NP-MRD: Showing NP-Card for Arctigenin 4'-O-beta-gentiobioside (NP0138722)

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Record Information

Version

2.0

Created at

2022-06-29 18:33:11 UTC

Updated at

2022-06-29 18:33:12 UTC

NP-MRD ID

NP0138722

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Arctigenin 4'-O-beta-gentiobioside

Description

Arctigenin 4'-O-beta-gentiobioside belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones. Arctigenin 4'-O-beta-gentiobioside is found in Trachelospermum asiaticum. Based on a literature review very few articles have been published on Arctigenin 4'-O-beta-gentiobioside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292220332D          

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M  END

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M  END


  Mrv1652306292220332D          

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    4.8946   -5.4241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946   -6.2491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801   -6.6616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -6.2491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -5.4241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -6.6616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -7.4866    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4186   -7.9715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1637   -8.7562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -8.7562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8538   -9.4236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0837   -7.9715    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2991   -7.7166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1276   -6.9096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7407   -6.3576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692   -5.5506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7845   -5.2957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1714   -5.8477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3430   -6.6547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6130   -4.4887    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1716   -4.2338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7847   -4.7858    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5693   -4.5309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7409   -3.7239    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1278   -3.1719    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3431   -3.4268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2993   -2.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6862   -1.8128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8577   -1.0059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6423   -0.7509    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8139    0.0560    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2008    0.6081    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4162    0.3531    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2446   -0.4538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1969    0.9052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0254    1.7121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3723    1.4150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5985    0.3110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2554   -1.3030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5255   -3.4689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1824   -5.0829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6132   -5.5928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1823   -4.9986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0107   -4.1916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6091   -6.6616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6091   -7.4866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 20 23  1  0  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 28 30  1  1  0  0  0
 30 31  1  0  0  0  0
 32 31  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 32 37  1  0  0  0  0
 36 38  1  1  0  0  0
 38 39  1  0  0  0  0
 35 40  1  6  0  0  0
 34 41  1  1  0  0  0
 33 42  1  6  0  0  0
 27 43  1  6  0  0  0
 26 44  1  1  0  0  0
 25 45  1  6  0  0  0
 19 46  1  0  0  0  0
 46 47  1  0  0  0  0
  4 48  1  0  0  0  0
 48 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0138722

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C=C(C[C@H]2COC(=O)[C@@H]2CC2=CC(OC)=C(O[C@@H]3O[C@H](CO[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@H](O)[C@H](O)[C@H]3O)C=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C33H44O16/c1-42-19-6-4-15(10-21(19)43-2)8-17-13-45-31(41)18(17)9-16-5-7-20(22(11-16)44-3)47-33-30(40)28(38)26(36)24(49-33)14-46-32-29(39)27(37)25(35)23(12-34)48-32/h4-7,10-11,17-18,23-30,32-40H,8-9,12-14H2,1-3H3/t17-,18+,23+,24+,25+,26+,27-,28-,29+,30+,32+,33+/m0/s1

> <INCHI_KEY>
FEQSYBHDHIPRKS-QWNZGVGBSA-N

> <FORMULA>
C33H44O16

> <MOLECULAR_WEIGHT>
696.699

> <EXACT_MASS>
696.262935337

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
70.01961777440319

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,4R)-4-[(3,4-dimethoxyphenyl)methyl]-3-[(3-methoxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one

