NP-MRD: Showing NP-Card for furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate (NP0279840)

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Record Information

Version

2.0

Created at

2022-09-09 05:22:27 UTC

Updated at

2022-09-09 05:22:27 UTC

NP-MRD ID

NP0279840

Secondary Accession Numbers

None

Natural Product Identification

Common Name

furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate

Description

Furan-3-yl (1S,2S,5R,6R,7S,8S,9R,12R)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecane-8-carboxylate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate is found in Celastrus paniculatus. Based on a literature review very few articles have been published on furan-3-yl (1S,2S,5R,6R,7S,8S,9R,12R)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]Dodecane-8-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092207222D          

 45 49  0  0  1  0            999 V2000
    4.4674    1.3392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1297    0.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9512    0.9989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5629   -0.0235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6782   -0.4183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8267    0.1195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4112   -0.6432    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6057   -1.5741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1875   -2.5027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4956   -3.0521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8287   -3.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6463   -2.9324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0039   -3.6759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4073   -4.2457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6810   -3.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5568   -0.6040    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9363   -1.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0173   -2.4543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0898   -1.5227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5593   -1.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5477   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3286    0.0352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8229   -0.6254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6582    0.0461    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4391   -0.7102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3464   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7043   -1.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2339   -0.9686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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 39 40  1  0  0  0  0
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  6 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
M  END

     RDKit          3D

 81 85  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309092207222D          

 45 49  0  0  1  0            999 V2000
    4.4674    1.3392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1297    0.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6463   -2.9324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0039   -3.6759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4073   -4.2457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6810   -3.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5568   -0.6040    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9363   -1.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0173   -2.4543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0898   -1.5227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5593   -1.0558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5477   -0.2309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3286    0.0352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8229   -0.6254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3475   -1.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1500    0.1616    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8099    0.4997    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0923   -0.2838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8153   -1.1652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1490   -1.9106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2840   -1.8509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4150    0.9000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7071    1.4552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9577    1.0058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4728    1.7693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0598    0.9570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9585    1.5568    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4077    2.2827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2423    2.4147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894    1.4796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1324    0.7246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6582    0.0461    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4391   -0.7102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3464   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7043   -1.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2339   -0.9686    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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 15  2  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  2  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  6  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  2  0  0  0  0
 26 31  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  1  1  0  0  0
 32 33  1  0  0  0  0
 25 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  1  0  0  0
 36 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
  6 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0279840

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@]12[C@@H](CC[C@](C)(O)[C@]11OC(C)(C)[C@@H]([C@H]1OC(C)=O)[C@@H]([C@@H]2OC(=O)C1=COC=C1)C(=O)OC1=COC=C1)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H36O14/c1-16(32)40-15-30-21(41-17(2)33)7-10-29(6,37)31(30)25(42-18(3)34)23(28(4,5)45-31)22(27(36)43-20-9-12-39-14-20)24(30)44-26(35)19-8-11-38-13-19/h8-9,11-14,21-25,37H,7,10,15H2,1-6H3/t21-,22+,23-,24+,25-,29+,30-,31+/m1/s1

> <INCHI_KEY>
ODCAMDJMGUTWOU-UFAKWALKSA-N

> <FORMULA>
C31H36O14

> <MOLECULAR_WEIGHT>
632.615

> <EXACT_MASS>
632.210505839

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
61.787161545500354

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
furan-3-yl (1S,2S,5R,6R,7S,8S,9R,12R)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecane-8-carboxylate

> <JCHEM_LOGP>
1.3063629289999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.270202344156537

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.75308828457564

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6512657435231604

> <JCHEM_POLAR_SURFACE_AREA>
187.23999999999998

> <JCHEM_REFRACTIVITY>
147.05740000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
furan-3-yl (1S,2S,5R,6R,7S,8S,9R,12R)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecane-8-carboxylate

> <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       8.339   2.500   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.575   1.174   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.109   1.865   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.517  -0.044   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.866  -0.781   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.277   0.223   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.501  -1.201   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.864  -2.938   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.083  -4.672   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.792  -5.697   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.280  -5.680   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.806  -5.474   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.474  -6.862   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.360  -7.925   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.005  -7.195   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.906  -1.128   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.748  -2.644   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.899  -4.581   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.168  -2.842   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.044  -1.971   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.022  -0.431   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.480   0.066   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.403  -1.167   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.515  -2.426   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.147   0.302   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.378   0.933   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.906  -0.530   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.389  -2.175   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.012  -3.566   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.397  -3.455   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.508   1.680   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.187   2.716   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.788   1.877   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.883   3.303   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.112   1.786   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.522   2.906   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.494   4.261   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       6.052   4.507   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       7.074   2.762   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.714   1.353   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.829   0.086   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.286  -1.326   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       9.980  -2.043   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      10.648  -3.513   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      11.637  -1.808   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   31   41                                             
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   11                                                       
CONECT   16    7   17   25                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20                                                       
CONECT   25   16   26   33                                                  
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   26    6   32   36                                             
CONECT   32   31   33                                                       
CONECT   33   32   25   34   35                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   31   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   36   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40    6   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
Furan-3-yl (1S,2S,5R,6R,7S,8S,9R,12R)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0,]dodecane-8-carboxylic acid	Generator

Chemical Formula

C₃₁H₃₆O₁₄

Average Mass

632.6150 Da

Monoisotopic Mass

632.21051 Da

IUPAC Name

furan-3-yl (1S,2S,5R,6R,7S,8S,9R,12R)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecane-8-carboxylate

Traditional Name

furan-3-yl (1S,2S,5R,6R,7S,8S,9R,12R)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecane-8-carboxylate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@]12[C@@H](CC[C@](C)(O)[C@]11OC(C)(C)[C@@H]([C@H]1OC(C)=O)[C@@H]([C@@H]2OC(=O)C1=COC=C1)C(=O)OC1=COC=C1)OC(C)=O

InChI Identifier

InChI=1S/C31H36O14/c1-16(32)40-15-30-21(41-17(2)33)7-10-29(6,37)31(30)25(42-18(3)34)23(28(4,5)45-31)22(27(36)43-20-9-12-39-14-20)24(30)44-26(35)19-8-11-38-13-19/h8-9,11-14,21-25,37H,7,10,15H2,1-6H3/t21-,22+,23-,24+,25-,29+,30-,31+/m1/s1

InChI Key

ODCAMDJMGUTWOU-UFAKWALKSA-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 paniculata	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
Furoic acid ester
Furoic acid or derivatives
Furan-3-carboxylic acid ester
Furan-3-carboxylic acid or derivatives
Oxepane
Cyclic alcohol
Heteroaromatic compound
Furan
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organooxygen compound
Carbonyl group
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	1.31	ChemAxon
pKa (Strongest Acidic)	13.75	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	187.24 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	147.06 m³·mol⁻¹	ChemAxon
Polarizability	61.79 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

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

163190446

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate (NP0279840)

MOL for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

3D MOL for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

3D SDF for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

3D-SDF for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

PDB for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

3D PDB for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

SMILES for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

INCHI for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

Structure for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)

3D Structure for NP0279840 (furan-3-yl (1s,2s,5r,6r,7s,8s,9r,12r)-5,12-bis(acetyloxy)-6-[(acetyloxy)methyl]-7-(furan-3-carbonyloxy)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-8-carboxylate)