NP-MRD: Showing NP-Card for [7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate (NP0234411)

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Record Information

Version

2.0

Created at

2022-09-06 16:26:05 UTC

Updated at

2022-09-06 16:26:05 UTC

NP-MRD ID

NP0234411

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate

Description

[7-(3-Methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]methyl butanoate belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton. [7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate is found in Cassinia uncata. Based on a literature review very few articles have been published on [7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]methyl butanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
    1.9010    2.6839   -0.8848 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7570    1.7421   -0.5700 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1499    2.0921   -0.2241 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4691    3.2942   -0.2508 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0757    1.1390    0.1200 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4191    1.4337    0.4657 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3119    0.3334   -0.5647 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7015   -0.4132    0.6869 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6360   -1.3291    1.1882 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0442   -2.0882    0.0201 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1413   -2.8259   -0.7466 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1107   -3.1837    0.5481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9772   -2.5571    1.3951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7241   -1.6366    0.4823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229   -1.0368   -0.5145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9049   -0.1252   -1.4046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2333   -0.0411   -0.9902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6911    0.5770    0.1739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8281    1.1202    0.9156 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1046    0.6219    0.5612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9548    1.4336   -0.3771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5600    2.8635   -0.5245 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3261   -1.1642   -0.8705 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8806    0.2413   -0.9015 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1871    3.7434   -0.9005 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8963    2.4809   -1.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5029    2.4434    0.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0195    1.4649   -0.4661 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8700    0.7270    1.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9377   -0.1473   -1.3939 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6461   -0.9786    0.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8540    0.3772    1.4704 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8234   -0.7156    1.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0693   -1.9778    1.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9021   -3.9039   -0.8571 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1234   -2.7690   -0.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2352   -2.4254   -1.7801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3593   -3.6819   -0.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6892   -3.8784    1.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5770   -2.0443    2.2610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6590   -3.3831    1.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7893   -1.5486    0.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4208    0.8821   -1.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9074   -0.4994   -2.4692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5855   -0.3914    0.6291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1907    1.0451    1.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0514    0.8821   -1.3556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9978    1.3875    0.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9578    3.2012   -1.5285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4654    3.0394   -0.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0102    3.5446    0.2342 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4054   -1.5838   -1.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6946    0.6472   -1.9068 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2926    0.8876   -0.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  6
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7 24  1  0
 24 23  1  0
  7  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
 23 15  1  0
 23 10  1  0
 22 49  1  0
 22 50  1  0
 22 51  1  0
 21 47  1  0
 21 48  1  0
 20 45  1  0
 20 46  1  0
 16 43  1  0
 16 44  1  0
 14 42  1  0
 13 40  1  0
 13 41  1  0
 12 38  1  0
 12 39  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
  9 33  1  0
  9 34  1  0
  8 31  1  0
  8 32  1  0
  7 30  1  6
 24 53  1  0
 24 54  1  0
 23 52  1  6
  1 25  1  0
  1 26  1  0
  6 27  1  0
  6 28  1  0
  6 29  1  0
M  END


  Mrv1652309062218262D          

 24 25  0  0  0  0            999 V2000
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  2  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
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15 23  1  0  0  0  0
 10 23  1  0  0  0  0
 23 24  1  0  0  0  0
  7 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0234411

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)OCC1=CCCC2(C)CCC(CC12)C(=C)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O4/c1-5-7-18(21)24-13-16-8-6-10-20(3)11-9-15(12-17(16)20)14(2)19(22)23-4/h8,15,17H,2,5-7,9-13H2,1,3-4H3

> <INCHI_KEY>
QMFZWTGKTJJOCF-UHFFFAOYSA-N

> <FORMULA>
C20H30O4

> <MOLECULAR_WEIGHT>
334.456

> <EXACT_MASS>
334.214409446

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.41195571965813

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]methyl butanoate

> <JCHEM_LOGP>
4.395688145666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.630421681359484

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
94.09279999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3H-naphthalen-1-yl]methyl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.667  -1.540   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -1.334  -3.850   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.000   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335   3.080   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.668   0.770   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669   3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5                                                            
CONECT    7    2    8   24                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   23                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   15   10   24                                                  
CONECT   24   23    7                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
[7-(3-Methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]methyl butanoic acid	Generator

Chemical Formula

C₂₀H₃₀O₄

Average Mass

334.4560 Da

Monoisotopic Mass

334.21441 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCC(=O)OCC1=CCCC2(C)CCC(CC12)C(=C)C(=O)OC

InChI Identifier

InChI=1S/C20H30O4/c1-5-7-18(21)24-13-16-8-6-10-20(3)11-9-15(12-17(16)20)14(2)19(22)23-4/h8,15,17H,2,5-7,9-13H2,1,3-4H3

InChI Key

QMFZWTGKTJJOCF-UHFFFAOYSA-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
Cassinia uncata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids

Alternative Parents

Substituents

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoid
Fatty acid ester
Fatty acyl
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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

162972314

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate (NP0234411)

MOL for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

3D MOL for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

3D SDF for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

3D-SDF for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

PDB for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

3D PDB for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

SMILES for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

INCHI for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

Structure for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)

3D Structure for NP0234411 ([7-(3-methoxy-3-oxoprop-1-en-2-yl)-4a-methyl-4,5,6,7,8,8a-hexahydro-3h-naphthalen-1-yl]methyl butanoate)