26287-69-4
26287-69-4
Chemical Structure
L-Uridine
- CAS No.: 26287-69-4
- Formula:C9H12N2O6
- Molecular Weight:244.20
IUPAC Name: 1-((2S,3S,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
InChIKey: DRTQHJPVMGBUCF-PSQAKQOGSA-N
SMILES: O=C(NC(C=C1)=O)N1[C@@H]2[C@@H](O)[C@@H](O)[C@H](CO)O2
Biological Activity: L-Uridine is an enantiomer of the normal RNA constituent D-uridine. L-Uridine can be isolated from the Polyporaceae fungus Poria cocos (Schw.). L-uridine acts as a phosphate acceptor for nucleoside phosphotransferases[1][2].
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L-Uridine | 99.81% | L-Uridine is an enantiomer of the normal RNA constituent D-uridine. L-Uridine can be isolated from the Polyporaceae fungus Poria cocos (Schw.). L-uridine acts as a phosphate acceptor for nucleoside phosphotransferases. | ||||||||||||||||||||
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L-Uridine (Standard) | ≥98% | L-Uridine (Standard) is the analytical standard of L-Uridine (HY-W006429). This product is intended for research and analytical applications. L-Uridine is an enantiomer of the normal RNA constituent D-uridine. L-Uridine can be isolated from the Polyporaceae fungus Poria cocos (Schw.). L-uridine acts as a phosphate acceptor for nucleoside phosphotransferases. | ||||||||||||||||||||
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References
- [1]. A F Wu, et al. L-uridine: synthesis and behavior as enzyme substrate. Proc Natl Acad Sci U S A. 1969 Aug;63(4):1222-6. [Content Brief]
- [2]. Yumei Wang, et al. Chemical Composition and Pharmacology Research Progress of Shenlingbaizhu Powder. 2019 Asia-Pacific Conference on Clinical Medicine and Public Health.
Keywords
