Drug intelligence / Profile preview

6-mercaptopurine riboside

Development stage
Unknown
Lead developer
Fox Chase Cancer Center
Modality
Small Molecules
Administration
(Not Explicitly Specified For 6-mercaptopurine Riboside In Humans; For Related Compounds, Oral And Intravenous Listed[5], But Route For 6-mercaptopurine Riboside Is Likely Investigational And Not Established Clinically.)
01

Overview

6-mercaptopurine riboside is a **small molecule purine analog** that is a riboside derivative of 6-mercaptopurine. Like its parent compound, it functions as an **inhibitor of de novo purine synthesis** and interconversion pathways. 6-mercaptopurine riboside acts primarily through inhibition of **phosphoribosyl amidotransferase (PPAT)**, which is key in the first step of purine nucleotide biosynthesis. It has been studied as an antineoplastic agent, particularly in the context of **neoplasms** and disorders related to **purine metabolism**. Its primary experimental indications relate to cancer, including pancreatic cancer and potentially other types of neoplasms[1][2].

Other names
6-MPR6-Methylmercaptopurine riboside6-(Methylthio)purine ribonucleoside6-S-methyl-6-thioinosine
02

Targets

PPAT (Amidophosphoribosyltransferase)

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