Catalogue Number
BD-P0122
Analysis Method
HPLC,NMR,MS
Specification
98.0%(HPLC)
Storage
2-8°C
Molecular Weight
808.783
Appearance
Yellow powder
Botanical Source
Structure Type
Flavonoids
Category
SMILES
CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)O)C)O)O)O)O)O
Synonyms
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
IUPAC Name
Density
1.6±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
330.9±27.8°C
Boiling Point
1082.7±65.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C38H48O19/c1-13(2)5-10-18-20(53-37-31(50)28(47)25(44)21(12-39)54-37)11-19(41)22-26(45)34(32(55-33(18)22)16-6-8-17(40)9-7-16)56-38-35(29(48)24(43)15(4)52-38)57-36-30(49)27(46)23(42)14(3)51-36/h5-9,11,14-15,21,23-25,27-31,35-44,46-50H,10,12H2,1-4H3/t14-,15-,21+,23-,24-,25+,27+,28-,29+,30+,31+,35+,36-,37+,38-/m0/s1
InChl Key
ABEPLDYBWOKMCT-KUBBBFTRSA-N
WGK Germany
RID/ADR
HS Code Reference
2933990000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
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No Technical Documents Available For This Product.
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Objective: To study the components of roots of Epimedium acuminatum.
Method: Column chromatography was employed for the isolation. The isolated compounds were elucidated by UV, IR, FAB-MS, 1HNMR and 13CNMR analysis.
Result: Four constituents were obtained and elucidated as epimedoside A(V), diphylloside B(VI), epimedin C(VII) and ikarisoside C(VIII).
Conclusion: Four constituents are all flavonol glycosides, of which VI, VII and VIII were separated from this plant for the first time.
[Chemical constituents of Epimedium acuminatum Franch. (II)]
X Jia 1, J Wu, Q Mao
1998 Dec
