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BDBM50357537 CHEMBL1914862

SMILES: CCOC(=O)c1ccc2n(CCCN3C[C@H](C)N[C@H](C)C3)c3ccccc3c2c1

InChI Key: InChIKey=OLMQTOGVUOQEDF-HDICACEKSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50357537   
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
Scavenger receptor class B member 1


(Homo sapiens (Human))
BDBM50357537
PNG
(CHEMBL1914862)
Show SMILES CCOC(=O)c1ccc2n(CCCN3C[C@H](C)N[C@H](C)C3)c3ccccc3c2c1 |r|
Show InChI InChI=1S/C24H31N3O2/c1-4-29-24(28)19-10-11-23-21(14-19)20-8-5-6-9-22(20)27(23)13-7-12-26-15-17(2)25-18(3)16-26/h5-6,8-11,14,17-18,25H,4,7,12-13,15-16H2,1-3H3/t17-,18+
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
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CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 600n/an/an/an/an/an/a



iTherX Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of human SRB1-mediated Hepatitis C virus genotype 2a entry into human 293T cells by immunoblotting


Bioorg Med Chem Lett 21: 6852-5 (2011)


Article DOI: 10.1016/j.bmcl.2011.09.019
BindingDB Entry DOI: 10.7270/Q2319W93
More data for this
Ligand-Target Pair