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关于此项目
经验公式(希尔记法):
C19H28O11
化学文摘社编号:
分子量:
432.42
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
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
SMILES string
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 key
IVRQZYXJBVMHCW-OTCFHACESA-N
form
solid
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
General description
Natural product derived from plant source.
Osmanthuside H is a chemical constituent, isolated from stem barks of Fraxinus paxiana.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
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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