NP-MRD: Showing NP-Card for (1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one (NP0309050)

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Record Information

Version

1.0

Created at

2022-09-11 03:20:26 UTC

Updated at

2022-09-11 03:20:27 UTC

NP-MRD ID

NP0309050

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one

Description

(1S,11R,12S,13S,14R)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]Hexadeca-3(16),4,6-trien-8-one 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. (1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one is found in Eucalyptus viminalis. Based on a literature review very few articles have been published on (1S,11R,12S,13S,14R)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]Hexadeca-3(16),4,6-trien-8-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          2D

 36 38  0  0  0  0  0  0  0  0999 V2000
   -0.8358   -6.3193    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9926   -4.8275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777   -4.2174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1277   -2.9184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500   -1.2990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8703   -0.6101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6203   -1.9091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4635   -3.4009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4598   -4.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9339   -4.8927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1474   -4.0110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5177   -4.6211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9906   -2.5192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2042   -1.6376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1595    1.8121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895    2.7762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6491    0.9642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1314   -4.0331    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8560   -2.5941    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3038   -1.8724    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9554   -0.3630    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9408   -3.6613    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0907   -6.3845    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7313   -3.7395    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0474   -0.1458    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4895    2.7762    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4200    3.2893    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1595    1.8121    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6386    3.7404    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6491   -0.9642    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0586    0.4512    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 15  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  7 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
  9 10  2  0
 19 21  1  0
  6  5  1  0
 10 11  1  0
 22 36  1  0
 21 35  1  1
  5 25  1  6
  4 23  1  0
  4 24  1  0
 12 28  1  0
 14 29  1  0
 16 30  1  0
  7 26  1  6
 17 31  1  1
 18 32  1  0
 19 33  1  6
 20 34  1  0
 10 27  1  0
M  END


  Mrv1652309112205202D          

 22 24  0  0  1  0            999 V2000
    2.3964    1.4836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8914    0.8236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6872    1.0414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4590    0.7499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9120    0.0605    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2737   -0.4622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4071   -1.2763    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5618   -1.6254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7900   -1.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9993   -0.5359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4128    0.0444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6170   -0.1735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4078   -0.9715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6121   -1.1893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9943   -1.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7851   -2.3497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1789   -1.5678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3124   -2.3819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8172   -1.0452    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5890   -1.3367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6838   -0.2310    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3221    0.2916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  6  0  0  0
  7  6  1  6  0  0  0
  7  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
  2 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0309050

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1[C@H]2COC(=O)C3=CC(O)=C(O)C(O[C@H](O2)[C@H](O)[C@H]1O)=C3

> <INCHI_IDENTIFIER>
InChI=1S/C13H14O9/c14-5-1-4-2-6(8(5)15)21-13-11(18)10(17)9(16)7(22-13)3-20-12(4)19/h1-2,7,9-11,13-18H,3H2/t7-,9-,10+,11-,13-/m1/s1

> <INCHI_KEY>
ZPIQZFYXEPWEAP-JEUROIALSA-N

> <FORMULA>
C13H14O9

> <MOLECULAR_WEIGHT>
314.246

> <EXACT_MASS>
314.063782031

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
27.398068789717588

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,11R,12S,13S,14R)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1^{3,7}]hexadeca-3(16),4,6-trien-8-one

> <JCHEM_LOGP>
-0.8834642096666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.813224512913218

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.595699365256525

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6491105016628502

> <JCHEM_POLAR_SURFACE_AREA>
145.91000000000003

> <JCHEM_REFRACTIVITY>
67.90910000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,11R,12S,13S,14R)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1^{3,7}]hexadeca-3(16),4,6-trien-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  O   UNK     0       4.473   2.769   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.397   1.537   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.883   1.944   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.323   1.400   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.169   0.113   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.978  -0.863   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.227  -2.382   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.649  -3.034   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.208  -2.490   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.599  -1.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.504   0.083   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.018  -0.324   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.628  -1.813   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.143  -2.220   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.723  -2.897   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.332  -4.386   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.667  -2.927   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.916  -4.446   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.859  -1.951   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.300  -2.495   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      10.610  -0.431   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      11.801   0.544   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10    2   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    9   16                                                  
CONECT   16   15                                                            
CONECT   17    7   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    5   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₁₄O₉

Average Mass

314.2460 Da

Monoisotopic Mass

314.06378 Da

IUPAC Name

(1S,11R,12S,13S,14R)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1^{3,7}]hexadeca-3(16),4,6-trien-8-one

Traditional Name

(1S,11R,12S,13S,14R)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1^{3,7}]hexadeca-3(16),4,6-trien-8-one

CAS Registry Number

Not Available

SMILES

O[C@@H]1[C@H]2COC(=O)C3=CC(O)=C(O)C(O[C@H](O2)[C@H](O)[C@H]1O)=C3

InChI Identifier

InChI=1S/C13H14O9/c14-5-1-4-2-6(8(5)15)21-13-11(18)10(17)9(16)7(22-13)3-20-12(4)19/h1-2,7,9-11,13-18H,3H2/t7-,9-,10+,11-,13-/m1/s1

InChI Key

ZPIQZFYXEPWEAP-JEUROIALSA-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
Eucalyptus viminalis	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
Gallic acid or derivatives
Dihydroxybenzoic acid
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Monosaccharide
Oxane
Carboxylic acid ester
Lactone
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Polyol
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organic oxide
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	-0.88	ChemAxon
pKa (Strongest Acidic)	8.6	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	145.91 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	67.91 m³·mol⁻¹	ChemAxon
Polarizability	27.4 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

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KNApSAcK ID

Not Available

Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

162861374

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one (NP0309050)

MOL for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

3D MOL for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

3D SDF for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

3D-SDF for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

PDB for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

3D PDB for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

SMILES for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

INCHI for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

Structure for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)

3D Structure for NP0309050 ((1s,11r,12s,13s,14r)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.1³,⁷]hexadeca-3(16),4,6-trien-8-one)