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

InChI Key: InChIKey=WGLJIVGIBDNIIT-NOATZLMBSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50026930   
Target/Host
(Institution)		LigandTarget/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		pHTemp
°C
fMet-Leu-Phe receptor


(Homo sapiens (Human))		BDBM50026930
PNG
(CHEMBL2372458)
Show SMILES CC(C)C[C@H]1N(C)C(=O)CN(C)C(=O)[C@@H](NC(=O)[C@H](CC(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](NC1=O)C(C)C)C(C)C |r|
Show InChI InChI=1S/C60H109N11O11/c1-32(2)26-42-53(75)64-49(38(13)14)59(81)67(21)43(27-33(3)4)52(74)61-40(17)51(73)62-41(18)55(77)69(23)45(29-35(7)8)56(78)70(24)46(30-36(9)10)57(79)71(25)50(39(15)16)60(82)68(22)44(28-34(5)6)54(76)63-48(37(11)12)58(80)65(19)31-47(72)66(42)20/h32-46,48-50H,26-31H2,1-25H3,(H,61,74)(H,62,73)(H,63,76)(H,64,75)/t40-,41+,42+,43+,44-,45-,46-,48-,49-,50-/m0/s1
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PubMed
n/an/a>1.00E+4n/an/an/an/an/an/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