BDBM50064268 CHEMBL44630::N-Cyclohexyl-N-isopropyl-formamide

SMILES CC(C)N(C=O)C1CCCCC1

InChI Key InChIKey=ZDNXEEKXUQSHTM-UHFFFAOYSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50064268   

TargetAlcohol dehydrogenase 1A(Homo sapiens (Human))
The University Of Iowa

Curated by ChEMBL
LigandPNGBDBM50064268(CHEMBL44630 | N-Cyclohexyl-N-isopropyl-formamide)
Affinity DataKi:  2.40E+4nMAssay Description:Inhibition of human alcohol dehydrogenase alpha activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAll-trans-retinol dehydrogenase [NAD(+)] ADH1B(Homo sapiens (Human))
The University Of Iowa

Curated by ChEMBL
LigandPNGBDBM50064268(CHEMBL44630 | N-Cyclohexyl-N-isopropyl-formamide)
Affinity DataKi:  4.60E+4nMAssay Description:Inhibition of human alcohol dehydrogenase beta 1 activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlcohol dehydrogenase 1C(Homo sapiens (Human))
The University Of Iowa

Curated by ChEMBL
LigandPNGBDBM50064268(CHEMBL44630 | N-Cyclohexyl-N-isopropyl-formamide)
Affinity DataKi:  8.30E+4nMAssay Description:Inhibition of human alcohol dehydrogenase gamma2 activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAll-trans-retinol dehydrogenase [NAD(+)] ADH4(Homo sapiens (Human))
The University Of Iowa

Curated by ChEMBL
LigandPNGBDBM50064268(CHEMBL44630 | N-Cyclohexyl-N-isopropyl-formamide)
Affinity DataKi:  1.50E+5nMAssay Description:Inhibition of human alcohol dehydrogenase pi activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAll-trans-retinol dehydrogenase [NAD(+)] ADH7(Homo sapiens (Human))
The University Of Iowa

Curated by ChEMBL
LigandPNGBDBM50064268(CHEMBL44630 | N-Cyclohexyl-N-isopropyl-formamide)
Affinity DataKi:  1.30E+6nMAssay Description:Inhibition of human alcohol dehydrogenase sigma activityMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed