The present study investigated the activity of pyrimidine derivatives against Aedes aegypti. Two compounds, 3c and 3d showed excellent larvicide activity. Additionally, quantitative structure-activity relationship (QSAR) models were built using multiple-linear regression and partial least squares with descriptors generated from Dragon and VolSurf+ software, respectively. The best model is obtained with multiple linear regression (MLR), leading to a robust model. Moreover, the QSAR model is validated by means of some internal validation techniques in order to check its reliability, quality and robustness for predicting the larvicidal activity against A. aegypti. The models confirmed that the three-dimensional structure of molecules, steric properties, hydrophobic polar surface area, log partition (logP) and a simple pattern of substituent groups as methyl, methoxy, and succinimide in the pyrimidine derivatives are responsible for the larvicidal activity of the pyrimidine derivatives. Even more, the activity decreases by an electron-withdrawing group in R1 and increases when it is replaced by an aromatic ring activator group. These findings will aid in further studies of new pyrimidine derivatives active against Aedes aegypti.

Laboratory bioassays on fumigation, ovicidal and oviposition deterrence activity of the essential oil from Indigofera suffruticosa and its constituents [eugenol, (E)-asarone, dill apiole, (Z)-asarone, thymol, (E)-nerolidol and safrole] against Tetranychus urticae were carried out. Components of Indigofera leaf oil were characterized by gas chromatography (GC) ad mass spectrometry (GC-MS), which revealed the identification of 17 components, representing 97.7 ± 0.6% of the total oil, with a high percentage of phenylpropanoids (89.9 ± 0.5%), among which eugenol (45.6 ± 0.4%) and (E)-asarone (17.4 ± 0.2%) were major constituents. The ovicidal activity and oviposition deterrence tests revealed that the essential oil as well as its main compounds affected the oviposition and hatchability of mite eggs. Eugenol and thymol were the most potent compounds and were approximately 225-fold more potent than the oil. The acaricidal action exerted by sesquiterpenes and phenylpropanoids of the leaf oil is also discussed. The results suggest that the Indigofera oil and selected components associated with ovicidal activity and oviposition deterrence can serve as the basis for a promising agent that could be used in the formulation of a product for use against the T. urticae.