BDBM50519494 CHEMBL1234234

SMILES CSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2[C@H](O)CNC=Nc12

InChI Key InChIKey=QLPPCUVJNCMYFD-SANHVUMCSA-N

Data  3 KI

PDB links: 4 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 3 hits for monomerid = 50519494   

TargetAdenosine deaminase(Plasmodium falciparum)
Universit£

Curated by ChEMBL
LigandPNGBDBM50519494(CHEMBL1234234)
Affinity DataKi:  0.430nMAssay Description:Inhibition of Plasmodium falciparum N-terminal thrombin cleavable His6-tagged ADA expressed in Escherichia coli BL21 assessed as equilibrium dissocia...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails ArticlePubMed
TargetAdenosine deaminase(Plasmodium falciparum)
Universit£

Curated by ChEMBL
LigandPNGBDBM50519494(CHEMBL1234234)
Affinity DataKi:  2.70nMAssay Description:Inhibition of Plasmodium falciparum N-terminal thrombin cleavable His6-tagged ADA expressed in Escherichia coli BL21 assessed as reduction in formati...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails ArticlePubMed
TargetAdenosine deaminase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50519494(CHEMBL1234234)
Affinity DataKi: >10nMAssay Description:Inhibition of human erythrocytes ADA assessed as reduction in formation of inosine using adenosine as substrateMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails ArticlePubMed