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1-[2,5-dideoxy-5-(methylamino)pentofuranosyl]-5-methylpyrimidine-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75191-50-3

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75191-50-3 Usage

Chemical class

Pyrimidine nucleosides

Explanation

The compound belongs to a class of nucleosides that contain a pyrimidine base.

Explanation

The compound is composed of a pyrimidine base (a type of nitrogen-containing ring structure) connected to a deoxyribose sugar (a sugar molecule lacking one oxygen atom).

Explanation

A methylamino group (a nitrogen atom bonded to a methyl group) is attached to the sugar ring, which is a modification of the standard deoxyribose sugar.

Explanation

The compound has potential applications in the development of pharmaceuticals due to its antiviral and antitumor properties.

Explanation

The compound is known to exhibit antiviral properties, which means it can help inhibit the replication of viruses within host cells.

Explanation

The compound also has antitumor properties, which means it can potentially help suppress the growth of tumors in the body.

Explanation

The compound serves as a precursor in the synthesis of various nucleoside analogs, which are modified versions of naturally occurring nucleosides.

Explanation

Research is currently being conducted to further explore the biological activities and potential therapeutic uses of 1-[2,5-dideoxy-5-(methylamino)pentofuranosyl]-5-methylpyrimidine-2,4(1H,3H)-dione in the field of medicine.

Structure

Pyrimidine base linked to a deoxyribose sugar

Modification

Methylamino group attached to the sugar ring

Applications

Pharmaceutical industry

Antiviral properties

Inhibits viral replication

Antitumor properties

Suppresses tumor growth

Precursor

Used in the synthesis of nucleoside analogs

Ongoing research

Biological activities and therapeutic uses

Check Digit Verification of cas no

The CAS Registry Mumber 75191-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,9 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75191-50:
(7*7)+(6*5)+(5*1)+(4*9)+(3*1)+(2*5)+(1*0)=133
133 % 10 = 3
So 75191-50-3 is a valid CAS Registry Number.

75191-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-hydroxy-5-(methylaminomethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5'-methylamino-5'-deoxythimidine

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:75191-50-3 SDS

75191-50-3Relevant academic research and scientific papers

Oligonucleotide analogues bearing an acyclonucleoside linked by an internucleotide amide bond

Kochetkova,Fillipova,Kolganova,Timofeev,Florentiev

, p. 207 - 214 (2008/09/19)

Oligonucleotide analogues bearing an acyclocytidine linked to thymidine with an amide (3′-O-CH2CO-N-5′) bond were synthesized. Melting curves of duplexes formed by modified oligonucleotides and complementary natural oligomers were obtained and

Synthesis and hybridization properties of amide-linked thymidine dimers incorporated into oligodeoxynucleotides

Idziak, Irene,Just, George,Damha, Masad J.,Giannaris, Paul A.

, p. 5417 - 5420 (2007/10/02)

Thymidine dimers, connected by amide or N-methyl amide linkages, have been prepared. The dimers have each been incorporated three times into normal strands of DNA by solid phase synthesis. Thermal denaturation studies indicated that these modifications ca

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