SMB01032
Jasminoside
≥90% (LC/MS-ELSD)
别名:
10-Cinnamoyloxyoleoside 7-methyl ester
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关于此项目
经验公式（希尔记法）:
C26H30O13
化学文摘社编号:
分子量:
550.51
UNSPSC Code:
12352205
NACRES:
NA.25
MDL number:
SMILES string
O1[C@H]([C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O)O[C@@H]2OC=C([C@H](\C\2=C/COC(=O)\C=C\c3ccccc3)CC(=O)OC)C(=O)O
InChI
1S/C26H30O13/c1-35-20(29)11-16-15(9-10-36-19(28)8-7-14-5-3-2-4-6-14)25(37-13-17(16)24(33)34)39-26-23(32)22(31)21(30)18(12-27)38-26/h2-9,13,16,18,21-23,25-27,30-32H,10-12H2,1H3,(H,33,34)/b8-7+,15-9+/t16-,18+,21+,22-,23+,25-,26-/m0/s1
InChI key
JGHUOJAZXGSFRI-UPJNDMORSA-N
biological source
plant
assay
≥90% (LC/MS-ELSD)
form
solid
mol wt
550.51
solubility
water: soluble
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
General description
Jasminoside, also known as 10-Cinnamoyloxyoleoside 7-methyl ester, is a natural compound classified as an iridoid glycoside. It is an analog of tolvaptan, a drug used in the treatment of polycystic kidney disease. Existing research suggests that this plant-derived metabolite exerts various biological activities, including antioxidant, anti-inflammatory, antimicrobial, and anticancer properties.
Application
It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical and biochemical research.
Biochem/physiol Actions
- Influences intracellular signaling pathways: MAPK, PI3K/Akt, and NF-κB
- Regulates gene expression and protein synthesis
- Inhibits tumor kinases and induces apoptosis in cancer cells
Features and Benefits
- High quality compound suitable for multiple research applications
- Compatible with HPLC and mass spectrometry techniques
Other Notes
For additional information on our range of Biochemicals, please complete this form.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
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