BDBM50026908 CHEMBL2372484

SMILES: [H][C@@]1([C@H](O)[C@H](C)C\C=C\CC)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)N(C)C(=O)[C@H](NC(=O)[C@H](Cc2ccccc2)N(C)C(=O)CN(C)C(=O)[C@H](CC)NC1=O)C(C)C

InChI Key: InChIKey=QFBHUTLKESKPGE-WZULUUDFSA-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 = 50026908   

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))	BDBM50026908 (CHEMBL2372484) Show SMILES [H][C@@]1([C@H](O)[C@H](C)C\C=C\CC)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)N(C)C(=O)[C@H](NC(=O)[C@H](Cc2ccccc2)N(C)C(=O)CN(C)C(=O)[C@H](CC)NC1=O)C(C)C |r| Show InChI InChI=1S/C66H111N11O12/c1-23-25-27-30-43(13)56(79)55-60(83)69-47(24-2)62(85)71(16)37-52(78)72(17)49(36-46-31-28-26-29-32-46)59(82)70-53(41(9)10)65(88)73(18)48(33-38(3)4)58(81)67-44(14)57(80)68-45(15)61(84)74(19)50(34-39(5)6)63(86)75(20)51(35-40(7)8)64(87)76(21)54(42(11)12)66(89)77(55)22/h25-29,31-32,38-45,47-51,53-56,79H,23-24,30,33-37H2,1-22H3,(H,67,81)(H,68,80)(H,69,83)(H,70,82)/b27-25+/t43-,44+,45-,47+,48-,49+,50+,51+,53-,54+,55+,56-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents 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