NP-MRD: Showing NP-Card for (2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid (NP0239153)

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Record Information

Version

2.0

Created at

2022-09-06 22:40:48 UTC

Updated at

2022-09-06 22:40:48 UTC

NP-MRD ID

NP0239153

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid

Description

(2E,6E,10E)-geranylgeranic acid, also known as geranylgeranate, 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. (2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid is found in Schisandra chinensis. Based on a literature review very few articles have been published on (2E,6E,10E)-geranylgeranic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 53  0  0  0  0  0  0  0  0999 V2000
    5.8914    2.5203    0.8981 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8596    1.0469    0.7427 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1012    0.2593    0.5178 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6548    0.4420    0.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5596   -1.0075    0.6670 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8564   -1.5430   -0.5397 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4651   -1.0759   -0.5949 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1016    0.3179   -0.8095 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4634   -1.9300   -0.5160 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0550   -1.7691   -0.5393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7370   -0.5796   -0.6672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1921   -1.0376   -0.5961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5805   -1.7413    0.6481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0640   -0.8577   -1.5400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4913   -1.2741   -1.5383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3750   -0.0952   -1.7656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1782    0.9056   -0.7012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4643    0.5443    0.6928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7592    2.0971   -1.0523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5453    3.1265   -0.0575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1359    4.2774   -0.4378 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7716    2.8944    1.2792 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6930    2.9563    0.2580 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1534    2.7932    1.9458 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8981    2.9651    0.6375 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9551    0.8861    0.2627 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3387   -0.3592    1.3894 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9001   -0.3717   -0.3933 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7749    1.0236    1.0043 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0612   -1.3809    1.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5939   -1.4330    0.7556 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8755   -2.6721   -0.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4300   -1.2646   -1.4631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6631    0.8769   -0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0102    0.9207   -1.1293 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5111    0.4091   -1.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7794   -2.9979   -0.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3390   -2.2798    0.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3520   -2.5104   -1.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6731    0.0630    0.2474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7486    0.0091   -1.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6214   -1.6305    0.9402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9325   -1.4034    1.4946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3044   -2.8144    0.4801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7072   -0.3375   -2.4465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7802   -1.8924   -0.6866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5850   -1.9650   -2.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4307   -0.4328   -1.7999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1450    0.3068   -2.7798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2869    1.1617    1.1278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5935    0.5976    1.3744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8176   -0.5215    0.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5654    2.3227   -2.1216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4690    3.4544    1.7809 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 22  1  0
 20 21  2  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  8 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 13 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 18 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
 22 54  1  0
M  END


  Mrv1652309072200402D          

 22 21  0  0  0  0            999 V2000
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    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
    0.8250    0.0000    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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  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
  7  8  1  0  0  0  0
  7  9  2  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
 14 15  1  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
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0239153

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O2/c1-16(2)9-6-10-17(3)11-7-12-18(4)13-8-14-19(5)15-20(21)22/h9,11,13,15H,6-8,10,12,14H2,1-5H3,(H,21,22)/b17-11+,18-13+,19-15+

> <INCHI_KEY>
SZNLKILVMCHHSD-OZFNKYQOSA-N

> <FORMULA>
C20H32O2

> <MOLECULAR_WEIGHT>
304.474

> <EXACT_MASS>
304.24023027

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.477965169876036

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid

> <JCHEM_LOGP>
6.142086383999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.12157483965426

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
98.65469999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      16.170   9.336   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      15.400   8.002   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.170   6.668   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.860   8.002   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.090   6.668   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.780   5.335   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.550   4.001   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.470   4.001   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.930   1.334   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.000  -2.667   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -2.310  -1.334   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   42    0
END

View in JSmol

Synonyms

Value	Source
Geranylgeranic acid	ChEBI
Geranylgeranate	Generator
(2E,6E,10E)-Geranylgeranate	Generator
Geranylgeranic acid, (e,e,e,)-isomer	MeSH
Geranylgeranoic acid	MeSH

Chemical Formula

C₂₀H₃₂O₂

Average Mass

304.4740 Da

Monoisotopic Mass

304.24023 Da

IUPAC Name

(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid

Traditional Name

(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\C(O)=O

InChI Identifier

InChI=1S/C20H32O2/c1-16(2)9-6-10-17(3)11-7-12-18(4)13-8-14-19(5)15-20(21)22/h9,11,13,15H,6-8,10,12,14H2,1-5H3,(H,21,22)/b17-11+,18-13+,19-15+

InChI Key

SZNLKILVMCHHSD-OZFNKYQOSA-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
Schisandra chinensis	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 acid
Branched fatty acid
Methyl-branched fatty acid
Fatty acyl
Fatty acid
Unsaturated fatty acid
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

alpha,beta-unsaturated monocarboxylic acid (CHEBI:84971 )
diterpenoid (CHEBI:84971 )
trienoic fatty acid (CHEBI:84971 )
methyl-branched fatty acid (CHEBI:84971 )

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	6.14	ChemAxon
pKa (Strongest Acidic)	5.12	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	10	ChemAxon
Refractivity	98.65 m³·mol⁻¹	ChemAxon
Polarizability	38.48 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

4439625

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5275521

PDB ID

Not Available

ChEBI ID

84971

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid (NP0239153)

MOL for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

3D MOL for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

3D SDF for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

3D-SDF for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

PDB for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

3D PDB for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

SMILES for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

INCHI for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

Structure for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)

3D Structure for NP0239153 ((2e,6e,10e)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenoic acid)