NP-MRD: Showing NP-Card for 1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid (NP0240426)

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Record Information

Version

2.0

Created at

2022-09-07 00:14:40 UTC

Updated at

2022-09-07 00:14:40 UTC

NP-MRD ID

NP0240426

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid

Description

Ent-8(17),13(16),14-Labdatrien-18-oic acid belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Ent-8(17),13(16),14-Labdatrien-18-oic acid is a weakly acidic compound (based on its pKa). Outside of the human body, ent-8(17),13(16),14-Labdatrien-18-oic acid has been detected, but not quantified in, fruits. 1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid is found in Callitris rhomboidea, Hymenaea courbaril, Juniperus sabina, Nepeta tuberosa, Torreya nucifera and Xylopia aromatica. This could make ent-8(17),13(16),14-labdatrien-18-Oic acid a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
    3.6649    2.1630   -1.3919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4264    1.1086   -1.2665 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1188   -0.1326   -0.6174 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0596   -1.0858   -0.5882 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8007   -0.4432    0.0566 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7317   -0.5904   -0.9539 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3682   -0.9340   -0.5393 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1724   -2.3325   -0.1212 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0930   -3.2225   -0.2380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1608   -2.6643    0.4424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1451   -1.6115   -0.1047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7733   -0.3087    0.5891 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7975    0.7516    0.3459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9819    0.1251   -0.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4094    1.2780    1.5835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9176    0.9798    2.6824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5137    2.0918    1.5319 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3384    1.8766   -0.5541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1035    2.4409    0.1160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0303    1.3991   -0.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3474    0.0353    0.4056 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2968   -0.0485    1.8028 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6592    2.2891   -1.0243 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0277    3.0710   -1.9259 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4270    1.2040   -1.7235 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8483   -2.0176   -0.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9970   -0.8792   -1.0614 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9742   -1.3608    0.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6722    0.3730    0.7979 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1212   -1.4274   -1.6505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7805    0.2827   -1.6724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2817   -0.8472   -1.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8571   -4.2569    0.0995 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0933   -3.1401   -0.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5438   -3.6374    0.1387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1701   -2.5266    1.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1397   -1.9746    0.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1430   -1.5429   -1.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9228   -0.5803    1.6925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6945   -0.2495   -1.3991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5751   -0.5353    0.2114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6502    1.0155   -0.6260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7041    2.8708    2.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1537    2.5896   -0.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0329    1.4516   -1.5097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2438    2.6989    1.1621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7975    3.3367   -0.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8622    1.7897    0.4147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2055    1.3994   -1.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0028   -0.8890    1.8887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7876    0.8697    2.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4766   -0.2527    2.5860 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  1  1
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 13  1  0
 13 14  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  2  3
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  3
  3  2  1  0
  2  1  2  3
 13 15  1  1
 15 17  1  0
 15 16  2  0
 12 21  1  0
  7 21  1  0
 22 50  1  0
 22 51  1  0
 22 52  1  0
 20 48  1  0
 20 49  1  0
 19 46  1  0
 19 47  1  0
 18 44  1  0
 18 45  1  0
 14 40  1  0
 14 41  1  0
 14 42  1  0
 12 39  1  1
 11 37  1  0
 11 38  1  0
 10 35  1  0
 10 36  1  0
  9 33  1  0
  9 34  1  0
  7 32  1  6
  6 30  1  0
  6 31  1  0
  5 28  1  0
  5 29  1  0
  4 26  1  0
  4 27  1  0
  2 25  1  0
  1 23  1  0
  1 24  1  0
 17 43  1  0
M  END


  Mrv0541 05061311112D          

 22 23  0  0  0  0            999 V2000
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.1250    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    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5690    2.5248    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
    3.5724    4.5375    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
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993    3.4433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3815    4.2185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6296    2.8113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  2  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12  7  1  0  0  0  0
 13  7  1  0  0  0  0
 14  2  2  0  0  0  0
 14  6  1  0  0  0  0
 14  8  1  0  0  0  0
 15  3  2  0  0  0  0
 15  9  1  0  0  0  0
 16 10  1  0  0  0  0
 16 15  1  0  0  0  0
 17 11  1  0  0  0  0
 19  4  1  0  0  0  0
 19 12  1  0  0  0  0
 19 16  1  0  0  0  0
 19 17  1  0  0  0  0
 20  5  1  0  0  0  0
 20 13  1  0  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21 18  2  0  0  0  0
 22 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240426

