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经验公式(希尔记法):
C26H30O11
化学文摘社编号:
分子量:
518.51
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)Oc2c(c3c(c(c2)O)C(=O)[C@@H]([C@H](O3)c4ccc(cc4)O)O)CC=C(C)C
InChI
1S/C26H30O11/c1-11(2)3-8-14-16(35-26-23(34)21(32)19(30)17(10-27)36-26)9-15(29)18-20(31)22(33)24(37-25(14)18)12-4-6-13(28)7-5-12/h3-7,9,17,19,21-24,26-30,32-34H,8,10H2,1-2H3/t17-,19-,21+,22+,23-,24-,26-/m1/s1
InChI key
GRDZTDZJQRPNCN-YIANMRPHSA-N
biological source
plant
assay
≥90% (LC/MS-ELSD)
form
solid
mol wt
518.51
solubility
water: slightly soluble
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
General description
Phellamurin, a trihydroxyflavanone, is a bioactive natural compound commonly sourced from Phellodendron amurense, Phellodendron chinense, and Commiphora africana plants. Current research indicates that this plant-derived metabolite acts as an inhibitor and may possess a range of biological activities, including antioxidant, anti-tumor, anti-inflammatory, and antimicrobial properties.
Application
Phellamurin is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.
Biochem/physiol Actions
Phellamurin induces cells apoptosis, has anti-tumor activity, exhibits inhibition of intestinal P-glycoprotein and it has a role as a metabolite.
Features and Benefits
- Suitable for Biochemical and Biomedical research
- Versatile and adaptable for wide variety of laboratory and research applications
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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