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  2. Oxazolidinone - Wikipedia

    en.wikipedia.org/wiki/Oxazolidinone

    2-Oxazolidinone is the parent compound of several protein synthesis inhibitor antibiotics and the Evans chiral auxiliaries for aldol reactions. Cycloserine is an antibiotic based on the 3-isoxazolidone parent.

  3. 2-Oxazolidinone - Wikipedia

    en.wikipedia.org/wiki/2-oxazolidinone

    Oxazolidinones are useful as Evans auxiliaries, which are of interest for chiral synthesis. In a common implementation, an acid chloride substrate reacts with a chiral oxazolidinone to form an imide. Substituents at the 4 and 5 position of the oxazolidinone direct any aldol reaction to the alpha position of the carbonyl of the substrate. [6]

  4. Linezolid - Wikipedia

    en.wikipedia.org/wiki/Linezolid

    Although many antibiotics work this way, the exact mechanism of action of linezolid appears to be unique in that it blocks the initiation of protein production, rather than one of the later steps. [14] As of 2014, bacterial resistance to linezolid has remained low. [15] Linezolid is a member of the oxazolidinone class of medications. [10]

  5. Oxazolidine - Wikipedia

    en.wikipedia.org/wiki/Oxazolidine

    Oxazolidine is a five-membered heterocycle ringwith the formula (CH 2) 3 (NH)O.The O atom and NH groups are not mutually bonded, in contrast to isoxazolidine. [2] [3] Oxazolidines (emphasis on plural) are derivatives of the parent oxazolidine owing to the presence of substituents on carbon and/or nitrogen.

  6. Contezolid - Wikipedia

    en.wikipedia.org/wiki/Contezolid

    Contezolid (trade name Youxitai) is an antibiotic of the oxazolidinone class. [ 1 ] [ 2 ] It is effective against Staphylococcus aureus , methicillin-resistant Staphylococcus aureus (MRSA), Streptococcus pyogenes , Streptococcus agalactiae , and other bacteria.

  7. Quinolone antibiotic - Wikipedia

    en.wikipedia.org/wiki/Quinolone_antibiotic

    See Mechanism of Action earlier.) The majority of quinolones in clinical use belong to the second generation class of "fluoroquinolones", which have a true quinoline framework, maintain the C-3 carboxylic acid group, and add a fluorine atom to the all-carbon containing ring, typically at the C-6 or C-8 positions. [73]

  8. Tedizolid - Wikipedia

    en.wikipedia.org/wiki/Tedizolid

    [6] [7] [8] [3] Tedizolid is a second-generation oxazolidinone derivative that is 4-to-16-fold more potent against staphylococci and enterococci compared to linezolid. [9] The recommended dosage for treatment is 200 mg once daily for a total duration of six days, either orally (with or without food) or through an intravenous injection (if ...

  9. Maropitant - Wikipedia

    en.wikipedia.org/wiki/Maropitant

    Maropitant (INN; [3] brand name: Cerenia, used as maropitant citrate , is a neurokinin-1 (NK 1) receptor antagonist developed by Zoetis specifically for the treatment of motion sickness and vomiting in dogs. It was approved by the FDA in 2007, for use in dogs [4] [5] and in 2012, for cats. [6]