NP-MRD: Showing NP-Card for (2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal (NP0248068)

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Record Information

Version

2.0

Created at

2022-09-07 10:10:22 UTC

Updated at

2022-09-07 10:10:22 UTC

NP-MRD ID

NP0248068

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal

Description

Gaudichaudione A belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. (2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal is found in Garcinia gaudichaudii. (2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal was first documented in 2002 (PMID: 11914953). Based on a literature review very few articles have been published on Gaudichaudione A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072212102D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309072212102D          

 40 44  0  0  1  0            999 V2000
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    3.5301   -2.2113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7385   -1.9494    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8969   -1.1183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7739   -0.1984    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1160    0.3417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2427    0.6786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4570    1.2697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6432   -0.3433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3906   -0.7820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6577    0.2806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3069    0.8082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1764    1.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4057    1.9171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8166    2.1432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6861    2.9578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0034   -1.5568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2367   -1.9962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3842   -0.6937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0504   -0.1206    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
  2  4  2  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 25 24  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 30 37  1  0  0  0  0
 23 37  1  0  0  0  0
 37 38  2  0  0  0  0
 30 39  1  0  0  0  0
 21 39  1  0  0  0  0
 25 39  1  0  0  0  0
 39 40  1  0  0  0  0
 15 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0248068

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C(O)C(CC=C(C)C)=C2OC34[C@@H]5C[C@H](C=C3C(=O)C2=C1O)C(=O)[C@@]4(C\C=C(/C)C=O)OC5(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C33H38O7/c1-17(2)8-10-21-26(35)22(11-9-18(3)4)29-25(27(21)36)28(37)23-14-20-15-24-31(6,7)40-32(30(20)38,33(23,24)39-29)13-12-19(5)16-34/h8-9,12,14,16,20,24,35-36H,10-11,13,15H2,1-7H3/b19-12+/t20-,24+,32+,33?/m0/s1

> <INCHI_KEY>
NTZQQDZXDGOJFE-HLGCXJDMSA-N

> <FORMULA>
C33H38O7

> <MOLECULAR_WEIGHT>
546.66

> <EXACT_MASS>
546.261753564

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
60.489945482456285

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-4-[(1R,13R,15S)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0^{2,11}.0^{2,15}.0^{4,9}]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal

> <JCHEM_LOGP>
6.411851167

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.296014702168344

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.5677866436868095

> <JCHEM_PKA_STRONGEST_BASIC>
-4.0157707038912775

> <JCHEM_POLAR_SURFACE_AREA>
110.13000000000001

> <JCHEM_REFRACTIVITY>
156.3409

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-4-[(1R,13R,15S)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0^{2,11}.0^{2,15}.0^{4,9}]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal

> <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      17.741   0.002   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.471  -0.869   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.590  -2.405   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.082  -0.205   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.773  -1.103   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.173  -0.883   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.637   0.561   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      12.642   1.786   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.119   0.818   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.942   2.480   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.683   3.904   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.855   5.203   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.566   6.569   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.317   5.135   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.137  -0.368   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.673  -1.812   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.191  -2.069   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      11.659  -3.591   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.773  -3.123   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.457  -4.631   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.249  -2.682   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.590  -4.128   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.112  -3.639   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.407  -2.088   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.178  -0.370   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.950   0.638   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.320   1.267   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.586   2.370   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.067  -0.641   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.462  -1.460   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.961   0.524   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.173   1.509   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.929   3.029   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.491   3.579   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.124   4.001   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       6.881   5.521   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       3.740  -2.906   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       2.308  -3.726   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       6.317  -1.295   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       7.561  -0.225   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                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    9   16   40                                                  
CONECT   16   15   17   19                                                  
CONECT   17   16    6   18                                                  
CONECT   18   17                                                            
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   39                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   37                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   39                                                  
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   30                                                       
CONECT   30   29   31   37   39                                             
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35                                                            
CONECT   37   30   23   38                                                  
CONECT   38   37                                                            
CONECT   39   30   21   25   40                                             
CONECT   40   39   15                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   88    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₃₈O₇

Average Mass

546.6600 Da

Monoisotopic Mass

546.26175 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(O)C(CC=C(C)C)=C2OC34[C@@H]5C[C@H](C=C3C(=O)C2=C1O)C(=O)[C@@]4(C\C=C(/C)C=O)OC5(C)C

InChI Identifier

InChI=1S/C33H38O7/c1-17(2)8-10-21-26(35)22(11-9-18(3)4)29-25(27(21)36)28(37)23-14-20-15-24-31(6,7)40-32(30(20)38,33(23,24)39-29)13-12-19(5)16-34/h8-9,12,14,16,20,24,35-36H,10-11,13,15H2,1-7H3/b19-12+/t20-,24+,32+,33?/m0/s1

InChI Key

NTZQQDZXDGOJFE-HLGCXJDMSA-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
Garcinia gaudichaudii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthones

Alternative Parents

Substituents

Xanthone
Chromone
Aromatic monoterpenoid
Monoterpenoid
Aryl ketone
Alkyl aryl ether
Phenol
Oxepane
Cyclohexenone
Benzenoid
Vinylogous acid
Alpha,beta-unsaturated aldehyde
Oxolane
Enal
Ketone
Ether
Dialkyl ether
Oxacycle
Organooxygen compound
Organic oxide
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Aldehyde
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00030118

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

101949804

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wu X, Cao S, Goh S, Hsu A, Tan BK: Mitochondrial destabilisation and caspase-3 activation are involved in the apoptosis of Jurkat cells induced by gaudichaudione A, a cytotoxic xanthone. Planta Med. 2002 Mar;68(3):198-203. doi: 10.1055/s-2002-23142. [PubMed:11914953 ]
LOTUS database [Link]

Showing NP-Card for (2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal (NP0248068)

MOL for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

3D MOL for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

3D SDF for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

3D-SDF for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

PDB for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

3D PDB for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

SMILES for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

INCHI for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

Structure for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)

3D Structure for NP0248068 ((2e)-4-[(1r,13r,15s)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-en-1-yl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.0²,¹¹.0²,¹⁵.0⁴,⁹]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal)