BDBM50565993 CHEMBL4797481

SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@@H](CC[C@]4(C)[C@@]3([H])CC[C@]12C)OC(=O)[C@@H](N)CC(O)=O)[C@H](C)CCC(O)=O

InChI Key InChIKey=NUUCRVJEHQBAKP-CNZWOIIDSA-N

Data  3 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 3 hits for monomerid = 50565993   

LigandPNGBDBM50565993(CHEMBL4797481)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of rat alpha-2,3-N-ST3GALIII assessed as reduction in sialylated-product formation using Gal-beta1-4Glc and CMP-NeuSAc incubated for 1.5 h...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSialyltransferase ST3Gal-I(Rattus norvegicus)
Academia Sinica

Curated by ChEMBL
LigandPNGBDBM50565993(CHEMBL4797481)
Affinity DataIC50:  3.90E+4nMAssay Description:Inhibition of rat alpha-2,3-O-ST3GALI assessed as reduction in sialylated-product formation using p-nitrophenyl T-antigen and CMP-NeuSAc incubated fo...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Academia Sinica

Curated by ChEMBL
LigandPNGBDBM50565993(CHEMBL4797481)
Affinity DataIC50:  1.58E+4nMAssay Description:Inhibition of human alpha-2,6-ST6GAL1 assessed as reduction in sialylated-product formation using Gal-beta1-4GlcNac and CMP-NeuSAc incubated for 15 m...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed