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

InChI Key: InChIKey=RXPSXDYPRNOFLI-BUOJKCARSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50026925   
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))		BDBM50026925
PNG
(CHEMBL2372456)
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)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)C(C)NC(=O)[C@@H](CC(C)C)N(C)C(=O)[C@H](CCC)NC(=O)[C@@H](CC(C)C)N(C)C(=O)CN(C)C(=O)[C@H](CCC)NC1=O |r|
Show InChI InChI=1S/C63H113N11O12/c1-24-27-30-41(14)53(76)52-57(80)67-44(28-25-2)59(82)68(17)35-50(75)69(18)46(31-36(4)5)56(79)66-45(29-26-3)60(83)70(19)47(32-37(6)7)55(78)64-42(15)54(77)65-43(16)58(81)71(20)48(33-38(8)9)61(84)72(21)49(34-39(10)11)62(85)73(22)51(40(12)13)63(86)74(52)23/h24,27,36-49,51-53,76H,25-26,28-35H2,1-23H3,(H,64,78)(H,65,77)(H,66,79)(H,67,80)/b27-24+/t41-,42?,43-,44+,45+,46-,47-,48+,49+,51+,52+,53-/m1/s1
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Similars
PubMed
n/an/a 3.40E+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