Acetamide, N-(2-aminoethyl)-2-[4-(2,3,6,9-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy]-, hydrochloride (1:1)

Modify Date: 2025-08-24 23:56:11

Acetamide, N-(2-aminoethyl)-2-[4-(2,3,6,9-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy]-, hydrochloride (1:1) Structure
Acetamide, N-(2-aminoethyl)-2-[4-(2,3,6,9-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy]-, hydrochloride (1:1) structure
Common Name Acetamide, N-(2-aminoethyl)-2-[4-(2,3,6,9-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy]-, hydrochloride (1:1)
CAS Number 1783977-95-6 Molecular Weight 464.95
Density N/A Boiling Point N/A
Molecular Formula C21H29ClN6O4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Acetamide, N-(2-aminoethyl)-2-[4-(2,3,6,9-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy]-, hydrochloride (1:1)


Xanthine amine congener (XAC) hydrochloride is a non-selective adenosine receptor antagonist. Xanthine amine congener hydrochloride induces convulsions in mice[1].

 Names

Name Acetamide, N-(2-aminoethyl)-2-[4-(2,3,6,9-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy]-, hydrochloride (1:1)

  Biological Activity

Description Xanthine amine congener (XAC) hydrochloride is a non-selective adenosine receptor antagonist. Xanthine amine congener hydrochloride induces convulsions in mice[1].
Related Catalog
References

[1]. Ukena D, et al. Functionalized congeners of 1,3-dipropyl-8-phenylxanthine: potent antagonists for adenosine receptors that modulate membrane adenylate cyclase in pheochromocytoma cells, platelets and fat cells. Life Sci. 1986 Mar 3;38(9):797-807.

 Chemical & Physical Properties

Molecular Formula C21H29ClN6O4
Molecular Weight 464.95
InChIKey IVOSTHCDPHGPAS-UHFFFAOYSA-N
SMILES CCCn1c(=O)c2[nH]c(-c3ccc(OCC(=O)NCCN)cc3)nc2n(CCC)c1=O.Cl
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.