NP-MRD: Showing NP-Card for [(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate (NP0218807)

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Record Information

Version

2.0

Created at

2022-09-05 19:35:35 UTC

Updated at

2022-09-05 19:35:36 UTC

NP-MRD ID

NP0218807

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate

Description

[(1R,9R,17R)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]Heptadeca-2,4,6,11,13,15-hexaen-17-yl]methyl acetate belongs to the class of organic compounds known as aryltetralin lignans. These are lignans with a structure based on the 1-phenyltetralin skeleton. [(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate is found in Cunninghamia lanceolata. Based on a literature review very few articles have been published on [(1R,9R,17R)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]Heptadeca-2,4,6,11,13,15-hexaen-17-yl]methyl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052221352D          

 37 40  0  0  1  0            999 V2000
   -2.4973    0.1045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9157   -0.5303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0447   -0.6765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5472   -0.0184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5939    0.0160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5927   -0.8802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0952   -1.5383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7235   -1.4365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1720   -2.1914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0152   -3.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2362   -3.2873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6400   -3.5543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3571   -1.1904    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1170   -0.8692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6240   -1.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4411   -1.4065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9275   -2.1252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8069   -2.9636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4554   -3.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0410   -3.2702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7513   -0.6421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5938   -0.4455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1498    0.1976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8791    0.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9600    0.0424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2444    0.0088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4273   -0.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1061    0.6552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3974    1.4618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3416    0.9654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5817    0.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0799   -0.1144    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1407    0.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3448    1.1675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1695    1.1445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5619    0.4188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6018    1.8472    0.0000 O   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  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
 10 12  2  0  0  0  0
 13  6  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 30 28  1  1  0  0  0
 30 31  1  0  0  0  0
  5 31  1  0  0  0  0
 30 32  1  0  0  0  0
 13 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
M  END


  Mrv1652309052221352D          

 37 40  0  0  1  0            999 V2000
   -2.4973    0.1045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9157   -0.5303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0447   -0.6765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5472   -0.0184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5939    0.0160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5927   -0.8802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0952   -1.5383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7235   -1.4365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1720   -2.1914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0152   -3.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2362   -3.2873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6400   -3.5543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3571   -1.1904    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1170   -0.8692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6240   -1.5201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4411   -1.4065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9275   -2.1252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8069   -2.9636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4554   -3.4736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0410   -3.2702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7513   -0.6421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5938   -0.4455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1498    0.1976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8791    0.9769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9600    0.0424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2444    0.0088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4273   -0.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1061    0.6552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3974    1.4618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3416    0.9654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5817    0.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0799   -0.1144    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1407    0.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3448    1.1675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1695    1.1445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5619    0.4188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6018    1.8472    0.0000 O   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  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
 10 12  2  0  0  0  0
 13  6  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 30 28  1  1  0  0  0
 30 31  1  0  0  0  0
  5 31  1  0  0  0  0
 30 32  1  0  0  0  0
 13 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0218807

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1OC(C)=O)[C@H]1[C@@H](COC(C)=O)[C@@H](C2)C(=O)C2=CC(OC(C)=O)=C(OC(C)=O)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C27H26O10/c1-12(28)34-11-21-19-6-16-7-22(33-5)23(35-13(2)29)8-17(16)26(21)18-9-24(36-14(3)30)25(37-15(4)31)10-20(18)27(19)32/h7-10,19,21,26H,6,11H2,1-5H3/t19-,21+,26-/m1/s1

> <INCHI_KEY>
KELYKXIEBFGAKA-BNIKKZEQSA-N

> <FORMULA>
C27H26O10

> <MOLECULAR_WEIGHT>
510.495

> <EXACT_MASS>
510.152597037

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
50.89640587224171

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(1R,9R,17R)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0^{2,7}.0^{11,16}]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate

> <JCHEM_LOGP>
1.883592114666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.144932673117832

> <JCHEM_PKA_STRONGEST_BASIC>
-4.89264160106453

> <JCHEM_POLAR_SURFACE_AREA>
131.5

> <JCHEM_REFRACTIVITY>
127.595

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,9R,17R)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0^{2,7}.0^{11,16}]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.662   0.195   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.576  -0.990   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.950  -1.263   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.021  -0.034   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.109   0.030   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.106  -1.643   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.178  -2.871   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.351  -2.681   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.188  -4.091   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.895  -5.629   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.441  -6.136   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.061  -6.635   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.533  -2.222   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.952  -1.623   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.898  -2.837   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.423  -2.626   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.331  -3.967   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.106  -5.532   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.317  -6.484   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.677  -6.104   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.003  -1.199   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.575  -0.832   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.613   0.369   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.108   1.824   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.125   0.079   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.056   0.016   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.531  -0.196   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.931   1.223   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.475   2.729   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.504   1.802   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.086   1.203   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.016  -0.214   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.263   0.706   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -0.644   2.179   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -2.183   2.136   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.916   0.782   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -2.990   3.448   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7   13                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    6   14   32                                                  
CONECT   14   13   15   27                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   27                                                       
CONECT   27   26   14   28                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30    5                                                       
CONECT   32   30   13   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Value	Source
[(1R,9R,17R)-4,5,14-Tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0,.0,]heptadeca-2,4,6,11,13,15-hexaen-17-yl]methyl acetic acid	Generator

Chemical Formula

C₂₇H₂₆O₁₀

Average Mass

510.4950 Da

Monoisotopic Mass

510.15260 Da

IUPAC Name

[(1R,9R,17R)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0^{2,7}.0^{11,16}]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate

Traditional Name

[(1R,9R,17R)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0^{2,7}.0^{11,16}]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1OC(C)=O)[C@H]1[C@@H](COC(C)=O)[C@@H](C2)C(=O)C2=CC(OC(C)=O)=C(OC(C)=O)C=C12

InChI Identifier

InChI=1S/C27H26O10/c1-12(28)34-11-21-19-6-16-7-22(33-5)23(35-13(2)29)8-17(16)26(21)18-9-24(36-14(3)30)25(37-15(4)31)10-20(18)27(19)32/h7-10,19,21,26H,6,11H2,1-5H3/t19-,21+,26-/m1/s1

InChI Key

KELYKXIEBFGAKA-BNIKKZEQSA-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
Cunninghamia lanceolata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aryltetralin lignans. These are lignans with a structure based on the 1-phenyltetralin skeleton.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Aryltetralin lignans

Sub Class

Not Available

Direct Parent

Aryltetralin lignans

Alternative Parents

Substituents

1-aryltetralin lignan
Tetracarboxylic acid or derivatives
Tetralin
Anisole
Aryl ketone
Aryl alkyl ketone
Alkyl aryl ether
Benzenoid
Ketone
Carboxylic acid ester
Ether
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	1.88	ChemAxon
pKa (Strongest Acidic)	15.14	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	131.5 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	127.6 m³·mol⁻¹	ChemAxon
Polarizability	50.9 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	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

163015422

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate (NP0218807)

MOL for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

3D MOL for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

3D SDF for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

3D-SDF for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

PDB for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

3D PDB for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

SMILES for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

INCHI for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

Structure for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)

3D Structure for NP0218807 ([(1r,9r,17r)-4,5,14-tris(acetyloxy)-13-methoxy-8-oxotetracyclo[7.7.1.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaen-17-yl]methyl acetate)