Pyrazofurin |
| Katalog-Nr.GC37042 |
Pyrazofurin, ein Pyrimidin-Nucleosid-Analogon mit antineoplastischer AktivitÄt, hemmt die Zellproliferation und die DNA-Synthese in Zellen durch Hemmung der Uridin-5'-Phosphat (UMP)-Synthase. Pyrazofurin ist ein aktiver, sensitiver Orotat-Phosphoribosyltransferase-Inhibitor mit IC50-Werten zwischen 0,06 und 0,37 μM in den drei Plattenepithelkarzinom (SCC)-Zelllinien Hep-2, HNSCC-14B und HNSCC-14C.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 30868-30-5
Sample solution is provided at 25 µL, 10mM.
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Pyrazofurin, a pyrimidine nucleoside analogue with antineoplastic activity, inhibits cell proliferation and DNA synthesis in cells by inhibiting uridine 5'-phosphate (UMP) synthase[1]. Pyrazofurin is an active, sensitive orotate-phosphoribosyltransferase inhibitor with IC50s between 0.06-0.37 µM in the three squamous cell carcinoma (SCC) cell lines Hep-2, HNSCC-14B and HNSCC-14C[2].
[1]. Ringer DP, et al. Alteration in de novo pyrimidine biosynthesis during uridine reversal of pyrazofurin-inhibited DNA synthesis. Neuropsychopharmacology. J Biochem Toxicol. 1991 Spring;6(1):19-27. [2]. Peters GJ, et al. Antipyrimidine effects of five different pyrimidine de novo synthesis inhibitors in three head and neck cancer cell lines. Nucleosides Nucleotides Nucleic Acids. 2018;37(6):329-339.
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