null

SMILES [H][C@]12O[C@H](COC)[C@@H](O)[C@H](O)[C@@]1([H])N=C(NCC)S2

InChI Key InChIKey=AVBFRSQZSIUFPO-JGKVKWKGSA-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 8 hits for monomerid = 50513936   

TargetProtein O-GlcNAcase(Homo sapiens (Human))
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50513936(CHEMBL4570378)copy SMILEScopy InChI
Affinity DataKi:  190nMAssay Description:Inhibition of recombinant human OGAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0QMHPubMed
TargetSodium channel protein type 5 subunit alpha(Homo sapiens (Human))
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50513936(CHEMBL4570378)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Nav1.5 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0QMHPubMed
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(Homo sapiens (Human))
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50513936(CHEMBL4570378)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of Cav1.2 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0QMHPubMed
TargetCytochrome P450 2D6(Homo sapiens (Human))
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50513936(CHEMBL4570378)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of CYP2D6 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0QMHPubMed
TargetCytochrome P450 2C9(Homo sapiens (Human))
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50513936(CHEMBL4570378)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of CYP2C9 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0QMHPubMed
TargetNuclear receptor subfamily 1 group I member 2(Homo sapiens (Human))
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50513936(CHEMBL4570378)copy SMILEScopy InChI
Affinity DataEC50: >3.00E+4nMAssay Description:Activation of PXR (unknown origin) assessed as CYP3A4 inductionMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0QMHPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50513936(CHEMBL4570378)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Displacement of MK-0499 from human ERGMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0QMHPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50513936(CHEMBL4570378)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21G0QMHPubMed