Convolutindole A
This article includes a list of references, related reading or external links, but its sources remain unclear because it lacks inline citations. (August 2015) |
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Preferred IUPAC name
N,N-Dimethyl-2-(2,4,6-tribromo-1,7-dimethoxy-1H-indol-3-yl)ethan-1-amine | |
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CompTox Dashboard (EPA)
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Properties | |
C14H17Br3N2O2 | |
Molar mass | 485.014 g·mol−1 |
Melting point | 61.5 to 62.5 °C (142.7 to 144.5 °F; 334.6 to 335.6 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
what is ?) | (|
Infobox references | |
Convolutindole A (2,4,6-tribromo-1,7-dimethoxy-N,N-dimethyltryptamine) is a brominated tryptamine alkaloid that was first identified in 2001 in , a marine bryozoan. Bryozoans are aquatic invertebrates that grow in colonies and may resemble coral.
Chemistry[]
Convolutamine A is the 2,4,6-tribromo-1,7-dimethoxy derivative of DMT, a hallucinogen that occurs naturally in many plants and animals. Convolutamine A is chemically related to 5-bromo-DMT which also occurs in many marine invertebrates.
Until the discovery of convolutindole A, the 1-methoxyindole moiety was unknown in the marine world. 1-Methoxyindoles, such as lespedamine, were previously only known to occur in legumes and the Brassicaceae, the plant family that cabbage and mustard belong to.
Biological activity[]
This chemical was tested for its ability to kill parasitic nematodes. It was found to be more effective than levamisole,[medical citation needed] a synthetic drug used to kill parasitic worms and to treat colon cancer.
References[]
- Narkowicz, C. K.; Blackman, A. J., (June 2001). Abstracts of Papers; 10th International Symposium on Marine Natural Products: Nago, Okinawa, Abstract OR1.
- Narkowicz, C. K.; Blackman, A. J.; Lacey, E.; Gill, J. H.; Heiland, K. (2002). "Convolutindole a and Convolutamine H, New Nematocidal Brominated Alkaloids from the Marine BryozoanAmathia convoluta". Journal of Natural Products. 65 (6): 938–941. doi:10.1021/np010574x. PMID 12088445.
- Tryptamine alkaloids
- Halogen-containing alkaloids
- Organobromides
- Indole ethers at the benzene ring
- Hydroxylamines