Limonexic acid structure
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Common Name | Limonexic acid | ||
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CAS Number | 99026-99-0 | Molecular Weight | 502.51 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | 783.6±60.0 °C at 760 mmHg | |
Molecular Formula | C26H30O10 | Melting Point | N/A | |
MSDS | N/A | Flash Point | 268.3±26.4 °C |
Use of Limonexic acidShihulimonin A is an alkaloid can be isolated from the fruit of Euodia rutaecarpa (Juss.) Benth[1]. |
Name | (4aS,6aR,8aR,8bR,9aS,12R,12aS,14aR,14bR)-12-(2-Hydroxy-5-oxo-2,5- dihydro-3-furanyl)-6,6,8a,12a-tetramethyldecahydro-3H-oxireno[d]p yrano[4',3':3,3a][2]benzofuro[5,4-f]isochromene-3,8,10(6H,9aH)-tr ione |
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Synonym | More Synonyms |
Description | Shihulimonin A is an alkaloid can be isolated from the fruit of Euodia rutaecarpa (Juss.) Benth[1]. |
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Related Catalog | |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 783.6±60.0 °C at 760 mmHg |
Molecular Formula | C26H30O10 |
Molecular Weight | 502.51 |
Flash Point | 268.3±26.4 °C |
Exact Mass | 502.183899 |
PSA | 137.96000 |
LogP | -0.93 |
Vapour Pressure | 0.0±6.2 mmHg at 25°C |
Index of Refraction | 1.621 |
Hazard Codes | Xi |
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~% Limonexic acid CAS#:99026-99-0 |
Literature: Melera et al. Helvetica Chimica Acta, 1957 , vol. 40, p. 1420,1433 |
Precursor 1 | |
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DownStream 0 |
hexylglutathione |
(4aS,6aR,8aR,8bR,9aS,12R,12aS,14aR,14bR)-12-(2-Hydroxy-5-oxo-2,5-dihydro-3-furanyl)-6,6,8a,12a-tetramethyldecahydro-3H-oxireno[d]pyrano[4',3':3,3a][2]benzofuro[5,4-f]isochromene-3,8,10(6H,9aH)-trione |
S-HEXYL-L-GLUTATHIONE REDUCED |
limonexic acid |
5-HEXYLGLUTATHIONE |
shihulimonin A |
S-hexyl GSH |
1H,3H-Oxireno[c]pyrano[4'',3'':2',3']furo[3',4':5,6]naphtho[1,2-d]pyran-3,8,10(6H,9aH)-trione, 12-(2,5-dihydro-2-hydroxy-5-oxo-3-furanyl)decahydro-6,6,8a,12a-tetramethyl-, (4aS,6aR,8aR,8bR,9aS,12R,12aS,14aR,14bR)- |
S-Hexyl-L-glutathione |