BDBM50160858 CHEMBL384970::Fullerene Derivative

SMILES C[N+]1(C)C[C@]23[C@H]4[C@@H]5C6=C7c8c4c4C2=C2[C@H]9[C@H]%10c4c-4c8[C@@H]8[C@@H]%11c%12c-4c%10c4c%10c9c9c2c2c%13c%14c(c5c5c6c6c%15c%16c(c%11c%11c%12c4c4c%10c%10c9c%13c9c%12c%14c5c%15c%12c5c%16c%11c4c5c%109)[C@]64C[N+](C)(C)C[C@@]784)[C@@]32C1

InChI Key InChIKey=SWOPXYYGQCBEHG-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50160858   

TargetRNA-directed RNA polymerase(Hepatitis C virus genotype 1b (isolate Con1) (HCV))
Kyoritsu University of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50160858(Fullerene Derivative | CHEMBL384970)
Affinity DataIC50: 310nMAssay Description:Inhibitory concentration against Hepatitis C virus-RNA-dependent RNA polymeraseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus type 1)
Kyoritsu University of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50160858(Fullerene Derivative | CHEMBL384970)
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibitory concentration against HIV-Reverse transcriptaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed