3’-O-(2-Methoxyethyl)-5-methylcytidine

Modify Date: 2025-08-29 07:45:40

3’-O-(2-Methoxyethyl)-5-methylcytidine structure	Common Name	3’-O-(2-Methoxyethyl)-5-methylcytidine
	CAS Number	2243311-50-2	Molecular Weight	315.32
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₃H₂₁N₃O₆	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of 3’-O-(2-Methoxyethyl)-5-methylcytidine

3’-O-(2-Methoxyethyl)-5-methylcytidine is a cytidine 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].

Name	3’-O-(2-Methoxyethyl)-5-methylcytidine

Description	3’-O-(2-Methoxyethyl)-5-methylcytidine is a cytidine 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].
Related Catalog	Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> Nucleoside Antimetabolite/Analog
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. [2]. 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.

Description

Related Catalog

Research Areas >> Cancer

Signaling Pathways >> Cell Cycle/DNA Damage >> Nucleoside Antimetabolite/Analog

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.

[2]. 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.

Molecular Formula	C₁₃H₂₁N₃O₆
Molecular Weight	315.32

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3’-O-(2-Methoxyethyl)-5-methylcytidine

Use of 3’-O-(2-Methoxyethyl)-5-methylcytidine

Names

3’-O-(2-Methoxyethyl)-5-methylcytidine Biological Activity

Chemical & Physical Properties

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.