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  2. Indole-3-carbaldehyde - Wikipedia

    en.wikipedia.org/wiki/Indole-3-carbaldehyde

    Indole can also be metabolized by the liver into indoxyl sulfate, a compound that is toxic in high concentrations and associated with vascular disease and renal dysfunction. [2] AST-120 ( activated charcoal ), an intestinal sorbent that is taken by mouth , adsorbs indole, in turn decreasing the concentration of indoxyl sulfate in blood plasma.

  3. Indole - Wikipedia

    en.wikipedia.org/wiki/Indole

    Indole is an organic compound with the formula C 6 H 4 CCNH 3. Indole is classified as an aromatic heterocycle. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered pyrrole ring. Indoles are derivatives of indole where one or more of the hydrogen atoms have been replaced by substituent groups.

  4. Indoleacetate decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Indoleacetate_decarboxylase

    The first one consists of the degradation of the amino acid into indole-3-acetate. And in the second step, IAD catalyzes the decarboxylation of the indole-3-acetate to form the final product, skatole. The decarboxylation of indole-3-acetate is chemically difficult since it leaves an unstable carbanion because of the direct elimination of CO 2.

  5. Indolepyruvate decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Indolepyruvate_decarboxylase

    The enzyme indolepyruvate decarboxylase (EC 4.1.1.74) catalyzes the chemical reaction. 3-(indol-3-yl)pyruvate 2-(indol-3-yl)acetaldehyde + CO 2. This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds.

  6. Chronic solvent-induced encephalopathy - Wikipedia

    en.wikipedia.org/wiki/Chronic_solvent-induced...

    Chronic solvent-induced encephalopathy (CSE) is a condition induced by long-term exposure to organic solvents, often—but not always—in the workplace, that lead to a wide variety of persisting sensorimotor polyneuropathies and neurobehavioral deficits even after solvent exposure has been removed.

  7. Indole-3-carbinol - Wikipedia

    en.wikipedia.org/wiki/Indole-3-carbinol

    Indole-3-carbinol is the subject of on-going biomedical research into its possible anticarcinogenic, [4] antioxidant, and anti-atherogenic effects. [5] Research on indole-3-carbinol has been conducted primarily using laboratory animals and cultured cells. [ 6 ]

  8. Naphthoylindoles - Wikipedia

    en.wikipedia.org/wiki/Naphthoylindoles

    This Cannabis -related article is a stub. You can help Wikipedia by expanding it.

  9. Indole-3-carboxylate decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Indole-3-carboxylate_de...

    Indole-3-carboxylate decarboxylase (EC 4.1.1.92) is an enzyme with systematic name indole-3-carboxylate carboxy-lyase. [1] This enzyme catalyses the following chemical reaction indole-3-carboxylate ⇌ {\displaystyle \rightleftharpoons } indole + CO 2