6-Mercaptopurine

Discontinued Product

4103 has been discontinued.

View all DNA, RNA and Protein Synthesis products.
Description: Purine analog; inhibits DNA and RNA synthesis
Chemical Name: Purine-6(1H)-thione
Purity: ≥99% (HPLC)
Datasheet
Citations (1)
Reviews
Literature (2)

Biological Activity for 6-Mercaptopurine

6-Mercaptopurine is an inhibitor of de novo purine synthesis through interference with DNA and RNA synthesis. Immunosuppressive and antileukemic drug; reduces the anticoagulation elicited by warfarin. Active metabolite of azathioprine (Cat. No. 4099). Also inhibits SARS-CoV papain-like protease (PLpro; IC50 = 21.6 μM for PLpro deubiquitination activity).

Technical Data for 6-Mercaptopurine

M. Wt 152.18
Formula C5H4N4S
Storage Store at RT
Purity ≥99% (HPLC)
CAS Number 50-44-2
PubChem ID 3000241
InChI Key GLYGRBPLZURLDD-UHFFFAOYSA-N
Smiles S=C1C2C(N=CN2)N=CN1

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

Tocris products are intended for laboratory research use only, unless stated otherwise.

Product Datasheets for 6-Mercaptopurine

References for 6-Mercaptopurine

References are publications that support the biological activity of the product.

Sahasranaman et al (2008) Clinical pharmacology and pharmacogenetics of thiopurines. Eur.J.Clin.Pharmacol. 64 753 PMID: 18506437

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Keywords: 6-Mercaptopurine, 6-Mercaptopurine supplier, 6-Mercaptopurine, thiopurine, immunosuppressant, drug, 6-MP, purine, analog, chemotherapeutics, DNA,, RNA, and, Protein, Synthesis, Immunosuppressants, Papain-like, Proteases, 4103, Tocris Bioscience

1 Citation for 6-Mercaptopurine

Citations are publications that use Tocris products. Selected citations for 6-Mercaptopurine include:

Ari et al (2021) Combined epigenetic and metabolic treatments overcome differentiation blockade in acute myeloid leukemia. iScience 24 102651 PMID: 34151238


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Literature in this Area

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

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