NP-MRD: Showing NP-Card for 2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0258333)

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Record Information

Version

2.0

Created at

2022-09-07 23:44:11 UTC

Updated at

2022-09-07 23:44:11 UTC

NP-MRD ID

NP0258333

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Description

Alyssonoside belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. 2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate is found in Ballota nigra, Phlomoides rotata, Lantana canescens, Marrubium alysson, Marrubium velutinum, Marrubium vulgare and Phlomis herba-venti. 2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate was first documented in 2014 (PMID: 25509294). Based on a literature review a small amount of articles have been published on Alyssonoside (PMID: 35153761) (PMID: 33916300) (PMID: 32298752) (PMID: 29058476).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082201442D          

 54 58  0  0  0  0            999 V2000
   -0.0576  -10.6776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5425  -10.0102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2070   -9.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6919   -8.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3563   -7.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8413   -7.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6617   -7.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1467   -6.5868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8111   -5.8331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9671   -6.6730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4521   -6.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1165   -5.2519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2960   -5.1657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605   -4.4120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4454   -3.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.6737   -3.6808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4942   -3.7670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6684   -9.5152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2792   -8.3528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  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  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
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 14 15  1  0  0  0  0
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 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
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 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 12 24  1  0  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
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 29 36  1  0  0  0  0
 25 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
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 41 49  1  0  0  0  0
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  5 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
  3 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END

     RDKit          3D

100104  0  0  0  0  0  0  0  0999 V2000
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    0.4819    2.7553    4.4534 O   0  0  0  0  0  0  0  0  0  0  0  0
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 51 98  1  0
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 54100  1  0
M  END


  Mrv1652309082201442D          

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   -2.6684   -9.5152    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0984   -9.8377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 29 36  1  0  0  0  0
 25 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
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 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
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 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 41 49  1  0  0  0  0
 49 50  1  0  0  0  0
  5 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
  3 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258333

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)OC2C(COC3OCC(O)(CO)C3O)OC(OCCC3=CC=C(O)C(O)=C3)C(O)C2OC2OC(C)C(O)C(O)C2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C35H46O19/c1-16-25(41)26(42)27(43)33(51-16)54-30-28(44)32(48-10-9-18-3-6-19(37)21(39)11-18)52-23(13-49-34-31(45)35(46,14-36)15-50-34)29(30)53-24(40)8-5-17-4-7-20(38)22(12-17)47-2/h3-8,11-12,16,23,25-34,36-39,41-46H,9-10,13-15H2,1-2H3/b8-5+

> <INCHI_KEY>
BVFLJHVBTFJPHJ-VMPITWQZSA-N

> <FORMULA>
C35H46O19

> <MOLECULAR_WEIGHT>
770.734

> <EXACT_MASS>
770.263329261

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
76.55403167441064

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
-0.3111796436666649

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.998991727354634

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.305296652762749

> <JCHEM_PKA_STRONGEST_BASIC>
-3.676505497283866

> <JCHEM_POLAR_SURFACE_AREA>
293.21

> <JCHEM_REFRACTIVITY>
179.55560000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.108 -19.932   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.013 -18.686   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.386 -17.279   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.292 -16.033   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.665 -14.626   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.570 -13.380   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.102 -13.541   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.007 -12.295   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.381 -10.888   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -5.539 -12.456   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -6.444 -11.210   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.817  -9.804   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.286  -9.643   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -3.660  -8.236   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -4.565  -6.990   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -6.105  -6.990   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -6.581  -5.525   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.365  -3.476   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.304  -3.476   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.798  -3.796   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.089  -5.525   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.624  -5.049   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -6.723  -8.558   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -8.254  -8.719   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -9.159  -7.473   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0     -10.691  -7.634   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -11.596  -6.388   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -13.128  -6.549   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -13.754  -7.956   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -15.286  -8.117   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -16.191  -6.871   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0     -17.722  -7.032   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0     -15.564  -5.464   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -16.470  -4.218   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0     -14.033  -5.303   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -8.881 -10.125   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -10.412 -10.286   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -7.975 -11.371   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -8.602 -12.778   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -7.697 -14.024   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -6.165 -13.863   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      -5.260 -15.109   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -3.728 -14.948   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -5.886 -16.516   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -4.981 -17.762   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -7.418 -16.677   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -8.044 -18.084   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -8.323 -15.431   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      -9.855 -15.592   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       0.866 -14.465   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       1.772 -15.711   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       1.145 -17.118   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0       2.050 -18.364   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   53                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   51                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   39                                                  
CONECT   12   11   13   24                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   22                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   18   15   23                                                  
CONECT   23   22                                                            
CONECT   24   12   25                                                       
CONECT   25   24   26   37                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   29                                                       
CONECT   37   25   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   11   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   49                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   41   50                                                  
CONECT   50   49                                                            
CONECT   51    5   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52    3   54                                                  
CONECT   54   53                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  116    0
END

