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112898-14-3

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  • 2′-3′-O-(4-Benzoylbenzoyl)guanosine 5′-triphosphate triethylammonium salt,Benzoylbenzoyl-GTP,

    Cas No: 112898-14-3

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112898-14-3 Usage

Structure

2'-3'-O-(4-benzoylbenzoyl)guanosine5'-triphosphate is a modified form of guanosine triphosphate with two benzoyl groups attached to the 2' and 3' positions of the ribose sugar moiety.

Role in cellular processes

The nucleotide is critical for cellular energy metabolism and RNA synthesis.

Unique properties

The addition of the two benzoyl groups imparts unique properties to the molecule, making it useful for studying RNA and protein interactions.

Applications in research

The modified nucleotide has been used in various biochemical and biophysical studies to investigate the structure and function of RNA and RNA-binding proteins, as well as to explore the mechanisms of RNA processing and translation.

Potential applications

It has potential applications in the design of new tools for manipulating and modulating RNA function in biological systems.

Modified form of guanosine triphosphate

2'-3'-O-(4-benzoylbenzoyl)guanosine5'-triphosphate is derived from guanosine triphosphate, a nucleotide essential for cellular processes.

Critical for cellular energy metabolism and RNA synthesis

The nucleotide plays a vital role in energy production and the creation of RNA molecules within the cell.

Attachment of two benzoyl groups

The addition of the benzoyl groups to the ribose sugar moiety of the nucleotide enhances its properties and applications in research.

Useful for studying RNA and protein interactions

The modified nucleotide facilitates the investigation of interactions between RNA and proteins, which is essential for understanding various cellular processes.

Investigating RNA structure and function

The modified nucleotide has been employed in research to better understand the structure and function of RNA molecules.

Exploring RNA processing and translation mechanisms

2'-3'-O-(4-benzoylbenzoyl)guanosine5'-triphosphate aids in the study of how RNA is processed and translated within the cell.

Designing new tools for RNA manipulation

The modified nucleotide has potential applications in the development of new tools for controlling and modulating RNA function in biological systems, which could lead to advances in research and therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 112898-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,9 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112898-14:
(8*1)+(7*1)+(6*2)+(5*8)+(4*9)+(3*8)+(2*1)+(1*4)=133
133 % 10 = 3
So 112898-14-3 is a valid CAS Registry Number.

112898-14-3SDS

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,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl 4-benzoyl-3-[[hydroxy-[hydroxy(phosphonooxy)phosphoryl]oxyphosphoryl]oxymethyl]benzoate,N,N-diethylethanamine

1.2 Other means of identification

Product number -
Other names 2 inverted exclamation marka-3 inverted exclamation marka-O-(4-Benzoylbenzoyl)guanosine 5 inverted exclamation marka-triphosphate triethylammonium salt

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:112898-14-3 SDS

112898-14-3Upstream product

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