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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. H3 receptor antagonist - Wikipedia

    en.wikipedia.org/wiki/H3_receptor_antagonist

    The structural diversity among H 3 R is limited and all known H 3 R agonists today contain an imidazole ring. [11] [10] The problem with the imidazole containing compounds was the inhibition of cytochrome P450 isoenzymes which resulted in severe drug interactions. [12] [11] They also had difficulty in crossing the blood-brain-barrier. Many ...

  4. 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 ...

  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. 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 ...

  7. 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.

  8. Imidazolidinone - Wikipedia

    en.wikipedia.org/wiki/Imidazolidinone

    Drugs featuring this ring system include emicerfont, ... Examples include imidazol-4-one-5-propionic acid, a product of the catabolism of histidine, ...

  9. Imidazothiazoles - Wikipedia

    en.wikipedia.org/wiki/Imidazothiazoles

    Imidazothiazoles are a class of chemical compounds containing a bicyclic heterocycle (a double ring system) consisting of an imidazole ring fused to a thiazole ring. [1] The structure contains three non- carbon or heteroatoms : two nitrogen atoms and one sulfur atom.