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Quantum Drug hit identification tool

Drug Hit Identification Tool calculates the IC50 (Kd, Ki, pKd) value of any protein-ligand complex, docks a small-molecule in the active site of a protein and performs screening a library of compounds against a target-protein or DNA/RNA. Hit Identification Tool consists of three modules: The IC50 module, 2) Ligand Docking and 3) Library Screening modules. Drug Hit Identification Tool can run both in Windows and Linux environments.

Hit Identification overview brochure

Quantum Receptor Based molecular modeling technology is applicable to any resolved 3D macromolecule structure. You can order our molecular docking and virtual screening services based on molecular structure indicated below or purchase Quantum software to do docking study and other research in-house:

PDB ID: 1H3C

Title: STRUCTURES OF HUMAN OXIDOSQUALENE CYCLASE INHIBITORS BOUND TO A HOMOLGOUS ENZYME

Functional Class: Isomerase

Primary citation: Lenhart, A.,Reinert, D.,Aebi, J.,Dehmlow, H.,Morand, O.,Schulz, G. Binding Structures and Potencies of Oxidosqualene Cyclase Inhibitors with the Homologous Squalene-Hopene Cyclase J.Med.Chem. v46 pp.2083, 2003

Keywords: Alpha/alpha, Proteins, Toroid, (hydroxyethyloxy)tri(ethyloxy)octane, Synthases, Intramolecular, Cyclase, N-(6-{[3-(4-bromophenyl)-1,2-benzisothiazol-, D1h3cb1, D1h3cb2, Squalene--hopene, Catalytic, Alpha/alpha, Prenyltransferases, 1h3cb1, Transferase, 1h3cb2, Terpene, Lyase, Alpha, Acidocaldarius, Metabolism, Cyclases/protein, Cyclase, Biosynthesis, Lyase, Glycosyltransferase, D1h3ca1, Alpha, D1h3ca2, Hopanoid, D1h3cc2, D1h3cc1, 6-yl]oxy}hexyl)-n-methylprop-2-en-1-amine, Terpenoid, Mainly, 1h3cc1, 1h3cc2, Alicyclobacillus, (1h3c:a,, Activity, Barrel, 1h3ca1, 1h3ca2, Squalene-hopene, Designing a ligand - a potential drug candidate, Interact specifically, Selected molecular target, Predict, In-vitro, Estimation, Determinate, Simulator, Lab, Bound, Small molecules faciliate, Modeling, Molecular modelling, Camm, Determination, Perform, Assisted, Computer assisted aided rational drug design, Structure based prediction, Estimate, Binds, 3d models, Coordinates, Measure, In-silico, Mechanisms, Advances, Inhibits, Inhibited, Bio, Biochem, Computational, Altered, Predicted values, Properties, Calculated, Appropriate, Scope, Set, Computing, Blocking, Docked, Virtual screening, Inhibiting, Native, Natural, Computational drug discovery technology, Automated, Limit, Automatic,