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

InChI Key: InChIKey=LPPAMBZXYZKEIN-AVDZQHQQSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50026909   
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))		BDBM50026909
PNG
(CHEMBL2372506)
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](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](CC(C)C)NC(=O)[C@@H](CC(C)C)N(C)C(=O)CN(C)C1=O)[C@@H](C)O |r|
Show InChI InChI=1S/C59H105N11O13/c1-23-24-25-36(12)49(73)48-54(78)64-46(40(16)71)58(82)65(17)30-45(72)66(18)42(27-32(4)5)53(77)63-41(26-31(2)3)57(81)68(20)44(29-34(8)9)51(75)60-37(13)50(74)61-38(14)55(79)67(19)43(28-33(6)7)52(76)62-39(15)56(80)69(21)47(35(10)11)59(83)70(48)22/h23-24,31-44,46-49,71,73H,25-30H2,1-22H3,(H,60,75)(H,61,74)(H,62,76)(H,63,77)(H,64,78)/b24-23+/t36-,37+,38-,39+,40-,41+,42-,43+,44-,46+,47+,48+,49-/m1/s1
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PubMed
n/an/a 3.25E+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