NP-MRD: Showing NP-Card for methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate (NP0280857)

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Record Information

Version

2.0

Created at

2022-09-09 06:52:51 UTC

Updated at

2022-09-09 06:52:51 UTC

NP-MRD ID

NP0280857

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate

Description

methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate is found in Khaya ivorensis.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092208522D          

 35 39  0  0  1  0            999 V2000
    4.1722    0.2589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5817   -0.3172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1067   -0.8883    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5198   -1.5096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6963   -1.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4904   -0.4920    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9575   -1.1218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6668   -0.4289    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1959   -1.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4671   -1.8854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8099   -2.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1325   -1.9132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3711   -1.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3221    0.3182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7914    1.0023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4397    1.7486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6251    0.9281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0560    0.1906    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7695    0.7428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6048    0.5066    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1480    1.1275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9722    1.0900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3636    1.8162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4567    0.4222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2367   -0.3729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0608   -0.4105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3835   -1.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4779   -0.6967    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4403   -1.5208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1353   -1.9654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8678   -1.5858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0977   -2.7895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7927   -3.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7516   -0.3053    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8507   -1.1243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  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
  9 13  2  0  0  0  0
  8 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  2  1  1  0  0  0
  6 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 28 34  1  0  0  0  0
 20 34  1  0  0  0  0
  3 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END

     RDKit          3D

 69 73  0  0  0  0  0  0  0  0999 V2000
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   -4.8688   -1.1664    0.3136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1096   -2.2004   -0.1320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6490   -3.1005   -0.8403 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6941   -2.3236    0.1699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9753   -1.0329    0.4039 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0615   -1.2472    1.3803 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2379   -1.1933    1.2214 C   0  0  1  0  0  0  0  0  0  0  0  0
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    2.1669   -2.5950    1.8568 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.3739    1.2986    1.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4063    2.3471   -0.0898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5526    1.6383   -0.7067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5280    2.2197    0.9770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5156    0.9257    2.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7290    0.4485    2.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0156   -0.7797    2.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8433    0.5551    1.3435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0345    2.9635    0.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5056    3.6922   -2.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
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 33 32  1  0
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M  END


  Mrv1652309092208522D          

 35 39  0  0  1  0            999 V2000
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 28 34  1  0  0  0  0
 20 34  1  0  0  0  0
  3 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0280857

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@H]1[C@@]2(C)[C@H](CC(=O)OC1(C)C)O[C@@]13CC(=O)O[C@H](C4=COC=C4)[C@]1(C)CC[C@@H]2C3=C

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O8/c1-15-17-7-9-25(4)23(16-8-10-32-14-16)33-22(30)13-27(15,25)34-19-12-21(29)35-24(2,3)18(26(17,19)5)11-20(28)31-6/h8,10,14,17-19,23H,1,7,9,11-13H2,2-6H3/t17?,18-,19+,23-,25+,26+,27-/m1/s1

> <INCHI_KEY>
DPBKKUVQRJSGOO-FRCLCOAUSA-N

> <FORMULA>
C27H34O8

> <MOLECULAR_WEIGHT>
486.561

> <EXACT_MASS>
486.225368055

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
49.60663105793249

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[(1R,3S,8S,9S,10S,13S,14S)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0^{1,13}.0^{3,9}]octadecan-8-yl]acetate

> <JCHEM_LOGP>
3.0449544749999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8695759192134607

> <JCHEM_POLAR_SURFACE_AREA>
101.27000000000002

> <JCHEM_REFRACTIVITY>
122.56329999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(1R,3S,8S,9S,10S,13S,14S)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0^{1,13}.0^{3,9}]octadecan-8-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       7.788   0.483   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.686  -0.592   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.666  -1.658   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.570  -2.818   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.033  -2.469   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.649  -0.918   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.654  -2.094   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.111  -0.801   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.232  -2.065   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.739  -3.519   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.512  -4.450   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.247  -3.571   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.693  -2.097   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.468   0.594   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.344   1.871   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.688   3.264   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.900   1.732   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.704   0.356   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.036   1.387   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.596   0.946   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.610   2.105   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.148   2.035   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.879   3.390   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      12.052   0.788   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.642  -0.696   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.180  -0.766   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.916  -2.212   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.225  -1.300   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.155  -2.839   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.452  -3.669   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.820  -2.960   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      11.382  -5.207   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      12.680  -6.037   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.870  -0.570   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.055  -2.099   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   18                                                  
CONECT    3    2    4   34                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   18                                             
CONECT    7    6                                                            
CONECT    8    6    9   14                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    9                                                       
CONECT   14    8   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    2    6   19                                             
CONECT   19   18   20                                                       
CONECT   20   19   21   34                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32                                                            
CONECT   34   28   20    3   35                                             
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₄O₈

Average Mass

486.5610 Da

Monoisotopic Mass

486.22537 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@H]1[C@@]2(C)[C@H](CC(=O)OC1(C)C)O[C@@]13CC(=O)O[C@H](C4=COC=C4)[C@]1(C)CC[C@@H]2C3=C

InChI Identifier

InChI=1S/C27H34O8/c1-15-17-7-9-25(4)23(16-8-10-32-14-16)33-22(30)13-27(15,25)34-19-12-21(29)35-24(2,3)18(26(17,19)5)11-20(28)31-6/h8,10,14,17-19,23H,1,7,9,11-13H2,2-6H3/t17?,18-,19+,23-,25+,26+,27-/m1/s1

InChI Key

DPBKKUVQRJSGOO-FRCLCOAUSA-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
Khaya ivorensis	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	3.04	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate (NP0280857)

MOL for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

3D MOL for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

3D SDF for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

3D-SDF for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

PDB for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

3D PDB for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

SMILES for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

INCHI for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

Structure for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)

3D Structure for NP0280857 (methyl 2-[(1r,3s,8s,9s,10s,13s,14r)-14-(furan-3-yl)-7,7,9,13-tetramethyl-18-methylidene-5,16-dioxo-2,6,15-trioxatetracyclo[8.7.1.0¹,¹³.0³,⁹]octadecan-8-yl]acetate)