CAS 223771-83-3

(2R,3S,4R,5S)-2-(Hydroxymethyl)-1-nonyl-3,4,5-piperidinetriol

Description:

The chemical substance known as (2R,3S,4R,5S)-2-(Hydroxymethyl)-1-nonyl-3,4,5-piperidinetriol, with the CAS number 223771-83-3, is a complex organic compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features multiple hydroxymethyl groups, contributing to its hydrophilicity and potential for forming hydrogen bonds, which can influence its solubility and reactivity. The stereochemistry indicated by the (2R,3S,4R,5S) configuration suggests that it has specific spatial arrangements of its substituents, which can significantly affect its biological activity and interactions with other molecules. Such compounds may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals, due to their ability to interact with biological targets. Additionally, the presence of a nonyl chain suggests potential lipophilicity, which can influence membrane permeability and bioavailability. Overall, this compound's unique structural features make it a subject of interest in various chemical and biological research fields.

Formula: C₁₅H₃₁NO₄

Synonyms:

• N-Nonyl-deoxygalactojirimycin
• N-nonyl-DGJ
• Alkovir
• 1,5-Dideoxy-1,5-(nonylimino)-D-galactitol

N-Nonyldeoxygalactonojirimycin

CAS: 223771-83-3

Ref: 7W-GC5993

N-(n-Nonyl)deoxygalactonojirimycin

Controlled Product

CAS: 223771-83-3

Formula: C₁₅H₃₁NO₄

Color and Shape: Neat

Molecular weight: 289.41

Ref: TR-N649900

N-Nonyldeoxygalactonojirimycin

CAS: 223771-83-3

N-Nonyldeoxygalactonojirimycin (NDGJ) is a novel antiviral agent that inhibits the activity of viral enzymes, such as polymerase chain reaction and reverse transcriptase. NDGJ has been shown to inhibit the replication of hepatitis viruses in primary cells and human macrophages. The drug also inhibits the replication of human pathogens, such as HIV-1, herpes simplex virus type 1, and cytomegalovirus in cell culture. NDGJ has an effect on hydrophobic amino acids in protein synthesis by binding to them and preventing their attachment to the ribosomal surface. This leads to cell lysis through a process called osmotic shock.

Formula: C₁₅H₃₁NO₄

Purity: Min. 95 Area-%

Color and Shape: White Off-White Powder

Molecular weight: 289.41 g/mol

Ref: 3D-MN04785