SKU: T001  / 
    CAS Number: 89786-04-9

    Tazobactam

    3,207,585.00₫ - 13,837,372.50₫

    Tazobactam is a penicillanic acid sulfone derivative and β-lactamase inhibitor with antibacterial activity. Tazobactam was discovered by Dr. R.G. Micetech at the University of Alberta in 1982. Tazobactam contains a β-lactam ring and irreversibly binds to β-lactamase at or near its active site. This protects other β-lactam antibiotics from β-lactamase catalysis. This drug is used in conjunction with β-lactamase susceptible penicillins to treat infections caused by β-lactamase producing organisms.

    Tazobactam alone showed an MIC of ≤ 8 mg/liter (range 2 to 32 mg/liter) against several Acinetobacter baumannii strains. Tazobactam in combination with piperacillin, successfully restored the activity of piperacillin against β-lactamase-producing bacteria. Tazobactam exhibited inhibitory activity and protected piperacillin against Richmond and Sykes types II, III, IV and V β-lactamases, staphylococcal penicillinase and extended-spectrum β-lactamases. Tazobactam showed species-specific activity against class I chromosomally-mediated enzymes.

    Tazobactam is slightly soluble in aqueous solution.

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    Mechanism of Action Tazobactam contains a β-lactam ring that binds strongly to β-lactamase at or near its activation site, thereby permanently inhibiting enzymatic activity.  This action protects other β-lactam antibiotics (penicillins, cephalosporins, etc.) from β-lactamase catalysis, thereby enhancing their antibacterial activity.
    Spectrum

    Tazobactam exhibits little useful antimicrobial activity, although weak activity against Acinetobacter spp. and Borrelia burgdorferi has been reported.

    Tazobactam inhibits a wide range of β-lactamases, including the group 2 penicillinases from Staphyloccus aureus, the TEM-1 and SHV-1 β-lactamases, many extended-spectrum enzymes, and the common group 2e cephalosporinases of Bacteroides fragilis. Against the group 1 cephalosporinases, activity is strongly influenced by the amount of enzyme produced. The inhibitor-resistant group 2br β-lactamases are poorly inhibited and group 3 metallo-β-lactamases are not inhibited at clinically useful levels. It is a poor inducer of β-lactamases of Gram-positive and Gram-negative organisms.

    Microbiology Applications Tazobactam is often combined with the extended-spectrum β-lactam antibiotic piperacillin in the compound Zosyn or Tazocin (piperacillin/tazobactam), used in infections due to Pseudomonas aeruginosa. Tazobactam broadens the spectrum of piperacillin by making it effective against organisms that express β-lactamase and would normally degrade piperacillin.
    Molecular Formula

    C10H12N4O5S

    References

    Bryson HM and Brogden RN (1994)  Piperacillin/tazobactam. A review of its antibacterial activity, pharmacokinetic properties and therapeutic potential. Drugs. 47(3):506-535  PMID 7514977

    Craig WA and Andes DR (2013)  In vivo activities of ceftolozane, a new cephalosporin, with and without tazobactam against Pseudomonas aeruginosa and Enterobacteriaceae, including strains with extended-spectrum β-lactamases, in the thighs of neutropenic mice. Antimicrob. Agents Chemother.57(4):1577-1582

    Drawz SM and Bonomo RA (2010)  Three decades of β-lactamase inhibitors. Clin.Microbiol.Rev. 23(1):160-201

    Frase H et al (2011) Identification of products of inhibition of GES-2 beta-lactamase by Tazobactam by x-ray crystallography and spectrometry. J Biol Chem. 286(16):14396-14409. PMID 21345789

    Jones RN et al (1989)  Piperacillin/tazobactam (YTR 830) combination. Comparative antimicrobial activity against 5889 recent aerobic clinical isolates and 60 Bacteroides fragilis group strains. Diagn. Microbiol. Infect. Dis. 12(6): 489-494

    Zhanel GG et al (2014)  Ceftolozane/tazobactam: a novel cephalosporin/β-lactamase inhibitor combination with activity against multidrug-resistant Gram-negative bacilli. Drugs. 74(1):31-51. PMID 24352909

    MIC Escherichia coli (DH5α + pBC-OXA-46)| 4 - ?| 660| Escherichia coli (DH5α + pBC-SK)| 4 - ?| 660|