5-Amino-1,5-dideoxy-1-(1,2,3,4-tetrahydro-5-hydroxymethyl-2,4-dioxopyrimidin-1-yl)-β-D-allofuranuronic acid

Modify Date: 2024-04-03 22:24:33

5-Amino-1,5-dideoxy-1-(1,2,3,4-tetrahydro-5-hydroxymethyl-2,4-dioxopyrimidin-1-yl)-β-D-allofuranuronic acid structure	Common Name	5-Amino-1,5-dideoxy-1-(1,2,3,4-tetrahydro-5-hydroxymethyl-2,4-dioxopyrimidin-1-yl)-β-D-allofuranuronic acid
	CAS Number	21027-33-8	Molecular Weight	317.25200
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₁₁H₁₅N₃O₈	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of 5-Amino-1,5-dideoxy-1-(1,2,3,4-tetrahydro-5-hydroxymethyl-2,4-dioxopyrimidin-1-yl)-β-D-allofuranuronic acid

Polyoxin C, the hybrid compound of nucleosides and R-amino acids, is important as the C-terminal amino acid component of Nikkomycin[1].

Name	5-amino-1-(5-hydroxymethyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-β-D-1,5-dideoxy-allofuranuronic acid
Synonym	More Synonyms

Description	Polyoxin C, the hybrid compound of nucleosides and R-amino acids, is important as the C-terminal amino acid component of Nikkomycin[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Isono K, et, al. The strucutre of polyoxin C. Tetrahedron Lett. 1968 Jan;2:203-8. [2]. Mita N, et, al. Nucleophilic addition reaction of 2-trimethylsilyloxyfuran to N-gulosyl-C-alkoxymethylnitrones: synthetic approach to polyoxin C. Org Lett. 2002 Apr 4;4(7):1111-4.

Description

Polyoxin C, the hybrid compound of nucleosides and R-amino acids, is important as the C-terminal amino acid component of Nikkomycin[1].

Related Catalog

Research Areas >> Others

Signaling Pathways >> Others >> Others

References

Polyoxin C, 1-<5'-Amino-5'-desoxy-β-D-allofuranuronosyl>-5-hydroxymethyl-uracil

Amino-[(2R,3S,4R,5R)-3,4-dihydroxy-5-(5-hydroxymethyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-acetic acid

Polyoxin-C

polyoxin C

Polyoxin C

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