BDBM50293661 CHEMBL556256::trans-(1S(R),2S(R))-2-Hydroxycyclooctyl nitrate::trans-(1S(R),2S(R))-2-Hydroxycyclooctylnitrate

SMILES O[C@H]1CCCCCC[C@@H]1O[N+]([O-])=O

InChI Key InChIKey=IWKAONCFSJZOOC-YUMQZZPRSA-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 = 50293661   

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

Curated by ChEMBL
LigandPNGBDBM50293661(CHEMBL556256 | trans-(1S(R),2S(R))-2-Hydroxycycloo...)
Affinity DataKi:  2.19E+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
LigandPNGBDBM50293661(CHEMBL556256 | trans-(1S(R),2S(R))-2-Hydroxycycloo...)
Affinity DataKi:  2.67E+5nMAssay 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
LigandPNGBDBM50293661(CHEMBL556256 | trans-(1S(R),2S(R))-2-Hydroxycycloo...)
Affinity DataKi:  4.52E+7nMAssay Description:Noncompetitive 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
LigandPNGBDBM50293661(CHEMBL556256 | trans-(1S(R),2S(R))-2-Hydroxycycloo...)
Affinity DataIC50:  1.42E+4nMAssay Description:Inhibition of human erythrocyte glutathione reductaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed