BDBM272800 (S)-2-((1-(2- aminobenzo[d]oxazol- 5-yl)-8,9-dihydro- 7H-6-oxa-2,9a- diazabenzo[cd]azulen-4- yl)amino)propanamide::US10065970, Compound 105::US10435414, Compound 105
SMILES: C[C@H](Nc1cc2OCCCn3c(nc(c1)c23)-c1ccc2oc(N)nc2c1)C(N)=O
InChI Key: InChIKey=IQKZEIMSEKFAGN-JTQLQIEISA-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)) | BDBM272800 ((S)-2-((1-(2- aminobenzo[d]oxazol- 5-yl)-8,9-dihyd...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | 0.0320 | 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)) | BDBM272800 ((S)-2-((1-(2- aminobenzo[d]oxazol- 5-yl)-8,9-dihyd...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | 0.0320 | 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 |