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Sigma-Aldrich/Tetracycline hydrochloride/T4062-1G/1G
  • Sigma-Aldrich/Tetracycline hydrochloride/T4062-1G/1G

Sigma-Aldrich/Tetracycline hydrochloride/T4062-1G/1G

價(jià)格: ¥178.60 市場(chǎng)價(jià): 232.18

貨號(hào): T4062-1G
品牌: Sigma-Aldrich
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      • CAS Number 64-75-5

      • Empirical Formula (Hill Notation) C22H24N2O8 · HCl

      • Molecular Weight 480.90

      •  Beilstein Registry Number 3844873

      •  EC Number 200-593-8

      •  MDL number MFCD00078142

      •  PubChem Substance ID 24900192

      • Popular Documents:  Specification Sheet (PDF)  

      Properties:

      Related Categories Analytical/Chromatography, Antibacterial, Antibiotics, Antibiotics A to Z, Antibiotics T-Z,
      More...
      biological source   from synthetic
      InChI Key   XMEVHPAGJVLHIG-FMZCEJRJSA-N
      form   solid
      optical activity   [α]/D -255 to 240° (Specific rotation )
      mp   220-223 °C(lit.)
      cation traces   heavy metals: ≤0.005%
      suitability   meets USP testing specifications
      Mode of action   protein synthesis | interferes
      antibiotic activity spectrum   Gram-negative bacteria
        Gram-positive bacteria
      storage temp.   −20°C

      Description:

      Application

      Tetracycline is a broad spectrum polyketide antibiotic with clinical uses in treating bacterial infections such as Rocky Mountain spotted fever, typush fever, tick fevers, Q fever, and Brill-Zinsser disease and to treat upper respiratory infections and acne. It has been used in studies of multidrug resistance and potential side effects including acute pancreatitis. It is recommended for use in cell culture applications at 10 mg/L.

      Biochem/physiol Actions

      Mode of Action: Tetracycline passively diffuses through proin channels in the cell membrane, binding to 30S ribosomes and inhibits protein synthesis by preventing access of aminoacyl tRNA to the acceptor site on the mRNA-ribosome complex. It also binds to the bacterial 50S ribosomal subunit, altering the membrane and causing intracellular components to leak from bacterial cells. The inhibitory effects can be reversed by washing, suggesting that it is the reversibly bound antibiotic, and not the irreversibly bound drug, that is responsible for antibacterial action.

      Mode of Resistance: The effects are inactivated via a loss of cell wall permeability.

      Antimicrobial spectrum: Includes a wide range of antimicrobial activity against gram-positive and gram-negative bacteria.

      Caution

      This product should be frozen below 0°C and protected from light and moisture. In these conditions, the product has been shown to retain activity for 4 years. Stock solutions should be stored at -20°C and are stable at 37°C for 4 days.

      Packaging

      1, 5 g in poly bottle

      Preparation Note

      The product is freely soluble in water, soluble in methanol and ethanol but is insoluble in ether and hydrocarbons. In water, the product yields a clear, yellow-orange solution with heating and in 95% ethanol, 50 mg dissolved in 4 mL with heating yields a clear, yellow-green solution. Tetracycline is rapidly destroyed by alkali hydroxide solutions and standing water solutions become turbid due to hydrolysis and precipitation. The potency of tetracycline is reduced in solutions with pH below 2.

      Other Notes

      Keep container tightly closed in a dry and well-ventilated place. Light sensitive.

      Safety:

      Symbol 
      GHS08GHS09  GHS08, GHS09
      Signal word 
      Warning
      Hazard statements 
      H361-H411
      Precautionary statements 
      P280
      Personal Protective Equipment 
      dust mask type N95 (US), Eyeshields, Gloves
      RIDADR 
      UN 3077 9 / PGIII
      WGK Germany 
      2
      RTECS 
      QI9100000
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