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  2. Antimicrobial - Wikipedia

    en.wikipedia.org/wiki/Antimicrobial

    Antimicrobial resistance The misuse and overuse of antimicrobials in humans, animals and plants are the main drivers in the development of drug-resistant pathogens. [4] It is estimated that bacterial antimicrobial resistance (AMR) was directly responsible for 1.27 million global deaths in 2019 and contributed to 4.95 million deaths.

  3. Fluorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzaldehyde

    Due to the aldehyde group, the fluorobenzaldehydes can be used to make a variety of schiff base compounds through a condensation reaction, some of which have antimicrobial properties. [ 2 ] [ 3 ] References

  4. Reuterin - Wikipedia

    en.wikipedia.org/wiki/Reuterin

    It is a bifunctional molecule, containing both a hydroxy and aldehyde functional groups. The name reuterin is derived from Lactobacillus reuteri , which produces the compound biosynthetically from glycerol as a broad-spectrum antibiotic ( bacteriocin ). [ 1 ]

  5. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group. Aldehydes are a common motif in many ...

  6. Disulfiram-like drug - Wikipedia

    en.wikipedia.org/wiki/Disulfiram-like_drug

    A number of drugs do not cause disulfiram-like reactions, but have other unintended interactions with alcoholic drinks. For example, alcohol interferes with the efficacy of erythromycin . Patients on linezolid and tedizolid may be sensitive to the tyramine present in tap beers and red wine.

  7. Dihydroneopterin aldolase - Wikipedia

    en.wikipedia.org/wiki/Dihydroneopterin_aldolase

    Dihydroneopterin aldolase (DHNA, EC 4.1.2.25) plays a key role in turning 7,8-dihydro-d-neopterin (DHNP) into 6-hydroxymethyl-7,8-dihydropterin (HP), which is part of the folate biosynthesis process—an important focus for creating new antimicrobial drugs [1]. Folate cofactors are vital for all living organisms [2].

  8. 1,3,4-Oxadiazole - Wikipedia

    en.wikipedia.org/wiki/1,3,4-Oxadiazole

    For example, raltegravir is an HIV drug which contains an 1,3,4-oxadiazole ring. Other pharmaceutical drugs containing the 1,3,4-oxadiazole ring include fenadiazole, zibotentan, and tiodazosin. 1,3,4-Oxadiazole derivatives can be synthesized in a variety of ways. [3] One pathway is from oxidation of tetrazoles in the presence of aldehydes. [4]

  9. Alkaloid - Wikipedia

    en.wikipedia.org/wiki/Alkaloid

    Many synthetic and semisynthetic drugs are structural modifications of the alkaloids, which were designed to enhance or change the primary effect of the drug and reduce unwanted side-effects. [208] For example, naloxone , an opioid receptor antagonist , is a derivative of thebaine that is present in opium .