BDBM50666327 CHEMBL6175937

SMILES O=c1[nH]c(=O)n([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@@H]2O)cc1CO

InChI Key InChIKey=WQCABYUOJVUOEC-UHFFFAOYSA-N

Data  1 IC50  1 Kd

  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 = 50666327   

Target2'-deoxynucleoside 5'-phosphate N-hydrolase 1(Human)
Albert Einstein College of Medicine

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666327BDBM50666327(CHEMBL6175937)
Affinity DataKd: >5.00E+4nMAssay Description:Competitive inhibition of wild-type truncated human DNPH1 extracted from Escherichia coli BL21DE3 using hmdUMP as substrate preincubated for 30 mins ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
Target2'-deoxynucleoside 5'-phosphate N-hydrolase 1(Human)
Albert Einstein College of Medicine

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666327BDBM50666327(CHEMBL6175937)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of wild-type truncated human DNPH1 extracted from Escherichia coli BL21DE3 assessed as decrease in hmdUMP hydrolysis preincubated for 30 m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed