These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
114 related articles for article (PubMed ID: 15670927)
21. QSAR of adenosine A3 receptor antagonist 1,2,4-triazolo[4,3-a]quinoxalin-1-one derivatives using chemometric tools. Bhattacharya P; Roy K Bioorg Med Chem Lett; 2005 Aug; 15(16):3737-43. PubMed ID: 15993066 [TBL] [Abstract][Full Text] [Related]
22. Exploring QSAR of thiazole and thiadiazole derivatives as potent and selective human adenosine A3 receptor antagonists using FA and GFA techniques. Bhattacharya P; Leonard JT; Roy K Bioorg Med Chem; 2005 Feb; 13(4):1159-65. PubMed ID: 15670924 [TBL] [Abstract][Full Text] [Related]
23. Exploring QSARs with Extended Topochemical Atom (ETA) indices for modeling chemical and drug toxicity. Roy K; Ghosh G Curr Pharm Des; 2010; 16(24):2625-39. PubMed ID: 20642426 [TBL] [Abstract][Full Text] [Related]
24. A best​ comprehension about the toxicity of phenylsulfonyl carboxylates in Vibrio fischeri using quantitative structure activity/property relationship methods. de Melo EB; Martins JP; Miranda EH; Ferreira MM J Hazard Mater; 2016 Mar; 304():233-41. PubMed ID: 26551227 [TBL] [Abstract][Full Text] [Related]
25. Exploring QSAR for substituted 2-sulfonyl-phenyl-indol derivatives as potent and selective COX-2 inhibitors using different chemometrics tools. Khoshneviszadeh M; Edraki N; Miri R; Hemmateenejad B Chem Biol Drug Des; 2008 Dec; 72(6):564-74. PubMed ID: 19090923 [TBL] [Abstract][Full Text] [Related]
26. Comparative QSAR modeling of COX-2 inhibitor 1,2-diarylimidazoles using E-state and physicochemical parameters. Chakraborty S; Sengupta C; Roy K Indian J Biochem Biophys; 2007 Jun; 44(3):169-75. PubMed ID: 17650586 [TBL] [Abstract][Full Text] [Related]
27. Structure-toxicity relationships for three mechanisms of action of toxicity to Vibrio fischeri. Cronin MT; Schultz TW Ecotoxicol Environ Saf; 1998 Jan; 39(1):65-9. PubMed ID: 9515077 [TBL] [Abstract][Full Text] [Related]
28. Exploring selectivity requirements for COX-2 versus COX-1 binding of 2-(5-phenyl-pyrazol-1-yl)-5-methanesulfonylpyridines using topological and physico-chemical parameters. Chakraborty S; Sengupta C; Roy K Indian J Biochem Biophys; 2005 Apr; 42(2):106-12. PubMed ID: 23923570 [TBL] [Abstract][Full Text] [Related]
29. Correlation weighting of valence shells in QSAR analysis of toxicity. Toropov AA; Benfenati E Bioorg Med Chem; 2006 Jun; 14(11):3923-8. PubMed ID: 16460943 [TBL] [Abstract][Full Text] [Related]
30. Comparative QSAR modeling of CCR5 receptor binding affinity of substituted 1-(3,3-diphenylpropyl)-piperidinyl amides and ureas. Thomas Leonard J; Roy K Bioorg Med Chem Lett; 2006 Sep; 16(17):4467-74. PubMed ID: 16806923 [TBL] [Abstract][Full Text] [Related]
31. A novel group contribution method in the development of a QSAR for predicting the toxicity (Vibrio fischeri EC50) of ionic liquids. Luis P; Ortiz I; Aldaco R; Irabien A Ecotoxicol Environ Saf; 2007 Jul; 67(3):423-9. PubMed ID: 16889829 [TBL] [Abstract][Full Text] [Related]
32. Exploring molecular shape analysis of styrylquinoline derivatives as HIV-1 integrase inhibitors. Leonard JT; Roy K Eur J Med Chem; 2008 Jan; 43(1):81-92. PubMed ID: 17452064 [TBL] [Abstract][Full Text] [Related]
33. Prediction of cellular toxicity of halocarbons from computed chemodescriptors: a hierarchical QSAR approach. Basak SC; Balasubramanian K; Gute BD; Mills D; Gorczynska A; Roszak S J Chem Inf Comput Sci; 2003; 43(4):1103-9. PubMed ID: 12870899 [TBL] [Abstract][Full Text] [Related]
34. Comparative QSTR studies for predicting mutagenicity of nitro compounds. Nair PC; Sobhia ME J Mol Graph Model; 2008 Feb; 26(6):916-34. PubMed ID: 17689994 [TBL] [Abstract][Full Text] [Related]
35. QSAR models for Daphnia toxicity of pesticides based on combinations of topological parameters of molecular structures. Toropov AA; Benfenati E Bioorg Med Chem; 2006 Apr; 14(8):2779-88. PubMed ID: 16377200 [TBL] [Abstract][Full Text] [Related]
36. Modeling dipeptides as ACE inhibitors and bitter-tasting compounds by means of E-state structure-information representation. Spasov B; Hall LH Chem Biodivers; 2007 Nov; 4(11):2528-39. PubMed ID: 18027352 [TBL] [Abstract][Full Text] [Related]
37. A new bioconcentration factor model based on SMILES and indices of presence of atoms. Toropova AP; Toropov AA; Lombardo A; Roncaglioni A; Benfenati E; Gini G Eur J Med Chem; 2010 Sep; 45(9):4399-402. PubMed ID: 20599297 [TBL] [Abstract][Full Text] [Related]
38. Toxicity prediction of dioxins and dioxins-like compounds based on the molecular fragments variable connectivity index. Chen Q; Sun J; Liu J Bull Environ Contam Toxicol; 2011 Aug; 87(2):134-7. PubMed ID: 21626111 [TBL] [Abstract][Full Text] [Related]
39. QSAR modeling of acute toxicity by balance of correlations. Toropov AA; Rasulev BF; Leszczynski J Bioorg Med Chem; 2008 Jun; 16(11):5999-6008. PubMed ID: 18482841 [TBL] [Abstract][Full Text] [Related]
40. Prediction of mutagenicity utilizing a hierarchical QSAR approach. Basak SC; Mills D SAR QSAR Environ Res; 2001; 12(6):481-96. PubMed ID: 11813801 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]