NP-MRD: Showing NP-Card for (2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol (NP0200135)

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Record Information

Version

2.0

Created at

2022-09-04 18:54:39 UTC

Updated at

2022-09-04 18:54:39 UTC

NP-MRD ID

NP0200135

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol

Description

(2E,7R,11R)-3,7,11,15-tetramethyloctadec-2-en-1-ol 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,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol is found in Akebia trifoliata. Based on a literature review very few articles have been published on (2E,7R,11R)-3,7,11,15-tetramethyloctadec-2-en-1-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 67 66  0  0  0  0  0  0  0  0999 V2000
   -6.3642    2.8728    1.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0043    2.2635    1.6054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5994    1.5637    0.3616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3638    0.3807   -0.0639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.8076    0.6764   -0.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8062   -0.2647   -1.3203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3778   -0.7377   -1.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2208   -1.7423   -0.0816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7585   -2.2354    0.0811 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3924   -2.8705   -1.2461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8788   -1.1036    0.4003 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5455   -1.3933    0.6746 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3936   -2.0116   -0.3768 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8259   -2.1822    0.1061 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6702   -2.8147   -0.9822 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3916   -0.8830    0.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3897    0.1396   -0.4923 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9020    1.4867   -0.1547 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2887    1.6020    0.3085 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7628    1.0013    1.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1980    2.3139   -0.3864 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6030    2.4914   -0.0141 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8080    3.8820    0.1512 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1754    2.1684    1.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5166    3.5707    0.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3664    3.5156    2.5923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9960    1.4723    2.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2170    2.9904    1.9483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5398    2.2891   -0.5204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5220    1.2225    0.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3597   -0.3502    0.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0545    1.7206   -0.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4881    0.2853    0.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1712    0.0585   -1.2395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4698   -1.0703   -1.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7992    0.5270   -2.1006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7252    0.1503   -1.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1047   -1.1835   -2.1357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4591   -1.2758    0.9033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8153   -2.6457   -0.1926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7042   -3.0089    0.8561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9623   -3.8906   -1.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3423   -2.9841   -1.8798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7643   -2.2118   -1.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2571   -0.4913    1.2744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8720   -0.4079   -0.5106 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6513   -2.0544    1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0466   -0.4316    1.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3878   -1.4045   -1.2993 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9982   -3.0516   -0.6041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8434   -2.8937    0.9668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7526   -2.1776   -1.8851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0846   -3.7184   -1.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6164   -3.2002   -0.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4731   -1.0776    0.9357 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8986   -0.5779    1.5193 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3154    0.2662   -0.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9063   -0.2010   -1.4189 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2309    2.0121    0.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7644    2.1225   -1.0826 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3930    1.7230    2.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4303    0.1398    1.3829 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9188    0.7678    2.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8260    2.7843   -1.2960 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9379    2.0112    0.8995 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3021    2.1282   -0.8270 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6995    3.9482    0.6178 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  1
  5 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  6 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  1
 10 42  1  0
 10 43  1  0
 10 44  1  0
 11 45  1  0
 11 46  1  0
 12 47  1  0
 12 48  1  0
 13 49  1  0
 13 50  1  0
 14 51  1  1
 15 52  1  0
 15 53  1  0
 15 54  1  0
 16 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 20 61  1  0
 20 62  1  0
 20 63  1  0
 21 64  1  0
 22 65  1  0
 22 66  1  0
 23 67  1  0
M  END


  Mrv1652309042220542D          

 23 22  0  0  1  0            999 V2000
    5.9961    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7105    4.6993    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
    8.1395    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1395    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8539    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5684    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2829    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9974    4.6993    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9974    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7118    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4263    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1408    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8552    4.6993    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.8552    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5697    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2842    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9987    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7131    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7131    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4276    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1421    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1421    5.5243    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0200135

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(C)CCC[C@@H](C)CCC[C@@H](C)CCC\C(C)=C\CO

> <INCHI_IDENTIFIER>
InChI=1S/C22H44O/c1-6-10-19(2)11-7-12-20(3)13-8-14-21(4)15-9-16-22(5)17-18-23/h17,19-21,23H,6-16,18H2,1-5H3/b22-17+/t19?,20-,21-/m1/s1

> <INCHI_KEY>
RJPVZHPAFRZZGC-JSVAJZLASA-N

> <FORMULA>
C22H44O

> <MOLECULAR_WEIGHT>
324.593

> <EXACT_MASS>
324.339216037

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
44.43089508744382

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E,7R,11R)-3,7,11,15-tetramethyloctadec-2-en-1-ol

> <JCHEM_LOGP>
7.9276876199999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.330030451338093

> <JCHEM_PKA_STRONGEST_BASIC>
-2.217044680584718

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
105.43929999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2E,7R,11R)-3,7,11,15-tetramethyloctadec-2-en-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      11.193   8.002   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.526   8.772   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.860   8.002   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.194   8.772   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.194  10.312   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.527   8.002   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.861   8.772   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      19.195   8.002   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.528   8.772   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.528  10.312   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      21.862   8.002   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      23.196   8.772   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.529   8.002   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      25.863   8.772   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      25.863  10.312   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      27.197   8.002   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      28.530   8.772   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      29.864   8.002   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      31.198   8.772   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      31.198  10.312   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      32.532   8.002   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      33.865   8.772   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      33.865  10.312   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₄₄O

Average Mass

324.5930 Da

Monoisotopic Mass

324.33922 Da

IUPAC Name

(2E,7R,11R)-3,7,11,15-tetramethyloctadec-2-en-1-ol

Traditional Name

(2E,7R,11R)-3,7,11,15-tetramethyloctadec-2-en-1-ol

CAS Registry Number

Not Available

SMILES

CCCC(C)CCC[C@@H](C)CCC[C@@H](C)CCC\C(C)=C\CO

InChI Identifier

InChI=1S/C22H44O/c1-6-10-19(2)11-7-12-20(3)13-8-14-21(4)15-9-16-22(5)17-18-23/h17,19-21,23H,6-16,18H2,1-5H3/b22-17+/t19?,20-,21-/m1/s1

InChI Key

RJPVZHPAFRZZGC-JSVAJZLASA-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
Akebia trifoliata	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

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	7.93	ChemAxon
pKa (Strongest Acidic)	16.33	ChemAxon
pKa (Strongest Basic)	-2.2	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	15	ChemAxon
Refractivity	105.44 m³·mol⁻¹	ChemAxon
Polarizability	44.43 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

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

163191143

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol (NP0200135)

MOL for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

3D MOL for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

3D SDF for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

3D-SDF for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

PDB for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

3D PDB for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

SMILES for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

INCHI for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

Structure for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)

3D Structure for NP0200135 ((2e,7r,11r)-3,7,11,15-tetramethyloctadec-2-en-1-ol)