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经验公式(希尔记法):
C33H40O20
化学文摘社编号:
分子量:
756.66
UNSPSC Code:
12352205
NACRES:
NA.25
MDL number:
SMILES string
O1[C@H]([C@@H]([C@@H]([C@H]([C@@H]1C)O)O)O)O[C@H]2[C@@H](O[C@@H]([C@@H]([C@@H]2O)O)CO[C@@H]6O[C@H]([C@@H]([C@H]([C@H]6O)O)O)C)OC3=C(Oc5c(c(cc(c5)O)O)C3=O)c4cc(c(cc4)O)O
InChI
1S/C33H40O20/c1-9-19(38)23(42)26(45)31(48-9)47-8-17-21(40)25(44)30(53-32-27(46)24(43)20(39)10(2)49-32)33(51-17)52-29-22(41)18-15(37)6-12(34)7-16(18)50-28(29)11-3-4-13(35)14(36)5-11/h3-7,9-10,17,19-21,23-27,30-40,42-46H,8H2,1-2H3/t9-,10-,17+,19-,20-,21-,23
InChI key
HKNBJSRIYRDSLB-MIORVHIISA-N
biological source
plant
assay
≥90% (LC/MS-ELSD)
form
solid
mol wt
756.66
solubility
water: slightly soluble
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
General description
Alcesefoliside is a flavonol tetraglycoside commonly available from Prunus mume, Monteverdia ilicifolia, Vicia amurensis, Chenopodium quinoa and Catharanthus roseus. Existing research suggests that this plant-derived secondary metabolite exerts various biological activities, including anti-inflammatory, antioxidant, antitumor and cytoprotective 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
- Inhibits the production of pro-inflammatory cytokines and reactive oxygen species, resulting in anti-inflammatory and antioxidant effects.
- Induces apoptosis in cancer cells, leading to antitumor effects.
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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