Palau'amine
Chemical structure of palau'amine | |
Names | |
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Systematic IUPAC name
2,2'-Diamino-11-(aminomethyl)-12-chloro-1,1',3a,5',10a,11,12,13a-octahydro-5'-hydroxy-spiro[8H-cyclopenta[3,4]pyrrolo[1,2-a]imidazo[4,5-b]pyrrolo[1,2-d]pyrazine-13(10H),4'-[4H]imidazol]-8-one[1]
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Identifiers | |
148717-58-2 | |
ChEMBL | ChEMBL2079438 |
ChemSpider | 17279008 |
Jmol 3D model | Interactive image |
MeSH | C438976 |
PubChem | 16122048 |
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Properties | |
C17H22ClN9O2 | |
Molar mass | 419.87 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Palau'amine is a toxic alkaloid compound synthesized naturally by Stylotella agminata, a species of sea sponge found in the southwest Pacific Ocean. The name of the molecule derives from the island nation of Palau, near which the sponges are found.
The substance was first isolated and described in 1993.[2] Containing nine nitrogen atoms, the molecule is considered highly complex. The precise atomic structure was pinned down in 2007,[3] and two years later the molecule was synthesized in the lab by a team at the Scripps Research Institute in La Jolla, California.[4][5]
Biosynthesis
A pathway to this dimeric pyrrole-imidazole alkaloid has been hypothesized to include a key oxidation of a β-ketoester with Mn(OAc)3 initiated a cascade radical cyclization sequence to deliver an ageliferin skeleton.[6]
References
- ↑ Chemical Abstracts, accessed via SciFinder, version 2004.2; Chemical Abstracts Service: Columbus, OH, 2004; RN 148717-58-2
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