NP-MRD: Showing NP-Card for (1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate (NP0289683)

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Record Information

Version

2.0

Created at

2022-09-09 19:59:36 UTC

Updated at

2022-09-09 19:59:37 UTC

NP-MRD ID

NP0289683

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate

Description

CHEMBL3577213 belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. (1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate is found in Celastrus vulcanicola. Based on a literature review very few articles have been published on CHEMBL3577213.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092221592D          

 51 55  0  0  1  0            999 V2000
    4.1650    2.5348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2969    2.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1406    1.3902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4569    2.6673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7043    2.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881    1.5419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8298    1.5673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7038    2.0666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2034    2.9947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2683    3.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9460    3.4971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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 50 92  1  0
 50 93  1  0
 32 80  1  1
 35 81  1  0
 35 82  1  0
 35 83  1  0
 37 84  1  6
 42 85  1  0
 43 86  1  0
 44 87  1  0
 45 88  1  0
 46 89  1  0
 17 62  1  0
 18 63  1  0
 19 64  1  0
 20 65  1  0
 21 66  1  0
M  END


  Mrv1652309092221592D          

 51 55  0  0  1  0            999 V2000
    4.1650    2.5348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2969    2.3156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1406    1.3902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4569    2.6673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7043    2.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881    1.5419    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8298    1.5673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7038    2.0666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2034    2.9947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2683    3.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9460    3.4971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    0.8674    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9888    0.3140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6698   -0.2939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5508   -1.1527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4762    0.1031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6954    0.8984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4938    1.1063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0729    0.5188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8537   -0.2766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0554   -0.4844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9060    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0812    0.0746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3355   -0.7769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5456   -0.6332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5808    0.7540    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1007    0.1726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8607    0.5953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4592   -0.0521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6987    0.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6954    1.4426    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3272    2.2252    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2763    2.5228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2009    2.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9398    2.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7450    3.2834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5304    2.2931    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5055    3.2522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0158    4.1287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7444    4.6187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5836    4.7061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1539    5.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5490    6.1346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3738    6.1546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8035    5.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    4.7261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0175    1.1439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2131    1.8980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1093    2.7532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9096    3.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2080    3.5443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  6  0  0  0
 23 26  1  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 31 28  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 32 37  1  0  0  0  0
  6 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 41 46  1  0  0  0  0
 31 47  1  0  0  0  0
 26 47  1  0  0  0  0
 47 48  1  1  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0289683

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@@]12[C@@H](OC(C)=O)[C@H](C[C@](C)(O)[C@]11OC(C)(C)[C@@H]([C@H]1OC(C)=O)[C@H](OC(C)=O)[C@@H]2OC(=O)C1=CC=CC=C1)OC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C37H42O14/c1-20(38)45-19-36-29(47-22(3)40)26(49-32(42)24-14-10-8-11-15-24)18-35(7,44)37(36)30(48-23(4)41)27(34(5,6)51-37)28(46-21(2)39)31(36)50-33(43)25-16-12-9-13-17-25/h8-17,26-31,44H,18-19H2,1-7H3/t26-,27+,28-,29-,30+,31-,35-,36-,37-/m0/s1

> <INCHI_KEY>
VLDOGFDAFSEYTM-YFNVFCEMSA-N

> <FORMULA>
C37H42O14

> <MOLECULAR_WEIGHT>
710.729

> <EXACT_MASS>
710.257456032

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
71.25371879441396

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,4S,5R,6S,7R,8S,9R,12R)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl benzoate

> <JCHEM_LOGP>
2.818270600333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.66862483787127

> <JCHEM_PKA_STRONGEST_BASIC>
-3.381143495915105

> <JCHEM_POLAR_SURFACE_AREA>
187.26

> <JCHEM_REFRACTIVITY>
172.69009999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4S,5R,6S,7R,8S,9R,12R)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       7.775   4.732   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.154   4.322   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.862   2.595   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       4.586   4.979   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.181   4.084   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.844   2.878   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.416   2.926   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.047   3.858   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.980   5.590   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.101   7.234   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.366   6.528   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.254   1.619   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.579   0.586   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.850  -0.549   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.628  -2.152   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.356   0.192   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.765   1.677   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.255   2.065   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.336   0.968   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.927  -0.516   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.437  -0.904   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.558   0.233   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.018   0.139   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.493  -1.450   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.018  -1.182   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.084   1.407   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.188   0.322   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.607   1.111   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.724  -0.097   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.171   1.544   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.298   2.693   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.611   4.154   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -2.382   4.709   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -4.108   4.827   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -5.488   4.020   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -5.124   6.129   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       0.990   4.280   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       0.944   6.071   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -0.030   7.707   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -1.390   8.622   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       1.089   8.785   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.287  10.099   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.025  11.451   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.564  11.489   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.366  10.174   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.629   8.822   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -0.033   2.135   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       0.398   3.543   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -0.204   5.139   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -1.698   5.629   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -0.388   6.616   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   26   37                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22   12   23                                                       
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23    6   27   47                                             
CONECT   27   26   28                                                       
CONECT   28   27   29   30   31                                             
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   28   32   47                                                  
CONECT   32   31   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   32    6   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   46                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   41                                                       
CONECT   47   31   26   48                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
MASTER        0    0    0    0    0    0    0    0   51    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₂O₁₄

Average Mass

710.7290 Da

Monoisotopic Mass

710.25746 Da

IUPAC Name

(1S,2S,4S,5R,6S,7R,8S,9R,12R)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl benzoate

Traditional Name

(1S,2S,4S,5R,6S,7R,8S,9R,12R)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl benzoate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@@]12[C@@H](OC(C)=O)[C@H](C[C@](C)(O)[C@]11OC(C)(C)[C@@H]([C@H]1OC(C)=O)[C@H](OC(C)=O)[C@@H]2OC(=O)C1=CC=CC=C1)OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C37H42O14/c1-20(38)45-19-36-29(47-22(3)40)26(49-32(42)24-14-10-8-11-15-24)18-35(7,44)37(36)30(48-23(4)41)27(34(5,6)51-37)28(46-21(2)39)31(36)50-33(43)25-16-12-9-13-17-25/h8-17,26-31,44H,18-19H2,1-7H3/t26-,27+,28-,29-,30+,31-,35-,36-,37-/m0/s1

InChI Key

VLDOGFDAFSEYTM-YFNVFCEMSA-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
Celastrus vulcanicola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
Agarofuran
Sesquiterpenoid
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Oxepane
Cyclitol or derivatives
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Cyclic alcohol
Tertiary alcohol
Carboxylic acid ester
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Ether
Alcohol
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
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
logP	2.82	ChemAxon
pKa (Strongest Acidic)	13.67	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	187.26 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	172.69 m³·mol⁻¹	ChemAxon
Polarizability	71.25 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

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

59005176

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122177553

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate (NP0289683)

MOL for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

3D MOL for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

3D SDF for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

3D-SDF for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

PDB for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

3D PDB for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

SMILES for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

INCHI for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

Structure for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)

3D Structure for NP0289683 ((1s,2s,4s,5r,6s,7r,8s,9r,12r)-5,8,12-tris(acetyloxy)-6-[(acetyloxy)methyl]-7-(benzoyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl benzoate)