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  2. Imidazole - Wikipedia

    en.wikipedia.org/wiki/Imidazole

    Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin. Imidazole-based histidine compounds play an important role in intracellular buffering. [17]

  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. 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 ...

  6. Transition metal imidazole complex - Wikipedia

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

    The free amino acid can coordinate through the imidazole and either or both of the carboxylate and amine. The imidazole side chain of histidine residues in proteins are common binding sites for metal ions. Unlike the free amino acid, the histidine residue (i.e., as a component of a peptide or protein), coordinates solely via the imidazole ...

  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. Imidazol-4-one-5-propionic acid - Wikipedia

    en.wikipedia.org/wiki/Imidazol-4-one-5-propionic...

    Imidazol-4-one-5-propionic acid is an intermediate in the metabolism of histidine. It is a colorless compound that is sensitive to light in air. It is a colorless compound that is sensitive to light in air.

  9. Histamine N-methyltransferase - Wikipedia

    en.wikipedia.org/wiki/Histamine_N-methyltransferase

    Histamine N-methyltransferase is encoded by a single gene, called HNMT, which has been mapped to chromosome 2 in humans. [5]Three transcript variants have been identified for this gene in humans, which produce different protein isoforms [6] [5] due to alternative splicing, which allows a single gene to code for multiple proteins by including or excluding particular exons of a gene in the final ...