102 related articles for article (PubMed ID: 12854651)
1. CoMFA of the acute toxicity of phenylsulfonyl carboxylates to Vibrio fischeri.
Liu X; Yang Z; Wang L
SAR QSAR Environ Res; 2003 Jun; 14(3):183-90. PubMed ID: 12854651
[TBL] [Abstract][Full Text] [Related]
2. Three-dimensional quantitative structure-activity relationship study for phenylsulfonyl carboxylates using CoMFA and CoMSIA.
Liu X; Yang Z; Wang L
Chemosphere; 2003 Dec; 53(8):945-52. PubMed ID: 14505717
[TBL] [Abstract][Full Text] [Related]
3. Three-dimensional, quantitative-structure-property-relationship study of aqueous solubility for phenylsulfonyl carboxylates using comparative-molecular-field analysis and comparative-molecular-similarity-indices analysis.
Liu X; Yang Z; Wang L
Water Environ Res; 2005; 77(5):519-24. PubMed ID: 16274086
[TBL] [Abstract][Full Text] [Related]
4. Influence of cyclodextrin complexation on the Vibrio fischeri toxicity of phenylsulfonyl carboxylates.
Liu XH; Hou J; Wang L; Luo WR; Cui BS
J Environ Sci Health A Tox Hazard Subst Environ Eng; 2007 Feb; 42(2):149-53. PubMed ID: 17182385
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. QSTR with extended topochemical atom indices. Part 5: Modeling of the acute toxicity of phenylsulfonyl carboxylates to Vibrio fischeri using genetic function approximation.
Roy K; Ghosh G
Bioorg Med Chem; 2005 Feb; 13(4):1185-94. PubMed ID: 15670927
[TBL] [Abstract][Full Text] [Related]
7. A new approach to QSAR modelling of acute toxicity.
Lagunin AA; Zakharov AV; Filimonov DA; Poroikov VV
SAR QSAR Environ Res; 2007; 18(3-4):285-98. PubMed ID: 17514571
[TBL] [Abstract][Full Text] [Related]
8. Modification of polychlorinated phenols and evaluation of their toxicity, biodegradation and bioconcentration using three-dimensional quantitative structure-activity relationship models.
Tong L; Guo L; Lv X; Li Y
J Mol Graph Model; 2017 Jan; 71():1-12. PubMed ID: 27825025
[TBL] [Abstract][Full Text] [Related]
9. Three-dimensional quantitative structure activity relationship (3D-QSAR) analysis for in vitro toxicity of chlorophenols to HepG2 cells.
Liu Y; Chen JN; Zhao JS; Yu HX; Wang XD; Jiang J; Jin HJ; Zhang JF; Wang LS
Chemosphere; 2005 Aug; 60(6):791-5. PubMed ID: 15946721
[TBL] [Abstract][Full Text] [Related]
10. The Acute toxicity of alpha-branched phenylsulfonyl acetates in Photobacterium phosphoreum test.
Liu X; Wu C; Han S; Wang L; Zhang Z
Ecotoxicol Environ Saf; 2001 Jul; 49(3):240-4. PubMed ID: 11440477
[TBL] [Abstract][Full Text] [Related]
11. 3D QSAR studies of AChE inhibitors based on molecular docking scores and CoMFA.
Akula N; Lecanu L; Greeson J; Papadopoulos V
Bioorg Med Chem Lett; 2006 Dec; 16(24):6277-80. PubMed ID: 17049234
[TBL] [Abstract][Full Text] [Related]
12. CoMFA and CoMSIA 3D-QSAR analysis of diaryloxy-methano-phenanthrene derivatives as anti-tubercular agents.
Shagufta ; Kumar A; Panda G; Siddiqi MI
J Mol Model; 2007 Jan; 13(1):99-109. PubMed ID: 16858589
[TBL] [Abstract][Full Text] [Related]
13. Dose-effect and structure-activity relationships of haloquinoline toxicity towards Vibrio fischeri.
Li M; Wang Y; Ma L; Yan X; Lei Q
Environ Sci Pollut Res Int; 2022 Feb; 29(7):10858-10864. PubMed ID: 34528206
[TBL] [Abstract][Full Text] [Related]
14. Topological study on the toxicity of ionic liquids on Vibrio fischeri by the quantitative structure-activity relationship method.
Yan F; Shang Q; Xia S; Wang Q; Ma P
J Hazard Mater; 2015 Apr; 286():410-5. PubMed ID: 25603290
[TBL] [Abstract][Full Text] [Related]
15. Acute toxicity and quantitative structure-activity relationships of alpha-branched phenylsulfonyl acetates to Daphnia magna.
Liu X; Wang B; Huang Z; Han S; Wang L
Chemosphere; 2003 Jan; 50(3):403-8. PubMed ID: 12656261
[TBL] [Abstract][Full Text] [Related]
16. Insight into the structural requirements of urokinase-type plasminogen activator inhibitors based on 3D QSAR CoMFA/CoMSIA models.
Bhongade BA; Gadad AK
J Med Chem; 2006 Jan; 49(2):475-89. PubMed ID: 16420035
[TBL] [Abstract][Full Text] [Related]
17. 3D-QSAR studies of farnesyltransferase inhibitors: a comparative molecular field analysis approach.
Puntambekar D; Giridhar R; Yadav MR
Bioorg Med Chem Lett; 2006 Apr; 16(7):1821-7. PubMed ID: 16455255
[TBL] [Abstract][Full Text] [Related]
18. 3D-QSAR comparative molecular field analysis on opioid receptor antagonists: pooling data from different studies.
Peng Y; Keenan SM; Zhang Q; Kholodovych V; Welsh WJ
J Med Chem; 2005 Mar; 48(5):1620-9. PubMed ID: 15743203
[TBL] [Abstract][Full Text] [Related]
19. Molecular Modeling Study on Diazine Indole Acetic Acid Derivatives for CRTH2 Inhibitory Activity.
Babu S; Rupa M; Nagarajan SK; Sohn H; Madhavan T
Comb Chem High Throughput Screen; 2016; 19(6):444-60. PubMed ID: 27137916
[TBL] [Abstract][Full Text] [Related]
20. Insight into the structural requirements of proton pump inhibitors based on CoMFA and CoMSIA studies.
Nayana MR; Sekhar YN; Nandyala H; Muttineni R; Bairy SK; Singh K; Mahmood SK
J Mol Graph Model; 2008 Oct; 27(3):233-43. PubMed ID: 18676164
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]