null

SMILES: Cc1nc(Nc2cccc(c2C)-c2cccc(-c3nc4cc(CN5CCC(CC5)C(O)=O)cc(C#N)c4o3)c2C)c2ncc(CN3CC[C@@H](O)C3)cc2n1

InChI Key: InChIKey=UWRISMWEBPQKNV-WJOKGBTCSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 446448   

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
Programmed cell death 1 ligand 1 [19-238]/protein 1 [25-167] (Homo sapiens (Human))	BDBM446448 ((R)-1-((7-cyano-2-(3′-(7-((3-hydroxypyrrolid...) Show SMILES Cc1nc(Nc2cccc(c2C)-c2cccc(-c3nc4cc(CN5CCC(CC5)C(O)=O)cc(C#N)c4o3)c2C)c2ncc(CN3CC[C@@H](O)C3)cc2n1 |r| Show InChI InChI=1S/C42H42N8O4/c1-24-32(6-4-8-34(24)41-48-37-17-27(16-30(19-43)39(37)54-41)21-49-13-10-29(11-14-49)42(52)53)33-7-5-9-35(25(33)2)47-40-38-36(45-26(3)46-40)18-28(20-44-38)22-50-15-12-31(51)23-50/h4-9,16-18,20,29,31,51H,10-15,21-23H2,1-3H3,(H,52,53)(H,45,46,47)/t31-/m1/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	<10	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation US Patent					Assay Description The assays were conducted in a standard black 384-well polystyrene plate with a final volume of 20 μL. Inhibitors were first serially diluted in...				US Patent US10669271 (2020) BindingDB Entry DOI: 10.7270/Q2MG7SJC
					More data for this Ligand-Target Pair
Programmed cell death 1 ligand 1 [19-238]/protein 1 [25-167] (Homo sapiens (Human))	BDBM446448 ((R)-1-((7-cyano-2-(3′-(7-((3-hydroxypyrrolid...) Show SMILES Cc1nc(Nc2cccc(c2C)-c2cccc(-c3nc4cc(CN5CCC(CC5)C(O)=O)cc(C#N)c4o3)c2C)c2ncc(CN3CC[C@@H](O)C3)cc2n1 |r| Show InChI InChI=1S/C42H42N8O4/c1-24-32(6-4-8-34(24)41-48-37-17-27(16-30(19-43)39(37)54-41)21-49-13-10-29(11-14-49)42(52)53)33-7-5-9-35(25(33)2)47-40-38-36(45-26(3)46-40)18-28(20-44-38)22-50-15-12-31(51)23-50/h4-9,16-18,20,29,31,51H,10-15,21-23H2,1-3H3,(H,52,53)(H,45,46,47)/t31-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	<10	n/a	n/a	n/a	n/a	n/a	n/a
TBA									Citation and Details BindingDB Entry DOI: 10.7270/Q2VT1W8C
					More data for this Ligand-Target Pair
Nuclear factor NF-kappa-B p105 subunit (Homo sapiens (Human))	BDBM446448 ((R)-1-((7-cyano-2-(3′-(7-((3-hydroxypyrrolid...) Show SMILES Cc1nc(Nc2cccc(c2C)-c2cccc(-c3nc4cc(CN5CCC(CC5)C(O)=O)cc(C#N)c4o3)c2C)c2ncc(CN3CC[C@@H](O)C3)cc2n1 |r| Show InChI InChI=1S/C42H42N8O4/c1-24-32(6-4-8-34(24)41-48-37-17-27(16-30(19-43)39(37)54-41)21-49-13-10-29(11-14-49)42(52)53)33-7-5-9-35(25(33)2)47-40-38-36(45-26(3)46-40)18-28(20-44-38)22-50-15-12-31(51)23-50/h4-9,16-18,20,29,31,51H,10-15,21-23H2,1-3H3,(H,52,53)(H,45,46,47)/t31-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	55	n/a	n/a	n/a	n/a
Incyte Corporation US Patent					Assay Description PD-L1 aAPC/CHO-Klcells (Promega) were maintained in F-12 medium with addition of 10% FBS, 200 μg/ml Hygromycin B, 250 μg/ml Geneticin (G418...				US Patent US10669271 (2020) BindingDB Entry DOI: 10.7270/Q2MG7SJC
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 11 (Homo sapiens (Human))	BDBM446448 ((R)-1-((7-cyano-2-(3′-(7-((3-hydroxypyrrolid...) Show SMILES Cc1nc(Nc2cccc(c2C)-c2cccc(-c3nc4cc(CN5CCC(CC5)C(O)=O)cc(C#N)c4o3)c2C)c2ncc(CN3CC[C@@H](O)C3)cc2n1 |r| Show InChI InChI=1S/C42H42N8O4/c1-24-32(6-4-8-34(24)41-48-37-17-27(16-30(19-43)39(37)54-41)21-49-13-10-29(11-14-49)42(52)53)33-7-5-9-35(25(33)2)47-40-38-36(45-26(3)46-40)18-28(20-44-38)22-50-15-12-31(51)23-50/h4-9,16-18,20,29,31,51H,10-15,21-23H2,1-3H3,(H,52,53)(H,45,46,47)/t31-/m1/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	<10	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation US Patent					Assay Description U2OS/PD-L1 cells (DiscoveRx Corporation) were maintained in McCoy's 5A medium with addition of 10% FBS, 0.25 μg/ml Puromycin. After removing...				US Patent US10669271 (2020) BindingDB Entry DOI: 10.7270/Q2MG7SJC
					More data for this Ligand-Target Pair