NP-MRD: Showing NP-Card for 3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal (NP0266119)

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Record Information

Version

2.0

Created at

2022-09-08 10:21:01 UTC

Updated at

2022-09-08 10:21:01 UTC

NP-MRD ID

NP0266119

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal

Description

3-[2,3,4,6-Tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxo-5H-benzo[7]annulen-7-yl]prop-2-enal belongs to the class of organic compounds known as tropolones. Tropolones are compounds containing tropone ring with a hydroxyl group at ring position 2. 3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal is found in Fomes fomentarius. 3-[2,3,4,6-Tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxo-5H-benzo[7]annulen-7-yl]prop-2-enal is a moderately basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
    6.8738   -1.9716   -0.0167 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6743   -2.2686    0.1306 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6086   -1.2810   -0.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3507   -1.5954    0.0185 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1727   -0.8076   -0.1824 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9348   -1.3810    0.1700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1834   -0.7012    0.5671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6634    0.5035    0.0510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0186    0.6127    0.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9280   -0.4187    0.5283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7555   -1.6883    0.4427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8471   -2.6269    0.9342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2353   -3.3854    1.9421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5507    1.8619   -0.2098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9274    2.0697   -0.1543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7558    2.9107   -0.6010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3269    4.1340   -0.9265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3931    2.7608   -0.6739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4798    3.7533   -1.0578 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1591    1.5438   -0.3450 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5496    1.5796   -0.5200 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1284    2.6726   -0.5026 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3319    0.4426   -0.7166 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3953    0.6497   -1.5724 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4033   -3.2487    0.4544 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9451   -0.3146   -0.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1757   -2.6373    0.3545 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9044   -2.4320    0.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7935   -1.0581    1.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8778   -0.0219    0.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9339   -2.1966    0.0103 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2226   -3.2318    0.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6893   -2.0497    1.3585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6809   -4.2479    2.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2822    2.9724   -0.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7772    4.9115   -1.2129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1619    4.6637   -1.3121 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5928    1.5214   -2.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 18 20  1  0
 20  8  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  2  0
  5 23  2  0
 23 24  1  0
 23 21  1  0
 21 22  2  0
  8  9  1  0
 21 20  1  0
 13 34  1  0
 12 32  1  0
 12 33  1  0
 11 31  1  0
 10 30  1  0
 15 35  1  0
 17 36  1  0
 19 37  1  0
  7 29  1  0
  6 28  1  0
  4 27  1  0
  3 26  1  0
  2 25  1  0
 24 38  1  0
M  END


  Mrv1533004171508502D          

 24 25  0  0  0  0            999 V2000
   -0.2228   -4.4191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4917   -4.0066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4917   -3.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2062   -2.7691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2062   -1.9441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4917   -1.5316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2228   -1.9441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4917   -0.7066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2228   -0.2941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2062   -0.2941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2062    0.5309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9206   -0.7066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5656   -0.1923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3821    0.6120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3700   -0.3758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7279   -1.1191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5529   -1.1191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9654   -1.8336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7904   -1.8336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2029   -1.1191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3700   -1.8624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5656   -2.0460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9206   -1.5316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8843    0.2692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
  5 23  1  0  0  0  0
 12 23  2  0  0  0  0
 15 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266119

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC=CC1=C(O)C(O)=C(O)C2=C1C=CC(C=CC=O)=C(O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O7/c18-7-1-3-9-5-6-10-11(4-2-8-19)14(21)17(24)16(23)12(10)15(22)13(9)20/h1-7,19,21,23-24H,8H2,(H,20,22)

> <INCHI_KEY>
DGZLOXRFKKMNBH-UHFFFAOYSA-N

> <FORMULA>
C17H14O7

> <MOLECULAR_WEIGHT>
330.292

> <EXACT_MASS>
330.073952791

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
32.91467351268423

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxo-5H-benzo[7]annulen-7-yl]prop-2-enal

> <ALOGPS_LOGP>
1.83

> <JCHEM_LOGP>
1.4308048333333332

> <ALOGPS_LOGS>
-3.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.630290493017224

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.282497624736511

> <JCHEM_PKA_STRONGEST_BASIC>
2.8871866939313704

> <JCHEM_POLAR_SURFACE_AREA>
135.29

> <JCHEM_REFRACTIVITY>
91.4995

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.49e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  O   UNK     0      -0.416  -8.249   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       0.918  -7.479   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.918  -5.939   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.251  -5.169   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.251  -3.629   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.918  -2.859   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.416  -3.629   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.918  -1.319   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.416  -0.549   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.251  -0.549   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.251   0.991   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.585  -1.319   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.789  -0.359   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.447   1.142   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.291  -0.702   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.959  -2.089   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.499  -2.089   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.269  -3.423   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.809  -3.423   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      11.579  -2.089   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.291  -3.477   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.789  -3.819   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.585  -2.859   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.251   0.502   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   23                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   24                                                  
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   16   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    5   12                                                  
CONECT   24   15                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₇

Average Mass

330.2920 Da

Monoisotopic Mass

330.07395 Da

IUPAC Name

3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxo-5H-benzo[7]annulen-7-yl]prop-2-enal

Traditional Name

3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal

CAS Registry Number

Not Available

SMILES

OCC=CC1=C(O)C(O)=C(O)C2=C1C=CC(C=CC=O)=C(O)C2=O

InChI Identifier

InChI=1S/C17H14O7/c18-7-1-3-9-5-6-10-11(4-2-8-19)14(21)17(24)16(23)12(10)15(22)13(9)20/h1-7,19,21,23-24H,8H2,(H,20,22)

InChI Key

DGZLOXRFKKMNBH-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
Fomes fomentarius	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tropolones. Tropolones are compounds containing tropone ring with a hydroxyl group at ring position 2.

Kingdom

Organic compounds

Super Class

Hydrocarbon derivatives

Class

Tropones

Sub Class

Tropolones

Direct Parent

Tropolones

Alternative Parents

Substituents

Tropolone
Styrene
Benzenoid
Vinylogous acid
Enal
Alpha,beta-unsaturated aldehyde
Polyol
Organic oxygen compound
Organic oxide
Primary alcohol
Organooxygen compound
Carbonyl group
Aldehyde
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	1.83	ALOGPS
logP	1.43	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	6.28	ChemAxon
pKa (Strongest Basic)	2.89	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	135.29 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	91.5 m³·mol⁻¹	ChemAxon
Polarizability	32.91 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal (NP0266119)

MOL for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

3D MOL for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

3D SDF for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

3D-SDF for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

PDB for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

3D PDB for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

SMILES for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

INCHI for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

Structure for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)

3D Structure for NP0266119 (3-[2,3,4,6-tetrahydroxy-1-(3-hydroxyprop-1-en-1-yl)-5-oxobenzo[7]annulen-7-yl]prop-2-enal)