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  2. Tetracycline antibiotics - Wikipedia

    en.wikipedia.org/wiki/Tetracycline_antibiotics

    Skeletal formula of tetracycline with atoms and four rings numbered and labeled.. Tetracyclines are a group of broad-spectrum antibiotic compounds that have a common basic structure and are either isolated directly from several species of Streptomyces bacteria or produced semi-synthetically from those isolated compounds. [1]

  3. Tetracycline - Wikipedia

    en.wikipedia.org/wiki/Tetracycline

    Tetracycline hydrochloride is available as yellow crystalline powder. Since tetracycline is absorbed into bone, it is used as a marker of bone growth for biopsies in humans. Tetracycline labeling is used to determine the amount of bone growth within a certain period of time, usually a period around 21 days.

  4. TetR - Wikipedia

    en.wikipedia.org/wiki/TetR

    The overall structure of TetR can be broken down into two DNA-binding domains (one per monomer) and a regulatory core, which is responsible for tetracycline recognition and dimerization. TetR dimerizes by making hydrophobic contacts within the regulatory core. There is a binding cavity for tetracycline in the outer helices of the regulatory domain.

  5. Tetracyclic - Wikipedia

    en.wikipedia.org/wiki/Tetracyclic

    Doxycycline, a tetracyclic antibiotic. Mirtazapine, a tetracyclic antidepressant. Tetracyclics are cyclic chemical compounds that contain four fused rings of atoms, for example, Tröger's base.

  6. Category:Tetracycline antibiotics - Wikipedia

    en.wikipedia.org/wiki/Category:Tetracycline...

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  7. Non-neutral plasma - Wikipedia

    en.wikipedia.org/wiki/Non-neutral_plasma

    Non-neutral plasmas are used for research into basic plasma phenomena such as cross-magnetic field transport, [6] nonlinear vortex interactions, [7] and plasma waves and instabilities. [8] They have also been used to create cold neutral antimatter , by carefully mixing and recombining cryogenic pure positron and pure antiproton plasmas.

  8. Tetracenomycin C - Wikipedia

    en.wikipedia.org/wiki/Tetracenomycin_C

    The structure of tetracenomycin C was established by chemical and spectroscopic methods. [3] The three hydroxy groups, at C-4, C-4a, and C-12a, are cis to each other. The two at C-4a and C-12a are involved in intramolecular hydrogen bonding to the carbonyl oxygen atoms at C-5 and C-1, respectively.

  9. Eravacycline - Wikipedia

    en.wikipedia.org/wiki/Eravacycline

    Eravacycline (TP-434, Xerava) is a synthetic halogenated tetracycline class antibiotic by Tetraphase Pharmaceuticals. It is closely related to tigecycline.It has a broad spectrum of activity including many multi-drug resistant strains of bacteria.