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  2. Doxycycline - Wikipedia

    en.wikipedia.org/wiki/Doxycycline

    Doxycycline, doxycycline monohydrate and doxycycline hyclate are yellow, crystalline powders with a bitter taste. The latter smells faintly of ethanol , a 1% aqueous solution has a pH of 2–3, and the specific rotation is [ α ] D 25 {\displaystyle [\alpha ]_{D}^{25}} −110° cm 3 /dm·g in 0.01 N methanolic hydrochloric acid .

  3. Metacycline - Wikipedia

    en.wikipedia.org/wiki/Metacycline

    It is used as a precursor in the industrial synthesis of doxycycline hyclate. [citation needed] It has been found to act as an agonist of the human pregnane X receptor ligand-binding domain and to induce CYP3A4 expression in vitro. [1]

  4. Tetracycline antibiotics - Wikipedia

    en.wikipedia.org/wiki/Tetracycline_antibiotics

    Partial exceptions to these rules occur for doxycycline and minocycline, which may be taken with food (though not iron, antacids, or calcium supplements). Minocycline can be taken with dairy products because it does not chelate calcium as readily, although dairy products do decrease absorption of minocycline slightly. [39]

  5. Talk:Doxycycline - Wikipedia

    en.wikipedia.org/wiki/Talk:Doxycycline

    Here are links to possibly useful sources of information about Doxycycline. PubMed provides review articles from the past five years (limit to free review articles) The TRIP database provides clinical publications about evidence-based medicine. Other potential sources include: Centre for Reviews and Dissemination and CDC

  6. Hyclate - Wikipedia

    en.wikipedia.org/wiki/Hyclate

    A hyclate (Latin: hyclas) is a pharmaceutical term for hydrochloride hemiethanolate hemihydrate [1] [2] (·HCl· ⁠ 1 / 2 ⁠ EtOH· ⁠ 1 / 2 ⁠ H 2 O), e.g. doxycycline hyclate. [ 3 ] [ 4 ] References

  7. Tetracycline - Wikipedia

    en.wikipedia.org/wiki/Tetracycline

    Tetracycline blocks the A-site so that a hydrogen bond is not formed between the amino acids. Tetracycline binds to the 30S and 50S subunit of microbial ribosomes. [3] Thus, it prevents the formation of a peptide chain. [25] The action is usually not inhibitory and irreversible even with the withdrawal of the drug.

  8. Oxytetracycline - Wikipedia

    en.wikipedia.org/wiki/Oxytetracycline

    Oxytetracycline, like other tetracyclines, is used to treat many infections, both common and rare.Its better absorption profile makes it preferable to tetracycline for moderately severe acne at a dosage of 250–500 mg four times a day for usually six to eight weeks at a time, but alternatives should be sought if no improvement occurs by three months.

  9. Dicloxacillin - Wikipedia

    en.wikipedia.org/wiki/Dicloxacillin

    Dicloxacillin is a narrow-spectrum β-lactam antibiotic of the penicillin class. [1] It is used to treat infections caused by susceptible (non-resistant) Gram-positive bacteria. [1]