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MedKoo product information:

Uridine triacetate

MedKoo Code#:  203090

Name:  Uridine triacetate

CAS#:  4105-38-8

 

Synonym:   vistonuridine,

 

IUPAC/Chemical name: 

(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3,4-diyl diacetate

 

Chemical structure Theoretical analysis

 

 

 

Chemical Formula: C15H18N2O9

Exact Mass: 370.10123

Molecular Weight: 370.31

m/z: 370.10123 (100.0%), 371.10459 (16.2%), 372.10548 (1.8%), 372.10794 (1.2%)

Elemental Analysis: C, 48.65; H, 4.90; N, 7.56; O, 38.88

 

 

Availability and price:

Uridine triacetate (98%)  is in stock.

 

To inquire quotation or to ask questions, please send email to sales@medkoo.com to describe your needs. A representative will respond your email shortly. We offer big discount for orders of bulk quantities.

 

 

Information about this agent

Uridine triacetate, formerly known as vistonuridine, is an orally active prodrug of uridine, meaning that uridine triacetate is converted to uridine in the body. Once uridine triacetate is converted to uridine, it reduces the incorporation of 5-FU metabolites into the genetic material of non-cancerous cells. Because of the poor bioavailability of oral uridine, however, and because of complications associated with intravenously administered uridine, uridine itself is not a clinically viable treatment for 5-FU overexposure. Uridine triacetate delivers about eight-fold more uridine into the bloodstream than does oral administration of uridine. Wellstat is also investigating the potential use of uridine triacetate when given after 5-FU administration to cancer patients to achieve higher, more effective doses of 5-FU while preserving an acceptable margin of safety.  see: http://www.medicalnewstoday.com/articles/189546.php.

 

According to news published in 21 May 2010, uridine triacetate has further demonstrated its life-saving potential in treating patients overexposed to the widely used cancer chemotherapy 5-fluorouracil (5-FU), according to clinical data to be presented June 7 at the annual meeting of the American Society of Clinical Oncology (ASCO) in Chicago. see http://www.medicalnewstoday.com/articles/189546.php.

 

Wellstat Releases Investigational Drug Uridine Triacetate Clinical Results
By PBR Staff Writer Published 21 May 2010
Wellstat Therapeutics has released clinical results of its investigational drug Uridine triacetate for treating patients overexposed to the widely used cancer chemotherapy 5-fluorouracil (5-FU). Wellstat Therapeutics said that while no antidote for 5-FU overexposure has been approved by regulatory authorities, Uridine triacetate (formerly known as vistonuridine) has been made available to physicians for emergency use. Wellstat Therapeutics' trial was made on 37 cases of 5-FU overexposure, all of them treated with Uridine triacetate. In all of these cases, the patients recovered from the overexposure, even though a fatal outcome for at least 27 of them would have been predicted by the dose and rate of 5-FU administration. In one extreme case, the patient survived after receiving a 5-FU dose 10 times higher than intended (10,000mg in three hours instead of 1,000mg in one hour). Reportedly, in all cases, the emergency treatment commenced as rapidly as possible after 5-FU overexposure (within 8 to 96 hours), depending on the timing of the request to Wellstat and the location of the treatment site.  Michael Bamat, vice president of research and development at Wellstat, said: “Since our first report on uridine triacetate at ASCO in 2009, the number of patients treated with this investigational antidote has more than doubled.”

Current developer:    Wellstat Therapeutics Corporation

 

References

 1: Morrey JD, Smee DF, Sidwell RW, Tseng C. Identification of active antiviral compounds against a New York isolate of West Nile virus. Antiviral Res. 2002 Jul;55(1):107-16. PubMed PMID: 12076755.

2: Tanaka H, Kawakita K, Suzuki H, Spiri-Nakagawa P, Omura S. The mode of action of cervinomycin in Staphylococcus aureus. J Antibiot (Tokyo). 1989 Mar;42(3):431-9. PubMed PMID: 2708137.

3: Cihák A, Vesely J, Skoda J. Azapyrimidine nucleosides: metabolism and inhibitory mechanisms. Adv Enzyme Regul. 1985;24:335-54. Review. PubMed PMID: 2424284.

4: Slavik M, Blanc O, Smith KJ, Slavik J. 6-azauridine triacetate induced hyper beta-alaninemia and its decrease by administration of pyridoxine. J Nutr Sci Vitaminol (Tokyo). 1983 Oct;29(5):631-5. PubMed PMID: 6198500.

5: Slavik M, Smith KJ, Blanc O. Decrease of serum pyridoxal phosphate levels and homocystinemia after administration of 6-azauridine triacetate and their prevention by administration of pyridoxine. Biochem Pharmacol. 1982 Dec 15;31(24):4089-92. PubMed PMID: 6186258.

6: Smee DF, Sidwell RW, Clark SM, Barnett BB, Spendlove RS. Inhibition of rotaviruses by selected antiviral substances: mechanisms of viral inhibition and in vivo activity. Antimicrob Agents Chemother. 1982 Jan;21(1):66-73. PubMed PMID: 6282209; PubMed Central PMCID: PMC181831.

7: Smee DF, Sidwell RW, Clark SM, Barnett BB, Spendlove RS. Inhibition of bluetongue and Colorado tick fever orbiviruses by selected antiviral substances. Antimicrob Agents Chemother. 1981 Oct;20(4):533-8. PubMed PMID: 6282197; PubMed Central PMCID: PMC181738.

8: Slavik M. Changes in amino acid metabolism caused by 6-azauridine triacetate: relevance to cancer treatment. Cancer Treat Rep. 1979 Jun;63(6):1041-4. PubMed PMID: 582429.

9: Deneau DG, Farber EM. The treatment of psoriasis with azaribine. Dermatologica. 1975;151(3):158-63. PubMed PMID: 1243822.

10: Catalanotto FA, Slavik M, Danilson D, Keiser HR, Henkin RI. Changes in preference for NaCl following administration of 6-azauridine and 6-azauridine triacetate. Pharmacol Ther Dent. 1975;2(1):25-32. PubMed PMID: 1054856.

11: Slavik M, Danilson DA, Keiser HR, Henkin RI. Alterations in metabolism of copper and zinc after administration of 6-azauridine triacetate. Biochem Pharmacol. 1973 Sep 15;22(18):2349-52. PubMed PMID: 4733685.

12: Perlík F, Elis J, Kubíková M. Antibody response in psoriatic patients treated with 6-azauridine-triacetate. Eur J Clin Pharmacol. 1973 Aug;6(2):141-3. PubMed PMID: 4769697.

13: Slavik M, Lovenberg W, Keiser HR. Changes in serum and urine amino acids in patients with progressive systemic sclerosis treated with 6-azauridine triacetate. Biochem Pharmacol. 1973 Jun 1;22(11):1295-300. PubMed PMID: 4727783. 

 

 

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