Limonexic acid

Names

[ Name ]:
Limonexic acid

[Synonym ]:
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

Biological Activity

[Description]:

Shihulimonin A is an alkaloid can be isolated from the fruit of Euodia rutaecarpa (Juss.) Benth[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[References]

[1]. Ma C, et al. A new quinolone alkaloid with cytotoxic activity from the fruits of Euodia Rutaecarpa[J]. Natural Product Communications, 2018, 13(3): 1934578X1801300317.

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ 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

Safety Information

[ Hazard Codes ]:
Xi

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Related Compounds

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