Kanamycin

From Wikipedia, the free encyclopedia

Kanamycin chemical structure
Kanamycin
Systematic (IUPAC) name
2-(aminomethyl)- 6-[4,6-diamino-3- [4-amino-3,5-dihydroxy-6-(hydroxymethyl) tetrahydropyran-

2-yl]oxy-2-hydroxy-cyclohexoxy]- tetrahydropyran-3,4,5-triol

Identifiers
CAS number 8063-07-8
ATC code A07AA08 J01GB04 S01AA24
PubChem 6032
DrugBank APRD00026
Chemical data
Formula C18H36N4O11
Mol. weight 484.499
Pharmacokinetic data
Bioavailability very low after oral delivery
Metabolism  ?
Half life 2 hours 30 minutes
Excretion  ?
Therapeutic considerations
Pregnancy cat.

?

Legal status

?

Routes Oral, intravenous, intramuscular

Kanamycin (marketed under the brand name Kantrex®) is an aminoglycoside antibiotic, available in both oral and intravenous forms, and used to treat a wide variety of infections.

[edit] Pharmacology

Kanamycin works by affecting 30S ribosomal subunit and causing a frame-shift. This means that instead of a codon CAT (for example in sequence CATG), a codon ATG is read by aminoacyil tRNA (aa-tRNA). Aminoacyil tRNA is consequently carrying a different amino acid, because the anticodon on the aa-tRNA is different. The protein needed cannot be synthesised - a completely different protein has been synthesised or a protein similar to the one needed, but not folded correctly; it depends of the site and severness of the frame-shift. A bacterium is destroyed because it cannot produce any of its proteins correctly.

Because of over usage of antibiotics in every possible (even viral) disease as a precaution many bacteria have developed a resistance against kanamycin, and, consequently, it is not being used much anymore.

[edit] Side effects

Common side effects include changes in hearing (either hearing loss or ringing in the ears), toxicity to kidneys, and allergic reactions to the drug.


[edit] External links


Aminoglycosides (J01G) edit

Amikacin, Gentamicin, Kanamycin, Neomycin, Netilmicin, Streptomycin, Tobramycin, Paromomycin, Hygromycin, spectinomycin


In other languages