Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H11N5O |
Molecular Weight | 241.2486 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC2=C(NC=C2CC3=CN=CC=C3)C(=O)N1
InChI
InChIKey=DOHVAKFYAHLCJP-UHFFFAOYSA-N
InChI=1S/C12H11N5O/c13-12-16-9-8(4-7-2-1-3-14-5-7)6-15-10(9)11(18)17-12/h1-3,5-6,15H,4H2,(H3,13,16,17,18)
Peldesine (also known as BCX-34) was developed as a purine nucleoside phosphorylase (PNP) inhibitor. It is known PNP inhibitors may be useful for treating a variety of T-cell related autoimmune diseases including psoriasis, rheumatoid arthritis, and Crohn s disease and T-cell cancers. Peldesine has undergone phase I trials for the treatment of human Immunodeficiency virus (HIV) infections. In addition, this drug participated in phase III clinical trial as a topical therapy for cutaneous T-cell lymphoma. This drug was also studied as a potential therapy for psoriasis, multiple sclerosis; rheumatoid arthritis; transplant rejection. However, all these indications were discontinued because of the lack of significant effects over placebo.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11369904
peldesine (BCX-34) in a 1% dermal cream formulation. BCX-34 dermal cream 1% or the vehicle cream (as a placebo control) was applied twice daily to the entire skin surface for up to 24 weeks.
Route of Administration:
Topical
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NCI_THESAURUS |
C2151
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FDA ORPHAN DRUG |
76293
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7405
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GG-27
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DTXSID10158107
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CHEMBL311300
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C1650
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135413525
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133432-71-0
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C104194
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DB02568
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7B646RJ70F
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SUB09649MIG
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100000083007
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ACTIVE MOIETY