SMB01064
Dimethylfraxetin
≥90% (LC/MS-ELSD)
别名:
6,7,8,-trimethoxycoumarin, 6,7,8-trimethoxychromen-2-one, Fraxidin Methyl Ether
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关于此项目
经验公式（希尔记法）:
C12H12O5
化学文摘社编号:
分子量:
236.22
UNSPSC Code:
12352205
NACRES:
NA.25
MDL number:
SMILES string
[o]1c2c(cc[c]1=O)cc(c(c2OC)OC)OC
InChI
1S/C12H12O5/c1-14-8-6-7-4-5-9(13)17-10(7)12(16-3)11(8)15-2/h4-6H,1-3H3
InChI key
RAYQKHLZHPFYEJ-UHFFFAOYSA-N
biological source
plant
assay
≥90% (LC/MS-ELSD)
form
solid
mol wt
236.22
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
General description
Dimethylfraxetin, also known as 6,7,8-Trimethoxycoumarin, a coumarin derivative, is a natural product commonly found in Pittosporum illicioides, Garcinia multiflora, and Cryptocarya bracteolata. It exhibits a range of biological activities, including anti-inflammatory, antioxidant, anticancer, and antimicrobial 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
- Binds to the CB2 receptor and induces immunomodulatory effects.
- Exhibits anti-inflammatory properties by inhibiting prostaglandin synthesis in the human erythroleukemia cell line K562.
- Inhibits the replication of both DNA and RNA.
- Blocks aminoacyl-tRNA binding to ribosomes, inhibiting protein synthesis.
- Binds to phenolic acid receptors on cultured cells.
Features and Benefits
- High quality compound suitable for multiple research applications
- Compatible with HPLC and mass spectrometry techniques
Other Notes
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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