Licoricesaponin H2

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(Spectroscopic Data)
 
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{{Metabolite
 
{{Metabolite
|SysName=(3.beta.,20.alpha.)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-.beta.-D-glucopyranuronosyl-.beta.-D-Glucopyranosiduronic acid
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|SysName=(3beta,20alpha)-20-Carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid
|Common Name=&&Licoricesaponin H2&&30-Noroleanane, .beta.-D-glucopyranosiduronic acid deriv.&& Saponin H2 from licorice
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|Common Name=&&Licoricesaponin H2&&30-Noroleanane beta-D-glucopyranosiduronic acid deriv.&&Saponin H2 from licorice
 
|CAS=118441-85-3
 
|CAS=118441-85-3
 
|KNApSAcK=
 
|KNApSAcK=
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==Mass Spectral Data==
 
==Mass Spectral Data==
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==Spectroscopic Data==
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{| class="wikitable" style="width:80%"
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'''Free acid'''
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|-
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| '''M.P.'''<sup>1</sup> || 209 - 210 °C
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|-
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| '''IR''' (KBr)<sup>2</sup>|| 3500-3300 (br), 2920, 1725, 1645, 1386, 1200, 1040 cm<sup>-1</sup>
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|-
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| '''<sup>1</sup>H-NMR''' (C<sub>5</sub>D<sub>5</sub>N, 500 MHz)<sup>2</sup>|| 0.87 (s, CH<sub>3</sub>), 1.06 (s, CH<sub>3</sub>), 1.19 (s, CH<sub>3</sub>), 1.20 (s, CH<sub>3</sub>), 1.35 (s, CH<sub>3</sub>), 1.36 (s, CH<sub>3</sub>), 1.38 (s, CH<sub>3</sub>), 3.00 (brd, ''J''= 13.0 Hz, H-18), 3.35 (dd, ''J''=4.0. 12.3 Hz, H-3), 4.97 (d, ''J''=7.6 Hz, H-1 of GlcUA I), 5.35 (d, ''J''=7.6 Hz, H-1 of GlcUA II), 5.79 (brs, H-12)
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|-
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| '''<sup>13</sup>C-NMR''' (C<sub>5</sub>D<sub>5</sub>N, 125MHz)<sup>1</sup>|| 105.0 (C-1 of Glc I), 106.8 (C-1 of Glc II), 128.8 (C-12), 169.0 (C-13), 180.6 (C-29), 199.4 (C-11)
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|}
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{| class="wikitable" style="width:80%"
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'''Trimethyl ester'''
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|-
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| '''M.P.'''<sup>1</sup> || 169 °C
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|-
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| '''IR''' (KBr)<sup>1</sup>|| 3362, 1722, 1654 cm<sup>-1</sup>
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|-
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| '''<sup>1</sup>H-NMR''' (C<sub>5</sub>D<sub>5</sub>N)<sup>1</sup>|| 4.95 (d, ''J''=7.3 Hz, H-1 of GlcUA I), 5.33 (d, ''J''=7.7 Hz, H-1 of GlcUA II)
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|-
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| '''<sup>13</sup>C-NMR''' (C<sub>5</sub>D<sub>5</sub>N, 22.5MHz)<sup>2</sup>|| C-3) 89.2, (11) 199.0, (12) 128.6, (13) 168.4, (18) 44.0, (22) 37.1, (24) 16.2, (29) 178.1, (30) 19.3, '''GlcUA I''' (1) 104.9, (2) 84.3, (3) 76.4, (4) 72.5, (5) 77.3, (6) 170.1, '''GlcUA II''' (1)106.8, (2) 76.6, (3) 77.4, (4) 72.9, (5) 77.6, (6) 170.2 
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|}
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<small>1) M. Yoshikawa et al., Chem.Pharm.Bull., 39, 244 (1991)., 2) M. Yoshikawa et al., Chem.Pharm.Bull., 41, 1337 (1993).</small>

Latest revision as of 12:13, 9 February 2010



Upper classes



Licoricesaponin H2
Licoricesaponin H2.png
Structural Information
Systematic Name (3beta,20alpha)-20-Carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid
Common Name
  • Licoricesaponin H2
  • 30-Noroleanane beta-D-glucopyranosiduronic acid deriv.
  • Saponin H2 from licorice
Symbol
Formula C42H62O16
Exact Mass 822.4037859360001
Average Mass 822.93208
SMILES C(C7(C)2)(=CC(C(C7(C)6)C(C5CC6)(CCC(C5(C)C)OC(C(OC(O4)C(O)C(O)C(O)C4C(O)=O)3)OC(C(O)C3O)C(O)=O)C)=O)C(C1(CC2)C)CC(CC1)(C)C(O)=O
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Reflactive Index
Solubility
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Chromatograms




Glycyrrhizae Radix LC-MS


[edit] Mass Spectral Data

[edit] Spectroscopic Data

Free acid
M.P.1 209 - 210 °C
IR (KBr)2 3500-3300 (br), 2920, 1725, 1645, 1386, 1200, 1040 cm-1
1H-NMR (C5D5N, 500 MHz)2 0.87 (s, CH3), 1.06 (s, CH3), 1.19 (s, CH3), 1.20 (s, CH3), 1.35 (s, CH3), 1.36 (s, CH3), 1.38 (s, CH3), 3.00 (brd, J= 13.0 Hz, H-18), 3.35 (dd, J=4.0. 12.3 Hz, H-3), 4.97 (d, J=7.6 Hz, H-1 of GlcUA I), 5.35 (d, J=7.6 Hz, H-1 of GlcUA II), 5.79 (brs, H-12)
13C-NMR (C5D5N, 125MHz)1 105.0 (C-1 of Glc I), 106.8 (C-1 of Glc II), 128.8 (C-12), 169.0 (C-13), 180.6 (C-29), 199.4 (C-11)
Trimethyl ester
M.P.1 169 °C
IR (KBr)1 3362, 1722, 1654 cm-1
1H-NMR (C5D5N)1 4.95 (d, J=7.3 Hz, H-1 of GlcUA I), 5.33 (d, J=7.7 Hz, H-1 of GlcUA II)
13C-NMR (C5D5N, 22.5MHz)2 C-3) 89.2, (11) 199.0, (12) 128.6, (13) 168.4, (18) 44.0, (22) 37.1, (24) 16.2, (29) 178.1, (30) 19.3, GlcUA I (1) 104.9, (2) 84.3, (3) 76.4, (4) 72.5, (5) 77.3, (6) 170.1, GlcUA II (1)106.8, (2) 76.6, (3) 77.4, (4) 72.9, (5) 77.6, (6) 170.2

1) M. Yoshikawa et al., Chem.Pharm.Bull., 39, 244 (1991)., 2) M. Yoshikawa et al., Chem.Pharm.Bull., 41, 1337 (1993).

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