ChemicalBook--->CAS DataBase List--->51768-38-8

51768-38-8

51768-38-8 Structure

51768-38-8 Structure
IdentificationBack Directory
[Name]

3-O-Methylellagic acid
[CAS]

51768-38-8
[Synonyms]

3-Methyl ellagic acid
3-O-Methylellagic acid
Ellagic acid 3-methyl ether
3-Methyl ellagic acid/3-O-Methylellagic acid
2,7,8-Trihydroxy-3-methoxychromeno[5,4,3-cde]chromene-5,10-dione
2,3,7-Trihydroxy-8-methoxy-[1]benzopyrano[5,4,3-cde][1]benzopyran-5,10-dione
[1]Benzopyrano[5,4,3-cde][1]benzopyran-5,10-dione, 2,3,7-trihydroxy-8-methoxy-
[Molecular Formula]

C15H8O8
[MOL File]

51768-38-8.mol
[Molecular Weight]

316.22
Chemical PropertiesBack Directory
[Boiling point ]

734.3±60.0 °C(Predicted)
[density ]

1.840±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[form ]

neat
[pka]

5.49±0.20(Predicted)
[BRN ]

1403110
[InChI]

1S/C15H8O8/c1-21-11-7(17)3-5-9-8-4(15(20)23-13(9)11)2-6(16)10(18)12(8)22-14(5)19/h2-3,16-18H,1H3
[InChIKey]

FAARLWTXUUQFSN-UHFFFAOYSA-N
[SMILES]

COc1c(O)cc2C(=O)Oc3c(O)c(O)cc4C(=O)Oc1c2-c34
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P501
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Uses]

3-O-Methylellagic acid is a nature product that can be isolated from Myrciaria cauliflora, with anti-inflammatory activity. 3-O-Methylellagic acid shows an inhibitory effect on glucose transport assay. 3-O-Methylellagic acid has antibacterial activity, with a MIC of 32 μg/mL for Staph. Aureus ATCC 25923[1][2][3].
[References]

[1] Da-Ke Zhao, et al. Jaboticabin and Related Polyphenols from Jaboticaba ( Myrciaria cauliflora) with Anti-inflammatory Activity for Chronic Obstructive Pulmonary Disease. J Agric Food Chem. 2019 Feb 6;67(5):1513-1520. DOI:10.1021/acs.jafc.8b05814
[2] Active compounds from Lagerstroemia speciosa, insulin-like glucose uptake-stimulatory/inhibitory and adipocyte differentiation-inhibitory activities in 3T3-L1 cells. J Agric Food Chem. 2008 Dec 24;56(24):11668-74. DOI:10.1021/jf802152z
[3] Sgariglia, M. A.,et al. Isolation of antibacterial components from infusion of Caesalpinia paraguariensis bark. A bio-guided phytochemical study. Food Chemistry, 2011. 126(2), 395–404.
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