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BDBM345890 US10202367, Compound 36

SMILES: CC1OC(=NC1CN1CCC(CC1)C(=O)NCCCN1C[C@@H](C)C[C@@H](C)C1)c1c2ccccc2cc2ccccc12

InChI Key: InChIKey=GQESQKOGNYWDGM-CFNAWJCCSA-N

Data: 1 EC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 345890   
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 genotype 2a (isolate HC-J6) (HCV...)
BDBM345890
PNG
(US10202367, Compound 36)
Show SMILES CC1OC(=NC1CN1CCC(CC1)C(=O)NCCCN1C[C@@H](C)C[C@@H](C)C1)c1c2ccccc2cc2ccccc12 |r,c:3|
Show InChI InChI=1S/C35H46N4O2/c1-24-19-25(2)22-39(21-24)16-8-15-36-34(40)27-13-17-38(18-14-27)23-32-26(3)41-35(37-32)33-30-11-6-4-9-28(30)20-29-10-5-7-12-31(29)33/h4-7,9-12,20,24-27,32H,8,13-19,21-23H2,1-3H3,(H,36,40)/t24-,25+,26?,32?
PDB

UniProtKB/SwissProt

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PC cid
PC sid
UniChem
US Patent
n/an/an/an/a 214n/an/an/an/a



The United States of America, as represented by the Secretary, Department of Health and Human Services; University of Kansas

US Patent


Assay Description
This example demonstrates the EC50 and CC50 values against HCV according to the HCVcc-RLuc reporter assay described in Example 5 and the cytotoxicity...


US Patent US10202367 (2019)


BindingDB Entry DOI: 10.7270/Q23B6277
More data for this
Ligand-Target Pair