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  2. Ceftriaxone - Wikipedia

    en.wikipedia.org/wiki/Ceftriaxone

    Ceftriaxone, sold under the brand name Rocephin, is a third-generation cephalosporin antibiotic used for the treatment of a number of bacterial infections. [4] These include middle ear infections, endocarditis, meningitis, pneumonia, bone and joint infections, intra-abdominal infections, skin infections, urinary tract infections, gonorrhea, and pelvic inflammatory disease. [4]

  3. ATC code J01 - Wikipedia

    en.wikipedia.org/wiki/ATC_code_J01

    ATC code J01 Antibacterials for systemic use is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products.

  4. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The word's meaning became restricted to "spirit of wine" (the chemical known today as ethanol) in the 18th century and was extended to the class of substances so-called as "alcohols" in modern chemistry after 1850. [16] The term ethanol was invented in 1892, blending "ethane" with the "-ol" ending of "alcohol", which was generalized as a libfix ...

  5. Cefuroxime axetil - Wikipedia

    en.wikipedia.org/wiki/Cefuroxime_axetil

    Cefuroxime axetil, sold under the brand name Ceftin among others, is a second generation oral cephalosporin antibiotic.. It is an acetoxyethyl ester prodrug of cefuroxime which is effective orally. [2]

  6. Sulbactam - Wikipedia

    en.wikipedia.org/wiki/Sulbactam

    PubChem CID: 130313; ... CHEBI:9321 ChEMBL: ChEMBL403 CompTox Dashboard (EPA) DTXSID1023605; ECHA InfoCard: 100.063.506: Chemical and physical data; Formula: C 8 H 11 ...

  7. Cefpodoxime - Wikipedia

    en.wikipedia.org/wiki/Cefpodoxime

    It also finds use as oral continuation therapy when intravenous cephalosporins (such as ceftriaxone) are no longer necessary for continued treatment. Cefpodoxime inhibits peptidoglycan synthesis in bacterial cell walls. It has an oral bioavailability of approximately 50%, which is increased when taken with food. It has an elimination half-life ...

  8. Allyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Allyl_alcohol

    Allyl alcohol is converted mainly to glycidol, which is a chemical intermediate in the synthesis of glycerol, glycidyl ethers, esters, and amines. Also, a variety of polymerizable esters are prepared from allyl alcohol, e.g. diallyl phthalate. [5] Allyl alcohol has herbicidal activity and can be used as a weed eradicant [9]) and fungicide. [8]

  9. Tazobactam - Wikipedia

    en.wikipedia.org/wiki/Tazobactam

    PubChem CID: 123630; ... Chemical and physical data; Formula: C 10 H 12 N 4 O 5 S: Molar mass: ... It is commonly used as its sodium salt, tazobactam sodium.