View in JSmol

Synonyms

Value	Source
beta-(3,4-Dihydroxyphenyl)ethyl-O-(alpha-L-rhamnopyranosyl-(1-3))-O-(beta-D-apiopyranosyl-(1-6))-4-feruloyl-beta-D-glucopyranoside	MeSH

Chemical Formula

C₃₅H₄₆O₁₉

Average Mass

770.7340 Da

Monoisotopic Mass

770.26333 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)OC2C(COC3OCC(O)(CO)C3O)OC(OCCC3=CC=C(O)C(O)=C3)C(O)C2OC2OC(C)C(O)C(O)C2O)=CC=C1O

InChI Identifier

InChI=1S/C35H46O19/c1-16-25(41)26(42)27(43)33(51-16)54-30-28(44)32(48-10-9-18-3-6-19(37)21(39)11-18)52-23(13-49-34-31(45)35(46,14-36)15-50-34)29(30)53-24(40)8-5-17-4-7-20(38)22(12-17)47-2/h3-8,11-12,16,23,25-34,36-39,41-46H,9-10,13-15H2,1-2H3/b8-5+

InChI Key

BVFLJHVBTFJPHJ-VMPITWQZSA-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
Ballota nigra	LOTUS Database	35616633
Lamiophlomis rotata	LOTUS Database	35616633
Lantana canescens	LOTUS Database	35616633
Marrubium alysson	LOTUS Database	35616633
Marrubium velutinum	LOTUS Database	35616633
Marrubium vulgare	LOTUS Database	35616633
Phlomis herba-venti	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Coumaric acid or derivatives
Cinnamic acid or derivatives
O-glycosyl compound
Glycosyl compound
Methoxyphenol
Tyrosol derivative
Anisole
Methoxybenzene
Catechol
Phenoxy compound
Phenol ether
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Fatty acid ester
Fatty acyl
Benzenoid
Oxane
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Oxolane
Secondary alcohol
Carboxylic acid ester
Ether
Acetal
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Polyol
Monocarboxylic acid or derivatives
Organic oxide
Alcohol
Carbonyl group
Primary alcohol
Hydrocarbon derivative
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

C00036035

Chemspider ID

4948177

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6444250

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li Y, Yang Y, Kang X, Li X, Wu Y, Xiao J, Ye Y, Yang J, Yang Y, Liu H: Study on The Anti-Inflammatory Effects of Callicarpa nudiflora Based on The Spectrum-Effect Relationship. Front Pharmacol. 2022 Jan 27;12:806808. doi: 10.3389/fphar.2021.806808. eCollection 2021. [PubMed:35153761 ]
Senol Deniz FS, Eren G, Orhan IE, Sener B, Ozgen U, Aldaba R, Calis I: Outlining In Vitro and In Silico Cholinesterase Inhibitory Activity of Twenty-Four Natural Products of Various Chemical Classes: Smilagenin, Kokusaginine, and Methyl Rosmarinate as Emboldening Inhibitors. Molecules. 2021 Apr 1;26(7). pii: molecules26072024. doi: 10.3390/molecules26072024. [PubMed:33916300 ]
Wu A, Yang Z, Huang Y, Yuan H, Lin C, Wang T, Zhao Z, Zhou Y, Zhu C: Natural phenylethanoid glycosides isolated from Callicarpa kwangtungensis suppressed lipopolysaccharide-mediated inflammatory response via activating Keap1/Nrf2/HO-1 pathway in RAW 264.7 macrophages cell. J Ethnopharmacol. 2020 Aug 10;258:112857. doi: 10.1016/j.jep.2020.112857. Epub 2020 Apr 13. [PubMed:32298752 ]
Frezza C, Venditti A, Matrone G, Serafini I, Foddai S, Bianco A, Serafini M: Iridoid glycosides and polyphenolic compounds from Teucrium chamaedrys L. Nat Prod Res. 2018 Jul;32(13):1583-1589. doi: 10.1080/14786419.2017.1392948. Epub 2017 Oct 23. [PubMed:29058476 ]
Ma YC, Zhang M, Xu WT, Feng SX, Lei M, Yi B: [Chemical constituents from Callicarpa nudiflora and their cytotoxic activities]. Zhongguo Zhong Yao Za Zhi. 2014 Aug;39(16):3094-101. [PubMed:25509294 ]
LOTUS database [Link]

Showing NP-Card for 2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate (NP0258333)

MOL for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D MOL for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D SDF for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D-SDF for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

PDB for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D PDB for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

SMILES for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

INCHI for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

Structure for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)

3D Structure for NP0258333 (2-({[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate)