推荐产品
等級
analytical standard
化驗
≥98.0% (HPLC)
儲存期限
limited shelf life, expiry date on the label
技術
HPLC: suitable
gas chromatography (GC): suitable
雜質
≤5.0% water
應用
food and beverages
格式
neat
儲存溫度
2-8°C
SMILES 字串
O=C1C=CC(C(OCC=C(C)C)=C(C=CO2)C2=C3)=C3O1
InChI
1S/C16H14O4/c1-10(2)5-7-19-16-11-3-4-15(17)20-14(11)9-13-12(16)6-8-18-13/h3-6,8-9H,7H2,1-2H3
InChI 密鑰
IGWDEVSBEKYORK-UHFFFAOYSA-N
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應用
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儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
Ah Yeon Park et al.
Biomedical chromatography : BMC, 23(10), 1034-1043 (2009-04-30)
Rapid, simple and reliable HPLC/UV and LC-ESI-MS/MS methods for the simultaneous determination of five active coumarins of Angelicae dahuricae Radix, byakangelicol (1), oxypeucedanin (2), imperatorin (3), phellopterin (4) and isoimperatorin (5) were developed and validated. The separation condition for HPLC/UV
Hong Nie et al.
Chinese journal of integrative medicine, 15(6), 442-447 (2010-01-19)
To demonstrate the vasodilatation activity of the coumarin-containing Angelica dahurica var. formosana and to further analyze active components in the herb extracts. (1) The vasodilatation effects induced by different extracts (cyclohexane, ethyl acetate, acetone, methanol, 95 % ethanol and water)
Zheng-jun Cai et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 31(8), 1160-1162 (2008-12-31)
To study chemical constituents of antibacterial activity fraction of Angelica polymorpha. Compounds were isolated by repeatedly silica gel column chromatography and recrystallization. Their structures were identified by physical and chemical evidences and spectral methods. Seven compounds were obtained from the
Jaroslaw Widelski et al.
Molecules (Basel, Switzerland), 14(8), 2729-2734 (2009-08-25)
The first phytochemical investigation of the fruits of Angelica lucida has led to the isolation and characterization of five known coumarins (imperatorin, isoimperatorin, heraclenol, oxypeucedanin hydrate and heraclenin). All isolated compounds were identified by means of spectral and literature data.
Shinsuke Marumoto et al.
Bioorganic & medicinal chemistry, 18(1), 455-459 (2009-11-27)
Biotransformation studies conducted on the furanocoumarins isoimperatorin (1) and imperatorin (3) have revealed that 1 was metabolized by Glomerella cingulata to give the corresponding reduced acid, 6,7-furano-5-prenyloxy hydrocoumaric acid (2), and 3 was transformed by G. cingulata to give the
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