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Virtual screening services
Quantum is a leading company providing drug screening services in-silico and, thus, delivering to it clients strong inhibitors against variety of target-proteins
We apply our proprietary developed computational technology QUANTUM, which shows outstanding accuracy in forecasting binding affinities. The hit rate of the QUANTUM performance is about 50%, it means that a half of found in silico strong inhibitors would be confirmed in in-vitro testing!!!
Click here to download a brochure about QUANTUM hit Identification technology.
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Title: STRUCTURAL INTERACTION OF NATURAL AND SYNTHETIC INHIBITORS WITH THE VENOM METALLOPROTEINASE, ATROLYSIN C (HT-D) |
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Functional Class: Metalloprotease Primary citation: Zhang, D.,Botos, I.,Gomis-Ruth, F.X.,Doll, R.,Blood, C.,Njoroge, F.G.,Fox, J.W.,Bode, W.,Meyer, E.F. Structural interaction of natural and synthetic inhibitors with the venom metalloproteinase, atrolysin C (form d). Proc.Natl.Acad.Sci.USA v91 pp.8447-8451, 1994 |
Abstract Title: Structural interaction of natural and synthetic inhibitors with the venom metalloproteinase, atrolysin C (form d).
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