NP-MRD: Showing NP-Card for (1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione (NP0266619)

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Record Information

Version

2.0

Created at

2022-09-08 11:01:10 UTC

Updated at

2022-09-08 11:01:11 UTC

NP-MRD ID

NP0266619

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione

Description

(1R,2R,6S,7R,9S,13Z)-5-amino-4-[(2E,4E)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]Trideca-4,10-diene-3,12-dione belongs to the class of organic compounds known as o-quinomethanes. These are organic compounds containing a benzene ring conjugated to a methylidene group and a ketone at carbon atoms 1 and 2, respectively. Based on a literature review very few articles have been published on (1R,2R,6S,7R,9S,13Z)-5-amino-4-[(2E,4E)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]Trideca-4,10-diene-3,12-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082213012D          

 37 39  0  0  1  0            999 V2000
   -1.5079   -0.3618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7009   -0.5334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4460   -1.3180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3610   -1.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6159   -2.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4229   -2.4457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6778   -3.2303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9749   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9130   -0.8764    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2720   -0.4349    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5724    0.0023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  8 36  1  0  0  0  0
 36 37  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309082213012D          

 37 39  0  0  1  0            999 V2000
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  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  6  0  0  0
 11 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 33 25  1  6  0  0  0
 17 33  1  0  0  0  0
 33 34  1  0  0  0  0
 14 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
  8 36  1  0  0  0  0
 36 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0266619

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C\C=C\C(\O)=C1/[C@H]2[C@](C)(O[C@]3(O)[C@@]2(C)C(=O)C(C(=O)\C=C\C=C\C)=C(N)[C@]3(C)O)C(O)=C(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H33NO8/c1-7-9-11-13-16(30)18-20(32)15(3)23(33)26(5)21(18)25(4)24(34)19(17(31)14-12-10-8-2)22(29)27(6,35)28(25,36)37-26/h7-14,21,30,33,35-36H,29H2,1-6H3/b9-7+,10-8+,13-11+,14-12+,18-16+/t21-,25-,26+,27+,28-/m1/s1

> <INCHI_KEY>
SBJOOLHBCGISRK-XIWQPWFWSA-N

> <FORMULA>
C28H33NO8

> <MOLECULAR_WEIGHT>
511.571

> <EXACT_MASS>
511.220617027

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
53.47659313038504

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,6S,7R,9S,13Z)-5-amino-4-[(2E,4E)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-4,10-diene-3,12-dione

> <JCHEM_LOGP>
2.4609154270000007

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.793022073736852

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.4603110942065105

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9929781260598576

> <JCHEM_POLAR_SURFACE_AREA>
167.38

> <JCHEM_REFRACTIVITY>
145.3417

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,6S,7R,9S,13Z)-5-amino-4-[(2E,4E)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-4,10-diene-3,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.815  -0.675   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.308  -0.996   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.833  -2.460   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.674  -2.780   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.150  -4.245   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.656  -4.565   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.132  -6.030   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.687  -3.421   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.211  -1.956   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       1.704  -1.636   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       4.241  -0.812   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.935   0.004   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.818   0.616   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.747  -1.132   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.427   0.374   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       6.993  -0.227   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.239  -1.132   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.559   0.374   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.746  -0.812   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.221   0.653   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      10.776  -1.956   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.282  -1.636   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.300  -3.421   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.331  -4.565   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.794  -3.741   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.318  -5.206   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.348  -6.350   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.812  -5.526   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.336  -6.990   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.829  -7.311   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.353  -8.775   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.847  -9.095   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.763  -2.597   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.223  -2.597   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.850  -4.003   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.193  -3.741   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.669  -5.206   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                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   36                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15   16   34                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19   33                                             
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   33                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31                                                            
CONECT   33   25   17   34                                                  
CONECT   34   33   14   35   36                                             
CONECT   35   34                                                            
CONECT   36   34    8   37                                                  
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₃NO₈

Average Mass

511.5710 Da

Monoisotopic Mass

511.22062 Da

IUPAC Name

(1R,2R,6S,7R,9S,13Z)-5-amino-4-[(2E,4E)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2E,4E)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-4,10-diene-3,12-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

C\C=C\C=C\C(\O)=C1/[C@H]2[C@](C)(O[C@]3(O)[C@@]2(C)C(=O)C(C(=O)\C=C\C=C\C)=C(N)[C@]3(C)O)C(O)=C(C)C1=O

InChI Identifier

InChI=1S/C28H33NO8/c1-7-9-11-13-16(30)18-20(32)15(3)23(33)26(5)21(18)25(4)24(34)19(17(31)14-12-10-8-2)22(29)27(6,35)28(25,36)37-26/h7-14,21,30,33,35-36H,29H2,1-6H3/b9-7+,10-8+,13-11+,14-12+,18-16+/t21-,25-,26+,27+,28-/m1/s1

InChI Key

SBJOOLHBCGISRK-XIWQPWFWSA-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 o-quinomethanes. These are organic compounds containing a benzene ring conjugated to a methylidene group and a ketone at carbon atoms 1 and 2, respectively.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

O-quinomethanes

Alternative Parents

Substituents

O-quinomethane
Cyclohexenone
Acryloyl-group
Enone
Oxolane
Vinylogous amide
Vinylogous acid
Alpha,beta-unsaturated ketone
Tertiary alcohol
Hemiacetal
Enamine
Enol
Oxacycle
Organoheterocyclic compound
Polyol
Primary aliphatic amine
Hydrocarbon derivative
Organic oxide
Alcohol
Organonitrogen compound
Amine
Organic nitrogen compound
Primary amine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.46	ChemAxon
pKa (Strongest Acidic)	3.46	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	167.38 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	145.34 m³·mol⁻¹	ChemAxon
Polarizability	53.48 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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

30829905

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione (NP0266619)

MOL for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

3D MOL for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

3D SDF for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

3D-SDF for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

PDB for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

3D PDB for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

SMILES for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

INCHI for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

Structure for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)

3D Structure for NP0266619 ((1r,2r,6s,7r,9s,13z)-5-amino-4-[(2e,4e)-hexa-2,4-dienoyl]-6,7,10-trihydroxy-13-[(2e,4e)-1-hydroxyhexa-2,4-dien-1-ylidene]-2,6,9,11-tetramethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-4,10-diene-3,12-dione)