NP-MRD: Showing NP-Card for 4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate (NP0253653)

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Record Information

Version

2.0

Created at

2022-09-07 17:35:21 UTC

Updated at

2022-09-07 17:35:21 UTC

NP-MRD ID

NP0253653

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

Description

4,5,8-Tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl benzoate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. 4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate is found in Euonymus japonicus. 4,5,8-Tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl benzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251513252D          

 43 46  0  0  0  0            999 V2000
    1.4374    3.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0652    3.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8426    3.7163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9154    2.6291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1379    2.3532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881    1.5419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8298    1.5673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2144    2.2972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0388    2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4233    3.0589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4786    1.6311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    0.8674    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  0  0  0  0  0  0  0  0  0  0
    1.2871   -0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3360   -0.2795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5808    0.7540    0.0000 C   0  0  0  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
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    0.3839    5.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5832    5.9242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0317    5.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6564    4.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1030    0.9107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5525    0.2189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3763    0.2622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1780   -0.5162    0.0000 C   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
  5  6  1  0  0  0  0
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  7  8  1  0  0  0  0
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  9 10  2  0  0  0  0
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  7 12  1  0  0  0  0
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  6 30  1  0  0  0  0
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 38 39  2  0  0  0  0
 34 39  1  0  0  0  0
 12 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
M  END

     RDKit          3D

 81 84  0  0  0  0  0  0  0  0999 V2000
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   -0.4896   -0.6671    2.0202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2876   -0.2949    0.5335 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1176   -0.7069    0.2346 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7897    0.1862   -0.5809 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9317    0.8823   -0.2120 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3222    0.6626    0.9601 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6839    1.8040   -1.0351 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004251513252D          

 43 46  0  0  0  0            999 V2000
    1.4374    3.9757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0652    3.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9154    2.6291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1379    2.3532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9881    1.5419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8298    1.5673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2144    2.2972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0388    2.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4233    3.0589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4786    1.6311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2792    0.8674    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  0  0  0  0  0  0  0  0  0  0
    1.2871   -0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3360   -0.2795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1839   -0.1637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6494    0.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6954    1.4426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0175    1.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3754    1.8694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3272    2.2252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7965    2.9038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6188    2.8367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9718    2.0910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0880    3.5152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5304    2.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9058    3.0278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4572    3.7201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3667    3.6778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8325    4.4548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3839    5.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7592    5.8819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5832    5.9242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0317    5.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6564    4.4971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1030    0.9107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5525    0.2189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3763    0.2622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1780   -0.5162    0.0000 C   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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
  6 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 34 39  1  0  0  0  0
 12 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0253653

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC12C(OC(C)=O)C(CC(C)(O)C11OC(C)(C)C(C1O)C(OC(C)=O)C2OC(=O)C1=CC=CC=C1)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H38O13/c1-15(31)38-14-29-24(41-18(4)34)20(39-16(2)32)13-28(7,37)30(29)23(35)21(27(5,6)43-30)22(40-17(3)33)25(29)42-26(36)19-11-9-8-10-12-19/h8-12,20-25,35,37H,13-14H2,1-7H3

> <INCHI_KEY>
NCGQUVSDYGMJGN-UHFFFAOYSA-N

> <FORMULA>
C30H38O13

> <MOLECULAR_WEIGHT>
606.621

> <EXACT_MASS>
606.231241284

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
59.58859768731759

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

> <ALOGPS_LOGP>
1.84

> <JCHEM_LOGP>
0.32297075166666733

> <ALOGPS_LOGS>
-3.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.985457156259919

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.268562436888853

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3804372251691985

> <JCHEM_POLAR_SURFACE_AREA>
181.18999999999997

> <JCHEM_REFRACTIVITY>
142.8681

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.97e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.683   7.421   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.855   6.422   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.306   6.937   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.575   4.908   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.124   4.393   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       4.134   4.288   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.672   4.348   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.390   5.710   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.493   3.045   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.254   1.619   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.558   0.233   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.018   0.139   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.403  -1.352   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.627  -0.522   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.084   1.407   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.188   0.322   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.607   1.111   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.210  -0.306   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.079   1.563   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.298   2.693   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.033   2.135   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.701   3.489   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.611   4.154   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.487   5.420   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -3.022   5.295   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -3.681   3.903   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -3.898   6.562   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.990   4.280   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.691   5.652   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.853   6.944   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.685   6.865   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.554   8.316   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.717   9.608   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.417  10.980   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.955  11.058   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.793   9.766   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.092   8.395   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       5.792   1.700   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       6.631   0.409   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.169   0.489   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       5.932  -0.964   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17   30                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13   40                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14    6   18   23                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23   25                                                  
CONECT   23   22   17   24                                                  
CONECT   24   23                                                            
CONECT   25   22   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25    6   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   34                                                       
CONECT   40   12   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

View in JSmol

Synonyms

Value	Source
4,5,8-Tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0,]dodecan-7-yl benzoic acid	Generator
4,5,8-Tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoic acid	Generator

Chemical Formula

C₃₀H₃₈O₁₃

Average Mass

606.6210 Da

Monoisotopic Mass

606.23124 Da

IUPAC Name

4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

Traditional Name

4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC12C(OC(C)=O)C(CC(C)(O)C11OC(C)(C)C(C1O)C(OC(C)=O)C2OC(=O)C1=CC=CC=C1)OC(C)=O

InChI Identifier

InChI=1S/C30H38O13/c1-15(31)38-14-29-24(41-18(4)34)20(39-16(2)32)13-28(7,37)30(29)23(35)21(27(5,6)43-30)22(40-17(3)33)25(29)42-26(36)19-11-9-8-10-12-19/h8-12,20-25,35,37H,13-14H2,1-7H3

InChI Key

NCGQUVSDYGMJGN-UHFFFAOYSA-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
Euonymus japonicus	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic 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
Secondary alcohol
Ether
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Alcohol
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
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	1.84	ALOGPS
logP	0.32	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	13.27	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	181.19 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	142.87 m³·mol⁻¹	ChemAxon
Polarizability	59.59 Å³	ChemAxon
Number of Rings	4	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate (NP0253653)

MOL for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D MOL for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D SDF for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D-SDF for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

PDB for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D PDB for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

SMILES for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

INCHI for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

Structure for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D Structure for NP0253653 (4,5,8-tris(acetyloxy)-6-[(acetyloxy)methyl]-2,12-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)