This can be done either prior to the HTS by subset design of compounds with known MoA or post HTS by data annotation and mining. To enable this process, we developed a tool that compares compounds solely on the basis of their bioactivity: screening library the chemical biological descriptor “high-throughput screening fingerprint” selelck kinase inhibitor (HTS-FP). In the current embodiment, data are aggregated from 195 biochemical and cell-based assays developed at Novartis and can be used to identify bioactivity relationships among the in-house collection comprising similar to 1.5 million compounds. We demonstrate the value of the HTS-FP for virtual screening and Inhibitors,Modulators,Libraries in particular scaffold hopping. HTS-FP outperforms state of the art methods in several aspects, retrieving bioactive compounds with remarkable chemical dissimilarity to a probe structure.
We also apply HTS-FP for the design of screening subsets in HTS. Using retrospective data, we show that a biodiverse selection of plates performs significantly better Inhibitors,Modulators,Libraries than a chemically Inhibitors,Modulators,Libraries diverse selection of plates, both in terms of number of hits and diversity of chemotypes retrieved. This is also true in, the case of hit expansion predictions using HTS-FP similarity. Sets Inhibitors,Modulators,Libraries of compounds clustered with HTS-FP are biologically meaningful, in the sense that these clusters enrich for genes and gene ontology (GO) terms, showing that compounds that are bioactively similar also tend to target proteins that operate together in the cell.
Inhibitors,Modulators,Libraries HTS-FP are valuable not only because of their predictive power but mainly because Inhibitors,Modulators,Libraries they relate compounds solely on the basis of bioactivity, Inhibitors,Modulators,Libraries harnessing the accumulated knowledge of a high-throughput screening facility toward Inhibitors,Modulators,Libraries the understanding of how compounds interact with the proteome.
Calpain 10 is a ubiquitously Inhibitors,Modulators,Libraries expressed mitochondrial and cytosolic Ca2+-regulated cysteine protease in which overexpression or knockdown leads to mitochondrial dysfunction and cell death. We previously identified a potent and specific calpain 10 peptide inhibitor (CYGAK), but it was not efficacious in cells. Therefore, we created a homology model using the calpain 10 amino acid sequence and calpain 1 3-D structure and docked CYGAK in the active site. Using this model we modified the inhibitor to improve potency 2-fold (CYGAbuK).
To increase cellular efficacy, we created CYGAK-S-phenyl-oleic Inhibitors,Modulators,Libraries acid heterodimers.
Using renal mitochondrial selleck inhibitor matrix CYGAK, purchase Dapagliflozin CYGAK-OC, and CYGAK-ON had IC50′s of 70, 90, and 875 nM, respectively. Using isolated whole renal mitochondria CYGAK, CYGAK-OC, and CYGAK-ON had IC50′s of 95, 196, and >10,000 nM, respectively. Using renal proximal tubular cells (RPTC) in primary culture, 30 min exposures to CYGAK-OC and CYGAbuK-OC decreased cellular calpain activity approximately 20% at 1 mu M, and concentrations up to 100 mu M had no additional effect.