BDBM50323798 CHEMBL1214336::N-[5-(3-pyridinyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide

SMILES CC(C)S(=O)(=O)NC1Cc2ccc(cc2C1)-c1cccnc1

InChI Key InChIKey=JYFFQMUEOPGGBU-UHFFFAOYSA-N

Data  5 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 5 hits for monomerid = 50323798   

TargetCytochrome P450 3A4(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50323798(CHEMBL1214336 | N-[5-(3-pyridinyl)-2,3-dihydro-1H-...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human CYP3A4 after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50323798(CHEMBL1214336 | N-[5-(3-pyridinyl)-2,3-dihydro-1H-...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human CYP2D6 after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 1A2(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50323798(CHEMBL1214336 | N-[5-(3-pyridinyl)-2,3-dihydro-1H-...)
Affinity DataIC50:  600nMAssay Description:Inhibition of human CYP1A2 after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50323798(CHEMBL1214336 | N-[5-(3-pyridinyl)-2,3-dihydro-1H-...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human CYP2C9 after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCytochrome P450 2C19(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50323798(CHEMBL1214336 | N-[5-(3-pyridinyl)-2,3-dihydro-1H-...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human CYP2C19 after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed