NP-MRD: Showing NP-Card for 3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one (NP0302082)

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Record Information

Version

2.0

Created at

2022-09-10 15:25:21 UTC

Updated at

2022-09-10 15:25:22 UTC

NP-MRD ID

NP0302082

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one

Description

3-(2,6-Dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]Hept-2-en-3-yl}-1,2-dihydropyridin-2-one belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group. 3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one is found in Coniochaeta cephalothecoides. Based on a literature review very few articles have been published on 3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]Hept-2-en-3-yl}-1,2-dihydropyridin-2-one.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309102217252D          

 31 35  0  0  0  0            999 V2000
    5.4776   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9066    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6571    2.1487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3342    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6197    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3342    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9066    2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6210    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9066    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6210    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 18 25  1  0  0  0  0
 17 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  2  0  0  0  0
  6 31  1  0  0  0  0
  2 31  1  0  0  0  0
M  END


  Mrv1652309102217252D          

 31 35  0  0  0  0            999 V2000
    5.4776   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9066    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6571    2.1487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4776    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3342    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6197    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3342    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0487    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1921    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9066    2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.6210    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9066    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6210    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 18 25  1  0  0  0  0
 17 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  2  0  0  0  0
  6 31  1  0  0  0  0
  2 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0302082

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C=CC2CC(C)=CCC2C1C(=O)C1=C(O)C(=CN(O)C1=O)C1=C(O)C2OC2CC1

> <INCHI_IDENTIFIER>
InChI=1S/C24H27NO6/c1-11-3-6-14-13(9-11)5-4-12(2)18(14)22(28)19-20(26)16(10-25(30)24(19)29)15-7-8-17-23(31-17)21(15)27/h3-5,10,12-14,17-18,23,26-27,30H,6-9H2,1-2H3

> <INCHI_KEY>
VULUABIEBSBZBB-UHFFFAOYSA-N

> <FORMULA>
C24H27NO6

> <MOLECULAR_WEIGHT>
425.481

> <EXACT_MASS>
425.183837593

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
45.15557032150001

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}-1,2-dihydropyridin-2-one

> <JCHEM_LOGP>
2.075515755

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.632833761439724

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.924751212825813

> <JCHEM_PKA_STRONGEST_BASIC>
-4.251555762151465

> <JCHEM_POLAR_SURFACE_AREA>
110.6

> <JCHEM_REFRACTIVITY>
117.63219999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      10.225  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.225  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.559  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.559  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.225  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.891  -1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.558  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.558   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.891   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.891   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.225   0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.559   1.540   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.892   0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.559   3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.225   3.850   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.693   4.011   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      10.225   5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.891   6.160   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.558   5.390   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.558   3.850   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.224   6.160   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.890   6.930   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.224   7.700   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.558   8.470   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.891   7.700   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.559   6.160   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0      12.892   5.390   0.000  0.00  0.00           N+0
HETATM   28  O   UNK     0      14.226   6.160   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      12.892   3.850   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      14.226   3.080   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.891  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7   31                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    5   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   29                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   26                                                  
CONECT   18   17   19   25                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21   23                                                       
CONECT   23   22   21   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   18                                                       
CONECT   26   17   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   14   30                                                  
CONECT   30   29                                                            
CONECT   31    6    2                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₇NO₆

Average Mass

425.4810 Da

Monoisotopic Mass

425.18384 Da

IUPAC Name

3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}-1,2-dihydropyridin-2-one

Traditional Name

3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one

CAS Registry Number

Not Available

SMILES

CC1C=CC2CC(C)=CCC2C1C(=O)C1=C(O)C(=CN(O)C1=O)C1=C(O)C2OC2CC1

InChI Identifier

InChI=1S/C24H27NO6/c1-11-3-6-14-13(9-11)5-4-12(2)18(14)22(28)19-20(26)16(10-25(30)24(19)29)15-7-8-17-23(31-17)21(15)27/h3-5,10,12-14,17-18,23,26-27,30H,6-9H2,1-2H3

InChI Key

VULUABIEBSBZBB-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Coniochaeta cephalothecoides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Aryl alkyl ketones

Alternative Parents

Substituents

Aryl alkyl ketone
Hydroxypyridine
Pyridinone
Dihydropyridine
Pyridine
Hydropyridine
Heteroaromatic compound
Vinylogous amide
Vinylogous acid
Lactam
Oxacycle
Azacycle
Organoheterocyclic compound
Ether
Oxirane
Enol
Dialkyl ether
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen 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	2.08	ChemAxon
pKa (Strongest Acidic)	5.92	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	110.6 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	117.63 m³·mol⁻¹	ChemAxon
Polarizability	45.16 Å³	ChemAxon
Number of Rings	5	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

162814722

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one (NP0302082)

MOL for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

3D MOL for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

3D SDF for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

3D-SDF for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

PDB for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

3D PDB for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

SMILES for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

INCHI for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

Structure for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)

3D Structure for NP0302082 (3-(2,6-dimethyl-1,2,4a,5,8,8a-hexahydronaphthalene-1-carbonyl)-1,4-dihydroxy-5-{2-hydroxy-7-oxabicyclo[4.1.0]hept-2-en-3-yl}pyridin-2-one)