BDBM272956 (S)-2-((1-(2-amino-4,7- difluorobenzo[d]oxazol- 5-yl)-7,8,9,10- tetrahydro-6-oxa-2,10a- diazacycloocta[cd]inden-4- yl)oxy)propanamide::US10065970, Example 261::US10435414, Example 261
SMILES: C[C@H](Oc1cc2OCCCCn3c(nc(c1)c23)-c1cc(F)c2oc(N)nc2c1F)C(N)=O
InChI Key: InChIKey=OXJYVRTYBXXGLP-VIFPVBQESA-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)) | BDBM272956![]() ((S)-2-((1-(2-amino-4,7- difluorobenzo[d]oxazol- 5-...) | PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | US Patent | <0.0200 | 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)) | BDBM272956![]() ((S)-2-((1-(2-amino-4,7- difluorobenzo[d]oxazol- 5-...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![]() | PC cid PC sid UniChem | US Patent | <0.0200 | 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 |