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SMB00252

Sigma-Aldrich

Osmanthuside H

≥95% (LC/MS-ELSD)

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About This Item

经验公式（希尔记法）:
C19H28O11
CAS号:
149155-70-4
分子量:
432.42
MDL编号:
MFCD24849382
UNSPSC代码:
12352200
PubChem化学物质编号:
329824904
NACRES:
NA.25

方案

≥95% (LC/MS-ELSD)

表单

solid

应用

metabolomics
vitamins, nutraceuticals, and natural products

储存温度

−20°C

SMILES字符串

OC[C@@]1(O)CO[C@@H](OC[C@H]2O[C@@H](OCCc3ccc(O)cc3)[C@H](O)[C@@H](O)[C@@H]2O)[C@@H]1O

InChI

1S/C19H28O11/c20-8-19(26)9-29-18(16(19)25)28-7-12-13(22)14(23)15(24)17(30-12)27-6-5-10-1-3-11(21)4-2-10/h1-4,12-18,20-26H,5-9H2/t12-,13-,14+,15-,16+,17-,18-,19-/m1/s1

InChI key

IVRQZYXJBVMHCW-OTCFHACESA-N

一般描述

Natural product derived from plant source.
Osmanthuside H is a chemical constituent, isolated from stem barks of Fraxinus paxiana.[1]

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H319

预防措施声明

P305 + P351 + P338

危险分类

Eye Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
12222854V
122228-54V

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M Sugiyama et al.
Phytochemistry, 32(6), 1553-1555 (1993-04-01)
Three new phenylethanoid glycosides, 2-(4-hydroxyphenyl)ethyl-beta-D-apiosyl-(1----6)-beta-D-glucopy ranoside(osmanthuside H), 2-(4-hydroxyphenyl)ethyl 5-O-trans-p-coumaroyl-beta-D-apiosyl(1----6)-beta-D-gluc+ ++ opy ranoside (osmanthuside I) and 2-(4-hydroxyphenyl)ethyl 5-O-trans-feruloyl-beta-D-apiosyl-(1----6)-beta-D-glucopy r ano side (osmanthuside J), were isolated from the bark of Osmanthus asiaticus. The structures were elucidated on the basis of spectroscopic evidence.
Phenolic compounds and their anti-oxidative properties and protein kinase inhibition from the Chinese mangrove plant Laguncularia racemosa.
Cui S, et al.
Phytochemistry, 71(4), 435-442 (2010)
Zhi-jing Ma et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 33(16), 1990-1993 (2008-12-18)
To investigate the chemical constituents of Fraxinus paxiana. The chemical constituents were isolated and purified by chromatographic techniques and the structures of the compounds were identified with or by spectroscopic methods. Fifteen compounds were obtained from the methanol extract of

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