所有图片(1)
About This Item
经验公式（希尔记法）:
C14H14O3
CAS号:
分子量:
230.26
Beilstein:
177877
MDL编号:
UNSPSC代码:
85151701
PubChem化学物质编号:
NACRES:
NA.24
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等级
analytical standard
质量水平
方案
≥95.0% (HPLC)
技术
HPLC: suitable
gas chromatography (GC): suitable
mp
142-148 °C
应用
food and beverages
包装形式
neat
SMILES字符串
COC1=CC(=O)OC(C1)\C=C\c2ccccc2
InChI
1S/C14H14O3/c1-16-13-9-12(17-14(15)10-13)8-7-11-5-3-2-4-6-11/h2-8,10,12H,9H2,1H3/b8-7+
InChI key
XEAQIWGXBXCYFX-BQYQJAHWSA-N
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一般描述
DL-Kavain, an analog of yangonin, is a kavalactone found in the kava plant.
应用
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Characterization of three small molecule inhibitors of enterovirus 71 identified from screening of a library of natural products
Li G, et al.
Antiviral Research, 143, 85-96 (2017)
Huaiping Yuan et al.
Journal of clinical periodontology, 38(11), 1029-1036 (2011-11-19)
The purpose of this study was to assess the role of anti-bone resorptive agents and an anti-inflammatory compound in murine Porphyromonas gingivalis (P. gingivalis)-induced periodontitis. Six randomly assigned groups were administered vehicle (saline, control) (n = 6), P. gingivalis infection only (untreated)
Roberto Cirilli et al.
Journal of separation science, 31(12), 2206-2210 (2008-06-20)
First baseline HPLC enantioseparation of kavain is described. Complete enantiodiscrimination was achieved on the immobilised-type Chiralpak IA chiral stationary phase (CSP) using pure methanol and simple methanol-water and ethanol-water mixtures as eluents. A water-dependent enantioselectivity was clearly demonstrated. Performance of
Peter A Whitton et al.
Phytochemistry, 64(3), 673-679 (2003-09-19)
Kava-kava is a traditional beverage of the South Pacific islanders and has had centuries of use without major side effects. Standardised extracts of kava-kava produced in Europe have led to many serious health problems and even to death. The extraction
Thomas E Smith et al.
Organic letters, 6(14), 2317-2320 (2004-07-02)
[reaction: see text] Three asymmetric pathways to the kavalactones have been developed. The first method is chiral auxiliary-based and utilizes aldol reactions of N-acetyl thiazolidinethiones followed by a malonate displacement/decarboxylation reaction. The second approach uses the asymmetric catalytic Mukaiyama additions
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