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    Gentamicin sulfate

    Available from stock

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      Gentamicin sulfate

      SKU
      G0050

      Category: Antibiotics

      Synonyms
      Apogen, Garamycin, Gentiomycin C, Refobacin, NSC-82261
      1405-41-0
      CAS-Number
      n/a
      Molecular Formula
      n/a
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Appearance
      White to off-white powder
      Optical Activity
      +107.0 to +121.0
      Water content (K.F.)
      ≤18.0%

      Properties

      Solvents
      water (50 mg/ml)
      Optical Activity
      +107°- +121°
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      +4°C
      Handling Advice
      Protect from light and air. Store under inert gas.
      Use / Stability
      Stable for at least 2 years after receipt when stored at +4°C.
      Hazard statements
      H317
      Precautionary statements
      P280
      GHS Symbol
      GHS07
      Signal word
      Warning
      Transportation
      Not dangerous goods
      Description
      Gentamicin sulfate is a broad-spectrum aminoglycoside antibiotic used to treat a wide range of bacterial infections. It is antibacterial against Gram-negative aerobic bacteria, Gram-positive bacteria and mycoplasmas. Gentamicin sulfate is a protein synthesis inhibitor. It causes codon misreading by binding to the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from the acceptor site to the donor site. Gentamicin sulfate is used as a selection agent (gentamicin-resistance gene) in molecular biology applications. It is a broad-spectrum cell culture antibiotic that is nontoxic to viruses and mammalian cells at antibacterial and antimycoplasmal concentrations. Due to its extended stability and slow development of bacterial resistance, it is a useful antibiotic in long-term virus und tissue culture studies.
      Smiles
      O=S(O)(O)=O.O[C@]1(C)[C@@H]([C@@H](O)[C@@H](O[C@@H]2[C@@H](O)[C@H](O[C@H]3O[C@@](CC[C@H]3N)([C@@H](C)NC)[H])[C@@H](N)C[C@H]2N)OC1)NC.O[C@]4(C)[C@@H]([C@@H](O)[C@@H](O[C@@H]5[C@@H](O)[C@H](O[C@H]6O[C@@](CC[C@H]6N)([C@@H](C)N)[H])[C@@H](N)C[C@H]5N)OC4)NC.O[
      InChi Key
      RDEIXVOBVLKYNT-HDZPSJEVSA-N
      References
      (1) M. Finland, Med. Times 97, 161 (1969) (Review) , (2) R.E. Hancock, J. Antimicrob. Chemother. 8, 249 (1981) (Review) , (3) E. Hancock, J. Antimicrob. Chemother. 8, 429 (1981) (Review) , (4) N.L. Martin & T.J. Beveridge, Antimicrob. Agents Chemother. 29, 1079 (1986) , (5) J.P. Montenez, et al., Toxicol. Lett. 73, 201 (1994) , (6) F.C. Luft, J. Mol. Med. 80, 543 (2002) (Review) , (7) Y. Quiros, et al., Toxicol. Sci. 119, 245 (2011) (Review)

      Gentamicin sulfate is a broad-spectrum aminoglycoside antibiotic used to treat a wide range of bacterial infections. It is antibacterial against Gram-negative aerobic bacteria, Gram-positive bacteria and mycoplasmas. Gentamicin sulfate is a protein synthesis inhibitor. It causes codon misreading by binding to the 30S ribosomal subunit, blocking the translocation of peptidyl-tRNA from the acceptor site to the donor site. Gentamicin sulfate is used as a selection agent (gentamicin-resistance gene) in molecular biology applications. It is a broad-spectrum cell culture antibiotic that is nontoxic to viruses and mammalian cells at antibacterial and antimycoplasmal concentrations. Due to its extended stability and slow development of bacterial resistance, it is a useful antibiotic in long-term virus und tissue culture studies.

      SKU: G0050 Category: Antibiotics
      • Additional information

      Additional information

      Synonyms

      Apogen, Garamycin, Gentiomycin C, Refobacin, NSC-82261

      Appearance

      White to off-white powder

      CAS-Number

      1405-41-0

      Molecular Formula

      n/a

      Molecular Weight

      n/a

      Solvents

      water (50 mg/ml)

      Optical Activity

      +107°- +121°

      Smiles

      O=S(O)(O)=O.O[C@]1(C)[C@@H]([C@@H](O)[C@@H](O[C@@H]2[C@@H](O)[C@H](O[C@H]3O[C@@](CC[C@H]3N)([C@@H](C)NC)[H])[C@@H](N)C[C@H]2N)OC1)NC.O[C@]4(C)[C@@H]([C@@H](O)[C@@H](O[C@@H]5[C@@H](O)[C@H](O[C@H]6O[C@@](CC[C@H]6N)([C@@H](C)N)[H])[C@@H](N)C[C@H]5N)OC4)NC.O[

      InChi Key

      RDEIXVOBVLKYNT-HDZPSJEVSA-N

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      +4°C

      Handling Advice

      Protect from light and air. Store under inert gas.

      Use / Stability

      Stable for at least 2 years after receipt when stored at +4°C.

      Hazard statements

      H317

      Precautionary statements

      P280

      GHS Symbol

      GHS07

      Signal word

      Warning

      Transportation

      Not dangerous goods

      References

      (1) M. Finland, Med. Times 97, 161 (1969) (Review), (2) R.E. Hancock, J. Antimicrob. Chemother. 8, 249 (1981) (Review), (3) E. Hancock, J. Antimicrob. Chemother. 8, 429 (1981) (Review), (4) N.L. Martin & T.J. Beveridge, Antimicrob. Agents Chemother. 29, 1079 (1986), (5) J.P. Montenez, et al., Toxicol. Lett. 73, 201 (1994), (6) F.C. Luft, J. Mol. Med. 80, 543 (2002) (Review), (7) Y. Quiros, et al., Toxicol. Sci. 119, 245 (2011) (Review)

      Quantity

      10 g, 50 g, Bulk

      cdx-Optical Activity

      +107.0 to +121.0

      cdx-Water content (K.F.)

      ≤18.0%

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