NP-MRD: Showing NP-Card for [(2s,4r,5s,6s,7s)-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 (NP0203142)

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Record Information

Version

2.0

Created at

2022-09-04 22:31:48 UTC

Updated at

2022-09-04 22:31:48 UTC

NP-MRD ID

NP0203142

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2s,4r,5s,6s,7s)-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

[(2S,4R,5S,6S,7S)-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 steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. [(2s,4r,5s,6s,7s)-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 Rodgersia podophylla. Based on a literature review very few articles have been published on [(2S,4R,5S,6S,7S)-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

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052200312D          

 45 49  0  0  1  0            999 V2000
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    4.0145   -1.0164    0.0000 O   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


  Mrv1652309052200312D          

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   -0.1105    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855    4.6993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    4.6993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    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
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  2  0  0  0  0
 18 26  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  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  1  0  0  0  0
 35 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 33 41  1  0  0  0  0
 29 42  1  0  0  0  0
 11 42  1  0  0  0  0
 42 43  1  1  0  0  0
 43 44  1  0  0  0  0
  7 44  1  0  0  0  0
 44 45  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0203142

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C2C(=O)O[C@@H]3[C@@H](OC(=O)C4=CC(O)=C(O)C(O)=C4)[C@@H](O)[C@@H](COC(=O)C4=CC(O)=C(O)C(O)=C4)O[C@H]3C2=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/t16-,20+,23+,24+,25+/m1/s1

> <INCHI_KEY>
LASUFZXDCFZCRI-WVUHNRQOSA-N

> <FORMULA>
C28H24O17

> <MOLECULAR_WEIGHT>
632.483

> <EXACT_MASS>
632.101349313

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
59.09269404405985

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2S,4R,5S,6S,7S)-5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate

> <JCHEM_LOGP>
1.9423848019999999

> <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

> <JCHEM_TRADITIONAL_IUPAC>
[(2S,4R,5S,6S,7S)-5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate

> <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       6.724  -3.231   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.494  -1.897   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.034   0.770   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.414  -1.897   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.104  -0.564   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.206  -1.897   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.564  -3.231   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.206  -4.565   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.746  -4.565   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.564  -5.898   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.104  -5.898   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.874  -7.232   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.414  -7.232   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.104  -8.566   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.874  -9.899   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.564  -8.566   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.206  -9.899   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.206  -7.232   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.746   3.437   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.516   2.104   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -2.516   4.771   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -4.056   4.771   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -4.826   6.105   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -6.366   6.105   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -4.056   7.438   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -4.826   8.772   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -2.516   7.438   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -1.746   8.772   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -1.746   6.105   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       2.874   3.437   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       5.184   4.771   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   44                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9                                                            
CONECT   11    8   12   42                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   18                                                       
CONECT   27   13   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   42                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   41                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   33                                                       
CONECT   42   29   11   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43    7   45                                                  
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
[(2S,4R,5S,6S,7S)-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

Chemical Formula

C₂₈H₂₄O₁₇

Average Mass

632.4830 Da

Monoisotopic Mass

632.10135 Da

IUPAC Name

[(2S,4R,5S,6S,7S)-5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate

Traditional Name

[(2S,4R,5S,6S,7S)-5,12,14-trihydroxy-13-methoxy-9-oxo-6-(3,4,5-trihydroxybenzoyloxy)-3,8-dioxatricyclo[8.4.0.0^{2,7}]tetradeca-1(14),10,12-trien-4-yl]methyl 3,4,5-trihydroxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C2C(=O)O[C@@H]3[C@@H](OC(=O)C4=CC(O)=C(O)C(O)=C4)[C@@H](O)[C@@H](COC(=O)C4=CC(O)=C(O)C(O)=C4)O[C@H]3C2=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/t16-,20+,23+,24+,25+/m1/s1

InChI Key

LASUFZXDCFZCRI-WVUHNRQOSA-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
Rodgersia podophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

Steroid lactone
3-hydroxysteroid
Oxosteroid
16-oxosteroid
1-hydroxysteroid
Hydroxysteroid
Galloyl ester
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
Benzoate ester
Benzopyran
Isochromane
2-benzopyran
Tricarboxylic acid or derivatives
Benzoic acid or derivatives
Pyrogallol derivative
Benzenetriol
Anisole
Benzoyl
Phenol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Oxane
Monosaccharide
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Lactone
Carboxylic acid ester
Polyol
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	1.94	ChemAxon
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	59.09 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

162878742

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2s,4r,5s,6s,7s)-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 (NP0203142)

MOL for NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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 NP0203142 ([(2s,4r,5s,6s,7s)-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)