NP-MRD: Showing NP-Card for (1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate (NP0324732)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 04:59:29 UTC

Updated at

2022-09-12 04:59:29 UTC

NP-MRD ID

NP0324732

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate

Description

Schiarisanrin C belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. (1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate is found in Schisandra arisanensis. (1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate was first documented in 2008 (PMID: 19023792). Schiarisanrin C is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309272006272D          

 37 42  0  0  0  0            999 V2000
   -1.7297   -1.4088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5935   -2.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7776   -2.3443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8214    2.0247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6647    3.2014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3997    1.4363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0864    3.7898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6797    0.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0789    0.0723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4008    1.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9892    0.8301    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9964    0.0051    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4181   -0.5832    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5931   -0.5904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0011   -0.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7885   -0.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989   -1.0239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4132   -1.6049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3829   -1.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5750    1.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0082    0.8072    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3656    2.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4402    2.4190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0302    1.8290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8142    1.0230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3975    0.4397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7486    1.1525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7613   -0.3039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7404   -1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5593   -1.4432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8816   -2.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0558   -0.7843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3967   -2.8699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7322   -3.6237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5527   -3.7100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0376   -3.0426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7021   -2.2888    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
  4  6  1  0  0  0  0
  5  7  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 14  2  0  0  0  0
 15 16  2  0  0  0  0
 17  1  1  0  0  0  0
 18  3  1  0  0  0  0
  8  9  1  0  0  0  0
  9 16  1  0  0  0  0
 21 20  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 20 22  2  0  0  0  0
 21 25  1  0  0  0  0
 23  5  1  0  0  0  0
 24  4  1  0  0  0  0
 10 20  1  0  0  0  0
 21 15  1  0  0  0  0
 21  8  1  6  0  0  0
 25 26  2  0  0  0  0
 11 27  1  1  0  0  0
 12 28  1  1  0  0  0
 13 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 33 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
 31 33  2  0  0  0  0
 37 31  1  0  0  0  0
M  END


  Mrv1652309272006272D          

 37 42  0  0  0  0            999 V2000
   -1.7297   -1.4088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5935   -2.2225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7776   -2.3443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8214    2.0247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6647    3.2014    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3997    1.4363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0864    3.7898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6797    0.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0789    0.0723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4008    1.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9892    0.8301    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9964    0.0051    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4181   -0.5832    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5931   -0.5904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0011   -0.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7885   -0.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989   -1.0239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4132   -1.6049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3829   -1.3881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5750    1.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0082    0.8072    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3656    2.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4402    2.4190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0302    1.8290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8142    1.0230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3975    0.4397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7486    1.1525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7613   -0.3039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7404   -1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5593   -1.4432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8816   -2.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0558   -0.7843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3967   -2.8699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7322   -3.6237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5527   -3.7100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0376   -3.0426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7021   -2.2888    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
  4  6  1  0  0  0  0
  5  7  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 14  2  0  0  0  0
 15 16  2  0  0  0  0
 17  1  1  0  0  0  0
 18  3  1  0  0  0  0
  8  9  1  0  0  0  0
  9 16  1  0  0  0  0
 21 20  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 20 22  2  0  0  0  0
 21 25  1  0  0  0  0
 23  5  1  0  0  0  0
 24  4  1  0  0  0  0
 10 20  1  0  0  0  0
 21 15  1  0  0  0  0
 21  8  1  6  0  0  0
 25 26  2  0  0  0  0
 11 27  1  1  0  0  0
 12 28  1  1  0  0  0
 13 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 33 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
 31 33  2  0  0  0  0
 37 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0324732

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C(=O)[C@]23COC4=C2C(=CC2=C4OCO2)[C@H](OC(=O)C2=CC=CC=C2)[C@H](C)[C@H](C)CC3=C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H28O8/c1-15-10-18-11-20(32-3)25(33-4)27(30)29(18)13-34-26-22(29)19(12-21-24(26)36-14-35-21)23(16(15)2)37-28(31)17-8-6-5-7-9-17/h5-9,11-12,15-16,23H,10,13-14H2,1-4H3/t15-,16-,23-,29+/m1/s1

> <INCHI_KEY>
RMKQIKRRIGHWHR-HUEIWROHSA-N

> <FORMULA>
C29H28O8

> <MOLECULAR_WEIGHT>
504.535

> <EXACT_MASS>
504.178417862

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
51.85169297498392

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,12R,13R,14R)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0^{1,16}.0^{4,21}.0^{5,9}]henicosa-4(21),5(9),10,16,18-pentaen-12-yl benzoate

> <ALOGPS_LOGP>
3.82

> <JCHEM_LOGP>
4.195093755666667

> <ALOGPS_LOGS>
-5.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.291846587829674

