null

SMILES NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O

InChI Key InChIKey=SBUJHOSQTJFQJX-NOAMYHISSA-N

PDB links: 26 PDB IDs match this monomer.

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50031282   

TargetPhospholipase A1 member A(Rattus norvegicus)
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50031282(CHEBI:17630 | Kanamycin)copy SMILEScopy InChI
Affinity DataIC50: 8.04E+4nMAssay Description:IC50 was measured as concentration causing 50% inhibition of lysosomal phospholipase A1 activity.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7MD4PubMed