Cyclopenta[c]pyran-4-carboxylic acid, 1-(β-D-glucopyranosyloxy)-1,4a,5,7a-tetrahydro-7-(hydroxymethyl)-5-[[3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, methyl ester, (1S,4aS,5R,7aS)-
(E)-6-O-(p-coumaroyl)scandoside methyl ester
CAS: 83946-90-1
Molecular Formula: C26H30O13
Cyclopenta[c]pyran-4-carboxylic acid, 1-(β-D-glucopyranosyloxy)-1,4a,5,7a-tetrahydro-7-(hydroxymethyl)-5-[[3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, methyl ester, (1S,4aS,5R,7aS)- - Names and Identifiers
Cyclopenta[c]pyran-4-carboxylic acid, 1-(β-D-glucopyranosyloxy)-1,4a,5,7a-tetrahydro-7-(hydroxymethyl)-5-[[3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, methyl ester, (1S,4aS,5R,7aS)- - Physico-chemical Properties
| Molecular Formula | C26H30O13 |
| Molar Mass | 550.51 |
| Density | 1.56±0.1 g/cm3(Predicted) |
| Boling Point | 803.0±65.0 °C(Predicted) |
| Appearance | Powder |
| pKa | 8.58±0.15(Predicted) |
| Storage Condition | 2-8℃ |
Cyclopenta[c]pyran-4-carboxylic acid, 1-(β-D-glucopyranosyloxy)-1,4a,5,7a-tetrahydro-7-(hydroxymethyl)-5-[[3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, methyl ester, (1S,4aS,5R,7aS)- - Reference
| Reference Show more | 1. He, Jingyu, et al. "Asperuloside and asperulosidic acid exert an anti-inflammatory effect via suppression of the NF-κB and MAPK signaling pathways in LPS-induced RAW 264.7 macrophages." International journal of molecular sciences 19.7 (2018): 2027.https:// 2. [IF=4.183] Jingyu He et al."Asperuloside and Asperulosidic Acid Exert an Anti-Inflammatory Effect via Suppression of the NF-κB and MAPK Signaling Pathways in LPS-Induced RAW 264.7 Macrophages."Int J Mol Sci. 2018 Jul;19(7):2027 3. [IF=2.419] Lu Wang et al."Characterization of interaction property of multi-components in Gardenia jasminoides with aldose reductase by microdialysis combined with liquid chromatography coupled to mass spectrometry."Rapid Communications In Mass Spectrometry. 2016 Au 4. [IF=5.34] Wei Zou et al."Imperatae rhizoma-Hedyotis diffusa Willd. herbal pair alleviates nephrotic syndrome by integrating anti-inflammatory and hypolipidaemic effects."Phytomedicine. 2021 Sep;90:153644 |
Cyclopenta[c]pyran-4-carboxylic acid, 1-(β-D-glucopyranosyloxy)-1,4a,5,7a-tetrahydro-7-(hydroxymethyl)-5-[[3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, methyl ester, (1S,4aS,5R,7aS)- - Introduction
(E)-6-O-(p-coumaroyl)scandoside methyl ester is a natural compound that contains an acyl group and a methyl ester group in its chemical structure. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance:(E)-6-O-(p-coumaroyl)scandoside methyl ester is a white crystalline solid.
-Solubility: In some organic solvents, such as ethanol, dimethyl methyl sulfite, etc., it has good solubility.
-Melting point: about 190-195 ℃.
Use:
-Pharmacological activity: The compound has antioxidant, anti-inflammatory, antibacterial and anti-tumor pharmacological activities, and has potential therapeutic effects on a variety of diseases.
-Cosmetics: It can also be used in skin care products and cosmetics, with antioxidant and anti-inflammatory effects.
Method:
- (E)-6-O-(p-coumaroyl)scandoside methyl ester can be extracted from the roots, stems and leaves of the vine, and then extracted, separated, purification and crystallization process to obtain pure product.
Safety Information:
- (E)-6-O-(p-coumaroyl)scandoside methyl ester, as a natural product, is generally considered to be relatively safe. However, due to limited research, there is limited understanding of the long-term toxicity and side effects of this compound, so caution is still needed in its use. It is recommended to consult professional bodies or experts before use to ensure safe use.
This is a brief introduction to the nature, use, formulation and safety information of (E)-6-O-(p-coumaroyl)scandoside methyl ester.
Nature:
-Appearance:(E)-6-O-(p-coumaroyl)scandoside methyl ester is a white crystalline solid.
-Solubility: In some organic solvents, such as ethanol, dimethyl methyl sulfite, etc., it has good solubility.
-Melting point: about 190-195 ℃.
Use:
-Pharmacological activity: The compound has antioxidant, anti-inflammatory, antibacterial and anti-tumor pharmacological activities, and has potential therapeutic effects on a variety of diseases.
-Cosmetics: It can also be used in skin care products and cosmetics, with antioxidant and anti-inflammatory effects.
Method:
- (E)-6-O-(p-coumaroyl)scandoside methyl ester can be extracted from the roots, stems and leaves of the vine, and then extracted, separated, purification and crystallization process to obtain pure product.
Safety Information:
- (E)-6-O-(p-coumaroyl)scandoside methyl ester, as a natural product, is generally considered to be relatively safe. However, due to limited research, there is limited understanding of the long-term toxicity and side effects of this compound, so caution is still needed in its use. It is recommended to consult professional bodies or experts before use to ensure safe use.
This is a brief introduction to the nature, use, formulation and safety information of (E)-6-O-(p-coumaroyl)scandoside methyl ester.
Last Update：2024-04-09 21:04:16
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Product Name: (E)-6-O-(p-coumaroyl)scandoside methyl ester Visit Supplier Webpage Request for quotation
CAS: 83946-90-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 83946-90-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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