An inhibitor of uridine phosphorylase
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Cyclouridine is an inhibitor of uridine phosphorylase (apparent Ki = 2.268 ?M).1 It is selective for uridine phosphorylase over thymidine phosphorylase at 3.33 mM. Cyclouridine has also been used as a building block in the synthesis of compounds with anticancer or antiviral activities.2,3
1.Veres, Z., Szabolcs, A., Szinai, I., et al.5-Substituted-2,2'-anhydrouridines, potent inhibitors of uridine phosphorylaseBiochem. Pharmacol.34(10)1737-1740(1985) 2.Ogawa, A., Tanaka, M., Sasaki, T., et al.Nucleosides and nucleotides. 180. Synthesis and antitumor activity of nucleosides that have a hydroxylamino group instead of a hydroxyl group at the 2'- or 3'-position of the sugar moietyJ. Med. Chem.41(25)5094-5107(1998) 3.Sato, Y., Utsumi, K., Maruyama, T., et al.Synthesis and hypnotic and anti-human immunodeficiency virus-1 activities of N3-substituted 2'-deoxy-2'-fluorouridinesChem. Pharm. Bull. (Tokyo)42(3)595-598(1994)
LX1606 Hippurate (Telotristat etiprate)
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