Chemodex

Amikacin disulfate salt

CHF 155.00
In stock
CDX-A0286-G0011 gCHF 155.00
CDX-A0286-G0055 gCHF 464.00
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Product Details
Synonyms Amikacin disulfate; Biodacyn; Selemycin; Amiglyde; BB-K 8; Novamin; Amikin
Product Type Chemical
Properties
Formula C22H43N5O13 . 2H2SO4
MW 781.76
CAS 39831-55-5
RTECS WK1961200
Source/Host Chemicals Synthetic.
Purity Chemicals ≥97% (NMR)
Appearance White to off-white powder.
Solubility Soluble in water (50mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key FXKSEJFHKVNEFI-GCZBSULCSA-N
Smiles OS(O)(=O)=O.OS(O)(=O)=O.O[C@@H]([C@@H]([C@H]1N)O[C@H]([C@@H]([C@H]2O)O)O[C@H](CN)[C@H]2O)[C@H]([C@@H](C1)N([H])C([C@H](CCN)O)=O)O[C@H]([C@@H]([C@H]3N)O)O[C@H](CO)[C@H]3O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
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Product Specification Sheet
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Description

Amikacin is a broad-spectrum aminoglycoside antibiotic and a semisynthetic analog of kanamycin. It irreversibly binds to 16S rRNA and the RNA-binding S12 protein of the 30S subunit and 50S subunit of prokaryotic ribosome and inhibits protein synthesis. It works in a concentration-dependent manner, and has better action in an alkaline environment. Amikacin disulfate is very active against most Gram-negative bacteria including gentamicin- and tobramycin-resistant strains, due to its resistance to inactivating enzymes. Amikacin disulfate also inhibits the infections caused by susceptible Nocardia and nontuberculous mycobacteria. Amikacin can be used to treat non-tubercular mycobacterial infections and tuberculosis when first-line drugs fail to control the infection.

Product References

[1] H. Kawaguchi, et al.; J. Antibiot. 25, 695 (1972) | [2] P.K. Yu, et al.; Antimicrob. Agents Chemother. 4, 133 (1973) | [3] D. Zaske & K. Crossley; Minn. Med. 61, 123 (1978) (Review) | [4] F.D. Pien & P.W. Ho; Am. J. Hosp. Pharm. 38, 981 (1981) (Review) | [5] A.M. Ristuccia & B.A.Cunha; Ther. Drug Monit. 7, 12 (1985) (Review) | [6] M.S. Ramirez & M.E. Tolmasky; Molecules 22, 2267 (2017) (Review)

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