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30414-00-7

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30414-00-7 Usage

Description

5-(Hydroxymethyl)uridine is a naturally occurring modified nucleoside and a derivative of uridine, which is found in various human tissues and fluids. It plays a significant role in RNA modification and biosynthesis, and has potential therapeutic applications in treating mitochondrial disorders and as a neuroprotective agent. It also has potential effects on mitochondrial biogenesis and improving energy metabolism in cells.

Uses

Used in Pharmaceutical Industry:
5-(Hydroxymethyl)uridine is used as a therapeutic agent for the treatment of mitochondrial disorders due to its potential role in improving mitochondrial function and energy metabolism in cells.
Used in Neuroprotection:
5-(Hydroxymethyl)uridine is used as a neuroprotective agent to protect neurons from damage and degeneration, potentially offering benefits in the treatment of neurodegenerative diseases.
Used in Research:
5-(Hydroxymethyl)uridine is used as a research tool to study RNA modification, biosynthesis, and its effects on cellular processes, contributing to a better understanding of its biological significance and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 30414-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,1 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30414-00:
(7*3)+(6*0)+(5*4)+(4*1)+(3*4)+(2*0)+(1*0)=57
57 % 10 = 7
So 30414-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O7/c13-2-4-1-12(10(18)11-8(4)17)9-7(16)6(15)5(3-14)19-9/h1,5-7,9,13-16H,2-3H2,(H,11,17,18)/t5-,6-,7-,9-/m1/s1

30414-00-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(Hydroxymethyl)uridine

1.2 Other means of identification

Product number -
Other names 5-Hydroxymethyl-uridin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30414-00-7 SDS

30414-00-7Relevant articles and documents

SYNTHESIS AND STRUCTURE OF HIGH POTENCY RNA THERAPEUTICS

-

, (2019/01/15)

This invention provides expressible polynucleotides, which can express a target protein or polypeptide. Synthetic mRNA constructs for producing a protein or polypeptide can contain one or more 5′ UTRs, where a 5′ UTR may be expressed by a gene of a plant. In some embodiments, a 5′ UTR may be expressed by a gene of a member of Arabidopsis genus. The synthetic mRNA constructs can be used as pharmaceutical agents for expressing a target protein or polypeptide in vivo.

Alternative synthetic routes to 2′,3′-didehydro-2′,3′-dideoxy-5-hydroxymethyluridine

Chung, Raymond,Anderson, Karen S.

, p. 8361 - 8363 (2007/10/03)

Alternative syntheses for the nucleoside analogue 2′,3′-didehydro-2′,3′-dideoxy-5-hydroxymethyluridine starting from 5-methyluridine and uridine are described.

Synthesis of 5-(2-amino-2-deoxy-β-D-glucopyranosyloxymethyl)-2'- deoxyuridine and its incorporation into oligothymidylates

Hunziker, Juerg

, p. 201 - 204 (2007/10/03)

The protected 5-(2-amino-2-deoxy-β-D-glucopyranosyloxymethyl)-2'- deoxyuridine phosphoramidite 15 has been prepared from uridine in 12 steps. When incorporated into oligodeoxyribonucleotides the novel nucleoside analog 5 leads to decreased binding affinit

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