SKU: M062  / 
    CAS Number: 10118-90-8

    Minocycline

    €122,03 - €398,19

    Minocycline is a broad-spectrum, second-generation tetracycline. Like all tetracyclines, Minocycline shows broad spectrum antibacterial and antiprotozoan activity. It was patented in 1961 (American cyanamid), synthesized in 1966 (Lederle Labs). Formulations containing Minocycline have been used for acne vulgaris, Current research is reviewing its neuroprotective and anti-inflammatory effects. Minocycline has been found to have many non-antibiotic biological effects in experimental models wtih inflammatory basis and autoimmune disorders. It is an indirect inhibitor of inducible nitric oxide synthase. Minocycline is soluble in ethanol, methanol, DMF or DMSO but has limited water solubility.

    We also offer:
    Minocycline Hydrochloride (M008)

    Mechanism of Action Minocycline acts by binding to the 30S and 50S ribosomal sub-units, inhibiting the binding of aminoacyl-tRNA to the ribosomal acceptor (A) site thus blocking protein synthesis. It has many non-antibiotic effects, multiple mechanisms of action have been proposed. A better understanding of the in vivo activity is needed before its therapeutic potential can be accurately assessed.
    Spectrum Minocycline has broad-spectrum antibacterial activity and antiprotozoan activity. It has bacteriostatic activity against both Gram-positive and Gram-negative bacteria. It can also be used for methicillin-resistant Staphylococcus aureus (MRSA) and carbapenem-resistant Acinetobacter baumannii.
    Microbiology Applications

    Minocycline is commonly used in clinical in vitro microbiological antimicrobial susceptibility tests (Etest, disk diffusion, and broth microdilution methods) against Gram-positive and Gram-negative microbial isolates. Medical microbiologists use AST results to recommend antibiotic treatment options. Representative MIC values include:

    Staphylococcus aureus (methicillin-resistant) 0.25 µg/mL - 8 µg/mL
    For a representative list of Minocycline MIC values, click here http://antibiotics.toku-e.com/antimicrobial_821_9.html.

    Pharmacokinetic/pharmacodynamic studies on Minocycline are scarce. A hollow-fibre in vitro model to simulate free-drug serum concentration with MRSA strains confimed that this agent is an AUC/MIC-driven agent. The estimation of MIC breakpoints is even more complex since tetracyclines including minocycline have an atypical non-linear protein binding pattern, meaning that the free fraction of the Minocycline

    Cancer Applications

    Minocycline inhibits in vitro invasion and experimental pulmonary metastatis in mouse renal adenocarcinoma (MRAC-PM2) cells (Masumori et al, 1994). It has been described to inhibit tumor growht in the xenograft tumor model of C6 glioma cells, inducing autophagic cell death. Its anti-proliferative activiites increase its anti-tumor potential.

    References

    Bishburg E, Bishburg K (2009) Minocycline--an old drug for a new century: Emphasis on methicillin-resistant Staphylococcus aureus (MRSA) and Acinetobacter baumannii. Int. J. Antimicrob. Agents. 34(5):395-401 PMID 19665876

    Church RFR et al (1971) Synthesis of 7-dimethylamino-6-demethyl-6-deoxytetracycline (Minocycline) via 9-nitro-6-demethyl-6-
    deoxytetracycline. J. Org. Chem. 36:723

    Fischer J, Ganellin CR (2006) Analogue-based Drug Discovery. John Wiley & Sons. p. 489 ISBN: 978-3-527-60749-5

    Garrido-Mesa N, Zarzuelo A, Gálvez J. Minocycline: far beyond an antibiotic. Br J Pharmacol. 2013 May;169(2):337-52. doi: 10.1111/bph.12139. PMID: 23441623; PMCID: PMC3651660.

    Martel MJ and Boothe JH (1967) The 6-deoxytetracyclines. VII. Alkylated aminotetracyclines possessing unique antibacterial activity. J. Med. Chem. 10:44

    Tsakris A, Koumaki V, Dokoumetzidis A (2019) Minocycline susceptibility breakpoints for Acinetobacter baumannii: Do we need to re-evaluate them? J. Antimicrob. Chemother. 74 (2):295-297

    Wang P et al (2016) Comparison of Minocycline susceptibility testing methods for Carbapenem-resistant Acinetobacter baumannii. J Clin Microbiol. 54(12):2937-2941