M.F.
C21H34D7N5O11โขxCH4O2
Storage Condition
Refer MSDS for complete information
Synonyms
O-4-Amino-4-deoxy-ฮฑ-D-glucopyranosyl-(18)-O-(8R)-2-amino-2,3,7-trideoxy-7-(methylamino)-D-glycero-ฮฑ-D-allo-octodialdo-1,5:8,4-dipyranosyl-(14)-2-deoxy-D-streptamine-d7 Acetate
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Refer MSDS for complete information
Apramycin Acetate-d7 (Major) is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
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Apramycin Acetate-d7 (Major) usage and description
Apramycin Acetate-d7 (Major) is a deuterated form of Apramycin Acetate, which is an aminoglycoside antibiotic. It is mainly used in the treatment of bacterial infections caused by Gram-negative organisms, including Escherichia coli, Salmonella, and Klebsiella. Apramycin Acetate-d7 (Major) is used for research purposes only and is not approved for human use.
Chemically, Apramycin Acetate-d7 (Major) is a deuterated form of the parent compound, Apramycin Acetate. Deuterium is a stable isotope of hydrogen with a neutron in its nucleus, which makes it heavier than the normal hydrogen atom. The incorporation of deuterium into the molecule of Apramycin Acetate-d7 (Major) makes it useful in various research applications, such as metabolic studies, pharmacokinetics, and drug-drug interactions.
The mechanism of action of Apramycin Acetate-d7 (Major) is similar to that of other aminoglycoside antibiotics. It binds to the bacterial ribosome and inhibits protein synthesis, leading to bacterial cell death. Apramycin Acetate-d7 (Major) is effective against bacteria that are resistant to other antibiotics, making it a valuable tool in antibiotic research.
In conclusion, Apramycin Acetate-d7 (Major) is a deuterated form of Apramycin Acetate that is used for research purposes only. It is effective against Gram-negative bacterial infections and is useful in various research applications. Its incorporation of deuterium makes it a useful tool in the study of pharmacokinetics and drug-drug interactions.