NP-MRD: Showing NP-Card for (1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate (NP0160414)

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Record Information

Version

2.0

Created at

2022-09-02 18:21:53 UTC

Updated at

2022-09-02 18:21:53 UTC

NP-MRD ID

NP0160414

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate

Description

Excavatolide J belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate is found in Briareum excavatum. Based on a literature review very few articles have been published on Excavatolide J.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022220212D          

 45 48  0  0  1  0            999 V2000
    4.4763   -4.7535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4387   -3.9294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7061   -3.5499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6685   -2.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3634   -2.2811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9360   -2.3462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8984   -1.5221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    4.2506    0.1913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.6781    0.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8232    0.1262    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 41 42  1  6  0  0  0
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 43 45  2  0  0  0  0
M  END

     RDKit          2D

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M  END


  Mrv1652309022220212D          

 45 48  0  0  1  0            999 V2000
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    4.9832   -0.1882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6781    0.2565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0208   -1.0123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8232    0.1262    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5181    0.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1283   -0.3184    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1659   -1.1426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4709   -1.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3957    0.0611    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6862   -0.7111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626   -1.3487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4531   -2.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700   -1.3003    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7008   -0.3836    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3384   -0.9071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5662   -1.1975    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7744   -1.9958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2495   -1.3211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6290   -2.0536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6190   -0.5835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0317   -0.0041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0693    0.8201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256    1.2647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5880    2.0889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3581    0.8852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0530    1.3298    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0154    2.1540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9463    2.8572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6728    3.4228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6789    2.4776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7856    0.9503    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4805    1.3950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4429    2.2191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7104    2.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1378    2.6638    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  1  0  0  0
 16 14  1  6  0  0  0
 16 17  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  1  6  0  0  0
 16 19  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 31 30  1  1  0  0  0
 24 31  1  0  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  1  0  0  0  0
 36 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 36 41  1  0  0  0  0
 14 41  1  0  0  0  0
 41 42  1  6  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0160414

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)O[C@H]1C[C@H](OC(C)=O)[C@]2(C)[C@H]([C@H]1C)[C@@H](OC(C)=O)[C@@]13O[C@@]1(C)C(=O)O[C@H]3\C=C(C)/C[C@H](OC(C)=O)[C@@H]2OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H44O13/c1-10-11-25(37)43-21-14-23(40-18(5)34)30(8)26(16(21)3)28(42-20(7)36)32-24(44-29(38)31(32,9)45-32)13-15(2)12-22(39-17(4)33)27(30)41-19(6)35/h13,16,21-24,26-28H,10-12,14H2,1-9H3/b15-13-/t16-,21-,22-,23-,24-,26+,27-,28+,30+,31-,32+/m0/s1

> <INCHI_KEY>
RDDNEKXKTMRLDN-LGLZCAIPSA-N

> <FORMULA>
C32H44O13

> <MOLECULAR_WEIGHT>
636.691

> <EXACT_MASS>
636.278191477

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
35.18002922306552

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3S,4R,5S,7S,8S,9R,10S,12Z,14S,17R)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0^{1,17}.0^{3,8}]octadec-12-en-5-yl butanoate

> <ALOGPS_LOGP>
2.80

> <JCHEM_LOGP>
2.2261714506666657

> <ALOGPS_LOGS>
-4.72

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.359277505914933

> <JCHEM_POLAR_SURFACE_AREA>
170.32999999999998

> <JCHEM_REFRACTIVITY>
151.7404

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.21e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3S,4R,5S,7S,8S,9R,10S,12Z,14S,17R)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0^{1,17}.0^{3,8}]octadec-12-en-5-yl butanoate

> <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       8.356  -8.873   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.285  -7.335   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.918  -6.626   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.848  -5.088   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.145  -4.258   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       5.481  -4.380   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.410  -2.841   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.708  -2.011   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.637  -0.473   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.935   0.357   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.302  -0.351   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.599   0.479   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.372  -1.890   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.270   0.236   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.567   1.066   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.973  -0.594   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.043  -2.133   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.746  -2.963   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.605   0.114   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.147  -1.327   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.170  -2.518   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.712  -3.959   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.504  -2.427   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.308  -0.716   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.498  -1.693   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.057  -2.235   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.445  -3.726   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.466  -2.466   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.174  -3.833   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -1.156  -1.089   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.059  -0.008   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.129   1.531   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.168   2.361   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.098   3.899   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.535   1.652   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.832   2.482   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       3.762   4.021   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       5.500   5.333   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.989   6.389   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       6.867   4.625   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       5.200   1.774   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.497   2.604   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       6.427   4.142   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.059   4.851   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       7.724   4.972   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15   16   41                                             
CONECT   15   14                                                            
CONECT   16   14   17   19                                                  
CONECT   17   16    7   18                                                  
CONECT   18   17                                                            
CONECT   19   16   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   26   31                                             
CONECT   25   24   26                                                       
CONECT   26   25   24   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   24   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   36   14   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₄O₁₃

Average Mass

636.6910 Da

Monoisotopic Mass

636.27819 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCC(=O)O[C@H]1C[C@H](OC(C)=O)[C@]2(C)[C@H]([C@H]1C)[C@@H](OC(C)=O)[C@@]13O[C@@]1(C)C(=O)O[C@H]3\C=C(C)/C[C@H](OC(C)=O)[C@@H]2OC(C)=O

InChI Identifier

InChI=1S/C32H44O13/c1-10-11-25(37)43-21-14-23(40-18(5)34)30(8)26(16(21)3)28(42-20(7)36)32-24(44-29(38)31(32,9)45-32)13-15(2)12-22(39-17(4)33)27(30)41-19(6)35/h13,16,21-24,26-28H,10-12,14H2,1-9H3/b15-13-/t16-,21-,22-,23-,24-,26+,27-,28+,30+,31-,32+/m0/s1

InChI Key

RDDNEKXKTMRLDN-LGLZCAIPSA-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
Briareum excavatum	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

Briarane diterpenoid
Hexacarboxylic acid or derivatives
Diterpenoid
Diterpene lactone
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Para-dioxane
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	2.8	ALOGPS
logS	-4.7	ALOGPS

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00049376

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

100967688

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,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate (NP0160414)

MOL for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

3D MOL for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

3D SDF for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

3D-SDF for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

PDB for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

3D PDB for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

SMILES for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

INCHI for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

Structure for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)

3D Structure for NP0160414 ((1r,2r,3s,4r,5s,7s,8s,9r,10s,12z,14s,17r)-2,7,9,10-tetrakis(acetyloxy)-4,8,12,17-tetramethyl-16-oxo-15,18-dioxatetracyclo[12.4.0.0¹,¹⁷.0³,⁸]octadec-12-en-5-yl butanoate)