Amikacin drug data and news

Amikacin drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Amikacin
Brand Names/Synonyms ANTIBIOTIC BB-K8; Amicacin; Amiglyde-V; Amikacin; Amikacin Base; Amikacin Dihydrate; Amikacin Sulfate; Amikacin [Usan:Ban:Inn]; Amikacina [Inn-Spanish]; Amikacine [Inn-French]; Amikacinum [Inn-Latin]; Amikavet; Amikin; BB-K8; Briclin; Novamin
Indication For short-term treatment of serious infections due to susceptible strains of Gram-negative bacteria, including Pseudomonas species, Escherichia coli, species of indole-positive and indole-negative Proteus, Providencia species, Klebsiella-Enterobacter-Serratia species, and Acinetobacter (Mima-Herellea) species.
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Description Not Available
Pharmacology Amikacin is an aminoglycoside antibiotic. Aminoglycosides work by binding to the bacterial 30S ribosomal subunit, causing misreading of t-RNA, leaving the bacterium unable to synthesize proteins vital to its growth. Aminoglycosides are useful primarily in infections involving aerobic, Gram-negative bacteria, such as Pseudomonas, Acinetobacter, and Enterobacter. In addition, some mycobacteria, including the bacteria that cause tuberculosis, are susceptible to aminoglycosides. Infections caused by Gram-positive bacteria can also be treated with aminoglycosides, but other types of antibiotics are more potent and less damaging to the host. In the past the aminoglycosides have been used in conjunction with penicillin-related antibiotics in streptococcal infections for their synergistic effects, particularly in endocarditis. Aminoglycosides are mostly ineffective against anaerobic bacteria, fungi and viruses.
Mechanism Of Action Aminoglycosides like Amikacin "irreversibly" bind to specific 30S-subunit proteins and 16S rRNA. Amikacin inhibits protein synthesis by binding to the 30S ribosomal subunit to prevent the formation of an initiation complex with messenger RNA. Specifically Amikacin binds to four nucleotides of 16S rRNA and a single amino acid of protein S12. This interferes with decoding site in the vicinity of nucleotide 1400 in 16S rRNA of 30S subunit. This region interacts with the wobble base in the anticodon of tRNA. This leads to interference with the initiation complex, misreading of mRNA so incorrect amino acids are inserted into the polypeptide leading to nonfunctional or toxic peptides and the breakup of polysomes into nonfunctional monosomes.
Amikacin News
(When available)

Nektar Announces Financial Results for the Year and Fourth Quarter ...  Feb 28, 2006
...which was in proof-of-concept for prevention of ventilator-associatedpneumonia, with Aerogen's ongoing Phase II program, that usesaerosolized amikacin to treat ... - Finanzen.net,

Nektar Announces Financial Results for the Year and Fourth Quarter ...  Feb 28, 2006
...was in proof-of-concept for prevention of ventilator-associated pneumonia, with Aerogen's ongoing Phase II program, that uses aerosolized amikacin to treat ... - Genetic Engineering News,

Dosage Forms IV Infusion; IM Injection
Drug_Category Anti-bacterial Agents; Aminoglycosides; ATC:D06AX12; ATC:J01GB06; ATC:S01AA21
Absorption Rapidly absorbed after intramuscular administration
Interactions Interactions for Amikacin:

No information provided.

Toxicity Not Available
Organisms Affected Enteric bacteria and other eubacteria
Chemical IUPAC Name 4-amino-N-[5-amino-2-[4-amino-3,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4-[6-(aminomethyl)-3,4,5-trihydroxy-tetrahydropyran-2-yl]oxy-3-hydroxy-cyclohexyl]-2-hydroxy-butanamide
Chemical Formula C22H43N5O13
Molecular Weight 585.603 g/mol
Smiles String C1C(C(C(C(C1NC(=O)C(CCN)O)OC2C(C(C(C(O2)CO)O)N)O)O)OC3C(C(C(C(O3)CN)O)O)O)N
Melting Point 203-204 °C
Water Solubility 1.85E+005 mg/L
State Solid
LogP/Hphobicity -9.048
Isoelectric Point Not Available
Biotransformation Not Available
Half Life 2-3 hours
Protein Binding [%] 0-11%
RxList Link RXlist
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Drug Reference http://www.drugs.com/cons/Amikacin.html
http://www.rxlist.com/cgi/generic3/amikacin.htm
Drug Type Approved Drug
Accession No APRD00550
CAS Registry Number 37517-28-5
KEGG Compound ID C06820
PubChem ID SID:9038
PharmGKB ID PA448366
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 2242971

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