NP-MRD: Showing NP-Card for (8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate (NP0175442)

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Record Information

Version

2.0

Created at

2022-09-03 12:54:44 UTC

Updated at

2022-09-03 12:54:45 UTC

NP-MRD ID

NP0175442

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate

Description

CHEMBL563299 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. (8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate is found in Schisandra propinqua. Based on a literature review very few articles have been published on CHEMBL563299.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032214542D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309032214542D          

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    1.3315   -4.8263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0035   -4.3123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8101   -4.5427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5415   -5.3228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6429   -4.3809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3856   -4.8089    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0348   -4.2999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7112   -3.5410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2066   -2.8813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0256   -2.9805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3492   -3.7394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3071   -3.3673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7554   -2.5970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8538   -4.3991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3628   -5.0483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2637   -5.8674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9234   -6.3628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6822   -6.0391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3371   -6.6410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4876   -7.4896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7814   -5.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6717   -5.1149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4970   -5.4428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1217   -4.7247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3603   -3.9148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2109   -3.4540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6144   -6.3764    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7819   -7.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7220   -8.0921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6353   -7.3762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1760   -6.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9860   -6.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2552   -7.6897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7145   -8.3128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9045   -8.1561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7954   -6.2772    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4715   -7.1130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0666   -6.7791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2864   -5.6279    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4491   -5.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3730   -2.2322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7687   -1.6706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0478   -2.0718    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  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
 15 16  1  0  0  0  0
 14 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 24 27  2  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 19 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
 30 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  1  0  0  0
 39 42  1  0  0  0  0
  9 42  1  0  0  0  0
 42 43  1  1  0  0  0
 13 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 12 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0175442

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC(=O)O[C@@H]1[C@H](C)[C@](C)(O)[C@@H](C(=O)C2=CC=CC=C2)C2=C(C(OC)=C(OC)C(OC)=C2)C2=C(OC)C3=C(OCO3)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C36H42O10/c1-8-9-11-16-26(37)46-31-20(2)36(3,39)29(30(38)21-14-12-10-13-15-21)22-17-24(40-4)32(41-5)34(42-6)27(22)28-23(31)18-25-33(35(28)43-7)45-19-44-25/h10,12-15,17-18,20,29,31,39H,8-9,11,16,19H2,1-7H3/t20-,29+,31+,36-/m0/s1

> <INCHI_KEY>
UHZVOOFMWZABRC-BHNQFKMUSA-N

> <FORMULA>
C36H42O10

> <MOLECULAR_WEIGHT>
634.722

> <EXACT_MASS>
634.277797552

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
67.407417518155

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(8S,9S,10S,11R)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0^{2,7}.0^{14,18}]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate

> <ALOGPS_LOGP>
5.31

> <JCHEM_LOGP>
5.743108691333336

> <ALOGPS_LOGS>
-5.74

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.162257491633888

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.779489713217249

> <JCHEM_PKA_STRONGEST_BASIC>
-3.168699199819928

> <JCHEM_POLAR_SURFACE_AREA>
118.98000000000003

> <JCHEM_REFRACTIVITY>
169.9765

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.17e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(8S,9S,10S,11R)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0^{2,7}.0^{14,18}]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.546  -8.202   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.208  -8.966   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.143  -8.178   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.485  -9.009   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.740  -8.050   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.246  -8.480   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.744  -9.936   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       6.800  -8.178   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.186  -8.977   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.398  -8.027   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.794  -6.610   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.719  -5.378   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.248  -5.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.852  -6.980   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.640  -6.286   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      14.477  -4.848   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.927  -8.212   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.877  -9.424   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.692 -10.952   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.924 -11.877   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.340 -11.273   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      15.563 -12.397   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      15.844 -13.981   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.525  -9.744   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      16.187  -9.548   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      17.728 -10.160   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.294  -8.819   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.739  -7.308   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      15.327  -6.448   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.480 -11.903   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.793 -13.461   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      10.681 -15.105   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      12.386 -13.769   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.395 -12.606   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.907 -12.898   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      15.410 -14.354   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.400 -15.517   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.888 -15.225   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.951 -11.717   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.347 -13.278   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       7.591 -12.654   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.001 -10.505   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       6.438 -10.809   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      11.896  -4.167   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      10.768  -3.118   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       9.423  -3.867   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   42                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   46                                                  
CONECT   13   12   14   44                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   10   18                                                  
CONECT   18   17   19   27                                                  
CONECT   19   18   20   30                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   18   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   19   31   39                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   33                                                       
CONECT   39   30   40   41   42                                             
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   39    9   43                                                  
CONECT   43   42                                                            
CONECT   44   13   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   12                                                       
MASTER        0    0    0    0    0    0    0    0   46    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₄₂O₁₀

Average Mass

634.7220 Da

Monoisotopic Mass

634.27780 Da

IUPAC Name

(8S,9S,10S,11R)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0^{2,7}.0^{14,18}]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate

Traditional Name

(8S,9S,10S,11R)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0^{2,7}.0^{14,18}]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate

CAS Registry Number

Not Available

SMILES

CCCCCC(=O)O[C@@H]1[C@H](C)[C@](C)(O)[C@@H](C(=O)C2=CC=CC=C2)C2=C(C(OC)=C(OC)C(OC)=C2)C2=C(OC)C3=C(OCO3)C=C12

InChI Identifier

InChI=1S/C36H42O10/c1-8-9-11-16-26(37)46-31-20(2)36(3,39)29(30(38)21-14-12-10-13-15-21)22-17-24(40-4)32(41-5)34(42-6)27(22)28-23(31)18-25-33(35(28)43-7)45-19-44-25/h10,12-15,17-18,20,29,31,39H,8-9,11,16,19H2,1-7H3/t20-,29+,31+,36-/m0/s1

InChI Key

UHZVOOFMWZABRC-BHNQFKMUSA-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
Schisandra propinqua	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
Dibenzocyclooctane lignan
Alkyl-phenylketone
Benzodioxole
Phenylketone
Anisole
Aryl alkyl ketone
Aryl ketone
Benzoyl
Alkyl aryl ether
Fatty acid ester
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Tertiary alcohol
Carboxylic acid ester
Ketone
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Oxacycle
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Alcohol
Aldehyde
Hydrocarbon derivative
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	5.31	ALOGPS
logP	5.74	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	13.78	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	118.98 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	169.98 m³·mol⁻¹	ChemAxon
Polarizability	67.41 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

24627666

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

45270921

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate (NP0175442)

MOL for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

3D MOL for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

3D SDF for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

3D-SDF for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

PDB for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

3D PDB for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

SMILES for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

INCHI for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

Structure for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)

3D Structure for NP0175442 ((8s,9s,10s,11r)-8-benzoyl-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(19),2(7),3,5,12,14(18)-hexaen-11-yl hexanoate)