BDBM50293660 CHEMBL563619::trans-(R(S))-2-Hydroxy-1-phenylethyl nitrate::trans-(R(S))-2-Hydroxy-1-phenylethylnitrate

SMILES OC[C@H](O[N+]([O-])=O)c1ccccc1

InChI Key InChIKey=HJZAIMHRCPGGNJ-QMMMGPOBSA-N

Data  3 KI  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50293660   

TargetGlutathione reductase, mitochondrial(Homo sapiens (Human))
Atat£Rk University

Curated by ChEMBL
LigandPNGBDBM50293660(CHEMBL563619 | trans-(R(S))-2-Hydroxy-1-phenylethy...)
Affinity DataKi:  2.56E+4nMAssay Description:Inhibition of human erythrocyte glutathione reductaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Atat£Rk University

Curated by ChEMBL
LigandPNGBDBM50293660(CHEMBL563619 | trans-(R(S))-2-Hydroxy-1-phenylethy...)
Affinity DataKi:  1.14E+6nMAssay Description:Noncompetitive inhibition of human carbonic anhydrase 2 esterase activity by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Atat£Rk University

Curated by ChEMBL
LigandPNGBDBM50293660(CHEMBL563619 | trans-(R(S))-2-Hydroxy-1-phenylethy...)
Affinity DataKi:  2.88E+8nMAssay Description:Uncompetitive inhibition of human carbonic anhydrase 1 esterase activity by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione reductase, mitochondrial(Homo sapiens (Human))
Atat£Rk University

Curated by ChEMBL
LigandPNGBDBM50293660(CHEMBL563619 | trans-(R(S))-2-Hydroxy-1-phenylethy...)
Affinity DataIC50:  1.60E+4nMAssay Description:Inhibition of human erythrocyte glutathione reductaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed