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Inactivation is the rarest type of resistance, [32] where NADPH-dependent oxidoreductase, a class of antibiotic destructase, modifies the tetracycline antibiotic at their oxidative soft spot leading to an inactivation of the tetracycline antibiotic. For example, the oxireductase makes a modification on the C11a site of oxytetracycline.
Tetracycline displayed higher potency, better solubility, and more favorable pharmacology than the other antibiotics in its class, leading to its FDA approval in 1954. The new compound was one of the first commercially successful semi-synthetic antibiotics that was used, and laid the foundation for the development of Sancycline, Minocycline ...
Pages in category "Tetracycline antibiotics" The following 20 pages are in this category, out of 20 total. This list may not reflect recent changes. ...
The following is a list of antibiotics. ... Similar structure with tetracycline, but five times stronger, big volume distribution and long half-time in the body
Some tricyclic compounds having three fused and one tethered ring (connected to main nucleus by a single bond) can also classified as tetracyclic, for example, ciclazindol. [1] Tetracyclic compounds have various pharmaceutical uses, such as: tetracycline antibiotics. Doxycycline; Tigecycline; Omadacycline; Eravacycline; tetracyclic ...
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.
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