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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](CO)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](CC)NC1=O)C(C)C

InChI Key: InChIKey=HNJSIYQWJAJGOC-YZEMNDORSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50026933   
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))		BDBM50026933
PNG
(CHEMBL2372491)
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](CO)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](CC)NC1=O)C(C)C |r|
Show InChI InChI=1S/C63H113N11O13/c1-24-26-27-28-41(15)53(77)52-57(81)65-43(25-2)58(82)68(17)33-49(76)69(18)45(29-35(3)4)56(80)67-50(39(11)12)62(86)70(19)46(30-36(5)6)55(79)64-42(16)54(78)66-44(34-75)59(83)71(20)47(31-37(7)8)60(84)72(21)48(32-38(9)10)61(85)73(22)51(40(13)14)63(87)74(52)23/h26-27,35-48,50-53,75,77H,24-25,28-34H2,1-23H3,(H,64,79)(H,65,81)(H,66,78)(H,67,80)/b27-26+/t41-,42+,43+,44-,45-,46-,47+,48+,50-,51+,52+,53-/m1/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