BDBM50565988 CHEMBL4785533

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](CC(O)=O)Nc1ccc([N+]([O-])=O)c2nonc12)[C@H](C)CCC(=O)OCCN=[N+]=[N-]

InChI Key InChIKey=PEAYJMZIZUBTMO-WNRPKZJSSA-N

Data  2 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 2 hits for monomerid = 50565988   

TargetBeta-galactoside alpha-2,6-sialyltransferase 1(Homo sapiens (Human))
Academia Sinica

Curated by ChEMBL
LigandPNGBDBM50565988(CHEMBL4785533)
Affinity DataIC50:  4.20E+3nMAssay 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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
LigandPNGBDBM50565988(CHEMBL4785533)
Affinity DataIC50:  800nMAssay 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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed