BDBM50026894 CHEMBL2372465

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](CC(C)(C)O)N(C)C(=O)CN(C)C(=O)[C@H](CC)NC1=O)C(C)C

InChI Key: InChIKey=KVUFLOXJKUYFMQ-HQCNNLQUSA-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 = 50026894   

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))	BDBM50026894 (CHEMBL2372465) 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](CC(C)(C)O)N(C)C(=O)CN(C)C(=O)[C@H](CC)NC1=O)C(C)C |r| Show InChI InChI=1S/C63H113N11O13/c1-25-27-28-29-40(13)52(76)51-56(80)66-43(26-2)58(82)68(18)34-48(75)69(19)47(33-63(16,17)87)55(79)67-49(38(9)10)61(85)70(20)44(30-35(3)4)54(78)64-41(14)53(77)65-42(15)57(81)71(21)45(31-36(5)6)59(83)72(22)46(32-37(7)8)60(84)73(23)50(39(11)12)62(86)74(51)24/h27-28,35-47,49-52,76,87H,25-26,29-34H2,1-24H3,(H,64,78)(H,65,77)(H,66,80)(H,67,79)/b28-27+/t40-,41+,42-,43+,44-,45+,46+,47+,49-,50+,51+,52-/m1/s1	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