NP-MRD: Showing NP-Card for 1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione (NP0254665)

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Record Information

Version

2.0

Created at

2022-09-07 18:54:03 UTC

Updated at

2022-09-07 18:54:03 UTC

NP-MRD ID

NP0254665

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione

Description

Lucidin-omega-methyl ether belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. 1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione is found in Galium aparine, Morinda elliptica and Gynochthodes officinalis. 1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione was first documented in 2010 (PMID: 20966871). Based on a literature review a small amount of articles have been published on Lucidin-omega-methyl ether (PMID: 31876434) (PMID: 30286869) (PMID: 29970094) (PMID: 21979929).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
    5.5540    0.0006   -0.2520 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6490   -0.8904   -0.7719 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7921   -0.4197   -1.7051 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8688    0.5606   -1.4314 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7817    0.5702   -0.6111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7754    0.9919    0.6725 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9204    1.4719    1.2732 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5994    0.9645    1.4585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5669    0.5062    0.9279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5959    0.0764   -0.3584 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5436    0.1058   -1.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4878   -0.3296   -2.4072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8573   -0.4175   -0.9277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8908   -0.8184   -2.1229 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0846   -0.4579   -0.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2577   -0.9282   -0.7054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4396   -0.9823    0.0046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4156   -0.5474    1.3101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2330   -0.0743    1.8746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0572   -0.0237    1.1584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7998    0.4677    1.7230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7840    0.8584    2.9003 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1294    0.8783    0.2291 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3232    0.3061   -1.0401 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1652   -0.5612    0.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4475    0.0040   -2.5532 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2987   -1.2910   -2.2721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9040    1.7834    2.2304 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6462    1.3142    2.4871 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3034   -0.3033   -2.9886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2798   -1.2690   -1.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3724   -1.3443   -0.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3378   -0.5856    1.8764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2171    0.2643    2.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 21  1  0
 21 22  2  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  2  0
 15 13  1  0
 13 14  2  0
 13 10  1  0
 10 11  2  0
 11 12  1  0
 11  5  1  0
 10  9  1  0
 15 20  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  7 28  1  0
  8 29  1  0
 19 34  1  0
 18 33  1  0
 17 32  1  0
 16 31  1  0
 12 30  1  0
M  END


  Mrv1652309072220542D          

 22 24  0  0  0  0            999 V2000
    7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    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  1  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  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 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
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0254665

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COCOC1=C(O)C=C2C(=O)C3=CC=CC=C3C(=O)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C16H12O6/c1-21-7-22-16-11(17)6-10-12(15(16)20)14(19)9-5-3-2-4-8(9)13(10)18/h2-6,17,20H,7H2,1H3

> <INCHI_KEY>
JKWCMFFAFBMEMW-UHFFFAOYSA-N

> <FORMULA>
C16H12O6

> <MOLECULAR_WEIGHT>
300.266

> <EXACT_MASS>
300.063388106

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
29.567716849327418

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,3-dihydroxy-2-(methoxymethoxy)-9,10-dihydroanthracene-9,10-dione

> <JCHEM_LOGP>
2.867029599666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.401595114215027

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.819382575340571

> <JCHEM_PKA_STRONGEST_BASIC>
-4.220918220848204

> <JCHEM_POLAR_SURFACE_AREA>
93.06

> <JCHEM_REFRACTIVITY>
77.429

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      13.337  -0.000   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      12.003  -0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.001   3.850   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   11                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   21                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10    5   12                                                  
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15   21                                                  
CONECT   21   20    9   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

C₁₆H₁₂O₆

Average Mass

300.2660 Da

Monoisotopic Mass

300.06339 Da

IUPAC Name

1,3-dihydroxy-2-(methoxymethoxy)-9,10-dihydroanthracene-9,10-dione

Traditional Name

1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione

CAS Registry Number

Not Available

SMILES

COCOC1=C(O)C=C2C(=O)C3=CC=CC=C3C(=O)C2=C1O

InChI Identifier

InChI=1S/C16H12O6/c1-21-7-22-16-11(17)6-10-12(15(16)20)14(19)9-5-3-2-4-8(9)13(10)18/h2-6,17,20H,7H2,1H3

InChI Key

JKWCMFFAFBMEMW-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
Galium aparine	LOTUS Database	35616633
Morinda elliptica	LOTUS Database	35616633
Morinda officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Hydroxyanthraquinones

Alternative Parents

Substituents

Hydroxyanthraquinone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Vinylogous acid
Ketone
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aldehyde
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	2.87	ChemAxon
pKa (Strongest Acidic)	7.82	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	77.43 m³·mol⁻¹	ChemAxon
Polarizability	29.57 Å³	ChemAxon
Number of Rings	3	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

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102138994

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Chokchaisiri S, Siriwattanasathien Y, Thongbamrer C, Suksamrarn A, Rukachaisirikul T: Morindaquinone, a new bianthraquinone from Morinda coreia roots. Nat Prod Res. 2021 Oct;35(20):3439-3445. doi: 10.1080/14786419.2019.1705820. Epub 2019 Dec 26. [PubMed:31876434 ]
Khanh PN, Huong TT, Spiga O, Trezza A, Son NT, Cuong TD, Ha VT, Cuong NM: In silico screening of anthraquinones from Prismatomeris memecyloides as novel phosphodiesterase type-5 inhibitors (PDE-5Is). Rev Int Androl. 2018 Oct - Dec;16(4):147-158. doi: 10.1016/j.androl.2017.07.001. Epub 2017 Dec 20. [PubMed:30286869 ]
Bajpai VK, Alam MB, Quan KT, Choi HJ, An H, Ju MK, Lee SH, Huh YS, Han YK, Na M: Cytotoxic properties of the anthraquinone derivatives isolated from the roots of Rubia philippinensis. BMC Complement Altern Med. 2018 Jul 3;18(1):200. doi: 10.1186/s12906-018-2253-2. [PubMed:29970094 ]
Endale M, Alao JP, Akala HM, Rono NK, Eyase FL, Derese S, Ndakala A, Mbugua M, Walsh DS, Sunnerhagen P, Erdelyi M, Yenesew A: Antiplasmodial quinones from Pentas longiflora and Pentas lanceolata. Planta Med. 2012 Jan;78(1):31-5. doi: 10.1055/s-0031-1280179. Epub 2011 Oct 6. [PubMed:21979929 ]
Osman CP, Ismail NH, Ahmad R, Ahmat N, Awang K, Jaafar FM: Anthraquinones with antiplasmodial activity from the roots of Rennellia elliptica Korth. (Rubiaceae). Molecules. 2010 Oct 20;15(10):7218-26. doi: 10.3390/molecules15107218. [PubMed:20966871 ]
LOTUS database [Link]

Showing NP-Card for 1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione (NP0254665)

MOL for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

3D MOL for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

3D SDF for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

3D-SDF for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

PDB for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

3D PDB for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

SMILES for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

INCHI for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

Structure for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)

3D Structure for NP0254665 (1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione)