Relationships between molecular properties and log P and soil sorption (Koc) of substituted phenylureas: QSAR models
- 1 June 1994
- journal article
- Published by Elsevier in Chemosphere
- Vol. 28 (11) , 1929-1941
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Relationships between molecular properties and biological activities of O-phenyl pyrrolidino- and piperidinocarbamate herbicidesJournal of Agricultural and Food Chemistry, 1992
- Quantitative structure-activity relationships of protoporphyrinogen oxidase-inhibiting diphenyl ether herbicidesPesticide Biochemistry and Physiology, 1992
- The role of property-reactivity relationships in meeting the EPA's needs for environmental fate constantsEnvironmental Toxicology and Chemistry, 1992
- Quantitative modeling of environmental fate and impact of commercial chemicalsEnvironmental Toxicology and Chemistry, 1992
- Synthesis and activity optimization of herbicidal substituted 4-aryl-1,2,4-triazole-5(1H)-thionesJournal of Agricultural and Food Chemistry, 1992
- Linear solvation energy relationships: "rule of thumb" for estimation of variable valuesEnvironmental Science & Technology, 1991
- Photodynamic herbicides. 9. Structure activity study of substituted 1,10-phenanthrolines as potent photodynamic herbicide modulatorsPesticide Biochemistry and Physiology, 1991
- Structure-activity relationships in the Hill inhibitory activity of substituted phenylureasJournal of Agricultural and Food Chemistry, 1987
- Intrinsic Molecular Volume as a Measure of the Cavity Term in Linear Solvation Energy Relationships: Octanol-Water Partition Coefficients and Aqueous SolubilitiesJournal of Pharmaceutical Sciences, 1986
- Solubility Properties in Polymers and Biological Media 5: An Analysis of the Physicochemical Properties Which Influence Octanol–Water Partition Coefficients of Aliphatic and Aromatic SolutesJournal of Pharmaceutical Sciences, 1985