SXD - Solvent eXtraction Database
A database for metal extraction
Web-based virtual screening
Here you may submit long term background jobs to :
(A) search our collection of > 3 million registered commercially available and reference compounds (Maybridge, Zinc, QSAR reference sets from the literature) by substructure or virtually screen by similarity - based on various original descriptors - starting from one or several queries (consensus similarity screening is supported).
Searching can be performed either with ChemAxon standard tools, or using our original and complementary fragment and pharmacophore ISIDA descriptors.
While ISIDA fragments capture topological similarity, fuzzy pharmacophore triplets support "scaffold hopping" - retrieval of original skeletons carrying a same pharmacophore pattern as in the query compounds.
Several similarity/substructure-based queries can be processed independently and resulting lists combined (Boolean operators).
Please note that fuzzy pharmacophore fingerprints (FPT) are information-rich high-dimensional integer value vectors : their comparison is nowhere close in speed to binary fingerprint matching (count several hours for a complete FPT-based similarity screening of the data base - albeit access to partial results is quick, and you may disconnect any time and revisit the page later).
(B) predict compound properties based on large-scale consensus models obtained by the Stochastic QSAR Sampler.
In complement to the quick, in-line Predictor tool, these approaches rely on thousands of linear and non-linear equations for each prediction, and must be run as a background task.
The methodology returns .csv files and/or .html result pages, regrouping the predicted property and the confidence level associated to each prediction.
The latter is based on an analysis of the situation of the compound to predict with respect to the Applicability Domain of each individual equation, and is associated to explicative remarks.
A legacy engine to apply published QSAR models to query compounds
Web service for some chemoinformatics tools.
Click here to access our Mobyle Portal.
Protection groups reactivity analysis
This model analyses reactivity of protection group(s) in user’s reaction. As input you should give to model your reaction in which you want to cleave/remain protection group(s). As output the model will give back recommendations of using catalysts. The first row shows catalysts that you should use to carry out the reaction. The second row says which group(s) model has found. Then you can see detailed analysis for each identified protection group(s).
If you need an account for this model, please contact us.