1-(Acetyloxy)-1,2-dihydroobacunoic Acid e-Lactone

Modify Date: 2024-01-02 13:36:00

1-(Acetyloxy)-1,2-dihydroobacunoic Acid e-Lactone Structure
1-(Acetyloxy)-1,2-dihydroobacunoic Acid e-Lactone structure
Common Name 1-(Acetyloxy)-1,2-dihydroobacunoic Acid e-Lactone
CAS Number 1063-77-0 Molecular Weight 514.564
Density 1.3±0.1 g/cm3 Boiling Point 657.7±55.0 °C at 760 mmHg
Molecular Formula C28H34O9 Melting Point 278-279°
MSDS Chinese USA Flash Point 351.6±31.5 °C

 Use of 1-(Acetyloxy)-1,2-dihydroobacunoic Acid e-Lactone


Nomilin is a limonoid compound obtained from the extracts of citrus fruits. Nomilin is an anti-obesity and anti-hyperglycemic agent [1][2].

 Names

Name Nomilin
Synonym More Synonyms

  Biological Activity

Description Nomilin is a limonoid compound obtained from the extracts of citrus fruits. Nomilin is an anti-obesity and anti-hyperglycemic agent [1][2].
Related Catalog
In Vitro Nomilin treatment significantly mitigated cell death and decreased lactate dehydrogenase (LDH) release and ROS production in SH-SY5Y cells induced by oxygen-glucose deprivation (OGD), which was almost abolished by Nrf2 knockdown[1].
In Vivo Nomilin attenuated blood-brain barrier (BBB) disruption in MCAO rats, which might be associated with alleviating the loss of tight junction proteins, including ZO-1 and occludin-5[1].
References

[1]. Shi YS, et al. Nomilin protects against cerebral ischemia-reperfusion induced neurological deficits and blood-brain barrier disruption via the Nrf2 pathway. Food Funct. 2019 Sep 1;10(9):5323-5332.

[2]. Sato R, et al. Nomilin as an anti-obesity and anti-hyperglycemic agent. Vitam Horm. 2013;91:425-39.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 657.7±55.0 °C at 760 mmHg
Melting Point 278-279°
Molecular Formula C28H34O9
Molecular Weight 514.564
Flash Point 351.6±31.5 °C
Exact Mass 514.220276
PSA 121.64000
LogP 2.47
Vapour Pressure 0.0±2.0 mmHg at 25°C
Index of Refraction 1.575

 Safety Information

Hazard Codes Xi
Safety Phrases 24/25
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles6

More Articles
Comparative metabolic and transcriptional analysis of a doubled diploid and its diploid citrus rootstock (C. junos cv. Ziyang xiangcheng) suggests its potential value for stress resistance improvement.

BMC Plant Biol. 15 , 89, (2015)

Polyploidy has often been considered to confer plants a better adaptation to environmental stresses. Tetraploid citrus rootstocks are expected to have stronger stress tolerance than diploid. Plenty of...

Development of delayed bitterness and effect of harvest date in stored juice from two complex citrus hybrids.

J. Sci. Food Agric. 96 , 422-9, (2015)

Mandarins and mandarin hybrids have excellent flavor and color attributes, making them good candidates for consumption as fresh fruit. When processed into juice, however, they are less palatable, as t...

Evaluation of Physiological Activities of the Citron (Citrus junos Sieb. ex TANAKA) Seed Extracts.

Prev. Nutr. Food Sci. 18 , 196-202, (2014)

Citron seed extracts (CSEs) were made using distilled water (CSEW), ethanol (CSEE), and n-hexane (CSEH), to measure the total polyphenol contents, DPPH and ABTS radical scavenging activities, and anti...

 Synonyms

fromcitrusseeds
1-(Acetyloxy)-1,2-dihydroobacunoic Acid e-Lactone
Oxireno[4',5']pyrano[4',3':5,6]naphth[2,1-c]oxepin-3,10,12(1H,4H,10aH)-trione, 5-(acetyloxy)-8-(3-furanyl)decahydro-1,1,5a,7a,11b-pentamethyl-, (5S,5aR,5bR,7aS,8S,10aS,11aR,11bR,13aR)-
(5S,5aR,5bR,7aS,8R,10aS,11aR,11bR,13aR)-8-(furan-3-yl)-1,1,5a,7a,11b-pentamethyl-3,10,12-trioxohexadecahydrooxireno[4,4a]isochromeno[6,5-g][2]benzoxepin-5-yl acetate
(5S,5aR,5bR,7aS,8S,10aS,11aR,11bR,13aR)-8-(3-Furyl)-1,1,5a,7a,11b-pentamethyl-3,10,12-trioxohexadecahydrooxireno[4,4a]isochromeno[6,5-g][2]benzoxepin-5-yl acetate
1-(3-Furyl)decahydro-11-hydroxy-4b,7,7,11a,13a-pentamethyloxireno(4,4a)-2-benzopyrano[6,5-g](2)benzoxepin-3,5,9(3aH,4bH,6H)-trione Acetate
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