BDBM272882 (S)-2-((1-(2- aminoquinoxalin-6- yl)-8,9-dihydro-7H- 6-oxa-2,9a- diazabenzo[cd]azulen- 4-yl)amino)-2- cyclopropylacetamide::US10065970, Compound 187::US10435414, Compound 187
SMILES: NC(=O)[C@@H](Nc1cc2OCCCn3c(nc(c1)c23)-c1ccc2nc(N)cnc2c1)C1CC1
InChI Key: InChIKey=VEIHMYIJHCUERO-FQEVSTJZSA-N
Data: 2 KI
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PI3-kinase class I (Homo sapiens (Human)) | BDBM272882 ((S)-2-((1-(2- aminoquinoxalin-6- yl)-8,9-dihydro-7...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | 0.0560 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Genentech, Inc. US Patent | Assay Description TBD | US Patent US10435414 (2019) BindingDB Entry DOI: 10.7270/Q2GX4DXV | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform (Homo sapiens (Human)) | BDBM272882 ((S)-2-((1-(2- aminoquinoxalin-6- yl)-8,9-dihydro-7...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | 0.0560 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Genentech, Inc. US Patent | Assay Description PI3K Binding assays are intended for determining the biochemical potency of small molecule PI3K inhibitors. The PI3K lipid kinase reaction is perform... | US Patent US10065970 (2018) BindingDB Entry DOI: 10.7270/Q27P91FB | |||||||||||
More data for this Ligand-Target Pair |