NP-MRD: Showing NP-Card for (1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate (NP0155738)

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Record Information

Version

2.0

Created at

2022-09-02 12:50:56 UTC

Updated at

2022-09-02 12:50:56 UTC

NP-MRD ID

NP0155738

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate

Description

(1S,2R,5R,6S,9R,10S,11S,14R,15S,16S,17R)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]Octadec-12-en-17-yl acetate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate is found in Erythropodium caribaeorum. Based on a literature review very few articles have been published on (1S,2R,5R,6S,9R,10S,11S,14R,15S,16S,17R)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]Octadec-12-en-17-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022214502D          

 37 40  0  0  1  0            999 V2000
    2.1086    3.5177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6281    2.8767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4318    3.1067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1591    2.6797    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8101    3.1864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3987    1.8556    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7749    1.3685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2508    0.8261    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8592    0.0556    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2691   -0.6604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0279    0.1060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5042   -0.5314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.5248    1.3308    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.4123    2.1938    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
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    4.3103   -1.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1030   -1.9362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7712    0.4139    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9676    1.2152    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    7.5469   -0.2666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7433    0.5347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1426   -0.8374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3669   -0.1569    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8173   -0.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5696   -0.9566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3636   -1.1809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1036   -0.8163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5663   -1.9806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
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  4  5  1  1  0  0  0
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  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
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 14 13  1  1  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  1  0  0  0
  8 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
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 22 17  1  6  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
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 32 34  1  1  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309022214502D          

 37 40  0  0  1  0            999 V2000
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    7.1036   -0.8163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5663   -1.9806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  1  6  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  1  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  1  0  0  0
  8 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 22 17  1  6  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 27 32  1  0  0  0  0
 22 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  1  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0155738

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C(=O)O[C@H]2[C@@H](Cl)C(=C)C[C@@H](O)[C@H]3O[C@]12[C@H](OC(C)=O)[C@H]1[C@](C)(OC(C)=O)[C@H](OC(C)=O)C=C[C@]31C

> <INCHI_IDENTIFIER>
InChI=1S/C26H33ClO10/c1-11-10-16(31)20-24(6)9-8-17(33-13(3)28)25(7,36-15(5)30)19(24)22(34-14(4)29)26(37-20)12(2)23(32)35-21(26)18(11)27/h8-9,12,16-22,31H,1,10H2,2-7H3/t12-,16+,17+,18-,19+,20+,21-,22+,24-,25+,26+/m0/s1

> <INCHI_KEY>
KXNLSRXVKAYMIV-RYKOITHNSA-N

> <FORMULA>
C26H33ClO10

> <MOLECULAR_WEIGHT>
540.99

> <EXACT_MASS>
540.176225

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
52.382394829207925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5R,6S,9R,10S,11S,14R,15S,16S,17R)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0^{1,5}.0^{11,16}]octadec-12-en-17-yl acetate

> <ALOGPS_LOGP>
2.28

> <JCHEM_LOGP>
1.3416647286666674

> <ALOGPS_LOGS>
-3.94

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.100142145287354

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1923978256513115

> <JCHEM_POLAR_SURFACE_AREA>
134.66000000000003

> <JCHEM_REFRACTIVITY>
126.99249999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.20e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5R,6S,9R,10S,11S,14R,15S,16S,17R)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0^{1,5}.0^{11,16}]octadec-12-en-17-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       3.936   6.566   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.906   5.370   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.406   5.799   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.764   5.002   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.979   5.948   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.211   3.464   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.046   2.555   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.068   1.542   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.337   0.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.102  -1.233   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.785   0.198   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.808  -0.992   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       3.396   1.687   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.713   2.484   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.172   3.986   0.000  0.00  0.00           C+0
HETATM   16 Cl   UNK     0       2.636   4.095   0.000  0.00  0.00          Cl+0
HETATM   17  C   UNK     0       7.336   0.447   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.949  -1.043   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.046  -2.124   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.530  -1.714   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.659  -3.614   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.906   0.773   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.273   2.268   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.699   3.748   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.752   2.699   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.864   1.633   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.497   0.137   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.609  -0.928   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      14.088  -0.498   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.454   0.998   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      15.200  -1.563   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      10.018  -0.293   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.992  -1.441   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      10.397  -1.786   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      11.879  -2.204   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.260  -1.524   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.257  -3.697   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14   17                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14    2   16                                                  
CONECT   16   15                                                            
CONECT   17    8   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23   32                                                  
CONECT   23   22    6   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   27   22   33   34                                             
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,5R,6S,9R,10S,11S,14R,15S,16S,17R)-14,15-Bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0,.0,]octadec-12-en-17-yl acetic acid	Generator

Chemical Formula

C₂₆H₃₃ClO₁₀

Average Mass

540.9900 Da

Monoisotopic Mass

540.17622 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1C(=O)O[C@H]2[C@@H](Cl)C(=C)C[C@@H](O)[C@H]3O[C@]12[C@H](OC(C)=O)[C@H]1[C@](C)(OC(C)=O)[C@H](OC(C)=O)C=C[C@]31C

InChI Identifier

InChI=1S/C26H33ClO10/c1-11-10-16(31)20-24(6)9-8-17(33-13(3)28)25(7,36-15(5)30)19(24)22(34-14(4)29)26(37-20)12(2)23(32)35-21(26)18(11)27/h8-9,12,16-22,31H,1,10H2,2-7H3/t12-,16+,17+,18-,19+,20+,21-,22+,24-,25+,26+/m0/s1

InChI Key

KXNLSRXVKAYMIV-RYKOITHNSA-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
Erythropodium caribaeorum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Briarane diterpenoid
Tetracarboxylic acid or derivatives
Gamma butyrolactone
Oxane
Tetrahydrofuran
Carboxylic acid ester
Lactone
Secondary alcohol
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Organochloride
Organohalogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Alkyl halide
Alkyl chloride
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	2.28	ALOGPS
logS	-3.9	ALOGPS

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

163050553

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate (NP0155738)

MOL for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

3D MOL for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

3D SDF for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

3D-SDF for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

PDB for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

3D PDB for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

SMILES for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

INCHI for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

Structure for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)

3D Structure for NP0155738 ((1s,2r,5r,6s,9r,10s,11s,14r,15s,16s,17r)-14,15-bis(acetyloxy)-6-chloro-9-hydroxy-2,11,15-trimethyl-7-methylidene-3-oxo-4,18-dioxatetracyclo[8.7.1.0¹,⁵.0¹¹,¹⁶]octadec-12-en-17-yl acetate)