NP-MRD: Showing NP-Card for (1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate (NP0223490)

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Record Information

Version

2.0

Created at

2022-09-06 01:36:12 UTC

Updated at

2022-09-06 01:36:12 UTC

NP-MRD ID

NP0223490

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate

Description

(1R,2S,3S,5R,8E,11R,14R)-5,9,14-trimethyl-14-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]Tetradec-8-en-2-yl (2Z)-2-methylbut-2-enoate belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate is found in Daucus rouyi. Based on a literature review very few articles have been published on (1R,2S,3S,5R,8E,11R,14R)-5,9,14-trimethyl-14-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]Tetradec-8-en-2-yl (2Z)-2-methylbut-2-enoate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062203362D          

 32 34  0  0  1  0            999 V2000
    6.0728    0.9738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3538    1.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8353    1.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0793    1.4014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7816    0.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8111   -0.4799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1175   -0.4207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2094   -1.2405    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8735   -0.7510    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5376   -0.2615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6295   -1.0813    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4493   -0.9894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7214   -1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0573   -2.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3013   -2.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373   -2.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7292   -3.3698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8813   -2.2196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7894   -1.3997    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1186   -0.9194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3681   -0.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8786    0.5310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1931   -0.1273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9989    0.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1012    0.6925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7653    1.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5212    0.8517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6734    2.0019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3374    2.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9174    2.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2533    1.8427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4534   -0.9102    0.0000 C   0  0  1  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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 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
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  0  0  0  0
 32 23  1  1  0  0  0
  8 32  1  0  0  0  0
 19 32  1  0  0  0  0
M  END


  Mrv1652309062203362D          

 32 34  0  0  1  0            999 V2000
    6.0728    0.9738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3538    1.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8353    1.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0793    1.4014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7816    0.0689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8111   -0.4799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1175   -0.4207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2094   -1.2405    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8735   -0.7510    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5376   -0.2615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6295   -1.0813    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4493   -0.9894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7214   -1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0573   -2.3907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3013   -2.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373   -2.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7292   -3.3698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8813   -2.2196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7894   -1.3997    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1186   -0.9194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3681   -0.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8786    0.5310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1931   -0.1273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9989    0.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1012    0.6925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7653    1.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5212    0.8517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6734    2.0019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3374    2.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9174    2.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2533    1.8427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4534   -0.9102    0.0000 C   0  0  1  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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 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
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  0  0  0  0
 32 23  1  1  0  0  0
  8 32  1  0  0  0  0
 19 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223490

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@@H]1[C@@H]2O[C@]2(C)CC\C=C(C)\C[C@H]2OC(=O)[C@](C)(OC(=O)C(\C)=C/C)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O7/c1-8-15(4)21(26)30-19-18-17(13-14(3)11-10-12-24(6)20(19)31-24)29-23(28)25(18,7)32-22(27)16(5)9-2/h8-9,11,17-20H,10,12-13H2,1-7H3/b14-11+,15-8-,16-9-/t17-,18-,19+,20+,24-,25-/m1/s1

> <INCHI_KEY>
KXCUYZCPRWSGBR-SVGBSFFKSA-N

> <FORMULA>
C25H34O7

> <MOLECULAR_WEIGHT>
446.54

> <EXACT_MASS>
446.230453435

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.07867439407897

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,3S,5R,8E,11R,14R)-5,9,14-trimethyl-14-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0^{3,5}]tetradec-8-en-2-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
5.290143401333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.241412949923408

> <JCHEM_POLAR_SURFACE_AREA>
91.43

> <JCHEM_REFRACTIVITY>
119.25

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3S,5R,8E,11R,14R)-5,9,14-trimethyl-14-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0^{3,5}]tetradec-8-en-2-yl (2Z)-2-methylbut-2-enoate

> <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      11.336   1.818   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.994   2.573   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.026   1.999   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.615   2.616   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.926   0.129   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.847  -0.896   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       7.686  -0.785   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.858  -2.316   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.097  -1.402   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.337  -0.488   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.508  -2.019   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.039  -1.847   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.680  -3.549   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.440  -4.463   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.029  -3.846   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.790  -4.760   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.961  -6.290   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.378  -4.143   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.207  -2.613   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.955  -1.716   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.420  -0.248   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.507   0.991   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.960  -0.238   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.465   0.093   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.789   1.293   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.028   2.206   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.440   1.590   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       6.857   3.737   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.097   4.651   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.446   4.354   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.206   3.440   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.446  -1.699   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                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   32                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9   11                                                       
CONECT   11   10    9   12   13                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   32                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25   32                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30                                                            
CONECT   32   23    8   19                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
(1R,2S,3S,5R,8E,11R,14R)-5,9,14-Trimethyl-14-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0,]tetradec-8-en-2-yl (2Z)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₅H₃₄O₇

Average Mass

446.5400 Da

Monoisotopic Mass

446.23045 Da

IUPAC Name

(1R,2S,3S,5R,8E,11R,14R)-5,9,14-trimethyl-14-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0^{3,5}]tetradec-8-en-2-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(1R,2S,3S,5R,8E,11R,14R)-5,9,14-trimethyl-14-{[(2Z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0^{3,5}]tetradec-8-en-2-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@@H]1[C@@H]2O[C@]2(C)CC\C=C(C)\C[C@H]2OC(=O)[C@](C)(OC(=O)C(\C)=C/C)[C@@H]12

InChI Identifier

InChI=1S/C25H34O7/c1-8-15(4)21(26)30-19-18-17(13-14(3)11-10-12-24(6)20(19)31-24)29-23(28)25(18,7)32-22(27)16(5)9-2/h8-9,11,17-20H,10,12-13H2,1-7H3/b14-11+,15-8-,16-9-/t17-,18-,19+,20+,24-,25-/m1/s1

InChI Key

KXCUYZCPRWSGBR-SVGBSFFKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Daucus rouyi	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Germacrane sesquiterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	5.29	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	91.43 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	119.25 m³·mol⁻¹	ChemAxon
Polarizability	47.08 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

162855914

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate (NP0223490)

MOL for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

PDB for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

Structure for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0223490 ((1r,2s,3s,5r,8e,11r,14r)-5,9,14-trimethyl-14-{[(2z)-2-methylbut-2-enoyl]oxy}-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradec-8-en-2-yl (2z)-2-methylbut-2-enoate)