Description

4-O-(2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl)-5-O-[3-O-(2,6-diamino-2,6-dideoxy-β-L-idopyranosyl)-5-O-(β-D-glucopyranosyl)-β-D-ribofuranosyl]-2-deoxy-D-streptamine is a structurally complex aminoglycoside antibiotic derivative of significant research interest. Its intricate glycosidic architecture makes it a valuable reference standard and key intermediate in pharmaceutical development and biochemical studies. This compound is primarily utilized by research institutions, pharmaceutical R&D laboratories, and fine chemical manufacturers engaged in antibiotic research, mechanism of action studies, and the synthesis of novel therapeutic agents.

Application

• Pharmaceutical Reference Standard: Used for analytical method development, validation, and quality control in antibiotic production.
• Biochemical Research: Serves as a critical tool for studying aminoglycoside mechanisms of action, bacterial resistance, and ribosomal interactions.
• Intermediate for Synthesis: Acts as a key building block in the semi-synthesis of novel or modified antibiotic compounds.
• Microbiology Studies: Employed in research to evaluate antimicrobial activity spectra and potency against various bacterial strains.
• Academic Research: Utilized in university and institutional labs for fundamental studies in medicinal chemistry and glycobiology.

Basic Information

Product Name	4-O-(2,6-Diamino-2,6-dideoxy-α-D-glucopyranosyl)-5-O-[3-O-(2,6-diamino-2,6-dideoxy-β-L-idopyranosyl)-5-O-(β-D-glucopyranosyl)-β-D-ribofuranosyl]-2-deoxy-D-streptamine
CAS No.	53861-54-4
Molecular Formula	C31H55N5O19
Molecular Weight	801.80 g/mol
Synonyms	2-Deoxy-4-O-(2,6-diamino-2,6-dideoxy-α-D-glucopyranosyl)-5-O-[3-O-(2,6-diamino-2,6-dideoxy-β-L-idopyranosyl)-5-O-(β-D-glucopyranosyl)-β-D-ribofuranosyl]streptamine; Antibiotic G-418 related compound; Geneticin intermediate; Aminoglycoside antibiotic derivative; 4-O-(Paromaminyl)-5-O-[3-O-(2,6-diamino-2,6-dideoxy-β-L-idopyranosyl)-5-O-(β-D-glucopyranosyl)-β-D-ribofuranosyl]-2-deoxystreptamine
EINECS	Contact for details

Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards for research and development. Each batch is characterized using advanced analytical techniques including HPLC, NMR, and mass spectrometry to confirm identity and purity. Certificates of Analysis (COA) detailing batch-specific results are available upon request. We adhere to a cGMP-compliant quality management system to ensure traceability and consistency for our pharmaceutical and research customers.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This compound is hygroscopic (moisture-sensitive) and should be handled under anhydrous conditions when possible to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms to reference standard
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 95.0%
Water Content (KF)	≤ 5.0%
Residue on Ignition	≤ 1.0%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.