> <JCHEM_POLAR_SURFACE_AREA>
89.52000000000001

> <JCHEM_REFRACTIVITY>
135.81409999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.61e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,12R,13R,14R)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0^{1,16}.0^{4,21}.0^{5,9}]henicosa-4(21),5(9),10,16,18-pentaen-12-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-20         0                                  
HETATM    1  O   UNK     0      -3.229  -2.630   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -2.975  -4.149   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.452  -4.376   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -3.400   3.779   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -1.241   5.976   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.479   2.681   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.161   7.074   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.269   1.221   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.014   0.135   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.615   2.629   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.713   1.550   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.727   0.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.647  -1.089   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.107  -1.102   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.002  -0.001   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.472  -0.422   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.865  -1.911   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.771  -2.996   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.715  -2.591   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.073   2.596   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.015   1.507   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.682   4.113   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.822   4.515   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.923   3.414   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.520   1.910   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.609   0.821   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.131   2.151   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.154  -0.567   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.249  -2.506   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.777  -2.694   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.379  -4.112   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.704  -1.464   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.474  -5.357   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.100  -6.764   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.632  -6.925   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.537  -5.680   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.911  -4.272   0.000  0.00  0.00           C+0
CONECT    1    2   17                                                       
CONECT    2    1    3                                                       
CONECT    3    2   18                                                       
CONECT    4    6   24                                                       
CONECT    5    7   23                                                       
CONECT    6    4                                                            
CONECT    7    5                                                            
CONECT    8    9   21                                                       
CONECT    9    8   16                                                       
CONECT   10   11   20                                                       
CONECT   11   10   12   27                                                  
CONECT   12   11   13   28                                                  
CONECT   13   12   14   29                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16   21                                                  
CONECT   16   17   15    9                                                  
CONECT   17   16   18    1                                                  
CONECT   18   17   19    3                                                  
CONECT   19   18   14                                                       
CONECT   20   21   22   10                                                  
CONECT   21   20   25   15    8                                             
CONECT   22   23   20                                                       
CONECT   23   22   24    5                                                  
CONECT   24   23   25    4                                                  
CONECT   25   24   21   26                                                  
CONECT   26   25                                                            
CONECT   27   11                                                            
CONECT   28   12                                                            
CONECT   29   13   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30   33   37                                                  
CONECT   32   30                                                            
CONECT   33   34   31                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   31                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Value	Source
Benzoyl oxokadsurane	PhytoBank
Schiarisanrin C	PhytoBank

Chemical Formula

C₂₉H₂₈O₈

Average Mass

504.5350 Da

Monoisotopic Mass

504.17842 Da

IUPAC Name

(1S,12R,13R,14R)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0^{1,16}.0^{4,21}.0^{5,9}]henicosa-4(21),5(9),10,16,18-pentaen-12-yl benzoate

Traditional Name

(1S,12R,13R,14R)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0^{1,16}.0^{4,21}.0^{5,9}]henicosa-4(21),5(9),10,16,18-pentaen-12-yl benzoate

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C(=O)[C@]23COC4=C2C(=CC2=C4OCO2)[C@H](OC(=O)C2=CC=CC=C2)[C@H](C)[C@H](C)CC3=C1

InChI Identifier

InChI=1S/C29H28O8/c1-15-10-18-11-20(32-3)25(33-4)27(30)29(18)13-34-26-22(29)19(12-21-24(26)36-14-35-21)23(16(15)2)37-28(31)17-8-6-5-7-9-17/h5-9,11-12,15-16,23H,10,13-14H2,1-4H3/t15-,16-,23-,29+/m1/s1

InChI Key

RMKQIKRRIGHWHR-HUEIWROHSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Schisandra arisanensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Benzoate ester
Coumaran
Benzoic acid or derivatives
Benzodioxole
Benzoyl
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Vinylogous ester
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	3.82	ALOGPS
logP	4.2	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	89.52 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	135.81 m³·mol⁻¹	ChemAxon
Polarizability	51.85 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

145709592

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lu Y, Chen DF: Kadsutherin D, a new dibenzocyclooctadiene lignan from Kadsura species. Nat Prod Res. 2008;22(15):1344-9. doi: 10.1080/14786410601133525. [PubMed:19023792 ]
LOTUS database [Link]

Showing NP-Card for (1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate (NP0324732)

MOL for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

3D MOL for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

3D SDF for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

3D-SDF for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

PDB for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

3D PDB for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

SMILES for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

INCHI for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

Structure for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)

3D Structure for NP0324732 ((1s,12r,13r,14r)-18,19-dimethoxy-13,14-dimethyl-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl benzoate)