A Forsby, E Walum
Index: Neurosci. Lett. 217(1) , 50-4, (1996)
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The pungent sesquiterpenoid unsaturated dialdehydes polygodial and isovelleral, have previously been shown to increase the intracellular free calcium concentration [Ca2+]i in human neuroblastoma SH-SY5Y cells, partly by a release from intracellular Ca2+ stores, whereas the non-pungent compound epipolygodial, had no effect on the [Ca2+]i. In this study, we investigated the effect of isovelleral, polygodial and epipolygodial on inositol phosphate (IP) formation on the assumption that there might be a correlation between the release of intracellular Ca2+ and pungency of the compounds. It was found that polygodial induced IP mobilization in a concentration dependent way, whereas isovelleral had no effect on the IP formation in the SH-SY5Y cells. Phosphoinositide (PPI) turnover was activated by epipolygodial, but only at concentrations 40-fold higher than for polygodial, which emphasizes the importance of the correct stereometry in the dialdehyde configuration for the biological activity of polygodial. The polygodial-induced formation of IP1 was reduced by 71% under extracellular calcium-free conditions, which suggests feedback interactions between the IP formation and the increase in [Ca2+]i to account for a periodic activation of phospholipase C(PLC).
| Structure | Name/CAS No. | Molecular Formula | Articles |
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Cycloprop[e]indene-1a,2(1H)-dicarboxaldehyde,3a,4,5,6,6a,6b-hexahydro-5,5,6b-trimethyl-, (1aS,3aS,6aS,6bR)-
CAS:37841-91-1 |
C15H20O2 |
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Structure-activity relationships for unsaturated dialdehydes...
1995-07-01 [Acta Chem. Scand. 49(7) , 530-5, (1995)] |
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Sesquiterpenoid unsaturated dialdehydes increase the concent...
1994-01-01 [Nat. Toxins 2(2) , 89-95, (1994)] |
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The preparation and bioactivities of (-)-isovelleral.
1997-07-01 [Bioorg. Med. Chem. 5(7) , 1363-7, (1997)] |
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A novel route to the marasmane skeleton via a tandem rearran...
2001-04-06 [J. Org. Chem. 66(7) , 2350-7, (2001)] |
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![Cycloprop[e]indene-1a,2(1H)-dicarboxaldehyde,3a,4,5,6,6a,6b-hexahydro-5,5,6b-trimethyl-, (1aS,3aS,6aS,6bR)- Structure](https://image.chemsrc.com/caspic/048/37841-91-1.png)