NP-MRD: Showing NP-Card for 5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate (NP0244785)

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Record Information

Version

2.0

Created at

2022-09-07 05:39:32 UTC

Updated at

2022-09-07 05:39:32 UTC

NP-MRD ID

NP0244785

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate

Description

2-{13-[5-(Acetyloxy)-2-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-5-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate belongs to the class of organic compounds known as p-benzoquinones. These are benzoquinones where the two C=O groups are attached at the 1- and 4-positions, respectively. 5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate is found in Ardisia teysmanniana. 2-{13-[5-(Acetyloxy)-2-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-5-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241502532D          

 41 42  0  0  0  0            999 V2000
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 11 39  1  0  0  0  0
  5 39  1  0  0  0  0
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 10 41  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004241502532D          

 41 42  0  0  0  0            999 V2000
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   12.1460   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 O   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
  2  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
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 26 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  2  0  0  0  0
 33 38  1  0  0  0  0
 11 39  1  0  0  0  0
  5 39  1  0  0  0  0
 39 40  2  0  0  0  0
 10 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0244785

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1=C(C)C(=O)C(O)=C(CCCCCCCCCCCCCC2=C(OC(C)=O)C(=O)C(C)=C(O)C2=O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H40O10/c1-18-24(34)28(38)23(31(26(18)36)41-21(4)33)17-15-13-11-9-7-5-6-8-10-12-14-16-22-27(37)25(35)19(2)30(29(22)39)40-20(3)32/h34,37H,5-17H2,1-4H3

> <INCHI_KEY>
AVPDKIQZUGDDMG-UHFFFAOYSA-N

> <FORMULA>
C31H40O10

> <MOLECULAR_WEIGHT>
572.651

> <EXACT_MASS>
572.262147488

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
63.393205729080805

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate

> <ALOGPS_LOGP>
4.30

> <JCHEM_LOGP>
5.803980859000001

> <ALOGPS_LOGS>
-6.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.777988598473479

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.175452207086164

> <JCHEM_PKA_STRONGEST_BASIC>
-5.326450382481416

> <JCHEM_POLAR_SURFACE_AREA>
161.34

> <JCHEM_REFRACTIVITY>
154.46740000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.19e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       5.335 -23.100   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335 -21.560   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.001 -20.790   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.668 -20.790   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.668 -19.250   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335 -18.480   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001 -19.250   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335 -16.940   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.001 -16.170   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002 -16.940   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336 -16.170   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669 -16.940   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.003 -16.170   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.337 -16.940   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.670 -16.170   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.004 -16.940   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      17.338 -16.170   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      18.672 -16.940   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.005 -16.170   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.339 -16.940   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      22.673 -16.170   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      24.006 -16.940   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.340 -16.170   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.674 -16.940   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      28.007 -16.170   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      28.007 -14.630   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      29.341 -13.860   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      29.341 -12.320   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      30.675 -14.630   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      29.341 -16.940   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      30.675 -16.170   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      29.341 -18.480   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      28.007 -19.250   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      28.007 -20.790   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      26.674 -18.480   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      25.340 -19.250   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      30.675 -19.250   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.002 -18.480   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       9.336 -19.250   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       6.668 -14.630   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   39                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   41                                                  
CONECT   11   10   12   39                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   36                                                  
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   26   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   38                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   25   37                                                  
CONECT   37   36                                                            
CONECT   38   33                                                            
CONECT   39   11    5   40                                                  
CONECT   40   39                                                            
CONECT   41   10                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

View in JSmol

Synonyms

Value	Source
2-{13-[5-(acetyloxy)-2-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-5-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetic acid	Generator

Chemical Formula

C₃₁H₄₀O₁₀

Average Mass

572.6510 Da

Monoisotopic Mass

572.26215 Da

IUPAC Name

5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate

Traditional Name

5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1=C(C)C(=O)C(O)=C(CCCCCCCCCCCCCC2=C(OC(C)=O)C(=O)C(C)=C(O)C2=O)C1=O

InChI Identifier

InChI=1S/C31H40O10/c1-18-24(34)28(38)23(31(26(18)36)41-21(4)33)17-15-13-11-9-7-5-6-8-10-12-14-16-22-27(37)25(35)19(2)30(29(22)39)40-20(3)32/h34,37H,5-17H2,1-4H3

InChI Key

AVPDKIQZUGDDMG-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
Ardisia teysmanniana Scheff.	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as p-benzoquinones. These are benzoquinones where the two C=O groups are attached at the 1- and 4-positions, respectively.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

P-benzoquinones

Alternative Parents

Substituents

P-benzoquinone
Dicarboxylic acid or derivatives
Vinylogous acid
Enol ester
Carboxylic acid ester
Enol
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	4.3	ALOGPS
logP	5.8	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	5.18	ChemAxon
pKa (Strongest Basic)	-5.3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	161.34 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	154.47 m³·mol⁻¹	ChemAxon
Polarizability	63.39 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

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

636534

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate (NP0244785)

MOL for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

3D MOL for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

3D SDF for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

3D-SDF for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

PDB for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

3D PDB for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

SMILES for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

INCHI for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

Structure for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)

3D Structure for NP0244785 (5-{13-[2-(acetyloxy)-5-hydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl]tridecyl}-4-hydroxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl acetate)