Streptomycin drug data and news

Streptomycin 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 Streptomycin
Brand Names/Synonyms Amikin; G-Mycin; Garamycin; Jenamicin; Kantrex; Nebcin; Netromycin; Streptomycin; Streptomycin Sesquisulfate Hydrate; Streptomycin Sulfate; Streptomycin Sulphate; Streptomycin a Sulfate; Streptomycin, Sulfate Salt
Indication For the treatment of Tuberculosis
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Description Not Available
Pharmacology Streptomycin 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 Streptomycin "irreversibly" bind to specific 30S-subunit proteins and 16S rRNA. Specifically Streptomycin 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.
Streptomycin News
(When available)
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Dosage Forms POWDER FOR SOLUTION
Drug_Category Anti-bacterial Agents; Aminoglycosides; ATC:A07AA04; ATC:J01GA01; ATC:S01AA15
Absorption Not Available
Interactions Not Available
Toxicity Oral rat LD50: 430 mg/kg (Streptomycin Sulfate).Side effect include nausea, vomiting, and vertigo, paresthesia of face, rash; fever, urticaria, angioneurotic edema, and eosinophilia.
Organisms Affected Enteric bacteria and other eubacteria
Chemical IUPAC Name 5-(2,4-diguanidino-3,5,6-trihydroxy-cyclohexoxy)-4-[4,5-dihydroxy-6-(hydroxymethyl)-3-methylamino-tetrahydropyran-2-yl]oxy-3-hydroxy-2-methyl-tetrahydrofuran-3-carbaldehyde
Chemical Formula C21H39N7O12
Molecular Weight 581.574 g/mol
Smiles String CC1C(C(C(O1)OC2C(C(C(C(C2O)O)N=C(N)N)O)N=C(N)N)OC3C(C(C(C(O3)CO)O)O)NC)(C=O)O
Melting Point Not Available
Water Solubility Not Available
State Solid
LogP/Hphobicity -8.005
Isoelectric Point Not Available
Biotransformation Not Available
Half Life Not Available
Protein Binding [%] Not Available
RxList Link RXlist
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Drug Reference http://www.drugs.com/cons/Streptomycin.html
Drug Type Approved Drug
Accession No APRD00412
CAS Registry Number 57-92-1
KEGG Compound ID C00413
PubChem ID SID:3703
PharmGKB ID PA451512
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 2243660

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