NP-MRD: Showing NP-Card for (6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol (NP0319200)

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Record Information

Version

2.0

Created at

2022-09-11 20:06:50 UTC

Updated at

2022-09-11 20:06:50 UTC

NP-MRD ID

NP0319200

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol

Description

Geranylcitronellol belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle. Thus, geranylcitronellol is considered to be a fatty alcohol lipid molecule. Geranylcitronellol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, Geranylcitronellol has been detected, but not quantified in, fruits. (6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol is found in Bupleurum fruticescens. This could make geranylcitronellol a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 57 56  0  0  0  0  0  0  0  0999 V2000
    6.6370   -0.5602   -1.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2554   -0.7594   -0.0256 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7331   -0.8033    0.0684 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4724   -0.8905    1.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9972   -0.8410    0.8975 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4898    0.2896    1.7217 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0522    0.4993    1.7168 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4755    1.6093    2.5159 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1851   -0.2576    1.0234 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7123   -0.0189    1.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2623    0.2633   -0.3831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1986    0.5070   -0.4180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7755    1.6157    0.3511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0156   -0.2620   -1.1380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4887    0.0449   -1.1265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1851   -1.1642   -0.5931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6798   -1.0059   -0.5218 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0280    0.1399    0.3744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3312   -0.9459   -1.8663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8392   -0.9531   -1.6455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5071   -0.8991   -2.8513 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4189   -0.4245   -2.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0865    0.4027   -1.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9422   -1.3939   -1.6332 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2235   -0.2339   -0.7549 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0933   -0.3349    1.0255 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1227   -1.8469    0.0963 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9562   -1.0367    2.0092 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5165   -1.8133    1.1097 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7682   -0.6136   -0.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9888    1.2262    1.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8103    0.1332    2.7926 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2593    2.0696    3.1127 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7036    1.2404    3.2378 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9477    2.3073    1.8334 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6436   -1.0551    0.4547 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4475    0.8180    1.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2094   -0.9247    1.4495 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5650   -0.5998   -1.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8061    1.1684   -0.7212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798    2.4313   -0.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0016    2.0746    0.9987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5704    1.2537    1.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6139   -1.0854   -1.7135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7747    0.1705   -2.2010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7039    0.9792   -0.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7993   -1.3742    0.4248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8885   -2.0301   -1.2188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0669   -1.9401   -0.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1644    0.4045    1.0395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2941    1.0706   -0.1648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8643   -0.1203    1.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0990   -1.8977   -2.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0561   -0.0717   -2.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0852   -0.0334   -1.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1342   -1.8165   -1.0157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4363   -0.6004   -2.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 12  2  0
 12 13  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  7  2  0
  7  8  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
 18 50  1  0
 18 51  1  0
 18 52  1  0
 17 49  1  1
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 21 57  1  0
 16 47  1  0
 16 48  1  0
 15 45  1  0
 15 46  1  0
 14 44  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 11 39  1  0
 11 40  1  0
 10 37  1  0
 10 38  1  0
  9 36  1  0
  8 33  1  0
  8 34  1  0
  8 35  1  0
  6 31  1  0
  6 32  1  0
  5 29  1  0
  5 30  1  0
  4 28  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
M  END


  Mrv0541 05061306232D          

 21 20  0  0  0  0            999 V2000
   -5.5243    7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0954    7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664    4.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0954    5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664    3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    6.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0954    4.8395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6204    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8099    6.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3809    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9520    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  6  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 12  7  1  0  0  0  0
 13  8  1  0  0  0  0
 14  8  1  0  0  0  0
 16 15  1  0  0  0  0
 17  1  1  0  0  0  0
 17  2  1  0  0  0  0
 17  9  2  0  0  0  0
 18  3  1  0  0  0  0
 18 10  1  0  0  0  0
 18 11  2  0  0  0  0
 19  4  1  0  0  0  0
 19 12  1  0  0  0  0
 19 13  2  0  0  0  0
 20  5  1  0  0  0  0
 20 14  1  0  0  0  0
 20 15  1  0  0  0  0
 21 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319200

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCO)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H36O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h9,11,13,20-21H,6-8,10,12,14-16H2,1-5H3/b18-11+,19-13+

> <INCHI_KEY>
ZKWFMIAGZQACFE-NWLVNBMCSA-N

> <FORMULA>
C20H36O

> <MOLECULAR_WEIGHT>
292.4992

> <EXACT_MASS>
292.276615774

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
38.481082383940425

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6E,10E)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol

> <ALOGPS_LOGP>
6.50

> <JCHEM_LOGP>
6.071483867333333

> <ALOGPS_LOGS>
-4.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.109791816239

> <JCHEM_PKA_STRONGEST_BASIC>
-1.8759770595770613

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
98.09129999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.26e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(6E,10E)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

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     -10.312  13.654   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.645  13.654   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.977   9.034   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.310   4.414   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.357  -0.206   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.645  10.574   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.977   5.954   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.310   1.334   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.978  11.344   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -7.645   9.034   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.311   6.724   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.977   4.414   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.644   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.976   2.104   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.691   2.104   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.025   1.334   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.978  12.884   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.311   8.264   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.644   3.644   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.357   1.334   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.358   2.104   0.000  0.00  0.00           O+0
CONECT    1   17                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   19                                                            
CONECT    5   20                                                            
CONECT    6    9   10                                                       
CONECT    7   11   12                                                       
CONECT    8   13   14                                                       
CONECT    9    6   17                                                       
CONECT   10    6   18                                                       
CONECT   11    7   18                                                       
CONECT   12    7   19                                                       
CONECT   13    8   19                                                       
CONECT   14    8   20                                                       
CONECT   15   16   20                                                       
CONECT   16   15   21                                                       
CONECT   17    1    2    9                                                  
CONECT   18    3   10   11                                                  
CONECT   19    4   12   13                                                  
CONECT   20    5   14   15                                                  
CONECT   21   16                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
(6E,10E)-3,7,11,15-Tetramethyl-6,10,14-hexadecatrien-1-ol	HMDB
Geranylcitronellol	MeSH

Chemical Formula

C₂₀H₃₆O

Average Mass

292.4992 Da

Monoisotopic Mass

292.27662 Da

IUPAC Name

(6E,10E)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol

Traditional Name

(6E,10E)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol

CAS Registry Number

Not Available

SMILES

CC(CCO)CC\C=C(/C)CC\C=C(/C)CCC=C(C)C

InChI Identifier

InChI=1S/C20H36O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h9,11,13,20-21H,6-8,10,12,14-16H2,1-5H3/b18-11+,19-13+

InChI Key

ZKWFMIAGZQACFE-NWLVNBMCSA-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
Bupleurum fruticescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Acyclic diterpenoids

Alternative Parents

Substituents

Acyclic diterpenoid
Long chain fatty alcohol
Fatty alcohol
Fatty acyl
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Fatty alcohols (LMFA05000210 )

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	6.5	ALOGPS
logP	6.07	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	17.11	ChemAxon
pKa (Strongest Basic)	-1.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	98.09 m³·mol⁻¹	ChemAxon
Polarizability	38.48 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0032147

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB008875

KNApSAcK ID

Not Available

Chemspider ID

4517812

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5365870

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol (NP0319200)

MOL for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

3D MOL for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

3D SDF for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

3D-SDF for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

PDB for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

3D PDB for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

SMILES for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

INCHI for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

Structure for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)

3D Structure for NP0319200 ((6e,10e)-3,7,11,15-tetramethylhexadeca-6,10,14-trien-1-ol)