N4-(n-Palmitoyl)-4’-azido-2’-deoxy-2’-fluoro-arabinocytidine

N4-(n-Palmitoyl)-4’-azido-2’-deoxy-2’-fluoro-arabinocytidine

• UNSPSC Description: N4-(n-Palmitoyl)-4’-azido-2’-deoxy-2’-fluoro-arabinocytidine is a cytidine nucleoside analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities[1]. N4-(n-Palmitoyl)-4’-azido-2’-deoxy-2’-fluoro-arabinocytidine 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.
• Target Antigen: Nucleoside Antimetabolite/Analog
• Type: Oligonucleotides
• Related Pathways: Cell Cycle/DNA Damage
• Applications: Cancer-programmed cell death
• Field of Research: Others
• Assay Protocol: https://www.medchemexpress.com/n4-n-palmitoyl-4-azido-2-deoxy-2-fluoro-arabinocytidine.html
• Solubility: 10 mM in DMSO
• Smiles: O=C1N([C@H]2[C@@H](F)[C@H](O)[C@](CO)(N=[N+]=[N-])O2)C=CC(NC(CCCCCCCCCCCCCCC)=O)=N1
• Molecular Weight: 524.63
• References & Citations: [1]Gowher H, et al. Mechanism of inhibition of DNA methyltransferases by cytidine analogs in cancer therapy. Cancer Biol Ther. 2004 Nov;3(11):1062-8.
• Shipping Conditions: Room temperature
• Clinical Information: No Development Reported