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCCC(C)(C1CCC(=C)C2CCC(=C)C=C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O2/c1-6-14(2)8-10-16-15(3)9-11-17-19(16,4)12-7-13-20(17,5)18(21)22/h6,16-17H,1-3,7-13H2,4-5H3,(H,21,22)

> <INCHI_KEY>
JEGUVXRNDRXUDN-UHFFFAOYSA-N

> <FORMULA>
C20H30O2

> <MOLECULAR_WEIGHT>
302.451

> <EXACT_MASS>
302.224580204

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
35.816319389512365

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-decahydronaphthalene-1-carboxylic acid

> <ALOGPS_LOGP>
4.82

> <JCHEM_LOGP>
5.385719886

> <ALOGPS_LOGS>
-5.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.878129897406169

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
90.96789999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.61e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2H-naphthalene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.529   4.713   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335   7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   7.700   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668   5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.519   6.427   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.045   7.875   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      10.509   5.248   0.000  0.00  0.00           O+0
CONECT    1    6                                                            
CONECT    2   14                                                            
CONECT    3   15                                                            
CONECT    4   19                                                            
CONECT    5   20                                                            
CONECT    6    1   14                                                       
CONECT    7   12   13                                                       
CONECT    8   10   14                                                       
CONECT    9   11   15                                                       
CONECT   10    8   16                                                       
CONECT   11    9   17                                                       
CONECT   12    7   19                                                       
CONECT   13    7   20                                                       
CONECT   14    2    6    8                                                  
CONECT   15    3    9   16                                                  
CONECT   16   10   15   19                                                  
CONECT   17   11   19   20                                                  
CONECT   18   20   21   22                                                  
CONECT   19    4   12   16   17                                             
CONECT   20    5   13   17   18                                             
CONECT   21   18                                                            
CONECT   22   18                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
ent-8(17),13(16),14-Labdatrien-18-Oate	Generator
1,4a-Dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-decahydronaphthalene-1-carboxylate	Generator

Chemical Formula

C₂₀H₃₀O₂

Average Mass

302.4510 Da

Monoisotopic Mass

302.22458 Da

IUPAC Name

1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-decahydronaphthalene-1-carboxylic acid

Traditional Name

1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2H-naphthalene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

CC12CCCC(C)(C1CCC(=C)C2CCC(=C)C=C)C(O)=O

InChI Identifier

InChI=1S/C20H30O2/c1-6-14(2)8-10-16-15(3)9-11-17-19(16,4)12-7-13-20(17,5)18(21)22/h6,16-17H,1-3,7-13H2,4-5H3,(H,21,22)

InChI Key

JEGUVXRNDRXUDN-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
Callitris rhomboidea	LOTUS Database	35616633
Hymenaea courbaril	LOTUS Database	35616633
Juniperus sabina	LOTUS Database	35616633
Nepeta tuberosa	LOTUS Database	35616633
Torreya nucifera	LOTUS Database	35616633
Xylopia aromatica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Labdane diterpenoid
Monocarboxylic acid or derivatives
Carboxylic acid
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
logP	4.82	ALOGPS
logP	5.39	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	4.88	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	90.97 m³·mol⁻¹	ChemAxon
Polarizability	35.82 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0039486

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB019092

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

72780956

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid (NP0240426)

MOL for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

3D MOL for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

3D SDF for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

3D-SDF for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

PDB for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

3D PDB for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

SMILES for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

INCHI for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

Structure for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)

3D Structure for NP0240426 (1,4a-dimethyl-6-methylidene-5-(3-methylidenepent-4-en-1-yl)-hexahydro-2h-naphthalene-1-carboxylic acid)