NP-MRD: Showing NP-Card for (8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione (NP0322976)

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Record Information

Version

2.0

Created at

2022-09-12 02:06:00 UTC

Updated at

2022-09-12 02:06:00 UTC

NP-MRD ID

NP0322976

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione

Description

Alpha,beta-Dehydrocurvularin, also known as α,β-dehydrocurvularin, belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. (8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione was first documented in 2003 (PMID: 14577643). Based on a literature review a small amount of articles have been published on alpha,beta-Dehydrocurvularin (PMID: 33902419) (PMID: 16190620).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
   -3.1723    2.6446    0.6547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4346    2.0692   -0.5613 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6810    0.5784   -0.5464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4416    0.0502    0.8094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4838   -1.1306    0.8522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4482   -1.7673   -0.4945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4655   -2.2066   -1.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9596   -2.2412   -0.9380 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5667   -3.2742   -1.4280 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8576   -1.3324   -0.2213 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8893   -1.9067    0.5633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9984   -3.2923    0.6283 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8069   -1.1897    1.2768 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7210    0.1830    1.2280 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6472    0.9234    1.9481 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7233    0.7619    0.4693 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7930    0.0281   -0.2535 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8033    0.8652   -0.9932 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0158    1.7146   -0.0834 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4909    1.8290    1.1162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1061    2.3340   -0.4422 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9699    1.9677    0.9996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4784    2.8224    1.4990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5656    3.6392    0.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9198    2.4173   -1.5014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1532    0.0678   -1.3761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7672    0.4535   -0.8026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0115    0.8370    1.4565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4314   -0.1861    1.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9423   -1.8079    1.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4985   -0.8715    1.2514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4725   -1.8573   -0.9052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7770   -2.6397   -2.2049 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7279   -3.6937    1.1831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5898   -1.6239    1.8726 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3988    1.1560    2.9001 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7046    1.8646    0.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3313    1.5787   -1.6954 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1948    0.2350   -1.6252 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  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21  2  1  0
 17 10  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  6
  3 26  1  0
  3 27  1  0
  4 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  7 33  1  0
 12 34  1  0
 13 35  1  0
 15 36  1  0
 16 37  1  0
 18 38  1  0
 18 39  1  0
M  END


  Mrv1652309122204062D          

 21 22  0  0  0  0            999 V2000
    7.4701    1.7627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6906    1.4927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5347    0.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1583    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0024   -0.6677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2228   -0.9377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5992   -0.3976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8196   -0.6677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6637   -1.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1960   -0.1276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4164   -0.3976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2605   -1.2078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7928    0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9487    0.9526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3251    1.4927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7283    1.2226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3519    0.6825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1315    0.9526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2874    1.7627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6637    2.3028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0669    2.0328    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  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
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
  2 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322976

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC\C=C\C(=O)C2=C(O)C=C(O)C=C2CC(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C16H18O5/c1-10-5-3-2-4-6-13(18)16-11(8-15(20)21-10)7-12(17)9-14(16)19/h4,6-7,9-10,17,19H,2-3,5,8H2,1H3/b6-4+

> <INCHI_KEY>
AVIRMQMUBGNCKS-GQCTYLIASA-N

> <FORMULA>
C16H18O5

> <MOLECULAR_WEIGHT>
290.315

> <EXACT_MASS>
290.11542368

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
29.045082220764783

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11,13-dihydroxy-4-methyl-2,4,5,6,7,10-hexahydro-1H-3-benzoxacyclododecine-2,10-dione

> <JCHEM_LOGP>
3.332512509999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.730255217482085

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.889643954561168

> <JCHEM_PKA_STRONGEST_BASIC>
-5.025747186283387

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
78.7097

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1H-3-benzoxacyclododecine-2,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      13.944   3.290   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.489   2.786   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.198   1.274   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.362   0.266   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.071  -1.246   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.616  -1.750   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.452  -0.742   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.997  -1.246   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.706  -2.759   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.833  -0.238   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.377  -0.742   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.086  -2.254   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.213   0.266   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.504   1.778   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.340   2.786   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.959   2.282   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.124   1.274   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.579   1.778   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.870   3.290   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.706   4.299   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      11.325   3.794   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   17                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   10   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    2                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Value	Source
a,b-Dehydrocurvularin	Generator
Α,β-dehydrocurvularin	Generator
beta,gamma-Dehydrocurvularin	MeSH
Dehydrocurvularin	MeSH

Chemical Formula

C₁₆H₁₈O₅

Average Mass

290.3150 Da

Monoisotopic Mass

290.11542 Da

IUPAC Name

11,13-dihydroxy-4-methyl-2,4,5,6,7,10-hexahydro-1H-3-benzoxacyclododecine-2,10-dione

Traditional Name

11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1H-3-benzoxacyclododecine-2,10-dione

CAS Registry Number

Not Available

SMILES

CC1CCC\C=C\C(=O)C2=C(O)C=C(O)C=C2CC(=O)O1

InChI Identifier

InChI=1S/C16H18O5/c1-10-5-3-2-4-6-13(18)16-11(8-15(20)21-10)7-12(17)9-14(16)19/h4,6-7,9-10,17,19H,2-3,5,8H2,1H3/b6-4+

InChI Key

AVIRMQMUBGNCKS-GQCTYLIASA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Vinylogous acid
Carboxylic acid ester
Ketone
Lactone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
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	3.33	ChemAxon
pKa (Strongest Acidic)	7.89	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	78.71 m³·mol⁻¹	ChemAxon
Polarizability	29.05 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

C00016018

Chemspider ID

20058741

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14314897

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Singh S, Verma S, Yadav DK, Kumar A, Tyagi R, Gupta P, Bawankule DU, Darokar MP, Srivastava SK, Kalra A: The Bioactive Potential of Culturable Fungal Endophytes Isolated From the Leaf of Catharanthus roseus (L.) G. Don. Curr Top Med Chem. 2021;21(10):895-907. doi: 10.2174/1568026621666210426123437. [PubMed:33902419 ]
Gutierrez M, Theoduloz C, Rodriguez J, Lolas M, Schmeda-Hirschmann G: Bioactive metabolites from the fungus Nectria galligena, the main apple canker agent in Chile. J Agric Food Chem. 2005 Oct 5;53(20):7701-8. doi: 10.1021/jf051021l. [PubMed:16190620 ]
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LOTUS database [Link]

Showing NP-Card for (8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione (NP0322976)

MOL for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

3D MOL for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

3D SDF for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

3D-SDF for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

PDB for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

3D PDB for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

SMILES for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

INCHI for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

Structure for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)

3D Structure for NP0322976 ((8e)-11,13-dihydroxy-4-methyl-4,5,6,7-tetrahydro-1h-3-benzoxacyclododecine-2,10-dione)