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  2. Imidazole - Wikipedia

    en.wikipedia.org/wiki/Imidazole

    This ring system is present in important biological building blocks, such as histidine and the related hormone histamine. Many drugs contain an imidazole ring, such as certain antifungal drugs , the nitroimidazole series of antibiotics , and the sedative midazolam .

  3. Histidine - Wikipedia

    en.wikipedia.org/wiki/Histidine

    Histidine ball and stick model spinning. Histidine (symbol His or H) [2] is an essential amino acid that is used in the biosynthesis of proteins.It contains an α-amino group (which is in the protonated –NH 3 + form under biological conditions), a carboxylic acid group (which is in the deprotonated –COO − form under biological conditions), and an imidazole side chain (which is partially ...

  4. Histamine - Wikipedia

    en.wikipedia.org/wiki/Histamine

    Histamine base, obtained as a mineral oil mull, melts at 83–84 °C. [8] Hydrochloride [9] and phosphorus [10] salts form white hygroscopic crystals and are easily dissolved in water or ethanol, but not in ether. In aqueous solution, the imidazole ring of histamine exists in two tautomeric forms, identified by which of the two nitrogen atoms ...

  5. Transition metal imidazole complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_imidazole...

    Structure of the histidine complex [Ni(κ 3-histidinate) 2] 2-. [1] A transition metal imidazole complex is a coordination complex that has one or more imidazole ligands. Complexes of imidazole itself are of little practical importance. In contrast, imidazole derivatives, especially histidine, are pervasive ligands in biology where they bind ...

  6. His-tag - Wikipedia

    en.wikipedia.org/wiki/His-tag

    Imidazole is the side chain of histidine and is typically used at a concentration of 150 - 500 mM for elution. Histidine or histamine can also be used. Decrease in pH; When the pH decreases, the histidine residue is protonated and can no longer coordinate the metal tag, allowing the protein to be eluted.

  7. Histidine decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Histidine_decarboxylase

    The enzyme histidine decarboxylase (EC 4.1.1.22, HDC) is transcribed on chromosome 15, region q21.1-21.2, and catalyzes the decarboxylation of histidine to form histamine.In mammals, histamine is an important biogenic amine with regulatory roles in neurotransmission, gastric acid secretion and immune response.

  8. Imidazole alkaloids - Wikipedia

    en.wikipedia.org/wiki/Imidazole_alkaloids

    In nature, imidazole alkaloids are found both as secondary plant compounds and as byproducts of histidine metabolism in marine organisms. One well-known imidazole alkaloid is pilocarpine , which is present in the leaves of Paraguay jaborandi .

  9. Imidazole-4-acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Imidazole-4-acetaldehyde

    In a study of imidazole-4-acetaldehyde presence in the reaction mixture during the coupling reaction of fungal amine oxidase and bacterial aldehyde oxidase for histamine elimination, imidazole 4-acetaldehyde was not detected, which suggests that imidazole 4-acetaldehyde was not produced as a result of the coupling reaction between fungal amine oxidase and aldehyde oxidase, as such, its absence ...