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BDBM50500140 CHEMBL3103854

SMILES: COc1cccc2C(=O)C3=C([C@@H](C)O[C@@H](Cn4cc(nn4)-c4ccccc4)C3)C(=O)c12

InChI Key: InChIKey=RHGXPWJMJQUARQ-GDBMZVCRSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50500140   
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
Indoleamine 2,3-dioxygenase


(Homo sapiens (Human))
BDBM50500140
PNG
(CHEMBL3103854)
Show SMILES COc1cccc2C(=O)C3=C([C@@H](C)O[C@@H](Cn4cc(nn4)-c4ccccc4)C3)C(=O)c12 |r,t:9|
Show InChI InChI=1S/C24H21N3O4/c1-14-21-18(23(28)17-9-6-10-20(30-2)22(17)24(21)29)11-16(31-14)12-27-13-19(25-26-27)15-7-4-3-5-8-15/h3-10,13-14,16H,11-12H2,1-2H3/t14-,16-/m1/s1
PDB
MMDB

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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 6.00E+3n/an/an/an/an/an/a



SIB Swiss Institute of Bioinformatics

Curated by ChEMBL


Assay Description
Inhibition of 6His-tagged human recombinant IDO1 expressed in Escherichia coli EC 539 using L-tryptophan as substrate after 1 hr by plate reader anal...


J Med Chem 58: 9421-37 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00326
BindingDB Entry DOI: 10.7270/Q28K7D3X
More data for this
Ligand-Target Pair