Compound:Ephemeranthoside

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Upper classes




Ephemeranthoside
Ephemeranthoside.png
Structural Information
Systematic Name 1-[(2R,4aS,4bR,6R,7S,8aR)-2,3,4,4a,4b,5,6,7,8,8a,9,10-dodecahydro-6,7-dihydroxy-2,4b,8,8-tetramethyl-2-phenanthrenyl]-2-(β-D-glucopyranosyloxy)- (9CI) Ethanone
Common Name
  • Ephemeranthoside
Symbol
Formula
Exact Mass
Average Mass
SMILES
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Reflactive Index
Solubility
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Chromatograms


Related Atomic Mappings, Enzymes, and Pathways



NMR Data

1H-NMR spectrum
13C-NMR spectrum
Difference NOE Experiments of Ephemeranthoside
1H-1H COSY spectrum of Ephemeranthoside
HMQC spectrum of Ephemeranthoside
HMBC spectrum of Ephemeranthoside
Table 1. 400MH 1H-and 100MHz 13C-NMR Data for Ephemeranthoside in C5D5N
Position Ginsenoside La
δH δC
11.72 dd (12, 4.5)40.5 t
1.93 t (12)
24.18 ddd (12, 4.5, 2.5)66.1 d
33.73 d (2.5)79.2 d
438.7 s
51.75 dd (12, 2.5)47.6 d
61.27 m22.0 t
1.52 m
72.07 td (14, 5)35.9 t
8141.9 s
91.84 dd (10, 7)50.8 d
1039.7 s
111.31 dddd (13.5, 12.5, 10, 3.5)20.5 t
1.54 ddt (13.5, 7, 3.5)
120.97 td (12.5, 3.5)32.9 t
2.37 dt (12.5, 3.5)
1347.6 s
145.47 brs124.6 d
15210.5 s
164.96 d (18)71.5 t
5.06d (18)
171.01 s27.0 q
181.21 s29.4 q
190.87 s22.4 q
200.73 s15.4 q
1'5.01 d (7.5)104.3 d
2'4.11 t (7.5)75.1 d
3'4.23 m78.3 d
4'4.26 m71.3 d
5'3.90 m78.6 d
6'4.36 dd (12, 5)62.5 t
4.50 dd (12, 2)
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