NP-MRD: Showing NP-Card for (11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate (NP0305531)

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Record Information

Version

1.0

Created at

2022-09-10 21:26:30 UTC

Updated at

2022-09-10 21:26:31 UTC

NP-MRD ID

NP0305531

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate

Description

Angustifolin A 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. (11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate is found in Kadsura angustifolia. Based on a literature review very few articles have been published on Angustifolin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102223262D          

 46 52  0  0  1  0            999 V2000
    1.5692    1.0074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3206    1.8705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4188    2.6383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0021    3.2217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7886    4.0186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    4.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    3.6488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    3.6488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309102223262D          

 46 52  0  0  1  0            999 V2000
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   -0.8016    1.9033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6164    2.0323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7455    2.8472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    5.0571    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7643    5.4891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8966    6.3199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2559    6.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6671    6.6149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3078    6.0951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0782    6.3901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2080    7.2049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5673    7.7246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7968    7.4296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5834    5.6405    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2879    6.4785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4084    5.6405    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6810    6.4506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9917    5.0571    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7566    5.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0482    6.3015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5196    6.9348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8611    6.4426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1452    7.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9580    7.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4867    6.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2026    5.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3897    5.8093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7372    2.8472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6082    2.0323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7933    1.9033    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  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 12 19  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 24 29  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
  7 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 38 43  1  0  0  0  0
  5 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
  4 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0305531

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2OCOC2=CC2=C1C1=C(C=C3OCOC3=C1OC)[C@H](OC(=O)C1=CC=CC=C1)[C@@H](C)[C@@H](C)[C@@H]2OC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C36H32O10/c1-19-20(2)30(46-36(38)22-13-9-6-10-14-22)24-16-26-32(44-18-42-26)34(40-4)28(24)27-23(15-25-31(33(27)39-3)43-17-41-25)29(19)45-35(37)21-11-7-5-8-12-21/h5-16,19-20,29-30H,17-18H2,1-4H3/t19-,20+,29+,30-

> <INCHI_KEY>
QIICHKIGEITIKP-MNVPHMDFSA-N

> <FORMULA>
C36H32O10

> <MOLECULAR_WEIGHT>
624.642

> <EXACT_MASS>
624.19954723

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
64.4106083298703

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(11R,12S,13R,14S)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0^{2,10}.0^{4,8}.0^{17,21}]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate

> <JCHEM_LOGP>
7.262773003999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.249124028176669

> <JCHEM_POLAR_SURFACE_AREA>
107.98000000000002

> <JCHEM_REFRACTIVITY>
164.75480000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(11R,12S,13R,14S)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0^{2,10}.0^{4,8}.0^{17,21}]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       2.929   1.880   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.465   3.492   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.028   5.323   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.515   4.925   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.604   6.014   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.205   7.501   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.718   7.900   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.629   6.811   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.089   6.811   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.000   7.900   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.488   7.501   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.886   6.014   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.797   4.925   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.690   5.323   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.661   4.101   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.245   2.386   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.496   3.553   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.017   3.794   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.258   5.315   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.000   9.440   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.427  10.246   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.674  11.797   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.478  12.767   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -3.112  12.348   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.308  11.378   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -5.746  11.928   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.988  13.449   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.792  14.419   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.354  13.869   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.089  10.529   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.537  12.093   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.629  10.529   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.138  12.041   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.718   9.440   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.146  10.279   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       5.690  11.763   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       4.703  12.945   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       7.207  12.026   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.738  13.472   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       9.255  13.736   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      10.242  12.553   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       9.711  11.108   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.194  10.844   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       6.976   5.315   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       6.735   3.794   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       5.214   3.553   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5   46                                                  
CONECT    5    4    6   44                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   34                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   20                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13    9   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   13   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   12                                                       
CONECT   20   10   21   30                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   24                                                       
CONECT   30   20   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32    7   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   43                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   38                                                       
CONECT   44    5   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45    4                                                       
MASTER        0    0    0    0    0    0    0    0   46    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₃₂O₁₀

Average Mass

624.6420 Da

Monoisotopic Mass

624.19955 Da

IUPAC Name

(11R,12S,13R,14S)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0^{2,10}.0^{4,8}.0^{17,21}]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate

Traditional Name

(11R,12S,13R,14S)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0^{2,10}.0^{4,8}.0^{17,21}]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate

CAS Registry Number

Not Available

SMILES

COC1=C2OCOC2=CC2=C1C1=C(C=C3OCOC3=C1OC)[C@H](OC(=O)C1=CC=CC=C1)[C@@H](C)[C@@H](C)[C@@H]2OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C36H32O10/c1-19-20(2)30(46-36(38)22-13-9-6-10-14-22)24-16-26-32(44-18-42-26)34(40-4)28(24)27-23(15-25-31(33(27)39-3)43-17-41-25)29(19)45-35(37)21-11-7-5-8-12-21/h5-16,19-20,29-30H,17-18H2,1-4H3/t19-,20+,29+,30-

InChI Key

QIICHKIGEITIKP-MNVPHMDFSA-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
Kadsura angustifolia	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
Benzoate ester
Benzodioxole
Benzoic acid or derivatives
Anisole
Benzoyl
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Oxacycle
Ether
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Organic oxide
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	7.26	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	107.98 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	164.75 m³·mol⁻¹	ChemAxon
Polarizability	64.41 Å³	ChemAxon
Number of Rings	7	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

102316916

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate (NP0305531)

MOL for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

3D MOL for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

3D SDF for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

3D-SDF for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

PDB for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

3D PDB for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

SMILES for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

INCHI for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

Structure for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)

3D Structure for NP0305531 ((11r,12s,13r,14s)-14-(benzoyloxy)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.0²,¹⁰.0⁴,⁸.0¹⁷,²¹]docosa-1(15),2(10),3,8,16,21-hexaen-11-yl benzoate)