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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)NC(=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)C(=O)[C@@H](NC1=O)C(C)C)C(C)C

InChI Key: InChIKey=UYPPEWHLQQUDPM-PNVMGJOXSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50026899   
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))		BDBM50026899
PNG
(CHEMBL2372468)
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)NC(=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)C(=O)[C@@H](NC1=O)C(C)C)C(C)C |r|
Show InChI InChI=1S/C62H111N11O12/c1-25-26-27-40(16)52(75)51-57(80)67-48(37(10)11)60(83)68(19)32-47(74)69(20)44(29-34(4)5)56(79)66-49(38(12)13)61(84)71(22)45(30-35(6)7)54(77)63-41(17)53(76)64-42(18)58(81)70(21)46(31-36(8)9)55(78)65-43(28-33(2)3)59(82)72(23)50(39(14)15)62(85)73(51)24/h25-26,33-46,48-52,75H,27-32H2,1-24H3,(H,63,77)(H,64,76)(H,65,78)(H,66,79)(H,67,80)/b26-25+/t40-,41+,42-,43+,44-,45-,46+,48+,49-,50+,51+,52-/m1/s1
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Similars
PubMed
n/an/a>3.00E+3n/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