NP-MRD: Showing NP-Card for 14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate (NP0303532)

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Record Information

Version

2.0

Created at

2022-09-10 17:57:35 UTC

Updated at

2022-09-10 17:57:36 UTC

NP-MRD ID

NP0303532

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate

Description

SALANNOLIDE belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. 14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate is found in Azadirachta indica. Based on a literature review very few articles have been published on SALANNOLIDE.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102219572D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309102219572D          

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    1.6379   -3.6410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9112   -2.4107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1926   -2.0053    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6215   -1.9911    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6133   -1.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8948   -0.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8866    0.0642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1680    0.4696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5423    0.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5341   -0.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2608    0.4554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5969    0.4838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9247    0.9620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7604    1.2924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5800    1.3868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230    0.6365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7101    0.3894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4205    0.8090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0390    0.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8603    0.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0399   -0.6202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7968   -0.9483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5072   -0.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1257   -1.0746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9309   -0.8950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7977   -1.8316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9764   -1.7535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4305   -2.3721    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3295   -1.0398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2515   -1.8611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7110   -0.4939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8897   -0.4158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1524   -1.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2821   -0.9739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4902   -1.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9029   -2.3517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1075   -2.1327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1110   -3.1500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5237   -3.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3236   -0.7465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4472   -1.5622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3154    0.0784    0.0000 C   0  0  0  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  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
 19 20  1  0  0  0  0
 20 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
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  2  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 22 34  1  0  0  0  0
 34 35  1  0  0  0  0
 20 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 37 43  1  0  0  0  0
  8 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 19 45  1  0  0  0  0
 15 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303532

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CC1C2(C)C(OC3CC(C(C)=C23)C2=CC(O)OC2=O)C2OCC3(C)C2C1(C)C(CC3OC(C)=O)OC(=O)C(\C)=C\C

> <INCHI_IDENTIFIER>
InChI=1S/C34H44O11/c1-9-15(2)30(38)44-23-13-22(42-17(4)35)32(5)14-41-27-28(32)33(23,6)21(12-24(36)40-8)34(7)26-16(3)18(10-20(26)43-29(27)34)19-11-25(37)45-31(19)39/h9,11,18,20-23,25,27-29,37H,10,12-14H2,1-8H3/b15-9+

> <INCHI_KEY>
FVEVYGNIVRCALL-OQLLNIDSSA-N

> <FORMULA>
C34H44O11

> <MOLECULAR_WEIGHT>
628.715

> <EXACT_MASS>
628.288362237

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
66.84112409674

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-(acetyloxy)-6-(5-hydroxy-2-oxo-2,5-dihydrofuran-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0^{2,9}.0^{4,8}.0^{15,18}]octadec-7-en-12-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
2.8988706760000005

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.526843432891066

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.819512377517619

> <JCHEM_PKA_STRONGEST_BASIC>
-3.891840677507622

> <JCHEM_POLAR_SURFACE_AREA>
143.89

> <JCHEM_REFRACTIVITY>
159.1085

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
14-(acetyloxy)-6-(5-hydroxy-2-oxo-5H-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0^{2,9}.0^{4,8}.0^{15,18}]octadec-7-en-12-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       0.406  -8.363   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.390  -6.823   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.716  -6.040   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.057  -6.797   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.701  -4.500   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.360  -3.743   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.027  -3.717   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.012  -2.177   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.670  -1.420   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.655   0.120   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.314   0.877   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.012   0.093   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.997  -1.447   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -2.354   0.850   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.981   0.903   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.726   1.796   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.286   2.413   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.816   2.589   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.456   1.188   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.926   0.727   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.252   1.510   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.406   0.491   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.939   0.345   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.274  -1.158   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.687  -1.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.013  -0.987   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.168  -2.006   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      16.671  -1.671   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      14.556  -3.419   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      13.023  -3.273   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      12.004  -4.428   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       9.948  -1.941   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.803  -3.474   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.794  -0.922   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.261  -0.776   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.751  -2.236   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.127  -1.818   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.515  -3.308   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.419  -4.390   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.934  -3.981   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       5.807  -5.880   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       4.711  -6.961   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.337  -1.394   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       4.568  -2.916   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.322   0.146   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   43                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   17   45                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   45                                                  
CONECT   20   19   21   35                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   34                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   32                                                  
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   25   31                                                  
CONECT   31   30                                                            
CONECT   32   24   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   22   35                                                  
CONECT   35   34   20   36   37                                             
CONECT   36   35                                                            
CONECT   37   35   38   43                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41                                                            
CONECT   43   37    8   44   45                                             
CONECT   44   43                                                            
CONECT   45   43   19   15                                                  
MASTER        0    0    0    0    0    0    0    0   45    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₄O₁₁

Average Mass

628.7150 Da

Monoisotopic Mass

628.28836 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)CC1C2(C)C(OC3CC(C(C)=C23)C2=CC(O)OC2=O)C2OCC3(C)C2C1(C)C(CC3OC(C)=O)OC(=O)C(\C)=C\C

InChI Identifier

InChI=1S/C34H44O11/c1-9-15(2)30(38)44-23-13-22(42-17(4)35)32(5)14-41-27-28(32)33(23,6)21(12-24(36)40-8)34(7)26-16(3)18(10-20(26)43-29(27)34)19-11-25(37)45-31(19)39/h9,11,18,20-23,25,27-29,37H,10,12-14H2,1-8H3/b15-9+

InChI Key

FVEVYGNIVRCALL-OQLLNIDSSA-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
Azadirachta indica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Naphthofuran
Tetracarboxylic acid or derivatives
Fatty acid ester
2-furanone
Fatty acyl
Dihydrofuran
Tetrahydrofuran
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Ether
Dialkyl ether
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
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

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

101320286

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate (NP0303532)

MOL for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

PDB for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

Structure for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0303532 (14-(acetyloxy)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-10-(2-methoxy-2-oxoethyl)-7,9,11,15-tetramethyl-3,17-dioxapentacyclo[9.6.1.0²,⁹.0⁴,⁸.0¹⁵,¹⁸]octadec-7-en-12-yl (2e)-2-methylbut-2-enoate)