BDBM50026898 CHEMBL2372467

SMILES: [H][C@@]1([C@H](O)[C@H](C)C\C=C\C)N(C)C(=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)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)N(C)C(=O)CN(C)C(=O)[C@H](CCC)NC1=O)C(C)C

InChI Key: InChIKey=UUKQNWJVWJLTEU-AJOHPCJESA-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 = 50026898   

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))	BDBM50026898 (CHEMBL2372467) Show SMILES [H][C@@]1([C@H](O)[C@H](C)C\C=C\C)N(C)C(=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)NC(=O)[C@H](NC(=O)[C@@H](CC(C)C)N(C)C(=O)CN(C)C(=O)[C@H](CCC)NC1=O)C(C)C |r| Show InChI InChI=1S/C62H111N11O12/c1-24-26-28-40(15)52(75)51-57(80)65-43(27-25-2)59(82)68(18)33-48(74)69(19)45(30-35(5)6)55(78)67-49(38(11)12)56(79)66-44(29-34(3)4)54(77)63-41(16)53(76)64-42(17)58(81)70(20)46(31-36(7)8)60(83)71(21)47(32-37(9)10)61(84)72(22)50(39(13)14)62(85)73(51)23/h24,26,34-47,49-52,75H,25,27-33H2,1-23H3,(H,63,77)(H,64,76)(H,65,80)(H,66,79)(H,67,78)/b26-24+/t40-,41+,42-,43+,44+,45-,46+,47+,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