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Guanosine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-N-(2-methyl-1-oxopropyl)is a modified nucleoside with a unique chemical structure. It is derived from guanosine, a nucleoside composed of guanine and deoxyribose, and has been modified with a tert-butyldimethylsilyl group at the 5' position and an isobutyryl group at the 2' position. This modification enhances its binding affinity to protein targets and ion channels, making it a promising candidate for various applications in the pharmaceutical and biotechnology industries.

85326-10-9

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85326-10-9 Usage

Uses

Used in Pharmaceutical Industry:
Guanosine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-N-(2-methyl-1-oxopropyl)is used as a ligand for targeting protein receptors and ion channels. Its unique chemical structure allows it to bind to the receptor site on the cell membrane, inhibiting the binding of ligands and initiating signal transduction. This property makes it a potential candidate for the development of drugs targeting various diseases, including cancer, neurological disorders, and inflammatory conditions.
Used in Biotechnology Industry:
Guanosine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]-N-(2-methyl-1-oxopropyl)is used as a research tool for studying protein interactions and ion channel activity. Its ability to inhibit protein interactions, such as antibody binding and peptide binding, makes it a valuable tool for investigating the mechanisms of protein-protein interactions and their role in various biological processes. Additionally, its inhibitory effect on ion channel activity in a dose-dependent manner allows researchers to study the role of ion channels in cellular functions and develop potential therapeutic agents targeting these channels.

Check Digit Verification of cas no

The CAS Registry Mumber 85326-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,2 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85326-10:
(7*8)+(6*5)+(5*3)+(4*2)+(3*6)+(2*1)+(1*0)=129
129 % 10 = 9
So 85326-10-9 is a valid CAS Registry Number.

85326-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N2-isobutyryl-5'-O-(tert-butyldimethylsilyl)-2'deoxyguanosine

1.2 Other means of identification

Product number -
Other names N2-Isobutyryl-5-O-tert-butyldimethylsilyl-2-deoxyguanosine

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:85326-10-9 SDS

85326-10-9Relevant academic research and scientific papers

Potential application of thymidylate kinase in nucleoside analogue activation in Plasmodium falciparum

Cui, Huaqing,Ruiz-Pérez, Luis M.,González-Pacanowska, Dolores,Gilbert, Ian H.

experimental part, p. 7302 - 7309 (2010/11/18)

Plasmodium falciparum thymidylate kinase (PfTMPK) shows a broad range of substrate tolerance when compared to the corresponding human enzyme. Besides 2′-deoxythymidine monophosphate (dTMP), PfTMPK can phosphorylate 3′-azido-2′,3′-dideoxythymidine monophos

Convenient syntheses of 3′-amino-2′,3′- dideoxynucleosides, their 5′-monophosphates, and 3′-aminoterminal oligodeoxynucleotide primers

Eisenhuth, Ralf,Richert, Clemens

experimental part, p. 26 - 37 (2009/04/07)

(Chemical Equation Presented) 5′-Protected 3′-amino-2′, 3′-dideoxynucleosides containing any of the four canonical nucleobases (A/C/G/T) were prepared via azides in five to six steps, starting from deoxynucleosides. For pyrimidines, the synthetic route in

Method for purifying 5' -protected 2' -deoxypurine nucleosides

-

, (2008/06/13)

A method for efficiently purifying 5′ protected 2′-deoxypurine nucleosides, efficient production of which has previously been difficult. Impurities can be separated by obtaining the 5′ protected 2′-deoxypurine nucleoside as an inclusion crystal including a solvent such as that having a nitrile structure in order to purify the 5′ protected 2′-deoxypurine nucleoside at a high purity. This invention enables synthesis of highly purified protected deoxypurine nucleosides easily on a large scale, which has previously been performed by column chromatography method.

Method for purifying 5'-protected 2'-deoxypurine nucleosides

-

Example 2, (2008/06/13)

A method for efficiently purifying 5' protected 2'-deoxypurine nucleosides, efficient production of which has previously been difficult. Impurities can be separated by obtaining the 5' protected 2'-deoxypurine nucleoside as an inclusion crystal including a solvent such as that having a nitrile structure in order to purify the 5' protected 2'-deoxypurine nucleoside at a high purity. This invention enables synthesis of highly purified protected deoxypurine nucleosides easily on a large scale, which has previously been performed by column chromatography method.

Synthesis of 3'-azido-3'-deoxythymidine-terminated oligonucleotide

Esipov, Dmitriy S.,Esipova, Olga V.,Korobko, Vyacheslav G.

, p. 1697 - 1704 (2007/10/03)

A method of completely chemical synthesis of 3'-azido-3'- deoxythymidine-terminated oligonucleotides via 5'-H-phosphonate of AZT is described.

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