> <ALOGPS_LOGP>
0.18

> <JCHEM_LOGP>
-0.6012271719999998

> <ALOGPS_LOGS>
-3.01

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.428072653942852

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.905234565901791

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083422322401

> <JCHEM_POLAR_SURFACE_AREA>
232.51999999999995

> <JCHEM_REFRACTIVITY>
164.67440000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.81e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4R)-4-[(3,4-dimethoxyphenyl)methyl]-3-[(3-methoxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0      10.470  -7.815   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.470  -9.355   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.137 -10.125   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.137 -11.665   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.803 -12.435   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.469 -11.665   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.469 -10.125   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.803  -9.355   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.136 -12.435   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.136 -13.975   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.381 -14.880   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.906 -16.345   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.366 -16.345   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.460 -17.591   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.890 -14.880   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.425 -14.404   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.105 -12.898   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.249 -11.867   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.929 -10.361   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.464  -9.885   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.320 -10.916   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.640 -12.422   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.144  -8.379   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.320  -7.903   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.465  -8.933   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.929  -8.458   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.250  -6.951   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.105  -5.921   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -0.641  -6.397   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -2.425  -4.414   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -1.281  -3.384   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -1.601  -1.878   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -3.066  -1.402   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -3.386   0.105   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.241   1.135   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.777   0.659   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -0.457  -0.847   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       0.368   1.690   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       0.047   3.196   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      -2.562   2.641   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      -4.851   0.580   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      -4.210  -2.432   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      -4.714  -6.475   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      -4.074  -9.488   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      -1.145 -10.440   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       4.074  -9.331   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       3.753  -7.824   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      10.470 -12.435   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      10.470 -13.975   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5   48                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    6   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   10   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   46                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   20   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26   45                                                  
CONECT   26   25   27   44                                                  
CONECT   27   26   28   43                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28   24                                                       
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   37                                                  
CONECT   33   32   34   42                                                  
CONECT   34   33   35   41                                                  
CONECT   35   34   36   40                                                  
CONECT   36   35   37   38                                                  
CONECT   37   36   32                                                       
CONECT   38   36   39                                                       
CONECT   39   38                                                            
CONECT   40   35                                                            
CONECT   41   34                                                            
CONECT   42   33                                                            
CONECT   43   27                                                            
CONECT   44   26                                                            
CONECT   45   25                                                            
CONECT   46   19   47                                                       
CONECT   47   46                                                            
CONECT   48    4   49                                                       
CONECT   49   48                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Value	Source
Arctigenin 4'-O-b-gentiobioside	Generator
Arctigenin 4'-O-β-gentiobioside	Generator

Chemical Formula

C₃₃H₄₄O₁₆

Average Mass

696.6990 Da

Monoisotopic Mass

696.26294 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

41682-24-0

SMILES

COC1=C(OC)C=C(C[C@H]2COC(=O)[C@@H]2CC2=CC(OC)=C(O[C@@H]3O[C@H](CO[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@H](O)[C@H](O)[C@H]3O)C=C2)C=C1

InChI Identifier

InChI=1S/C33H44O16/c1-42-19-6-4-15(10-21(19)43-2)8-17-13-45-31(41)18(17)9-16-5-7-20(22(11-16)44-3)47-33-30(40)28(38)26(36)24(49-33)14-46-32-29(39)27(37)25(35)23(12-34)48-32/h4-7,10-11,17-18,23-30,32-40H,8-9,12-14H2,1-3H3/t17-,18+,23+,24+,25+,26+,27-,28-,29+,30+,32+,33+/m0/s1

InChI Key

FEQSYBHDHIPRKS-QWNZGVGBSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Trachelospermum asiaticum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan glycosides

Sub Class

Not Available

Direct Parent

Lignan glycosides

Alternative Parents

Substituents

Lignan glycoside
Dibenzylbutyrolactone
Lignan lactone
Tetrahydrofuran lignan
Furanoid lignan
9,9p-epoxylignan
Phenolic glycoside
Fatty acyl glycoside of mono- or disaccharide
Fatty acyl glycoside
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Disaccharide
O-dimethoxybenzene
Dimethoxybenzene
Phenoxy compound
Phenol ether
Methoxybenzene
Anisole
Alkyl aryl ether
Fatty acyl
Oxane
Gamma butyrolactone
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Lactone
Acetal
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Polyol
Ether
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxygen compound
Organic oxide
Primary alcohol
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

57620411

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14681436

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Arctigenin 4'-O-beta-gentiobioside (NP0138722)

MOL for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

3D MOL for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

3D SDF for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

3D-SDF for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

PDB for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

3D PDB for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

SMILES for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

INCHI for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

Structure for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)

3D Structure for NP0138722 (Arctigenin 4'-O-beta-gentiobioside)