null

SMILES: CCNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N2CCNCC2=O)nc1C

InChI Key: InChIKey=PZHYYDQKVVSTEG-KRWDZBQOSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 489277   

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))	BDBM489277 (2-[(1S)-1-Cyclopropylethyl]-N-ethyl-6-(4-methyl-2-...) Show SMILES CCNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N2CCNCC2=O)nc1C |r| Show InChI InChI=1S/C28H33N7O4S2/c1-4-30-41(38,39)21-13-19(12-20-15-35(27(37)25(20)21)17(3)18-8-9-18)26-16(2)31-28(40-26)33-22-6-5-7-23(32-22)34-11-10-29-14-24(34)36/h5-7,12-13,17-18,29-30H,4,8-11,14-15H2,1-3H3,(H,31,32,33)/t17-/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))	BDBM489277 (2-[(1S)-1-Cyclopropylethyl]-N-ethyl-6-(4-methyl-2-...) Show SMILES CCNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N2CCNCC2=O)nc1C |r| Show InChI InChI=1S/C28H33N7O4S2/c1-4-30-41(38,39)21-13-19(12-20-15-35(27(37)25(20)21)17(3)18-8-9-18)26-16(2)31-28(40-26)33-22-6-5-7-23(32-22)34-11-10-29-14-24(34)36/h5-7,12-13,17-18,29-30H,4,8-11,14-15H2,1-3H3,(H,31,32,33)/t17-/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	271	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))	BDBM489277 (2-[(1S)-1-Cyclopropylethyl]-N-ethyl-6-(4-methyl-2-...) Show SMILES CCNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N2CCNCC2=O)nc1C |r| Show InChI InChI=1S/C28H33N7O4S2/c1-4-30-41(38,39)21-13-19(12-20-15-35(27(37)25(20)21)17(3)18-8-9-18)26-16(2)31-28(40-26)33-22-6-5-7-23(32-22)34-11-10-29-14-24(34)36/h5-7,12-13,17-18,29-30H,4,8-11,14-15H2,1-3H3,(H,31,32,33)/t17-/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	54	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))	BDBM489277 (2-[(1S)-1-Cyclopropylethyl]-N-ethyl-6-(4-methyl-2-...) Show SMILES CCNS(=O)(=O)c1cc(cc2CN([C@@H](C)C3CC3)C(=O)c12)-c1sc(Nc2cccc(n2)N2CCNCC2=O)nc1C |r| Show InChI InChI=1S/C28H33N7O4S2/c1-4-30-41(38,39)21-13-19(12-20-15-35(27(37)25(20)21)17(3)18-8-9-18)26-16(2)31-28(40-26)33-22-6-5-7-23(32-22)34-11-10-29-14-24(34)36/h5-7,12-13,17-18,29-30H,4,8-11,14-15H2,1-3H3,(H,31,32,33)/t17-/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	1.40	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