null

SMILES: CN(C)C1CCN(C1)c1ccc(cc1F)N1CCC[C@@H](NC(=O)Nc2ccc(Cl)cc2)C1=O

InChI Key: InChIKey=OOJBFRLPFIZHEB-VGAJERRHSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 497409   

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
fMet-Leu-Phe receptor (Homo sapiens (Human))	BDBM497409 (US11008301, Example 83) Show SMILES CN(C)C1CCN(C1)c1ccc(cc1F)N1CCC[C@@H](NC(=O)Nc2ccc(Cl)cc2)C1=O |r| Show InChI InChI=1S/C24H29ClFN5O2/c1-29(2)19-11-13-30(15-19)22-10-9-18(14-20(22)26)31-12-3-4-21(23(31)32)28-24(33)27-17-7-5-16(25)6-8-17/h5-10,14,19,21H,3-4,11-13,15H2,1-2H3,(H2,27,28,33)/t19?,21-/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	1.10E+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 US11008301 (2021)
					More data for this Ligand-Target Pair
N-formyl peptide receptor 2 (Homo sapiens (Human))	BDBM497409 (US11008301, Example 83) Show SMILES CN(C)C1CCN(C1)c1ccc(cc1F)N1CCC[C@@H](NC(=O)Nc2ccc(Cl)cc2)C1=O |r| Show InChI InChI=1S/C24H29ClFN5O2/c1-29(2)19-11-13-30(15-19)22-10-9-18(14-20(22)26)31-12-3-4-21(23(31)32)28-24(33)27-17-7-5-16(25)6-8-17/h5-10,14,19,21H,3-4,11-13,15H2,1-2H3,(H2,27,28,33)/t19?,21-/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	0.390	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 US11008301 (2021)
					More data for this Ligand-Target Pair