NP-MRD: Showing NP-Card for (4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate (NP0240046)

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Record Information

Version

2.0

Created at

2022-09-06 23:45:41 UTC

Updated at

2022-09-06 23:45:41 UTC

NP-MRD ID

NP0240046

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate

Description

(4S,6R,7R,8S,9S)-4-hydroxy-9-{[(2S,3S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]Undecan-6-yl 4-hydroxybenzoate belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. (4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate is found in Catalpa ovata. Based on a literature review very few articles have been published on (4S,6R,7R,8S,9S)-4-hydroxy-9-{[(2S,3S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]Undecan-6-yl 4-hydroxybenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072201452D          

 34 38  0  0  1  0            999 V2000
    1.6635   -0.8677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8783   -1.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2666   -0.5670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4403    0.2396    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0204    0.9309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7100    1.2654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1014    1.8224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0053    2.0974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8628    2.2087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4729    1.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3132    1.0021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2977    0.7757    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2111    0.2895    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0362   -0.0358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1849   -0.8473    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9620   -1.1244    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5904   -0.5899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3675   -0.8669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9960   -0.3324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7731   -0.6094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5162   -1.6784    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2933   -1.9554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8877   -2.2129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0364   -3.0244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1106   -1.9359    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4822   -2.4703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7376    0.6019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7046   -1.9271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3162   -2.4808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1426   -3.2873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3573   -3.5402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1836   -4.3467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2544   -2.9865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0807   -2.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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  4 12  1  0  0  0  0
 13 12  1  1  0  0  0
  6 13  1  0  0  0  0
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  2 28  1  0  0  0  0
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 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 28 34  1  0  0  0  0
M  END

     RDKit          3D

 62 66  0  0  0  0  0  0  0  0999 V2000
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   -0.3421    2.6811   -1.7747 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4880    1.4277   -1.9245 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8745    0.8660   -0.5557 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2719    1.1624    0.3652 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5857    1.3158   -0.3721 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8829    0.1202   -0.9826 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0462   -0.4723   -0.4903 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7732   -1.6678    0.0797 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7731   -2.5501    0.2901 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2790   -2.4647    1.7330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2346   -2.7522    2.5887 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9438   -2.4947   -0.6081 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7158   -3.3190   -1.7335 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3317   -1.1075   -1.0408 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -1.4930    3.6402    0.2070 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4346    0.2168    0.2982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3341   -3.5903    0.2129 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7227   -4.2659   -1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309072201452D          

 34 38  0  0  1  0            999 V2000
    1.6635   -0.8677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8783   -1.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2666   -0.5670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4403    0.2396    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0204    0.9309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7100    1.2654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1014    1.8224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0053    2.0974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8628    2.2087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4729    1.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3132    1.0021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2977    0.7757    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2111    0.2895    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0362   -0.0358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.5904   -0.5899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3675   -0.8669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9960   -0.3324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7731   -0.6094    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5162   -1.6784    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.8877   -2.2129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0364   -3.0244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1106   -1.9359    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4822   -2.4703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7376    0.6019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3573   -3.5402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1836   -4.3467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2544   -2.9865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0807   -2.1800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
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  4 12  1  0  0  0  0
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 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
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 14 27  1  0  0  0  0
 10 27  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 28 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240046

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC1O[C@@H](O[C@@H]2OC3C[C@H]4[C@@H](C[C@@](O)(CO3)[C@@H]24)OC(=O)C2=CC=C(O)C=C2)[C@@H](O)C(O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O12/c23-7-13-16(25)17(26)18(27)21(32-13)34-20-15-11-5-14(33-20)30-8-22(15,29)6-12(11)31-19(28)9-1-3-10(24)4-2-9/h1-4,11-18,20-21,23-27,29H,5-8H2/t11-,12+,13?,14?,15+,16-,17?,18-,20-,21-,22+/m0/s1

> <INCHI_KEY>
VGNSHUAFKWSOOW-SKCMJWITSA-N

> <FORMULA>
C22H28O12

> <MOLECULAR_WEIGHT>
484.454

> <EXACT_MASS>
484.158076342

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
46.09033698254298

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,6R,7R,8S,9S)-4-hydroxy-9-{[(2S,3S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0^{4,8}]undecan-6-yl 4-hydroxybenzoate

> <JCHEM_LOGP>
-1.1546788543333337

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.186996472305657

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.496502120302749

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847587232487

> <JCHEM_POLAR_SURFACE_AREA>
184.6

> <JCHEM_REFRACTIVITY>
108.94450000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4S,6R,7R,8S,9S)-4-hydroxy-9-{[(2S,3S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0^{4,8}]undecan-6-yl 4-hydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  O   UNK     0       3.105  -1.620   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.639  -2.092   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.498  -1.058   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.822   0.447   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.038   1.738   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.325   2.362   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.189   3.402   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.877   3.915   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.477   4.123   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.616   2.927   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.318   1.871   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.422   1.448   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.261   0.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.801  -0.067   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.078  -1.582   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.529  -2.099   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.702  -1.101   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.153  -1.618   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.326  -0.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.776  -1.138   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.430  -3.133   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.881  -3.650   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.257  -4.131   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.535  -5.645   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.806  -3.614   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.633  -4.611   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       5.110   1.124   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.315  -3.597   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.457  -4.631   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.133  -6.136   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.667  -6.608   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.343  -8.114   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -0.475  -5.575   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.151  -4.069   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8   13                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   27                                                  
CONECT   11   10   12                                                       
CONECT   12   11    4   13                                                  
CONECT   13   12    6   14                                                  
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25                                                            
CONECT   27   14   10                                                       
CONECT   28    2   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   28                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Value	Source
(4S,6R,7R,8S,9S)-4-Hydroxy-9-{[(2S,3S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0,]undecan-6-yl 4-hydroxybenzoic acid	Generator

Chemical Formula

C₂₂H₂₈O₁₂

Average Mass

484.4540 Da

Monoisotopic Mass

484.15808 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OCC1O[C@@H](O[C@@H]2OC3C[C@H]4[C@@H](C[C@@](O)(CO3)[C@@H]24)OC(=O)C2=CC=C(O)C=C2)[C@@H](O)C(O)[C@H]1O

InChI Identifier

InChI=1S/C22H28O12/c23-7-13-16(25)17(26)18(27)21(32-13)34-20-15-11-5-14(33-20)30-8-22(15,29)6-12(11)31-19(28)9-1-3-10(24)4-2-9/h1-4,11-18,20-21,23-27,29H,5-8H2/t11-,12+,13?,14?,15+,16-,17?,18-,20-,21-,22+/m0/s1

InChI Key

VGNSHUAFKWSOOW-SKCMJWITSA-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
Catalpa ovata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Hexose monosaccharide
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
O-glycosyl compound
Benzoate ester
Benzoic acid or derivatives
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Oxepane
Dioxepane
1,3-dioxepane
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxide
Hydrocarbon derivative
Primary alcohol
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162969687

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate (NP0240046)

MOL for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

3D MOL for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

3D SDF for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

3D-SDF for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

PDB for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

3D PDB for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

SMILES for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

INCHI for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

Structure for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)

3D Structure for NP0240046 ((4s,6r,7r,8s,9s)-4-hydroxy-9-{[(2s,3s,5r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,10-dioxatricyclo[5.3.1.0⁴,⁸]undecan-6-yl 4-hydroxybenzoate)