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  2. Aminoglycoside - Wikipedia

    en.wikipedia.org/wiki/Aminoglycoside

    Aminoglycoside antibiotics display bactericidal activity against Gram-negative aerobes and some anaerobic bacilli where resistance has not yet arisen but generally not against Gram-positive and anaerobic Gram-negative bacteria. [3] Streptomycin is the first-in-class aminoglycoside antibiotic.

  3. Cross-resistance - Wikipedia

    en.wikipedia.org/wiki/Cross-resistance

    Cross-resistance can take place between compounds that are chemically similar, like antibiotics within similar and different classes. [9] That said, structural similarity is a weak predictor of antibiotic resistance, and does not predict antibiotic resistance at all when aminoglycosides are disregarded in the comparison. [10]

  4. Netilmicin - Wikipedia

    en.wikipedia.org/wiki/Netilmicin

    Netilmicin (1-N-ethylsisomicin) is a semisynthetic aminoglycoside antibiotic, and a derivative of sisomicin, produced by Micromonospora inyoensis. Aminoglycoside antibiotics have the ability to kill a wide variety of bacteria. Netilmicin is not absorbed from the gut and is therefore only given by injection or infusion.

  5. Streptothricin - Wikipedia

    en.wikipedia.org/wiki/Streptothricin

    Streptothricins are a group of antibiotics in the aminoglycoside class. [1] The first antibiotic in the group was isolated from Streptomyces lavendulae in 1942. [2] It was later determined to be a mixture of closely-related compounds, and is now known as nourseothricin.

  6. Sisomicin - Wikipedia

    en.wikipedia.org/wiki/Sisomicin

    Sisomicin (bactoCeaze, ensamycin, and initially antibiotic 6640 [1] and rickamicin [1]), is an aminoglycoside antibiotic, isolated from the fermentation broth of Micromonospora inositola. [1] It is a newer broad-spectrum aminoglycoside most structurally related to gentamicin .

  7. Amikacin - Wikipedia

    en.wikipedia.org/wiki/Amikacin

    Side-effects of amikacin are similar to those of other aminoglycosides. Kidney damage and ototoxicity (which can lead to hearing loss) are the most important effects, occurring in 1–10% of users. [17] The nephro- and ototoxicity are thought to be due to aminoglycosides' tendency to accumulate in the kidneys and inner ear. [8] Diagram of the ...

  8. Kanamycin A - Wikipedia

    en.wikipedia.org/wiki/Kanamycin_A

    Antibiotic resistance or development of multi-drug resistant bacterial strains is a key challenge for treating bacterial infections. With limited research being carried out to design and develop new antibiotics, novel approaches like functionalizing antibiotic to metal nanoparticles surface to treat resistant bacterial strains have been studied ...

  9. Aminocyclitol - Wikipedia

    en.wikipedia.org/wiki/Aminocyclitol

    Aminocyclitols are found as a component of aminoglycoside antibiotics which is also called as pseudosugars or pseudosaccharides. Aminocyclitols have chemical structures of a carbon ring with amine functional group(s). The class of aminocyclitol containing natural products can be divided by ring sizes or types of precursors.