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--> - A QSAR is of the form Biological Activity = Const + (C1 P1) + (C2 P2) + (C3 P3) + .. where the parameters P1 through Pn are computed for each molecule in the series and the coefficients C1 through Cn are calculated by fitting variations in the parameters and the biological activity.
- NOW these P1,P2,P3 and so on are the descriptor variables of the QSAR equation you would be interested.
- Many tools are available for generating these descriptors. Refer this link for calculating them : click here
- Once you know how to calculate the descriptors the next thing which you need to get the possible other STRUCTURALLY RELATED drugs (by searching a drug library) and get their activity on the target.This is where you generate the library. Note: This library must be large enough (choose at least 10.
- Calculate the descriptors(choose as many descriptors as you can and make sure that the descriptors you choose are varied enough ) for each compound from your library. (Also calculate the descriptors for your drug and keep it aside for now.)
- descriptor.csv : will contain the descriptor values for your library compounds
- activity.csv : will contain the activity value for your library compounds
- Now run the tool as per the instructions and generate the equation, the tool will guide you step by step for the analysis.
- Choose 'Analyze test data' option which will ask you to enter the descriptor values for an unknown sample (this is your drug). Enter the descriptor values in the .csv file in the same order as you entered for the library structures.This will predict the activity value for your drug compond based on the QSAR equation generated.
To get a better idea you can have a look into these published works (links provided below) that used EasyQSAR for their work
- Computational validation of 3-ammonio-3-(4-oxido- 1H-imidazol-1-ium-5-yl) propane-1, 1-bis (olate) as a potent anti-tubercular drug against mt-MetAP click here
- Synthesis, antimicrobial and QSAR studies of some new thiadiazepine derivatives click here
- Designing and screening of potent inhibitor against inha reductase of mycobacterium tuberculosis: a computational approach click here
- Molecular modeling and qsar analysis to explore therapeutic potentials of phytoestrogens in osteoporosis click here
- Resveratrol A Potent Angiotensin Converting Enzyme Inhibitor: AComputational Study in Relevance to Cardioprotective Activity. click here
- In-silico screening of potential inhibitors of gamma-secretase, a key enzyme of Alzheimer’s disease. click here
- Quantitative-Structure Activity Relationship (QSAR) Model for Abuse-liability Evaluation of Designer Drugs. click here
- Docking and QSAR based screening of some naturally occurring diterpenes as inhibitors of angiotensin converting enzyme (ACE) against cardiovascular diseases. click here
- An in silico insight into molecular mechanism of hypoglycemic activity of scoparic acid d, a diterpenoid from scoparia dulcis. click here
Developed by:
Kuntal Kumar Bhusan
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Reference to some of the content above is taken from :
Introduction to QSAR Methodolog
by AB Richon