null

SMILES: CS(=O)(=O)Nc1ccccc1-c1ccc(cc1)N1CCC[C@@H](NC(=O)Nc2ccc(cn2)C(F)(F)F)C1=O

InChI Key: InChIKey=VQOULAYTSCHUII-OAQYLSRUSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 454203   

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
N-formyl peptide receptor 2 (Homo sapiens (Human))	BDBM454203 (US10717708, Example 184 | US11186544, Example 184) Show SMILES CS(=O)(=O)Nc1ccccc1-c1ccc(cc1)N1CCC[C@@H](NC(=O)Nc2ccc(cn2)C(F)(F)F)C1=O |r| Show InChI InChI=1S/C25H24F3N5O4S/c1-38(36,37)32-20-6-3-2-5-19(20)16-8-11-18(12-9-16)33-14-4-7-21(23(33)34)30-24(35)31-22-13-10-17(15-29-22)25(26,27)28/h2-3,5-6,8-13,15,21,32H,4,7,14H2,1H3,(H2,29,30,31,35)/t21-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	8.10	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Company US Patent					Assay Description FPR2 and FPR1 Cyclic Adenosine Monophosphate (cAMP) Assays. A mixture of forskolin (5 μM final for FPR2 or 10 μM final for FPR1) and IBMX (...				US Patent US10717708 (2020)
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM454203 (US10717708, Example 184 | US11186544, Example 184) Show SMILES CS(=O)(=O)Nc1ccccc1-c1ccc(cc1)N1CCC[C@@H](NC(=O)Nc2ccc(cn2)C(F)(F)F)C1=O |r| Show InChI InChI=1S/C25H24F3N5O4S/c1-38(36,37)32-20-6-3-2-5-19(20)16-8-11-18(12-9-16)33-14-4-7-21(23(33)34)30-24(35)31-22-13-10-17(15-29-22)25(26,27)28/h2-3,5-6,8-13,15,21,32H,4,7,14H2,1H3,(H2,29,30,31,35)/t21-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
N-formyl peptide receptor 2 (Homo sapiens (Human))	BDBM454203 (US10717708, Example 184 | US11186544, Example 184) Show SMILES CS(=O)(=O)Nc1ccccc1-c1ccc(cc1)N1CCC[C@@H](NC(=O)Nc2ccc(cn2)C(F)(F)F)C1=O |r| Show InChI InChI=1S/C25H24F3N5O4S/c1-38(36,37)32-20-6-3-2-5-19(20)16-8-11-18(12-9-16)33-14-4-7-21(23(33)34)30-24(35)31-22-13-10-17(15-29-22)25(26,27)28/h2-3,5-6,8-13,15,21,32H,4,7,14H2,1H3,(H2,29,30,31,35)/t21-/m1/s1	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		n/a	n/a	n/a	n/a	8.10	n/a	n/a	n/a	n/a
TBA									Citation and Details
					More data for this Ligand-Target Pair
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM454203 (US10717708, Example 184 | US11186544, Example 184) Show SMILES CS(=O)(=O)Nc1ccccc1-c1ccc(cc1)N1CCC[C@@H](NC(=O)Nc2ccc(cn2)C(F)(F)F)C1=O |r| Show InChI InChI=1S/C25H24F3N5O4S/c1-38(36,37)32-20-6-3-2-5-19(20)16-8-11-18(12-9-16)33-14-4-7-21(23(33)34)30-24(35)31-22-13-10-17(15-29-22)25(26,27)28/h2-3,5-6,8-13,15,21,32H,4,7,14H2,1H3,(H2,29,30,31,35)/t21-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Company US Patent					Assay Description FPR2 and FPR1 Cyclic Adenosine Monophosphate (cAMP) Assays. A mixture of forskolin (5 μM final for FPR2 or 10 μM final for FPR1) and IBMX (...				US Patent US10717708 (2020)
					More data for this Ligand-Target Pair