NP-MRD: Showing NP-Card for (1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate (NP0260598)

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Record Information

Version

2.0

Created at

2022-09-08 02:48:58 UTC

Updated at

2022-09-08 02:48:58 UTC

NP-MRD ID

NP0260598

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate

Description

(E)-2-[(1R,7R,8S,11R,15S)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]Hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate belongs to the class of organic compounds known as cycloheptafurans. These are organic heterocyclic compounds containing a cycloheptane derivative fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. Based on a literature review very few articles have been published on (E)-2-[(1R,7R,8S,11R,15S)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]Hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082204482D          

 31 34  0  0  1  0            999 V2000
    2.4445   -1.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6962   -0.4406    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5997   -1.2923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -1.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1604   -1.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1674   -1.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472   -1.0192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1628   -0.3317    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3636    0.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0221    1.1754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8441    1.3382    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7045    2.1513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9255    0.6605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9426   -0.1150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7141    1.4734    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9162    2.2732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7099    2.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9120    3.2980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7058    3.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2974    2.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    4.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7016    4.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9037    5.3476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2933    3.9728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4064    0.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1994    1.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6608    0.4915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4853    0.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1529   -0.1586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3776    0.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  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  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 15 14  1  6  0  0  0
  9 15  1  0  0  0  0
  3 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
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 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
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 16 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 26 31  2  0  0  0  0
  3 31  1  0  0  0  0
M  END

     RDKit          3D

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   -2.0288    0.5916   -1.1803 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3746   -0.8828    0.3974 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5916   -0.0429    0.5048 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6050   -0.4079    1.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7608    0.3276    1.4080 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8232    0.1127    0.5561 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6684   -0.7813   -0.3394 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    0.8629    0.6568 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0842    0.6489   -0.1623 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0202   -0.3617   -1.2388 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3336    1.4620    0.0105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6447   -0.4420    1.3326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7264   -0.9656    2.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7810   -0.3672    3.2869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2373   -0.6225    4.6956 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3648   -1.9497    0.4323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0188   -2.6870   -1.0311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5185   -3.0221   -0.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4516    1.3204   -1.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
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 27 64  1  0
M  END


  Mrv1652309082204482D          

 31 34  0  0  1  0            999 V2000
    2.4445   -1.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9120    3.2980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7058    3.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2974    2.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    4.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7016    4.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9037    5.3476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2933    3.9728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1994    1.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6608    0.4915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4853    0.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  3 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0260598

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@]12COC(C)(C)[C@@H]3CC[C@@](C)(C[C@H]13)[C@@H](\C=C\OC(=O)C=C(C)C)C1=C2OC(C)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O5/c1-16(2)12-22(27)29-11-9-19-18-13-17(3)31-23(18)26(28-7)15-30-24(4,5)20-8-10-25(19,6)14-21(20)26/h9,11-13,19-21H,8,10,14-15H2,1-7H3/b11-9+/t19-,20+,21-,25-,26-/m0/s1

> <INCHI_KEY>
MQLDUXIMSMUVOZ-JWKHEBSUSA-N

> <FORMULA>
C26H36O5

> <MOLECULAR_WEIGHT>
428.569

> <EXACT_MASS>
428.256274259

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
48.114014273639306

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(E)-2-[(1R,7R,8S,11R,15S)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0^{2,6}.0^{11,15}]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate

> <JCHEM_LOGP>
4.863526279

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.840998579886468

> <JCHEM_POLAR_SURFACE_AREA>
57.900000000000006

> <JCHEM_REFRACTIVITY>
121.2978

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(E)-2-[(1R,7R,8S,11R,15S)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0^{2,6}.0^{11,15}]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       4.563  -3.095   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.521  -1.555   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.166  -0.822   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.986  -2.412   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.589  -3.121   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.299  -2.217   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.312  -3.630   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.208  -1.902   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.304  -0.619   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.679   0.688   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.041   2.194   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.576   2.498   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.315   4.016   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.728   1.233   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.760  -0.215   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.200   2.750   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.577   4.243   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.059   4.663   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.436   6.156   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.917   6.576   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.022   5.503   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.295   8.069   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.776   8.489   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.154   9.982   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.881   7.416   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.492   1.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.972   2.194   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.833   0.918   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.373   0.864   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.885  -0.296   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.438   0.231   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   15   31                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   16                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    9    3                                                  
CONECT   16   12   17   26                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   16   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   26    3                                                  
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Value	Source
(e)-2-[(1R,7R,8S,11R,15S)-1-Methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0,.0,]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₆H₃₆O₅

Average Mass

428.5690 Da

Monoisotopic Mass

428.25627 Da

IUPAC Name

(E)-2-[(1R,7R,8S,11R,15S)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0^{2,6}.0^{11,15}]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate

Traditional Name

(E)-2-[(1R,7R,8S,11R,15S)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0^{2,6}.0^{11,15}]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CO[C@@]12COC(C)(C)[C@@H]3CC[C@@](C)(C[C@H]13)[C@@H](\C=C\OC(=O)C=C(C)C)C1=C2OC(C)=C1

InChI Identifier

InChI=1S/C26H36O5/c1-16(2)12-22(27)29-11-9-19-18-13-17(3)31-23(18)26(28-7)15-30-24(4,5)20-8-10-25(19,6)14-21(20)26/h9,11-13,19-21H,8,10,14-15H2,1-7H3/b11-9+/t19-,20+,21-,25-,26-/m0/s1

InChI Key

MQLDUXIMSMUVOZ-JWKHEBSUSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cycloheptafurans. These are organic heterocyclic compounds containing a cycloheptane derivative fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Cycloheptafurans

Sub Class

Not Available

Direct Parent

Cycloheptafurans

Alternative Parents

Substituents

Cycloheptafuran
Fatty acid ester
Fatty acyl
Oxane
Enol ester
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Furan
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Monocarboxylic acid or derivatives
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	4.86	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	57.9 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	121.3 m³·mol⁻¹	ChemAxon
Polarizability	48.11 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

12068759

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate (NP0260598)

MOL for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

3D MOL for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

3D SDF for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

3D-SDF for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

PDB for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

3D PDB for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

SMILES for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

INCHI for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

Structure for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)

3D Structure for NP0260598 ((1e)-2-[(1r,7r,8s,11r,15s)-1-methoxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl]ethenyl 3-methylbut-2-enoate)