J. Willis, R. Bardsley, and J. Reid The synthesis and insecticidal activity of a series of 2-aryl-1,2,3-triazoles Pest Manage. Sci. 48 1996 189 196
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
T. Mossman Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J. Immunol. Methods 65 1983 55 63
Different polyphenolic components of soft fruits inhibit α-amylase and α-glucosidase
G.J. McDougall, F. Shpiro, P. Dobson, P. Smith, A. Blake, and D. Stewart Different polyphenolic components of soft fruits inhibit α-amylase and α-glucosidase J. Agric. Food Chem. 53 2005 2760 2766
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O. Trott, and A.J. Olson AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization and multithreading J. Comput. Chem. 31 2010 455 461
Development of QSAR model for immunomodulatory activity of natural coumarinolignoids
D.K. Yadav, A. Meena, A. Srivastava, D. Chanda, F. Khan, and S.K. Chattopadhyay Development of QSAR model for immunomodulatory activity of natural coumarinolignoids Drug Des. Dev. Ther. 4 2010 173 186
New glucosidase inhibitors from an ayurvedic herbal treatment for type 2 diabetes: Structures and inhibition of human intestinal maltase-glucoamylase with compounds from Salacia reticulate
L. Sim, K. Jayakanthan, S. Mohan, R. Nasi, B.D. Johnston, B.M. Pinto, and D.R. Rose New glucosidase inhibitors from an ayurvedic herbal treatment for type 2 diabetes: structures and inhibition of human intestinal maltase-glucoamylase with compounds from Salacia reticulate Biochemistry 49 2010 443 451