产品名称
5,7-二甲氧基香豆素, 98%
InChI key
NXJCRELRQHZBQA-UHFFFAOYSA-N
InChI
1S/C11H10O4/c1-13-7-5-9(14-2)8-3-4-11(12)15-10(8)6-7/h3-6H,1-2H3
SMILES string
COc1cc(OC)c2C=CC(=O)Oc2c1
assay
98%
form
solid
mp
146-149 °C (lit.)
functional group
ester
Quality Level
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Biochem/physiol Actions
5,7-二甲氧基香豆素诱导小鼠(B16) 和人类(A375) 的分化和黑色素生成过程。
General description
从茴香 H. Mann 的叶子和果实中分离和鉴定出 5,7-二甲氧基香豆素,该植物的果实用于构建莫霍克花环。它在细菌中诱导移码诱变。它还会在中国仓鼠细胞中引起致命的光敏化和姐妹染色单体交换的形成。
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
ppe
Eyeshields, Gloves, type N95 (US)
Earl Grey tea intoxication.
Josef Finsterer
Lancet (London, England), 359(9316), 1484-1484 (2002-05-04)
Tomonori Nakamura et al.
Journal of natural medicines, 63(1), 15-20 (2008-07-09)
We have investigated the structure-activity relationship between 63 natural oxycoumarin derivatives and their effects on the expression of inducible-nitric oxide synthase (iNOS) induced by lipopolysaccharide. The protein expression of iNOS was screened by Western blot analysis, and four 5,7-dimethoxycoumarins were
Ewa Chodurek et al.
Cellular & molecular biology letters, 17(4), 616-632 (2012-09-25)
Malignant melanoma (melanoma malignum) is one of the most dangerous types of tumor. It is very difficult to cure. In recent years, a lot of attention has been given to chemoprevention. This method uses natural and synthetic compounds to interfere
D Chouchi et al.
Journal of chromatography. A, 672(1-2), 177-183 (1994-06-24)
Generally on the gas chromatogram of a volatile essential oil, terpenes, oxygenated compounds and sesquiterpenes appear. With temperature programming, it was shown that some non-volatiles are present with the volatiles. They are simple coumarin (2H-1-benzopyran-2-one) derivatives such as citropten (5,7-dimethoxycoumarin)
Daniela Alesiani et al.
International journal of oncology, 32(2), 425-434 (2008-01-19)
In the present study we investigated the antiproliferative activity of 5,7-dimethoxycoumarin on the murine B16 and human A375 melanoma cell lines. The inhibitory concentration 50 (IC50) was estimated for each cell line by preliminary assay of tetrazolium salt reduction (MTT).
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