General description
Chemical structure: aminoglycoside
Application
Amikacin is an aminoglycoside antibiotic commonly used in the treatment of drug-resistant mycobacteria . It is used to study organism-directed delivery of antibiotics as well as drug resistance .
Biochem/physiol Actions
Amikacin prevents bacterial protein synthesis by binding to the 30S ribosome subunit and inducing mRNA misreading.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
Keep container tightly closed in a dry and well-ventilated place.
Molecular Weight: 781.76. Empirical Formula: C22H43N5O13 · 2H2SO4. biological source: synthetic. Quality Level: 200. form: powder or crystals. potency: 674-786 . μ. g per mg (as amikacin base). color: white to off-white. antibiotic activity spectrum: Gram-negative bacteria, mycobacteria. Mode of action: protein synthesis | interferes. storage temp.: 2-8°C. SMILES string: OS(O)(: O): O.OS(O)(: O): O.NCC[C@H](O)C(: O)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CN)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O. InChI: 1S/C22H43N5O13.2H2O4S/c23-2-1-8(29)20(36)27-7-3-6(25)18(39-22-16(34)15(33)13(31)9(4-24)37-22)17(35)19(7)40-21-14(32)11(26)12(30)10(5-28)38-21. 2*1-5(2,3)4/h6-19,21-22,28-35H,1-5,23-26H2,(H,27,36). 2*(H2,1,2,3,4)/t6-,7+,8-,9+,10+,11-,12+,13+,14+,15-,16+,17-,18+,19-,21+,22+. . /m0../s1. InChI key: FXKSEJFHKVNEFI-GCZBSULCSA-N. Pictograms: GHS07,GHS08. Signal Word: Warning. Hazard Statements: H317 - H361fd. Precautionary Statements: P202 - P261 - P272 - P280 - P302 + P352 - P308 + P313. Hazard Classifications: Repr. 2 - Skin Sens. 1. Storage Class Code: 11 - Combustible Solids. WGK: WGK 2. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: Eyeshields, Gloves, type N95 (US).- UPC:
- 51191506
- Condition:
- New
- HazmatClass:
- No
- MPN:
- A1774-250MG
- CAS:
- 39831-55-5
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