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  2. Indole-3-carbaldehyde - Wikipedia

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

    Indole-3-carbaldehyde (I3A), also known as indole-3-aldehyde and 3-formylindole, is a metabolite of dietary L-tryptophan which is synthesized by human gastrointestinal bacteria, particularly species of the Lactobacillus genus.

  3. 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] Limited and inconclusive human studies have been reported.

  4. Indole - Wikipedia

    en.wikipedia.org/wiki/Indole

    At very low concentrations, however, it has a flowery smell, [3] and is a constituent of many perfumes. It also occurs in coal tar. It has been identified in cannabis. [4] It is the main volatile compound in stinky tofu. [5] When indole is a substituent on a larger molecule, it is called an indolyl group by systematic nomenclature.

  5. Indolocarbazole - Wikipedia

    en.wikipedia.org/wiki/Indolocarbazole

    The process begins by producing 7-chloroindole-3-acetamide by treating 7-chloroindole with a series of reagents, shown farther down. This molecule is then glycosylated and reacted with methyl 7-chloroindole-3-glyoxylate to produce an intermediate that goes on to stabilize into the final product.

  6. β-Carboline - Wikipedia

    en.wikipedia.org/wiki/Β-Carboline

    The effects of these substances depend on their respective substituent. Natural β-carbolines primarily influence brain functions but can also exhibit antioxidant [1] effects. Synthetically designed β-carboline derivatives have recently been shown to have neuroprotective, [2] cognitive enhancing and anti-cancer properties. [3]

  7. 6-Formylindolo (3,2-b)carbazole - Wikipedia

    en.wikipedia.org/wiki/6-Formylindolo(3,2-b)carbazole

    In addition to the light- or H 2 O 2-induced formation of FICZ, a number of other enzymatic pathways have been identified to convert Trp to FICZ via the precursor I3A. [2] [3] Oxidative deamination of Trp by aromatic amino acid aminotransferases (ArAT) or L-amino oxidases (LAAO), one of which is the IL4-inducible enzyme IL4I1, converts Trp to indole-3-pyruvate, which after decarboxylation ...

  8. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    Some organochlorides are considered safe enough for consumption in foods and medicines. For example, peas and broad beans contain the natural chlorinated plant hormone 4-chloroindole-3-acetic acid (4-Cl-IAA); [16] [17] and the sweetener sucralose (Splenda) is widely used in diet products.

  9. Levonorgestrel-releasing implant - Wikipedia

    en.wikipedia.org/wiki/Levonorgestrel-releasing...

    It is generally well tolerated with few significant side effects. [1] Side effects may include irregular menstrual periods, no periods, headaches, and breast pain. [3] [4] Use is not recommended in people with significant liver disease. [3] The levonorgestrel implant is a type of long-acting reversible birth control. [5]