QSAR is an analytical application that can be used to interpret the quantitative relationship between biological activities of a particular molecule and its structure. The product will then produce useful equations, images or models in either 2D 3D form would relate their responses physical properties molecular Hologram (HQSAR) uses holograms PLS generate fragment-based structure-activity relat...

Quantitative Structure Activity Relationship (QSAR) for tylophorine derivatives acting as Plasmodium kinases inhibitors has been developed. The proposed 2D-QSAR model was found to be statistically significant with respect to training, cross-validation, and external validation. The contribution of carbon chains with aromatic and electronegative features are found to be the most important descrip...

The objective of the present investigation was to obtain a QSAR model predict antiurease activity series 1,2,4-triazole congeners with reported IC50 values in order design new and better congeners. calculation descriptors done using CDK package correlation matrix developed all descriptors. All variables were subjected blind simulation select independent least inter-correlation high anti-urease ...

Liver X receptor (LXR) is an attractive drug target for the development of novel therapeutic agents for the treatment of dyslipidaemia and cholestasis. In the present work, comparative molecular field analysis (CoMFA) and hologram quantitative structure-activity relationship (HQSAR) studies were conducted on a series of potent LXR ligands. Significant correlation coefficients (CoMFA, r(2) = 0.9...

Abstract Quantitative structure activity relationships (QSAR) modelling is a well-known computational tool, often used in wide variety of applications. Yet one the major drawbacks conventional QSAR that models are set up based on limited number experimental and/or theoretical conditions. To overcome this, so-called multitasking or multitarget (mt-QSAR) approaches have emerged as new tools able ...

3D-pharmacophore and 2D-QSAR modeling studies describe the anti-oncological properties of spiro-alkaloids. The dispiro[2H-indene-2,3'-pyrrolidine-2',3''-[3H]indole]-1,2''(1''H, 3H)-diones 20-38 were prepared via 1,3-dipolar cycloaddition reactions of azomethine ylides (generated in situ via decarboxylative condensation of isatins 7-9 with sarcosine 10) and 2-(arylmethylidene)-2,3-dihydro-1H-ind...