Indole-3-acetaldehyde: Difference between revisions
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Revision as of 18:27, 4 November 2016
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| Names | |
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| IUPAC name
2-(1H-indol-3-yl)acetaldehyde
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| Other names
Indoleacetaldehyde;1H-Indole-3-acetaldehyde; 2-(indol-3-yl)Acetaldehyde; Indole-3-acetaldehyde; Indoleacetaldehyde; 1H-indol-3-Ylacetaldehyde; 2-(3-Indolyl)acetaldehyde; indol-3-Ylacetaldehyde; Tryptaldehyde
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C10H9NO | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Indole-3-acetaldehyde belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
Indole-3-acetaldehyde is a substrate for Retina-specific copper amine oxidase, aldehyde dehydrogenase X (mitochondrial), amine oxidase B, amiloride-sensitive amine oxidase, aldehyde dehydrogenase (mitochondrial), fatty aldehyde dehydrogenase, 4-trimethylaminobutyraldehyde dehydrogenase, Aldehyde dehydrogenase (dimeric NADP-preferring), Aldehyde dehydrogenase family 7 member A1, Amine oxidase A, Aldehyde dehydrogenase 1A3 and Membrane copper amine oxidase.[1]
References
- ^ Nutaratat P, Srisuk N, Arunrattiyakorn P, Limtong S (2016). "Indole-3-acetic acid biosynthetic pathways in the basidiomycetous yeast Rhodosporidium paludigenum". Arch Microbiol. 198 (5): 429–37. doi:10.1007/s00203-016-1202-z.