Kanamycin
From Wikipedia, the free encyclopedia
Kanamycin
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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 |
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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 | ||
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Amikacin, Gentamicin, Kanamycin, Neomycin, Netilmicin, Streptomycin, Tobramycin, Paromomycin, Hygromycin, spectinomycin |