Convolutindole A

Convolutindole A (2,4,6-tribromo-1,7-dimethoxy-N,N-dimethyltryptamine) is a brominated tryptamine alkaloid that was first identified in 2001 in Amathia convoluta, a marine bryozoan. Bryozoans are aquatic invertebrates that grow in colonies and may resemble corals.

Convolutindole A

Names
Preferred IUPAC name N,N-Dimethyl-2-(2,4,6-tribromo-1,7-dimethoxy-1H-indol-3-yl)ethan-1-amine
Identifiers
CAS Number	443356-86-3 Y
3D model (JSmol)	Interactive image
ChemSpider	4481610 N
PubChem CID	5324072
UNII	D37997A5KB Y
CompTox Dashboard (EPA)	DTXSID50415867
InChI InChI=1S/C14H17Br3N2O2/c1-18(2)6-5-8-11-9(15)7-10(16)13(20-3)12(11)19(21-4)14(8)17/h7H,5-6H2,1-4H3 N Key: KPTXBOJWIDAMOS-UHFFFAOYSA-N N
SMILES CN(C)CCc2c1c(c(OC)c(Br)cc1Br)n(OC)c2Br
Properties
Chemical formula	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). N verify (what is YN ?) Infobox references

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 plants of the bean and mustard families.

Biological activity

This chemical was tested for its ability to kill parasitic nematodes. It was found to be more effective than levamisole - a synthetic drug used to kill parasitic worms and to treat colon cancer. ^{[citation needed]}