NP-MRD: Showing NP-Card for [5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate (NP0240171)

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Record Information

Version

2.0

Created at

2022-09-06 23:54:56 UTC

Updated at

2022-09-06 23:54:57 UTC

NP-MRD ID

NP0240171

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate

Description

[5,12,14-Trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]Tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. [5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate is found in Mallotus japonicus and Rodgersia podophylla. [5,12,14-Trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]Tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231514152D          

 45 49  0  0  0  0            999 V2000
    2.4454   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5079    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.3954    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3954    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 69 73  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004231514152D          

 45 49  0  0  0  0            999 V2000
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    6.1579   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9829   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -5.8263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -6.5408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -5.8263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -6.5408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    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
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  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  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  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
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 16 24  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 32 40  1  0  0  0  0
 27 41  1  0  0  0  0
 41 42  1  0  0  0  0
 11 42  1  0  0  0  0
 42 43  1  0  0  0  0
  7 43  1  0  0  0  0
 43 44  2  0  0  0  0
  3 44  1  0  0  0  0
 44 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240171

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C2C(=O)OC3C(OC(=O)C4=CC(O)=C(O)C(O)=C4)C(O)C(COC(=O)C4=CC(O)=C(O)C(O)=C4)OC3C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C28H24O17/c1-41-22-15(33)6-10-17(21(22)37)23-25(45-28(10)40)24(44-27(39)9-4-13(31)19(35)14(32)5-9)20(36)16(43-23)7-42-26(38)8-2-11(29)18(34)12(30)3-8/h2-6,16,20,23-25,29-37H,7H2,1H3

> <INCHI_KEY>
LASUFZXDCFZCRI-UHFFFAOYSA-N

> <FORMULA>
C28H24O17

> <MOLECULAR_WEIGHT>
632.483

> <EXACT_MASS>
632.101349313

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
58.91522711803418

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,12,14-trihydroxy-13-methoxy-9-oxo-4-[(3,4,5-trihydroxybenzoyloxy)methyl]-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-6-yl 3,4,5-trihydroxybenzoate

> <ALOGPS_LOGP>
2.24

> <JCHEM_LOGP>
1.9423848019999999

> <ALOGPS_LOGS>
-2.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.260527238960565

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.743047675267242

> <JCHEM_PKA_STRONGEST_BASIC>
-4.8610714097506245

> <JCHEM_POLAR_SURFACE_AREA>
279.42999999999995

> <JCHEM_REFRACTIVITY>
144.89469999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.11e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,12,14-trihydroxy-13-methoxy-9-oxo-4-[(3,4,5-trihydroxybenzoyloxy)methyl]-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-6-yl 3,4,5-trihydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       4.565  -5.541   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.795  -4.207   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.255  -1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.105   2.461   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       8.415   1.127   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.495   1.127   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.725   2.461   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.185   2.461   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      11.495   3.795   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.725   5.128   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.495   6.462   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.725   7.796   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      13.035   6.462   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      13.805   7.796   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      13.805   5.128   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      15.345   5.128   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      13.035   3.795   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      13.035  -1.540   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.495  -4.207   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.725  -5.541   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      11.495  -6.875   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      13.035  -6.875   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      10.725  -8.208   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.495  -9.542   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.725 -10.876   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      11.495 -12.209   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       9.185 -10.876   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       8.415 -12.209   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       8.415  -9.542   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       6.875  -9.542   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       9.185  -8.208   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       9.185  -2.874   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       6.875  -4.207   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   44                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   43                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   42                                                  
CONECT   12   11   13   25                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   16                                                       
CONECT   25   12   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   41                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   40                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   32                                                       
CONECT   41   27   42                                                       
CONECT   42   41   11   43                                                  
CONECT   43   42    7   44                                                  
CONECT   44   43    3   45                                                  
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
[5,12,14-Trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0,]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoic acid	Generator
[5,12,14-Trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoic acid	Generator

Chemical Formula

C₂₈H₂₄O₁₇

Average Mass

632.4830 Da

Monoisotopic Mass

632.10135 Da

IUPAC Name

5,12,14-trihydroxy-13-methoxy-9-oxo-4-[(3,4,5-trihydroxybenzoyloxy)methyl]-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-6-yl 3,4,5-trihydroxybenzoate

Traditional Name

5,12,14-trihydroxy-13-methoxy-9-oxo-4-[(3,4,5-trihydroxybenzoyloxy)methyl]-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-6-yl 3,4,5-trihydroxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C2C(=O)OC3C(OC(=O)C4=CC(O)=C(O)C(O)=C4)C(O)C(COC(=O)C4=CC(O)=C(O)C(O)=C4)OC3C2=C1O

InChI Identifier

InChI=1S/C28H24O17/c1-41-22-15(33)6-10-17(21(22)37)23-25(45-28(10)40)24(44-27(39)9-4-13(31)19(35)14(32)5-9)20(36)16(43-23)7-42-26(38)8-2-11(29)18(34)12(30)3-8/h2-6,16,20,23-25,29-37H,7H2,1H3

InChI Key

LASUFZXDCFZCRI-UHFFFAOYSA-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
Mallotus japonicus	LOTUS Database	35616633
Rodgersia podophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Dicarboxylic acid or derivatives
Tetrahydrofuran
Amino acid or derivatives
Carboxylic acid ester
Lactone
Tertiary amine
Tertiary aliphatic amine
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Amine
Organic oxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.24	ALOGPS
logP	1.94	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	7.74	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	279.43 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	144.89 m³·mol⁻¹	ChemAxon
Polarizability	58.92 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14464346

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate (NP0240171)

MOL for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

3D MOL for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

3D SDF for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

3D-SDF for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

PDB for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

3D PDB for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

SMILES for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

INCHI for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

Structure for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)

3D Structure for NP0240171 ([5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0²,⁷]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate)