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Tigecycline - NDSRI's

n-nitroso-tigecycline
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N-Nitroso Tigecycline

  • CAT NUMBER DCTI-C-2106
  • CAS NUMBER NA
  • MOLECULAR FORMULA C29H38N6O9
  • MOLECULAR WEIGHT 614.66
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References
FAQ's

References

  1. Sum, Phaik-Eng; Petersen, Peter, Synthesis and structure-activity relationship of novel glycylcycline derivatives leading to the discovery of GAR-936, Bioorganic & Medicinal Chemistry Letters, Volume: 9, Issue: 10, Pages: 1459-1462, 1999
  2. Li, Chonghua; Sutherland, Christina A.; Nightingale, Charles H.; Nicolau, David P., Quantitation of tigecycline, a novel glycyclcycline, by liquid chromatography, Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, Volume: 811, Issue: 2, Pages: 225-229, 2004

Frequently Asked Questions

Impurities in Tigecycline can affect the drug's bioavailability and its therapeutic effect.

 

The control of Tigecycline impurities during the manufacturing process involves monitoring and controlling the manufacturing process, conducting tests at multiple stages of production, and utilizing validated analytical methods.

Impurities in Tigecycline may arise from the starting materials, intermediates, degradation products, or residual solvents used in the manufacturing process.

Tigecycline impurities are stored at a controlled room temperature between 2-8 °C or as indicated on the Certificate of Analysis (CoA).

Note: Products protected by valid patents by a manufacturer are not offered for sale in countries having patent protection. The sale of such products constitutes a patent infringement, and its liability is at the buyer's risk.

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