BDBM50026907 CHEMBL2372461

SMILES: [H][C@]1(NC(=O)[C@]([H])([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)N(C)C(=O)[C@@]([H])(NC(=O)[C@@H](CC(C)C)N(C)C(=O)CN(C)C1=O)[C@@H](C)CC)[C@@H](C)O

InChI Key: InChIKey=IZUOWPDPGMBNCB-GPOCBZBZSA-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 = 50026907   

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))	BDBM50026907 (CHEMBL2372461) Show SMILES [H][C@]1(NC(=O)[C@]([H])([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)N(C)C(=O)[C@@]([H])(NC(=O)[C@@H](CC(C)C)N(C)C(=O)CN(C)C1=O)[C@@H](C)CC)[C@@H](C)O |r| Show InChI InChI=1S/C63H113N11O13/c1-25-27-28-40(14)53(77)52-57(81)67-50(43(17)75)61(85)68(18)33-48(76)69(19)44(29-34(3)4)56(80)66-49(39(13)26-2)62(86)70(20)45(30-35(5)6)55(79)64-41(15)54(78)65-42(16)58(82)71(21)46(31-36(7)8)59(83)72(22)47(32-37(9)10)60(84)73(23)51(38(11)12)63(87)74(52)24/h25,27,34-47,49-53,75,77H,26,28-33H2,1-24H3,(H,64,79)(H,65,78)(H,66,80)(H,67,81)/b27-25+/t39-,40+,41-,42+,43+,44+,45+,46-,47-,49-,50-,51-,52-,53+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.30E+3	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