3'-Azido-3'-deoxy-5-methyl-beta-L-uridine

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3'-Azido-3'-deoxy-5-methyl-beta-L-uridine manufacturers

3'-Azido-3'-deoxy-5-methyl-beta-L-uridine Basic information
Product Name:3'-Azido-3'-deoxy-5-methyl-beta-L-uridine
Synonyms:3'-Azido-3'-deoxy-5-methyl-beta-L-uridine;3’-Azido-3’-deoxy-5-methyl-β-L-uridine;3'-Azido-3'-deoxy-5-methyl-b-L-uridine;3’-Azido-3’-deoxy-5-methyl-beta-L-uridine;N-[(3-ethoxyphenyl)methyl]-4-[(4-methylphenyl)methyl]-5-oxomorpholine-3-carboxamide
CAS:2095417-10-8
MF:C10H13N5O5
MW:283.24
EINECS:
Product Categories:
Mol File:2095417-10-8.mol
3'-Azido-3'-deoxy-5-methyl-beta-L-uridine Structure
3'-Azido-3'-deoxy-5-methyl-beta-L-uridine Chemical Properties
Safety Information
MSDS Information
3'-Azido-3'-deoxy-5-methyl-beta-L-uridine Usage And Synthesis
Uses3’-Azido-3’-deoxy-5-methyl-beta-L-uridine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1]. 3’-Azido-3’-deoxy-5-methyl-beta-L-uridine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
References[1] Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88. DOI:10.2174/138161212801227005
3'-Azido-3'-deoxy-5-methyl-beta-L-uridine Preparation Products And Raw materials
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