null

SMILES: CNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N(C)C(=O)[C@H](C)OC)nc1C

InChI Key: InChIKey=DHEKPZQWFVQYSO-IRXDYDNUSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 489243   

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
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform (Homo sapiens (Human))	BDBM489243 ((2S)?N-{6-[(5-{2-[(1S)-1-Cyclopropylethyl]-7-(meth...) Show SMILES CNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N(C)C(=O)[C@H](C)OC)nc1C |r| Show InChI InChI=1S/C28H34N6O5S2/c1-15-25(40-28(30-15)32-22-8-7-9-23(31-22)33(5)26(35)17(3)39-6)19-12-20-14-34(16(2)18-10-11-18)27(36)24(20)21(13-19)41(37,38)29-4/h7-9,12-13,16-18,29H,10-11,14H2,1-6H3,(H,30,31,32)/t16-,17-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	0.800	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca AB US Patent					Assay Description The activity of recombinant human PI3Kγ ((aa144-1102)-6His) and PI3Kα, β, δ (6-His(p110-p85α)) was determined by measuring t...				US Patent US10961236 (2021)
					More data for this Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform (Homo sapiens (Human))	BDBM489243 ((2S)?N-{6-[(5-{2-[(1S)-1-Cyclopropylethyl]-7-(meth...) Show SMILES CNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N(C)C(=O)[C@H](C)OC)nc1C |r| Show InChI InChI=1S/C28H34N6O5S2/c1-15-25(40-28(30-15)32-22-8-7-9-23(31-22)33(5)26(35)17(3)39-6)19-12-20-14-34(16(2)18-10-11-18)27(36)24(20)21(13-19)41(37,38)29-4/h7-9,12-13,16-18,29H,10-11,14H2,1-6H3,(H,30,31,32)/t16-,17-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	539	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca AB US Patent					Assay Description The activity of recombinant human PI3Kγ ((aa144-1102)-6His) and PI3Kα, β, δ (6-His(p110-p85α)) was determined by measuring t...				US Patent US10961236 (2021)
					More data for this Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform (Homo sapiens (Human))	BDBM489243 ((2S)?N-{6-[(5-{2-[(1S)-1-Cyclopropylethyl]-7-(meth...) Show SMILES CNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N(C)C(=O)[C@H](C)OC)nc1C |r| Show InChI InChI=1S/C28H34N6O5S2/c1-15-25(40-28(30-15)32-22-8-7-9-23(31-22)33(5)26(35)17(3)39-6)19-12-20-14-34(16(2)18-10-11-18)27(36)24(20)21(13-19)41(37,38)29-4/h7-9,12-13,16-18,29H,10-11,14H2,1-6H3,(H,30,31,32)/t16-,17-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	55	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca AB US Patent					Assay Description The activity of recombinant human PI3Kγ ((aa144-1102)-6His) and PI3Kα, β, δ (6-His(p110-p85α)) was determined by measuring t...				US Patent US10961236 (2021)
					More data for this Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform [144-1102] (Homo sapiens (Human))	BDBM489243 ((2S)?N-{6-[(5-{2-[(1S)-1-Cyclopropylethyl]-7-(meth...) Show SMILES CNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N(C)C(=O)[C@H](C)OC)nc1C |r| Show InChI InChI=1S/C28H34N6O5S2/c1-15-25(40-28(30-15)32-22-8-7-9-23(31-22)33(5)26(35)17(3)39-6)19-12-20-14-34(16(2)18-10-11-18)27(36)24(20)21(13-19)41(37,38)29-4/h7-9,12-13,16-18,29H,10-11,14H2,1-6H3,(H,30,31,32)/t16-,17-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca AB US Patent					Assay Description The activity of recombinant human PI3Kγ ((aa144-1102)-6His) and PI3Kα, β, δ (6-His(p110-p85α)) was determined by measuring t...				US Patent US10961236 (2021)
					More data for this Ligand-Target Pair