null

SMILES CC(C)(C)c1ccc(SCC(C2CCNCC2)c2cnc[nH]2)cc1

InChI Key InChIKey=VGVKTKUHIJKMHS-UHFFFAOYSA-N

  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 4 hits for monomerid = 50326292   

TargetCytochrome P450 3A4(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326292(4-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+3nMAssay Description:Inhibition of CYP3A4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326292(4-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of CYP2C19More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326292(4-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of CYP2D6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by ChEMBL
LigandPNGBDBM50326292(4-(2-(4-tert-Butylphenylthio)-1-(1H-imidazol-4-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of CYP1A2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QF8T3XPubMed