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105281-08-1

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105281-08-1 Usage

Chemical class

Pyrimidine nucleosides

Natural occurrence

Synthetic derivative of arabinosylcytosine

Application

Antiviral and anticancer agent

Structural similarity

Cytosine, a nucleobase in DNA and RNA

Mechanism of action

Inhibits replication of viral and cancer cells by interfering with genetic material

Fluoro substitution

At the 2' position of the arabinose sugar

Enhanced properties

Stability and potency due to fluoro substitution

Importance

Therapeutic agent for certain viral infections and malignancies

Usage

Pharmaceutical formulations and research settings for its pharmacological properties

Check Digit Verification of cas no

The CAS Registry Mumber 105281-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,8 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105281-08:
(8*1)+(7*0)+(6*5)+(5*2)+(4*8)+(3*1)+(2*0)+(1*8)=91
91 % 10 = 1
So 105281-08-1 is a valid CAS Registry Number.

105281-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-methyloxolan-2-yl]pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5'-deoxy-FAU

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:105281-08-1 SDS

105281-08-1Relevant articles and documents

Nucleosides. 139. Synthesis and Anticytomegalovirus and Antiherpes Simplex Virus Activity of 5'-Modified Analogues of 2'-Fluoroarabinosylpyrimidine Nucleosides

Harada, Kazuho,Matulic-Adamic, Jasenka,Price, Richard W.,Schinazi, Raymond F.,Watanabe, Kyoichi A.,Fox, Jack J.

, p. 226 - 229 (2007/10/02)

In order to determine if modification of the 5'-position reduces or abolishes the antiviral activity of 2'-fluoro-5-iodo-ara-C (FIAC), 2'-fluoro-5-iodo-ara-U (FIAU), or 2'-fluoro-5-methyl-ara-U (FMAU) against human cytomegalovirus (HCMV) and herpes simple

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