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134444-47-6

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134444-47-6 Usage

General Description

2-Amino-2'-deoxy-2'-fluoro-D-adenosine, also known as 2'-F-adenosine, is a synthetic analogue of adenosine with potent anti-cancer activities. The presence of the Fluorine atom at the 2' position on the ribose sugar makes this compound resistant to adenosine deaminase, an enzyme that breaks down adenosine. As a result, it inhibits cell proliferation and induces apoptosis in cancer cells. Due to its pharmacological efficiency and stability, this compound has been utilized in the development of several anticancer drugs and therapies. However, like all medicines, it may also carry potential side effects and risks. In general, this chemical is significant in medical research and therapeutic developments for its potential anticancer properties.

Check Digit Verification of cas no

The CAS Registry Mumber 134444-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,4,4 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134444-47:
(8*1)+(7*3)+(6*4)+(5*4)+(4*4)+(3*4)+(2*4)+(1*7)=116
116 % 10 = 6
So 134444-47-6 is a valid CAS Registry Number.

134444-47-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R,4R,5R)-5-(2,6-diaminopurin-9-yl)-4-fluoro-2-(hydroxymethyl)oxolan-3-ol

1.2 Other means of identification

Product number -
Other names 2-Amino-2'-deoxy-2'-fluoroadenosine

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:134444-47-6 SDS

134444-47-6Relevant articles and documents

Chemical and enzymatic synthesis and antiviral properties of 2'-deoxy- 2'-fluoroguanosine

Zaitseva, Galina V.,Zinchenko, Anatoli I.,Barai, Vladimir N.,Pavlova,Boreko, Evgeny I.,Mikhailopulo, Igor A.

, p. 687 - 688 (1999)

Chemical and enzymatic methods were employed for the synthesis of the title compound, 2'F-Guo 7. High antiviral activity of 2'F-Guo was established in chick embryo cells infected with influenza virus FPV/Rostock/34 (H7N1) and herpes simplex virus (HSV) type I (1C strain).

Anti-HCV nucleoside derivatives

-

, (2008/06/13)

The present invention comprises nucleoside derivatives for use in the treatment or prophylaxis of hepatitis C virus infections. In particular, the present invention discloses the novel use of known 2'-deoxy-2'-fluoro nucleoside derivatives as inhibitors of hepatitis C virus (HCV) RNA replication and pharmaceutical compositions of such compounds. The compounds of this invention have potential use as therapeutic agents for the treatment of HCV infections.

Synthesis and biologic activity of purine 2'-deoxy-2'-fluoro- ribonucleosides

Thomas,Tiwari,Clayton,Secrist III,Montgomery

, p. 309 - 323 (2007/10/02)

The synthesis of 3,5-di-O-benzoyl-2-deoxy-2-fluoro-D-ribofuranosyl bromide (8) and its reaction with 2,6-dichloropurine by fusion and with mercuric cyanide catalysis is described. The resulting 2,6-dichloro-9-(3,5-di-O- benzoyl-2-deoxy-2-fluoro-β-D-ribofuranosyl)purine (13) was converted to the 2-fluoroadenine (16), the 2-chloroadenine (17), 2,6-diaminopurine (12), and guanine (14) nucleosides by standard procedures. These nucleosides were cytotoxic to a number of cell lines in culture. The 2-haloadenine nucleosides 16 and 17 gave modest increases in lifespan when tested against the P388 leukemia in mice.

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