5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine

Modify Date: 2025-09-07 14:22:44

5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine structure	Common Name	5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine
	CAS Number	1384253-67-1	Molecular Weight	627.69
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₃₄H₃₇N₅O₇	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of 5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine

5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277)[1].

Name	5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine

Description	5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277)[1].
Related Catalog	Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> Nucleoside Antimetabolite/Analog
References	[1]. Man S, et al. Potential and promising anticancer drugs from adenosine and its analogs. Drug Discov Today. 2021 Jun;26(6):1490-1500.

Molecular Formula	C₃₄H₃₇N₅O₇
Molecular Weight	627.69
InChIKey	JCXHIHKUTBGDNV-UHFFFAOYSA-N
SMILES	COCCOC1C(O)C(COC(c2ccccc2)(c2ccc(OC)cc2)c2ccc(OC)cc2)OC1n1cnc2c(N)ncnc21

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5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine

Use of 5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine

Names

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.