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BDBM50542149 CHEMBL4632607

SMILES: Cc1ccc(NC(=O)[C@@H]2CC3(CC3)CN2C(=O)[C@H](CC2CCCC2)CC(=O)NO)cc1

InChI Key: InChIKey=BJMIBMGVBBSKLH-QUCCMNQESA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50542149   
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
Peptide deformylase mitochondrial


(Homo sapiens (Human))
BDBM50542149
PNG
(CHEMBL4632607)
Show SMILES Cc1ccc(NC(=O)[C@@H]2CC3(CC3)CN2C(=O)[C@H](CC2CCCC2)CC(=O)NO)cc1 |r|
Show InChI InChI=1S/C24H33N3O4/c1-16-6-8-19(9-7-16)25-22(29)20-14-24(10-11-24)15-27(20)23(30)18(13-21(28)26-31)12-17-4-2-3-5-17/h6-9,17-18,20,31H,2-5,10-15H2,1H3,(H,25,29)(H,26,28)/t18-,20+/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
PubMed
n/an/a 3.60n/an/an/an/an/an/a



Sun Yat-sen University

Curated by ChEMBL


Assay Description
Inhibition of human PDF expressed in Escherichia coli BL21 pLysS using formyl-Met-Ala-His-Ala peptide as substrate measured after 1 hr by fluorescami...


J Med Chem 63: 6959-6978 (2020)

More data for this
Ligand-Target Pair