BDBM50026932 CHEMBL2370884

SMILES: C\C=C\C[C@@H](C)[C@@H](O)C1NC(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](CC(C)C)N(C)C(=O)[C@H](NC(=O)[C@@H](CC(C)C)N(C)C(=O)CN(C)C(=O)[C@@H](NC1=O)C(C)C)C(C)C

InChI Key: InChIKey=WRWNSMAXKRRZGB-PQTSBPMESA-N

Data: 1 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50026932   

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))	BDBM50026932 (CHEMBL2370884) Show SMILES C\C=C\C[C@@H](C)[C@@H](O)C1NC(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](CC(C)C)N(C)C(=O)[C@H](NC(=O)[C@@H](CC(C)C)N(C)C(=O)CN(C)C(=O)[C@@H](NC1=O)C(C)C)C(C)C Show InChI InChI=1S/C62H111N11O12/c1-25-26-27-40(16)52(75)50-56(79)66-48(37(10)11)61(84)68(19)32-47(74)69(20)43(28-33(2)3)55(78)65-49(38(12)13)62(85)70(21)44(29-34(4)5)54(77)63-41(17)53(76)64-42(18)58(81)71(22)45(30-35(6)7)59(82)72(23)46(31-36(8)9)60(83)73(24)51(39(14)15)57(80)67-50/h25-26,33-46,48-52,75H,27-32H2,1-24H3,(H,63,77)(H,64,76)(H,65,78)(H,66,79)(H,67,80)/b26-25+/t40-,41+,42-,43-,44-,45+,46+,48+,49-,50?,51+,52-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Strasbourg 1 University Curated by ChEMBL					Assay Description Inhibitory activity against human formylpeptide receptor (FPR) of human leukemia HL-60 cells				J Med Chem 45: 4613-28 (2002) BindingDB Entry DOI: 10.7270/Q2571CQX
					More data for this Ligand-Target Pair