BDBM60894 BDBM50392256::US9200020, Table 3 compound 9B
SMILES OC(=O)CCCN(CCn1cnc2c1nc[nH]c2=O)CCP(O)(O)=O
InChI Key InChIKey=OHSLVUIGAJNHRN-UHFFFAOYSA-N
Data 4 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 60894
Affinity DataKi: 1.60E+3nM ΔG°: -8.22kcal/moleT: 2°CAssay Description:The [3H]-hypoxanthine growth inhibition assay (Desjardins et al., 1979 Antimicrobial Agents Chemother 16: 710-718) was used to evaluate the in vitro ...More data for this Ligand-Target Pair
Affinity DataKi: 5.40E+3nM ΔG°: -7.47kcal/moleT: 2°CAssay Description:The [3H]-hypoxanthine growth inhibition assay (Desjardins et al., 1979 Antimicrobial Agents Chemother 16: 710-718) was used to evaluate the in vitro ...More data for this Ligand-Target Pair
Affinity DataKi: 5.40E+3nMAssay Description:Inhibition of human HGPRT using Prib-PP as substrate by spectrophotometric assay in presence of guanineMore data for this Ligand-Target Pair
TargetHypoxanthine-guanine-xanthine phosphoribosyltransferase(Plasmodium falciparum)
The University of Queensland
US Patent
The University of Queensland
US Patent
Affinity DataKi: >2.10E+5nM ΔG°: >-5.22kcal/moleT: 2°CAssay Description:The [3H]-hypoxanthine growth inhibition assay (Desjardins et al., 1979 Antimicrobial Agents Chemother 16: 710-718) was used to evaluate the in vitro ...More data for this Ligand-Target Pair