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Showing NP-Card for Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside] (NP0334899)

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Record Information
Version2.0
Created at2024-09-10 22:59:29 UTC
Updated at2024-09-10 22:59:29 UTC
NP-MRD IDNP0334899
Secondary Accession NumbersNone
Natural Product Identification
Common NameEugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside]
DescriptionEugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside] belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Based on a literature review very few articles have been published on Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside].
Structure
Thumb
MOLSDFPDBSMILESInChI

MOL for NP0334899 (Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside])


  Mrv2104 05262301312D          

 32 34  0  0  0  0            999 V2000
   -6.8569   -8.8455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6118   -5.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3719   -8.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7075   -7.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5581   -6.0032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0732   -5.3358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4021   -6.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2991   -0.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4691   -1.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2226   -6.7569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2527   -5.4220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9172   -6.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0837   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9540   -2.5798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7745   -2.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2594   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4186   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9239   -3.9147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1637   -1.3312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1034   -4.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1276    0.5154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1100   -1.7399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0799   -3.0748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2032   -0.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4088   -4.5821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0967   -6.2619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6486   -1.9986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7678   -4.7546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3387   -1.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6184   -3.3335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  4  3  1  0  0  0  0
  6  5  2  0  0  0  0
 10  4  1  0  0  0  0
 10  5  1  0  0  0  0
 10  7  2  0  0  0  0
 11  6  1  0  0  0  0
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 12 11  2  0  0  0  0
 13  8  1  0  0  0  0
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 15 13  1  0  0  0  0
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 18 15  1  0  0  0  0
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 31 13  1  0  0  0  0
 31 20  1  0  0  0  0
 32 14  1  0  0  0  0
 32 21  1  0  0  0  0
M  END
Download

3D MOL for NP0334899 (Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside])

Download
3D SDF for NP0334899 (Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside])

  Mrv2104 05262301312D          

 32 34  0  0  0  0            999 V2000
   -6.8569   -8.8455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6118   -5.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3719   -8.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7075   -7.4243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5581   -6.0032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0732   -5.3358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4021   -6.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2991   -0.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4691   -1.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2226   -6.7569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2527   -5.4220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9172   -6.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0837   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9540   -2.5798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7745   -2.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2594   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4186   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9239   -3.9147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1637   -1.3312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1034   -4.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1276    0.5154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1100   -1.7399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0799   -3.0748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2032   -0.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4088   -4.5821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0967   -6.2619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6486   -1.9986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7678   -4.7546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3387   -1.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6184   -3.3335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  4  3  1  0  0  0  0
  6  5  2  0  0  0  0
 10  4  1  0  0  0  0
 10  5  1  0  0  0  0
 10  7  2  0  0  0  0
 11  6  1  0  0  0  0
 12  7  1  0  0  0  0
 12 11  2  0  0  0  0
 13  8  1  0  0  0  0
 14  9  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 16  1  0  0  0  0
 18 15  1  0  0  0  0
 19 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 19  1  0  0  0  0
 22  8  1  0  0  0  0
 23 15  1  0  0  0  0
 24 16  1  0  0  0  0
 25 17  1  0  0  0  0
 26 18  1  0  0  0  0
 27 19  1  0  0  0  0
 28  2  1  0  0  0  0
 28 12  1  0  0  0  0
 29  9  1  0  0  0  0
 29 20  1  0  0  0  0
 30 11  1  0  0  0  0
 30 21  1  0  0  0  0
 31 13  1  0  0  0  0
 31 20  1  0  0  0  0
 32 14  1  0  0  0  0
 32 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0334899

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC2OC(COC3OC(CO)C(O)C3O)C(O)C(O)C2O)C=CC(CC=C)=C1

> <INCHI_IDENTIFIER>
InChI=1/C21H30O11/c1-3-4-10-5-6-11(12(7-10)28-2)30-21-19(27)17(25)16(24)14(32-21)9-29-20-18(26)15(23)13(8-22)31-20/h3,5-7,13-27H,1,4,8-9H2,2H3

> <INCHI_KEY>
VLKZOKSLKIEMBT-UHFFFAOYNA-N

> <FORMULA>
C21H30O11

> <MOLECULAR_WEIGHT>
458.46

> <EXACT_MASS>
458.178811786

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
45.598926669906305

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-methoxy-4-(prop-2-en-1-yl)phenoxy]oxane-3,4,5-triol

