|This article is an orphan, as no other articles link to it. Please introduce links to this page from ; try the Find link tool for suggestions. (July 2013)|
Both groups of compounds display a range of biological activities, such as cytotoxicity, inhibition of adenosine transfer into rabbit erythrocytes (red blood cells), Ca2+ channel antagonistic action, α1 adrenergic blockade and others.
Both compounds have been reproduced in the laboratory by organic synthesis.
- Fathi-Afshar R, Allen TM, Krueger CA et al. (April 1989). "Some pharmacological activities of novel adenine-related compounds isolated from a marine sponge Agelas mauritiana". Can. J. Physiol. Pharmacol. 67 (4): 276–81. doi:10.1139/y89-045. PMID 2758370.
- Fathi-Afshar, R.; Allen, T. M., Canadian Journal of Chemistry, 1988, 66(1), 45-50.
- Ohba, Masashi; Iizuka, Kazuaki; Ishibashi, Hiroyuki; Fujii, Tozo., Tetrahedron 1997, 53(50), 16977-16986.
|This article about an organic compound is a stub. You can help Wikipedia by expanding it.|