NP-MRD: Showing NP-Card for 3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate (NP0285721)

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Record Information

Version

2.0

Created at

2022-09-09 14:00:46 UTC

Updated at

2022-09-09 14:00:46 UTC

NP-MRD ID

NP0285721

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate

Description

Pterocaryanin B, also known as 5,5-dnads, 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. Pterocaryanin B is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, pterocaryanin b has been detected, but not quantified in, nuts. 3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate is found in Lotus corniculatus. This could make pterocaryanin b a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241220292D          

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M  END

     RDKit          3D

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M  END


  Mrv0541 02241220292D          

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    1.8142    1.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2264    2.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0514    2.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7940    3.0102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0715    2.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4843    3.3401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8142    3.3401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8861    0.1231    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8861   -0.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1440   -1.1134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1440   -1.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8861   -2.3505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5458   -1.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5458   -1.1134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2885   -0.7006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2885   -2.3505    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
  2 20  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4 22  1  0  0  0  0
  5  6  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 34  1  0  0  0  0
  9 10  1  0  0  0  0
  9 30  1  0  0  0  0
 10 11  2  0  0  0  0
 10 15  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 34  2  0  0  0  0
 14 15  1  0  0  0  0
 14 21  1  0  0  0  0
 15 16  2  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 29  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 40  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 32  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 36  1  0  0  0  0
 32 33  1  0  0  0  0
 34 35  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 43  2  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 42 45  1  0  0  0  0
 43 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0285721

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC1OC(O)C2OC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(O)C(O)=C(O)C=C3C(=O)OC2C1OC(=O)C1=CC(O)=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H22O18/c28-5-13-21(43-24(38)6-1-9(29)16(33)10(30)2-6)22-23(27(41)42-13)45-26(40)8-4-12(32)18(35)20(37)15(8)14-7(25(39)44-22)3-11(31)17(34)19(14)36/h1-4,13,21-23,27-37,41H,5H2

> <INCHI_KEY>
XFEDUHVHOZXTGB-UHFFFAOYSA-N

> <FORMULA>
C27H22O18

> <MOLECULAR_WEIGHT>
634.4528

> <EXACT_MASS>
634.0806139

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
56.45763292016616

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(22),2(7),3,5,18,20-hexaen-14-yl 3,4,5-trihydroxybenzoate

> <ALOGPS_LOGP>
1.70

> <JCHEM_LOGP>
1.095251979

> <ALOGPS_LOGS>
-2.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.927834095792827

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.4100682413372105

> <JCHEM_PKA_STRONGEST_BASIC>
-5.548940638051083

> <JCHEM_POLAR_SURFACE_AREA>
310.65999999999997

> <JCHEM_REFRACTIVITY>
142.29569999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.58e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(22),2(7),3,5,18,20-hexaen-14-yl 3,4,5-trihydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0       4.773  -3.617   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.233  -3.617   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.464  -4.848   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.924  -4.848   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.153  -6.235   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.385  -6.235   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.308   6.235   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.462   4.848   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.308   3.617   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.462   2.232   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.000   2.232   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.771   3.617   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -4.310   3.617   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       0.153  -0.847   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.615   0.385   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.155   0.385   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       5.696   0.385   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.002   0.385   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.233  -0.847   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.464  -2.232   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.924  -2.232   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.153  -3.617   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.385  -3.617   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.616  -4.388   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.616  -5.926   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.005   3.617   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.465   3.617   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.696   2.232   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.156   2.232   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.387   3.617   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.156   4.848   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.696   4.848   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.082   5.619   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -2.000   4.848   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -2.771   6.235   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       3.387   6.235   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -5.387   0.230   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -5.387  -1.308   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -4.002  -2.078   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -4.002  -3.617   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -5.387  -4.388   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -6.619  -3.617   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -6.619  -2.078   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -8.005  -1.308   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      -8.005  -4.388   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   22                                                  
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    8                                                            
CONECT    8    7    9   34                                                  
CONECT    9    8   10   30                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   34                                                  
CONECT   13   12                                                            
CONECT   14   15   21                                                       
CONECT   15   10   14   16                                                  
CONECT   16   15                                                            
CONECT   17   18                                                            
CONECT   18   17   19   29                                                  
CONECT   19   18   20                                                       
CONECT   20    2   19   21                                                  
CONECT   21   14   20   22                                                  
CONECT   22    4   21   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   40                                                  
CONECT   25   24                                                            
CONECT   26   27                                                            
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   18   28   30                                                  
CONECT   30    9   29   31                                                  
CONECT   31   30   32   36                                                  
CONECT   32   27   31   33                                                  
CONECT   33   32                                                            
CONECT   34    8   12   35                                                  
CONECT   35   34                                                            
CONECT   36   31                                                            
CONECT   37   38                                                            
CONECT   38   37   39   43                                                  
CONECT   39   38   40                                                       
CONECT   40   24   39   41                                                  
CONECT   41   40   42                                                       
CONECT   42   41   43   45                                                  
CONECT   43   38   42   44                                                  
CONECT   44   43                                                            
CONECT   45   42                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
5,5-Dnads	HMDB
3,4,5,11,20,21,22-Heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(22),2,4,6,18,20-hexaen-14-yl 3,4,5-trihydroxybenzoic acid	Generator

Chemical Formula

C₂₇H₂₂O₁₈

Average Mass

634.4528 Da

Monoisotopic Mass

634.08061 Da

IUPAC Name

3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(22),2(7),3,5,18,20-hexaen-14-yl 3,4,5-trihydroxybenzoate

Traditional Name

3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(22),2(7),3,5,18,20-hexaen-14-yl 3,4,5-trihydroxybenzoate

CAS Registry Number

Not Available

SMILES

OCC1OC(O)C2OC(=O)C3=C(C(O)=C(O)C(O)=C3)C3=C(O)C(O)=C(O)C=C3C(=O)OC2C1OC(=O)C1=CC(O)=C(O)C(O)=C1

InChI Identifier

InChI=1S/C27H22O18/c28-5-13-21(43-24(38)6-1-9(29)16(33)10(30)2-6)22-23(27(41)42-13)45-26(40)8-4-12(32)18(35)20(37)15(8)14-7(25(39)44-22)3-11(31)17(34)19(14)36/h1-4,13,21-23,27-37,41H,5H2

InChI Key

XFEDUHVHOZXTGB-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
Lotus corniculatus	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
Galloyl ester
Gallic acid or derivatives
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
Benzoate ester
Pyrogallol derivative
Benzenetriol
Benzoic acid or derivatives
Tricarboxylic acid or derivatives
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Phenol
Monosaccharide
Monocyclic benzene moiety
Oxane
Benzenoid
Carboxylic acid ester
Hemiacetal
Lactone
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Polyol
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
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	1.7	ALOGPS
logP	1.1	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	7.41	ChemAxon
pKa (Strongest Basic)	-5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	310.66 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	142.3 m³·mol⁻¹	ChemAxon
Polarizability	56.46 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	No	ChemAxon

External Links

HMDB ID

HMDB0039743

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB019389

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

14057218

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate (NP0285721)

MOL for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

3D MOL for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

3D SDF for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

3D-SDF for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

PDB for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

3D PDB for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

SMILES for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

INCHI for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

Structure for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)

3D Structure for NP0285721 (3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.0²,⁷.0¹⁰,¹⁵]docosa-1(18),2,4,6,19,21-hexaen-14-yl 3,4,5-trihydroxybenzoate)