NP-MRD: Showing NP-Card for 6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate (NP0271662)

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Record Information

Version

2.0

Created at

2022-09-08 18:02:00 UTC

Updated at

2022-09-08 18:02:00 UTC

NP-MRD ID

NP0271662

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

Description

6-[(Acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-7-yl benzoate belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene). 6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate is found in Euonymus nanoides. 6-[(Acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-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


  Mrv1533005011514052D          

 44 47  0  0  0  0            999 V2000
    7.8025   -2.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0187   -2.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1110   -2.3063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0651   -3.1702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4242   -1.7640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0256   -1.0975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4265   -1.5979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5838   -0.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351    0.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0677    1.4445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3038    1.2761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6531    0.4578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934    0.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0940   -1.4191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4839   -2.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2330   -3.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 41 42  1  0  0  0  0
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 43 44  1  0  0  0  0
M  END

     RDKit          3D

 92 95  0  0  0  0  0  0  0  0999 V2000
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    1.9198    3.1095    3.1891 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3186    1.7157    3.5096 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.0580    0.6636    1.4898 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1 47  1  0
M  END


  Mrv1533005011514052D          

 44 47  0  0  0  0            999 V2000
    7.8025   -2.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0187   -2.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0651   -3.1702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4242   -1.7640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0256   -1.0975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4265   -1.5979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5838   -0.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351    0.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0677    1.4445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3038    1.2761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6531    0.4578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934    0.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3768    0.7553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0322   -0.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0588   -0.8122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4269   -1.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2845   -1.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6651   -2.5124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0982   -3.2779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8930   -3.5650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7428   -4.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2807   -4.6904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0079   -5.4690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1972   -5.6220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6593   -4.9964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9321   -4.2178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -0.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4960   -1.4916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2724   -0.9584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8374   -0.3105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240    0.4697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7510   -0.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7368   -0.5133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7544   -1.3033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7487   -1.6832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0940   -1.4191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1423   -2.3677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4266   -3.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4839   -2.9746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2330   -3.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  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
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 25 30  1  0  0  0  0
 21 31  1  0  0  0  0
  8 31  1  0  0  0  0
 14 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 19 37  1  0  0  0  0
 14 37  1  0  0  0  0
 37 38  1  0  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  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0271662

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)OC1C2CC(OC(=O)C3=CC=CC=C3)C3(COC(C)=O)C(CCC(C)(O)C13OC2(C)C)OC(=O)C(C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C34H48O10/c1-9-20(3)28(36)41-25-16-17-32(8,39)34-27(43-29(37)21(4)10-2)24(31(6,7)44-34)18-26(33(25,34)19-40-22(5)35)42-30(38)23-14-12-11-13-15-23/h11-15,20-21,24-27,39H,9-10,16-19H2,1-8H3

> <INCHI_KEY>
UEGXNWYVIIAFGA-UHFFFAOYSA-N

> <FORMULA>
C34H48O10

> <MOLECULAR_WEIGHT>
616.748

> <EXACT_MASS>
616.324747746

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
65.99179107384369

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

> <ALOGPS_LOGP>
4.49

> <JCHEM_LOGP>
5.219548990999999

> <ALOGPS_LOGS>
-5.22

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.754781478731612

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3434585812027926

> <JCHEM_POLAR_SURFACE_AREA>
134.66000000000003

> <JCHEM_REFRACTIVITY>
159.00280000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.70e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-MAY-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-MAY-15         0                                  
HETATM    1  C   UNK     0      14.565  -3.866   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.102  -4.500   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.407  -4.305   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.322  -5.918   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.125  -3.293   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      11.248  -2.049   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       8.263  -2.983   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.690  -1.749   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.528  -0.443   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.832   0.943   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.292   1.038   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.726   2.696   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.300   2.382   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.358  -0.230   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.086   0.855   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.668   0.065   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.703   1.410   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.060  -0.147   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.976  -1.516   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.664  -2.977   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.264  -3.104   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.975  -4.690   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.783  -6.119   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.267  -6.655   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.120  -7.588   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.124  -8.755   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.615 -10.209   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.101 -10.494   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.097  -9.327   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.607  -7.873   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.118  -1.701   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.526  -2.784   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.975  -1.789   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       9.030  -0.580   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       8.072   0.877   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      10.735  -0.686   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.242  -0.958   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.275  -2.433   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       1.398  -3.142   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -0.175  -2.649   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       0.266  -4.420   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.796  -5.796   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -0.903  -5.553   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -2.302  -6.245   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   31                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15   31   37                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20   37                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   31                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25                                                       
CONECT   31   21    8   14   32                                             
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   19   14   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   94    0
END

View in JSmol

Synonyms

Value	Source
6-[(Acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0,]dodecan-7-yl benzoic acid	Generator
6-[(Acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoic acid	Generator

Chemical Formula

C₃₄H₄₈O₁₀

Average Mass

616.7480 Da

Monoisotopic Mass

616.32475 Da

IUPAC Name

6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

Traditional Name

6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)OC1C2CC(OC(=O)C3=CC=CC=C3)C3(COC(C)=O)C(CCC(C)(O)C13OC2(C)C)OC(=O)C(C)CC

InChI Identifier

InChI=1S/C34H48O10/c1-9-20(3)28(36)41-25-16-17-32(8,39)34-27(43-29(37)21(4)10-2)24(31(6,7)44-34)18-26(33(25,34)19-40-22(5)35)42-30(38)23-14-12-11-13-15-23/h11-15,20-21,24-27,39H,9-10,16-19H2,1-8H3

InChI Key

UEGXNWYVIIAFGA-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 nanoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Agarofurans

Alternative Parents

Substituents

Agarofuran
Tetracarboxylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Fatty acid ester
Oxepane
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	4.49	ALOGPS
logP	5.22	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	13.75	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	134.66 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	159 m³·mol⁻¹	ChemAxon
Polarizability	65.99 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

85426671

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate (NP0271662)

MOL for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D MOL for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D SDF for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D-SDF for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

PDB for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D PDB for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

SMILES for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

INCHI for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

Structure for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)

3D Structure for NP0271662 (6-[(acetyloxy)methyl]-2-hydroxy-2,10,10-trimethyl-5,12-bis[(2-methylbutanoyl)oxy]-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-7-yl benzoate)