Synthèse
Volume 20, Numéro 2, Pages 51-58
2014-10-31
Authors : Ziani Nadia . Amirat Khadidja . Messadi Djelloul .
A Quantitative Structure- Activity Relationship (QSAR) study was undertaken to evaluate the relative toxicity of a mixed series of 21 (linear and branched-chain) alcohols and 9 normal aliphatic amines in term of the 50% inhibitory growth concentration (IGC50) of Tetrahymena pyriformis. The applied simple linear regression approach is based on theoretical 3D (geometrical ) molecular descriptors from DRAGON package, and some calculated logP descriptors. The robustness and the predictive performance of the models were verified using both internal (cross-validation by LOO and LMO; bootstrap) and external statistical validations. ClogP turned out to be the best descriptor to model the considered endpoint. It may be interchanged with geometrical descriptor ADDD without relevant variations in the statistical parameters.
Alcohols and Amines –Aquatic toxicity – QSAR – Geometrical descriptors and hydrophobic character – Simple linear regression.
Djeradi H.
.
Rahmouni A.
.
Cheriti A.
.
pages 205-213.
Hadj Seyd Abdelkader
.
Lanez Touhami
.
Gharib Toufik
.
Herma Aida
.
pages 6-11.
Oumelkheir Rahim
.
Ali Ben Chenna
.
pages 190-197.
Souyei B.
.
Korichi M.
.
pages 166-170.
Amrouche Tahar
.
Djenane Djamel
.
Dziri Faiza
.
Danoune Kaissa
.
Djerbal Mouloud
.
Rabinal Pedro Roncalès
.
pages 01-10.