CAS 22318-10-1|Evodol

Introduction：Basic information about CAS 22318-10-1|Evodol, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Evodol BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Synonyms

Common Name	Evodol
CAS Number	22318-10-1	Molecular Weight	484.495
Density	1.5±0.1 g/cm3	Boiling Point	736.2±60.0 °C at 760 mmHg
Molecular Formula	C₂₆H₂₈O₉	Melting Point	/
MSDS	USA	Flash Point	399.0±32.9 °C

Names

Name	[(3S,8S,9S,10R,13S,14S,16R,17R)-17-acetyl-16-(aziridin-1-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
Synonym	More Synonyms

Evodol BiologicalActivity

Description	Evodol is a natural product isolated from the dried and nearly ripe fruits of Euodia rutaecarpa. Evodol shows inhibitory activity against NO production[1]. Evodol possesses larvicidal activity against the Asian tiger mosquitoes with a LC50 value of 32.43 μg/ml[2].
Related Catalog	Signaling Pathways >>Others >>Others
References	[1]. Yang XB, et al. Limonoid constituents of Euodia rutaecarpa var. bodinieri and their inhibition on NO production in lipopolysaccharide-activated RAW264.7 macrophages. J Asian Nat Prod Res. 2013;15(10):1130-8. [2]. Liu ZL, et al. Mosquito larvicidal activity of alkaloids and limonoids derived from Evodia rutaecarpa unripe fruits against Aedes albopictus (Diptera: Culicidae).Parasitol Res. 2012 Sep;111(3):991-6.

Description

Evodol is a natural product isolated from the dried and nearly ripe fruits of Euodia rutaecarpa. Evodol shows inhibitory activity against NO production[1]. Evodol possesses larvicidal activity against the Asian tiger mosquitoes with a LC50 value of 32.43 μg/ml[2].

Related Catalog

Signaling Pathways >>Others >>Others

References

[1]. Yang XB, et al. Limonoid constituents of Euodia rutaecarpa var. bodinieri and their inhibition on NO production in lipopolysaccharide-activated RAW264.7 macrophages. J Asian Nat Prod Res. 2013;15(10):1130-8.

[2]. Liu ZL, et al. Mosquito larvicidal activity of alkaloids and limonoids derived from Evodia rutaecarpa unripe fruits against Aedes albopictus (Diptera: Culicidae).Parasitol Res. 2012 Sep;111(3):991-6.

Chemical & Physical Properties

Density	1.5±0.1 g/cm3
Boiling Point	736.2±60.0 °C at 760 mmHg
Molecular Formula	C₂₆H₂₈O₉
Molecular Weight	484.495
Flash Point	399.0±32.9 °C
Exact Mass	484.173340
PSA	124.80000
LogP	2.38
Vapour Pressure	0.0±2.5 mmHg at 25°C
Index of Refraction	1.633
InChIKey	SNGHLUWTFLYPMT-JPRNBFAHSA-N
SMILES	CC1(C)OC2CC(=O)OCC23C1=C(O)C(=O)C1(C)C3CCC2(C)C(c3ccoc3)OC(=O)C3OC321
Storage condition	?20°C

Safety Information

Hazard Codes	Xi
RIDADR	NONH for all modes of transport

Synonyms

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-(3-furanyl)-4,4a,8a,12,12a,13,14,14a-octahydro-7-hydroxy-6,6,8a,12a-tetramethyl-, (4aS,8aR,8bR,9aS,12S,12aS,14aR,14bR)-

(4aS,8aR,8bR,9aS,12S,12aS,14aR,14bR)-12-(3-Furyl)-7-hydroxy-6,6,8a,12a-tetramethyl-4,4a,8a,12,12a,13,14,14a-octahydro-3H-oxireno[d]pyrano[4',3':3,3a][2]benzofuro[5,4-f]isochromene-3,8,10(6H,9aH)-trione

(4aS,8aR,8bR,9aS,12S,12aS,14aR,14bR)-12-(Furan-3-yl)-7-hydroxy-6,6,8a,12a-tetramethyl-4,4a,9a,12,12a,13,14,14a-octahydrooxireno[2,3-d]pyrano[4',3':3,3a]isobenzofuro[5,4-f]isochromene-3,8,10(1H,6H,8aH)-trione

Recommended......