forodesine   Click here for help

GtoPdb Ligand ID: 8272

Synonyms: BCX-1777 | BCX1777 | Fodosine® (proposed trade name) | immucillin H | immucillin-H
PDB Ligand Antimalarial Ligand
Compound class: Synthetic organic
Comment: Forodesine is a picomolar inhibitor of purine nucleoside phosphorylase (PNP) [1,4].

The Malaria tab on this ligand page provides additional curator comments of relevance to the Guide to MALARIA PHARMACOLOGY.
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2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 6
Hydrogen bond donors 6
Rotatable bonds 2
Topological polar surface area 134.26
Molecular weight 266.1
XLogP 0.72
No. Lipinski's rules broken 1
SMILES / InChI / InChIKey
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Canonical SMILES OCC1NC(C(C1O)O)c1c[nH]c2c1[nH]cnc2=O
Isomeric SMILES OC[C@H]1N[C@H]([C@@H]([C@@H]1O)O)c1c[nH]c2c1[nH]cnc2=O
InChI InChI=1S/C11H14N4O4/c16-2-5-9(17)10(18)7(15-5)4-1-12-8-6(4)13-3-14-11(8)19/h1,3,5,7,9-10,12,15-18H,2H2,(H,13,14,19)/t5-,7+,9-,10+/m1/s1
InChI Key IWKXDMQDITUYRK-KUBHLMPHSA-N
Selectivity at enzymes
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Target Sp. Type Action Value Parameter Concentration range (M) Reference
purine nucleoside phosphorylase Primary target of this compound Hs Inhibitor Inhibition 10.1 pKi - 4
pKi 10.1 (Ki 7.2x10-11 M) [4]
Selectivity at other protein targets
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Target Sp. Type Action Value Parameter Concentration range (M) Reference
Plasmodium falciparum purine nucleoside phosphorylase Pf Inhibitor - 9.2 pKi - 2
pKi 9.2 (Ki 6x10-10 M) [2]
Whole organism assay data
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MOA/likely target Sp. Assay description Type Action Value Parameter Concentration range (M) Reference
Plasmodium falciparum purine nucleoside phosphorylase Pf Parasite growth inhibition assay - - 7.5 pIC50 - 3
pIC50 7.5 (IC50 3.5x10-8 M) Tran35S incorporation [3]
Lifecycle stages: Plasmodium asexual blood stage (erythrocytic merozoite, trophozoite, erythrocytic schizont)