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SMILES: CN(C)[C@@H](C(=O)N1CCC[C@H]1C(=O)Nc1ccc2-c3[nH]c4ccc(NC(=O)[C@@H]5CCCN5C(=O)[C@H](N(C)C)c5ccccc5)cc4c3CCCc2c1)c1ccccc1

InChI Key:

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   Substructure
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 516553   
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
Genome polyprotein


(Hepatitis C Virus (Virus))
BDBM516553
PNG
((2S,2'S)-N,N'-5,6,7,12- tetrahydrobenzo[6,7]cycloh...)
Show SMILES CN(C)[C@@H](C(=O)N1CCC[C@H]1C(=O)Nc1ccc2-c3[nH]c4ccc(NC(=O)[C@@H]5CCCN5C(=O)[C@H](N(C)C)c5ccccc5)cc4c3CCCc2c1)c1ccccc1 |r|
PDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a 0.0100n/an/an/an/a


TBA

Assay Description
Measurement of inhibition by compounds was performed using the HCV replicon system. Several different replicons encoding different HCV genotypes or m...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2WW7MVZ
More data for this
Ligand-Target Pair