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CAS RN: 69304-47-8 | Product Number: B3404

(E)-5-(2-Bromovinyl)-2'-deoxyuridine


Purity: >98.0%(T)(HPLC)
Synonyms:
  • Brivudine
  • BVdU
Product Documents:
100MG
£99.00
1   5  

*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).


Supplemental Product Information:

This product is a sample for RUO (research use only). Do not use this product for any purpose other than testing and research.

Product Number B3404
Purity / Analysis Method >98.0%(T)(HPLC)
Molecular Formula / Molecular Weight C__1__1H__1__3BrN__2O__5 = 333.14 
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
Condition to Avoid Heat Sensitive
Packaging and Container 100MG-Glass Bottle with Plastic Insert (View image)
CAS RN 69304-47-8
Reaxys Registry Number 758153
PubChem Substance ID 87561214
Merck Index (14) 1378
MDL Number

MFCD00058585

Specifications
Appearance White to Almost white powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(Neutralization titration) min. 98.0 %
Specific rotation [a]20/D +8.0 to +10.0 deg(C=1, MeOH)
NMR confirm to structure
Properties (reference)
Melting Point 166 °C(dec.)
Specific Rotation 9° (C=1,MeOH)
GHS
Related Laws:
RTECS# YU7355000
Transport Information:
HS Number 2934999090
Application
Brivudine (BVdU): A Nucleoside Analogue Anti-Herpesvirus Agent

Brivudine (BVdU) is a nucleoside analogue anti-herpesvirus agent, and is often used for treatment of herpes simplex virus-1 (HSV-1) and varicella-zoster virus (VZV) infections. Brivudine blocks the action of DNA polymerases, thus inhibiting viral replication. Brivudine owes its effect to preferential phosphorylation by virus-encoded thymidine kinase to its 5'-diphosphate form. After further conversion to triphosphate form, it acts as an inhibitor or alternate substrate for the viral DNA polymerase. Brivudine is also characterized by a well described fatal drug interaction with antitumor agents such as 5-fluorouracil (5-FU) [F0151] and its prodrugs. This is caused by the main metabolite, bromovinyluracil (BVU), irreversibly inhibiting the enzyme dihydropyrimidine dehydrogenase (DPD) which is necessary for inactivating 5-FU. (The product is for research purpose only.)

References


PubMed Literature


TCIMAIL
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