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BDBM50051694 CHEMBL3311133

SMILES: CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(OC(C)(C)C)cc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O

InChI Key: InChIKey=QVULXCXSQLREIV-LVZHEHNUSA-N

Data: 1 Kd

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50051694   
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))
BDBM50051694
PNG
(CHEMBL3311133)
Show SMILES CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(OC(C)(C)C)cc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc1ccccc1)C(O)=O |r|
Show InChI InChI=1S/C48H67N5O9/c1-30(2)25-36(50-44(57)39(53-46(60)62-48(8,9)10)28-34-21-23-35(24-22-34)61-47(5,6)7)41(54)51-38(27-32-17-13-11-14-18-32)43(56)49-37(26-31(3)4)42(55)52-40(45(58)59)29-33-19-15-12-16-20-33/h11-24,30-31,36-40H,25-29H2,1-10H3,(H,49,56)(H,50,57)(H,51,54)(H,52,55)(H,53,60)(H,58,59)/t36-,37-,38+,39+,40+/m1/s1
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Article
PubMed
n/an/an/a 62n/an/an/an/an/a



Saga University

Curated by ChEMBL


Assay Description
Antagonist activity at formyl peptide receptor in human HL60 cells assessed as inhibition of intracellular calcium mobilization incubated for 5 mins ...


Bioorg Med Chem 22: 3824-8 (2014)


Article DOI: 10.1016/j.bmc.2014.06.048
BindingDB Entry DOI: 10.7270/Q28S4RK8
More data for this
Ligand-Target Pair