NP-MRD: Showing NP-Card for methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate (NP0223775)

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Record Information

Version

2.0

Created at

2022-09-06 01:57:52 UTC

Updated at

2022-09-06 01:57:52 UTC

NP-MRD ID

NP0223775

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate

Description

Methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]Tetradeca-2,4-diene-14-carboxylate belongs to the class of organic compounds known as cedrane and isocedrane sesquiterpenoids. These are sesquiternoids with a structure based on the cedrane or the isocedrane skeleton. Cedrane is a tricyclic molecules a 3,6,8,8-tetramethyl-1H-3a,7-methano-azulene moiety. Isocedrane is a rearranged cedrane arising from the migration of methyl group moved from the 6-position to the 4-position. methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate is found in Trixis antimenorrhoea. Based on a literature review very few articles have been published on methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]Tetradeca-2,4-diene-14-carboxylate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062203572D          

 26 29  0  0  0  0            999 V2000
   -1.5076    1.1887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6949    1.0468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1656    1.6797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4491    2.4545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7002    1.4339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2110    0.8374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6109    1.7064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9453    2.4606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7656    2.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2516    1.8816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0719    1.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5580    1.3025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2236    0.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7097   -0.1184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3753   -0.8726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5550   -0.9602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8614   -1.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5270   -2.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0131   -2.9601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7067   -2.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4033    0.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195   -0.2075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1344    0.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1862    0.7672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9173    1.1273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0970    1.0398    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 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  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 13 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
  5 24  1  0  0  0  0
 24 25  1  0  0  0  0
 10 25  1  0  0  0  0
 21 25  1  0  0  0  0
 25 26  1  0  0  0  0
  7 26  1  0  0  0  0
M  END


  Mrv1652309062203572D          

 26 29  0  0  0  0            999 V2000
   -1.5076    1.1887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6949    1.0468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1656    1.6797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4491    2.4545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7002    1.4339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2110    0.8374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6109    1.7064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9453    2.4606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7656    2.5482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2516    1.8816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0719    1.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5580    1.3025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2236    0.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7097   -0.1184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3753   -0.8726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5550   -0.9602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8614   -1.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5270   -2.2935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0131   -2.9601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7067   -2.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4033    0.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9195   -0.2075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1344    0.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1862    0.7672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9173    1.1273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0970    1.0398    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 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  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 13 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
  5 24  1  0  0  0  0
 24 25  1  0  0  0  0
 10 25  1  0  0  0  0
 21 25  1  0  0  0  0
 25 26  1  0  0  0  0
  7 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223775

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1(C)C2CC34C(CCC13)C(OC(=O)CC(C)C)OC=C4C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O5/c1-12(2)9-17(22)26-18-15-7-8-16-20(3,19(23)24-4)13-5-6-14(11-25-18)21(15,16)10-13/h5-6,11-13,15-16,18H,7-10H2,1-4H3

> <INCHI_KEY>
FNLVWVNGNLUSMJ-UHFFFAOYSA-N

> <FORMULA>
C21H28O5

> <MOLECULAR_WEIGHT>
360.45

> <EXACT_MASS>
360.193674002

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.49186726637198

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0^{4,12}.0^{8,12}]tetradeca-2,4-diene-14-carboxylate

> <JCHEM_LOGP>
3.2116982993333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.891291575573095

> <JCHEM_POLAR_SURFACE_AREA>
61.830000000000005

> <JCHEM_REFRACTIVITY>
96.5572

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0^{4,12}.0^{8,12}]tetradeca-2,4-diene-14-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.814   2.219   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.297   1.954   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.309   3.135   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.838   4.582   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.307   2.677   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.394   1.563   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.140   3.185   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.764   4.593   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.296   4.757   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.203   3.512   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.734   3.676   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.642   2.431   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.017   1.023   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.925  -0.221   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.301  -1.629   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.769  -1.792   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.208  -2.873   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.584  -4.281   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.491  -5.526   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.053  -4.445   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.486   0.860   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.583  -0.387   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.118   0.086   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.214   1.432   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.579   2.104   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.048   1.941   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   24                                             
CONECT    6    5                                                            
CONECT    7    5    8   26                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   25                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   13   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23    5   25                                                  
CONECT   25   24   10   21   26                                             
CONECT   26   25    7                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
Methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0,.0,]tetradeca-2,4-diene-14-carboxylic acid	Generator

Chemical Formula

C₂₁H₂₈O₅

Average Mass

360.4500 Da

Monoisotopic Mass

360.19367 Da

IUPAC Name

methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0^{4,12}.0^{8,12}]tetradeca-2,4-diene-14-carboxylate

Traditional Name

methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0^{4,12}.0^{8,12}]tetradeca-2,4-diene-14-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1(C)C2CC34C(CCC13)C(OC(=O)CC(C)C)OC=C4C=C2

InChI Identifier

InChI=1S/C21H28O5/c1-12(2)9-17(22)26-18-15-7-8-16-20(3,19(23)24-4)13-5-6-14(11-25-18)21(15,16)10-13/h5-6,11-13,15-16,18H,7-10H2,1-4H3

InChI Key

FNLVWVNGNLUSMJ-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
Trixis antimenorrhoea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cedrane and isocedrane sesquiterpenoids. These are sesquiternoids with a structure based on the cedrane or the isocedrane skeleton. Cedrane is a tricyclic molecules a 3,6,8,8-tetramethyl-1H-3a,7-methano-azulene moiety. Isocedrane is a rearranged cedrane arising from the migration of methyl group moved from the 6-position to the 4-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Cedrane and isocedrane sesquiterpenoids

Alternative Parents

Substituents

Isocedrane sesquiterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Methyl ester
Carboxylic acid ester
Oxacycle
Acetal
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
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	3.21	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	61.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	96.56 m³·mol⁻¹	ChemAxon
Polarizability	38.49 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163036134

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate (NP0223775)

MOL for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

3D MOL for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

3D SDF for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

3D-SDF for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

PDB for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

3D PDB for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

SMILES for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

INCHI for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

Structure for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)

3D Structure for NP0223775 (methyl 14-methyl-7-[(3-methylbutanoyl)oxy]-6-oxatetracyclo[9.2.1.0⁴,¹².0⁸,¹²]tetradeca-2,4-diene-14-carboxylate)