> <JCHEM_LOGP>
-0.7979888353333318

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.485256259452186

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.936815353352278

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981143337099244

> <JCHEM_POLAR_SURFACE_AREA>
167.52999999999997

> <JCHEM_REFRACTIVITY>
107.38459999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-({[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-methoxy-4-(prop-2-en-1-yl)phenoxy]oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0334899 (Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside])
Download
PDB for NP0334899 (Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside])
HEADER    PROTEIN                                 26-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-23         0                                  
HETATM    1  C   UNK     0     -12.800 -16.512   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.742 -10.443   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -11.894 -15.266   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -12.521 -13.859   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -12.242 -11.206   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -11.337  -9.960   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -10.084 -12.774   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.425  -0.544   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.342  -3.570   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -11.616 -12.613   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.805 -10.121   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -9.179 -11.528   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.890  -1.020   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.247  -4.816   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.136  -0.115   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.779  -4.655   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -11.684  -5.901   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.381  -1.020   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -11.058  -7.307   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.906  -2.485   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -9.526  -7.468   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.105   0.962   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -5.136   1.425   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0     -11.405  -3.248   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0     -13.216  -5.740   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -7.846  -0.544   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0     -11.963  -8.553   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -7.647 -11.689   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -6.811  -3.731   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -8.900  -8.875   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -4.366  -2.485   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -8.621  -6.223   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2   28                                                            
CONECT    3    1    4                                                       
CONECT    4    3   10                                                       
CONECT    5    6   10                                                       
CONECT    6    5   11                                                       
CONECT    7   10   12                                                       
CONECT    8   13   22                                                       
CONECT    9   14   29                                                       
CONECT   10    4    5    7                                                  
CONECT   11    6   12   30                                                  
CONECT   12    7   11   28                                                  
CONECT   13    8   15   31                                                  
CONECT   14    9   16   32                                                  
CONECT   15   13   18   23                                                  
CONECT   16   14   17   24                                                  
CONECT   17   16   19   25                                                  
CONECT   18   15   20   26                                                  
CONECT   19   17   21   27                                                  
CONECT   20   18   29   31                                                  
CONECT   21   19   30   32                                                  
CONECT   22    8                                                            
CONECT   23   15                                                            
CONECT   24   16                                                            
CONECT   25   17                                                            
CONECT   26   18                                                            
CONECT   27   19                                                            
CONECT   28    2   12                                                       
CONECT   29    9   20                                                       
CONECT   30   11   21                                                       
CONECT   31   13   20                                                       
CONECT   32   14   21                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

Download
3D PDB for NP0334899 (Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside])
Download
SMILES for NP0334899 (Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside])
COC1=C(OC2OC(COC3OC(CO)C(O)C3O)C(O)C(O)C2O)C=CC(CC=C)=C1
Download
INCHI for NP0334899 (Eugenol O-[a-L-Arabinofuranosyl-(1->6)-b-D-glucopyranoside])
InChI=1/C21H30O11/c1-3-4-10-5-6-11(12(7-10)28-2)30-21-19(27)17(25)16(24)14(32-21)9-29-20-18(26)15(23)13(8-22)31-20/h3,5-7,13-27H,1,4,8-9H2,2H3
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View in JSmol
SynonymsNot Available
Chemical FormulaC21H30O11
Average Mass458.4600 Da
Monoisotopic Mass458.17881 Da
IUPAC Name2-({[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-methoxy-4-(prop-2-en-1-yl)phenoxy]oxane-3,4,5-triol
Traditional Name2-({[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}methyl)-6-[2-methoxy-4-(prop-2-en-1-yl)phenoxy]oxane-3,4,5-triol
CAS Registry NumberNot Available
SMILES
COC1=C(OC2OC(COC3OC(CO)C(O)C3O)C(O)C(O)C2O)C=CC(CC=C)=C1
InChI Identifier
InChI=1/C21H30O11/c1-3-4-10-5-6-11(12(7-10)28-2)30-21-19(27)17(25)16(24)14(32-21)9-29-20-18(26)15(23)13(8-22)31-20/h3,5-7,13-27H,1,4,8-9H2,2H3
InChI KeyVLKZOKSLKIEMBT-UHFFFAOYNA-N
Experimental Spectra
Not Available
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of OriginNot Available
Chemical Taxonomy
DescriptionThis compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
KingdomOrganic compounds  
Super ClassOrganic oxygen compounds  
ClassOrganooxygen compounds  
Sub ClassCarbohydrates and carbohydrate conjugates  
Direct ParentPhenolic glycosides  
Alternative Parents
Substituents
  • Phenolic glycoside
    • 

  • Disaccharide
    • 

  • O-glycosyl compound
    • 

  • Phenoxy compound
    • 

  • Anisole
    • 

  • Methoxybenzene
    • 

  • Phenol ether
    • 

  • Alkyl aryl ether
    • 

  • Monocyclic benzene moiety
    • 

  • Benzenoid
    • 

  • Oxane
    • 

  • Tetrahydrofuran
    • 

  • Secondary alcohol
    • 

  • Acetal
    • 

  • Oxacycle
    • 

  • Organoheterocyclic compound
    • 

  • Ether
    • 

  • Polyol
    • 

  • Hydrocarbon derivative
    • 

  • Primary alcohol
    • 

  • Alcohol
    • 

  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-0.8ChemAxon
pKa (Strongest Acidic)11.94ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area167.53 ŲChemAxon
Rotatable Bond Count9ChemAxon
Refractivity107.38 m³·mol⁻¹ChemAxon
Polarizability45.6 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General ReferencesNot Available