201 related articles for article (PubMed ID: 19916114)
1. Quantitative structure-activity relationship (QSAR) for insecticides: development of predictive in vivo insecticide activity models.
Naik PK; Singh T; Singh H
SAR QSAR Environ Res; 2009 Jul; 20(5-6):551-66. PubMed ID: 19916114
[TBL] [Abstract][Full Text] [Related]
2. Molecular modeling and structure-activity relationship of podophyllotoxin and its congeners.
Naik PK; Alam A; Malhotra A; Rizvi O
J Biomol Screen; 2010 Jun; 15(5):528-40. PubMed ID: 20460251
[TBL] [Abstract][Full Text] [Related]
3. Development of predictive quantitative structure-activity relationship models of epipodophyllotoxin derivatives.
Naik PK; Dubey A; Kumar R
J Biomol Screen; 2010 Dec; 15(10):1194-203. PubMed ID: 20926843
[TBL] [Abstract][Full Text] [Related]
4. Predictive QSAR modeling of HIV reverse transcriptase inhibitor TIBO derivatives.
Mandal AS; Roy K
Eur J Med Chem; 2009 Apr; 44(4):1509-24. PubMed ID: 18760864
[TBL] [Abstract][Full Text] [Related]
5. Ligand-based virtual screening and in silico design of new antimalarial compounds using nonstochastic and stochastic total and atom-type quadratic maps.
Marrero-Ponce Y; Iyarreta-Veitía M; Montero-Torres A; Romero-Zaldivar C; Brandt CA; Avila PE; Kirchgatter K; Machado Y
J Chem Inf Model; 2005; 45(4):1082-100. PubMed ID: 16045304
[TBL] [Abstract][Full Text] [Related]
6. Linear indices of the "molecular pseudograph's atom adjacency matrix": definition, significance-interpretation, and application to QSAR analysis of flavone derivatives as HIV-1 integrase inhibitors.
Marrero-Ponce Y
J Chem Inf Comput Sci; 2004; 44(6):2010-26. PubMed ID: 15554670
[TBL] [Abstract][Full Text] [Related]
7. Quantitative structure-activity relationships for organophosphates binding to trypsin and chymotrypsin.
Ruark CD; Hack CE; Robinson PJ; Gearhart JM
J Toxicol Environ Health A; 2011; 74(1):1-23. PubMed ID: 21120745
[TBL] [Abstract][Full Text] [Related]
8. 3-Heterocycle-phenyl N-alkylcarbamates as FAAH inhibitors: design, synthesis and 3D-QSAR studies.
Käsnänen H; Myllymäki MJ; Minkkilä A; Kataja AO; Saario SM; Nevalainen T; Koskinen AM; Poso A
ChemMedChem; 2010 Feb; 5(2):213-31. PubMed ID: 20024981
[TBL] [Abstract][Full Text] [Related]
9. Quantitative structure-activity relationship (QSAR) of aryl alkenyl amides/imines for bacterial efflux pump inhibitors.
Nargotra A; Koul S; Sharma S; Khan IA; Kumar A; Thota N; Koul JL; Taneja SC; Qazi GN
Eur J Med Chem; 2009 Jan; 44(1):229-38. PubMed ID: 18395941
[TBL] [Abstract][Full Text] [Related]
10. TOMOCOMD-CARDD descriptors-based virtual screening of tyrosinase inhibitors: evaluation of different classification model combinations using bond-based linear indices.
Casañola-Martín GM; Marrero-Ponce Y; Khan MT; Ather A; Sultan S; Torrens F; Rotondo R
Bioorg Med Chem; 2007 Feb; 15(3):1483-503. PubMed ID: 17110117
[TBL] [Abstract][Full Text] [Related]
11. Quantitative structure-toxicity relationship (QSTR) studies on the organophosphate insecticides.
Can A
Toxicol Lett; 2014 Nov; 230(3):434-43. PubMed ID: 25149906
[TBL] [Abstract][Full Text] [Related]
12. Combinatorial QSAR modeling of chemical toxicants tested against Tetrahymena pyriformis.
Zhu H; Tropsha A; Fourches D; Varnek A; Papa E; Gramatica P; Oberg T; Dao P; Cherkasov A; Tetko IV
J Chem Inf Model; 2008 Apr; 48(4):766-84. PubMed ID: 18311912
[TBL] [Abstract][Full Text] [Related]
13. Quantitative structure activity relationship (QSAR) of piperine analogs for bacterial NorA efflux pump inhibitors.
Nargotra A; Sharma S; Koul JL; Sangwan PL; Khan IA; Kumar A; Taneja SC; Koul S
Eur J Med Chem; 2009 Oct; 44(10):4128-35. PubMed ID: 19523722
[TBL] [Abstract][Full Text] [Related]
14. Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors.
Chaudhaery SS; Roy KK; Saxena AK
J Chem Inf Model; 2009 Jun; 49(6):1590-601. PubMed ID: 19441865
[TBL] [Abstract][Full Text] [Related]
15. An investigation of structurally diverse carbamates for acetylcholinesterase (AChE) inhibition using 3D-QSAR analysis.
Roy KK; Dixit A; Saxena AK
J Mol Graph Model; 2008 Sep; 27(2):197-208. PubMed ID: 18515163
[TBL] [Abstract][Full Text] [Related]
16. Critical assessment of QSAR models of environmental toxicity against Tetrahymena pyriformis: focusing on applicability domain and overfitting by variable selection.
Tetko IV; Sushko I; Pandey AK; Zhu H; Tropsha A; Papa E; Oberg T; Todeschini R; Fourches D; Varnek A
J Chem Inf Model; 2008 Sep; 48(9):1733-46. PubMed ID: 18729318
[TBL] [Abstract][Full Text] [Related]
17. QSAR analyses of organophosphates for insecticidal activity and its in-silico validation using molecular docking study.
Niraj RR; Saini V; Kumar A
Environ Toxicol Pharmacol; 2015 Nov; 40(3):886-94. PubMed ID: 26492451
[TBL] [Abstract][Full Text] [Related]
18. Quantitative structure-activity relationships of mosquito larvicidal chalcone derivatives.
Pasquale G; Romanelli GP; Autino JC; García J; Ortiz EV; Duchowicz PR
J Agric Food Chem; 2012 Jan; 60(2):692-7. PubMed ID: 22217234
[TBL] [Abstract][Full Text] [Related]
19. Quantitative structure-activity relationships of monoterpenoid binding activities to the housefly GABA receptor.
Tong F; Coats JR
Pest Manag Sci; 2012 Aug; 68(8):1122-9. PubMed ID: 22461383
[TBL] [Abstract][Full Text] [Related]
20. Development of quantitative structure-activity relationships and classification models for anticonvulsant activity of hydantoin analogues.
Sutherland JJ; Weaver DF
J Chem Inf Comput Sci; 2003; 43(3):1028-36. PubMed ID: 12767162
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
