BDBM50247149 5'-Methylthio-ImmH::CHEMBL473929::US9290501, (A)
SMILES CSC[C@H]1N[C@H]([C@H](O)[C@@H]1O)c1c[nH]c2c1nc[nH]c2=O
InChI Key InChIKey=CEGIKIXYDFDYDN-UHFFFAOYSA-N
Data 4 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 50247149
TargetS-methyl-5'-thioinosine phosphorylase(Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 /...)
Albert Einstein College of Medicine
US Patent
Albert Einstein College of Medicine
US Patent
Affinity DataKi: 0.0760nM ΔG°: -13.8kcal/molepH: 7.4 T: 2°CAssay Description:Assays for slow-onset inhibitors were carried out by adding 1 nM PaMTIP into reaction mixtures at 25 °C. containing 100 mM Hepes, pH 7.4, 100 mM ...More data for this Ligand-Target Pair
TargetPurine nucleoside phosphorylase(malaria parasite P. falciparum)
University of Montpellier
Curated by ChEMBL
University of Montpellier
Curated by ChEMBL
Affinity DataKi: 2.70nMAssay Description:Inhibition of Plasmodium falciparum 3D7 PNP expressed in Escherichia coli assessed as reduction in uric acid formation by spectrophotometric methodMore data for this Ligand-Target Pair
TargetPurine nucleoside phosphorylase(Human)
Albert Einstein College of Medicine of Yeshiva University
Curated by ChEMBL
Albert Einstein College of Medicine of Yeshiva University
Curated by ChEMBL
Affinity DataKi: 101nMAssay Description:Initial binding affinity to wild type human PNPMore data for this Ligand-Target Pair
TargetPurine nucleoside phosphorylase(Human)
Albert Einstein College of Medicine of Yeshiva University
Curated by ChEMBL
Albert Einstein College of Medicine of Yeshiva University
Curated by ChEMBL
Affinity DataKi: 303nMAssay Description:Inhibition of human PNP expressed in Escherichia coli assessed as reduction in uric acid formation by spectrophotometric methodMore data for this Ligand-Target Pair
