NP-MRD: Showing NP-Card for (2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol (NP0283615)

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Record Information

Version

2.0

Created at

2022-09-09 10:57:11 UTC

Updated at

2022-09-09 10:57:11 UTC

NP-MRD ID

NP0283615

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol

Description

SCHEMBL16367020 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,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol is found in Artemisia gmelinii, Bidens pilosa, Parasenecio auriculatus, Caesalpinia pulcherrima, Carthamus tinctorius, Caulerpa racemosa, Glebionis coronaria, Cinnamomum kotoense, Desmarestia aculeata, Elodea canadensis, Farfugium japonicum, Fossombronia alaskana, Goniophlebium mengtzeense, Grangea maderaspatana, Hydrocotyle sibthorpioides, Laurencia nipponica, Lavandula latifolia, Lemna minor, Lindera glauca, Myriophyllum verticillatum, Paronychia kapela, Peperomia leptostachya, Picea abies, Piper aduncum, Piper auritum, Plagiochasma rupestre, Porella platyphylla, Pteris wallichiana, Pyrus communis, Schefflera arboricola, Tetragonia tetragonoides, Tetragonotheca repanda, Trichocolea tomentella and Xanthium strumarium. Based on a literature review very few articles have been published on SCHEMBL16367020.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 61 60  0  0  0  0  0  0  0  0999 V2000
    6.6626   -1.4961   -0.1532 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3629   -0.1890    0.4635 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3154    0.7143    0.6229 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7266    0.4853    0.2023 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5177    0.5934    1.3398 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9870    0.1251    0.9116 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0904    0.0370   -0.3308 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6918    0.3593    0.1416 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6900    0.3109   -0.9848 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7007   -0.9996   -1.7158 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2989    0.6266   -0.5398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2951   -0.3846    0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6828    0.0300    0.7625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6398    0.1789   -0.3759 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8759   -1.0831   -1.1397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9785    0.5996    0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9757    0.8256   -0.8797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3217    1.2502   -0.4377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0734    0.3423    0.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3358   -1.0274   -0.1206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5717    0.2754    1.8803 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5963   -1.9289    0.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8755   -2.2527    0.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7711   -1.4319   -1.2660 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1041    1.6821    1.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8924   -0.4701   -0.2909 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9885    1.3617   -0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8794    1.5137    1.4678 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9605    1.1297    1.3502 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6455   -0.5883    1.6851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3750    0.8077   -1.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1987   -1.0002   -0.6955 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7289    1.3854    0.5616 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4516   -0.3161    0.9718 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9938    1.0943   -1.7153 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3141   -1.8474   -1.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0767   -0.9313   -2.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7123   -1.2947   -2.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3282    0.6204   -1.4795 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1939    1.6262   -0.1160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3664   -1.4004   -0.0624 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2775   -0.5082    1.3234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5947    1.0381    1.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1482   -0.6755    1.4951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2768    0.9955   -1.0613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7420   -1.6241   -0.6948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0397   -1.7804   -1.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1249   -0.8465   -2.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8014    1.4896    0.8292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2551   -0.2391    0.9028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9829   -0.0182   -1.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5502    1.6867   -1.4781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9476    1.4253   -1.3544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2279    2.2311    0.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1128    0.8002    0.5492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0914   -1.5169    0.5590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4599   -1.6719   -0.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8427   -0.8903   -1.0823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3960    0.4547    2.6368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8303    1.0700    2.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2105   -0.7534    2.1586 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 21  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
 20 56  1  0
 20 57  1  0
 20 58  1  0
 19 55  1  0
 21 59  1  0
 21 60  1  0
 21 61  1  0
 18 53  1  0
 18 54  1  0
 17 51  1  0
 17 52  1  0
 16 49  1  0
 16 50  1  0
 14 45  1  6
 15 46  1  0
 15 47  1  0
 15 48  1  0
 13 43  1  0
 13 44  1  0
 12 41  1  0
 12 42  1  0
 11 39  1  0
 11 40  1  0
  9 35  1  6
 10 36  1  0
 10 37  1  0
 10 38  1  0
  8 33  1  0
  8 34  1  0
  7 31  1  0
  7 32  1  0
  6 29  1  0
  6 30  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
M  END


  Mrv1652309092212572D          

 21 20  0  0  1  0            999 V2000
    4.7586    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6151    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    3.9849    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
    6.9020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6164    3.5724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.6164    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3309    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4743    3.5724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4743    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  2  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  6  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  6  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  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0283615

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C20H40O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h15,17-19,21H,6-14,16H2,1-5H3/b20-15+/t18-,19-/m0/s1

> <INCHI_KEY>
BOTWFXYSPFMFNR-PFIWFTBQSA-N

> <FORMULA>
C20H40O

> <MOLECULAR_WEIGHT>
296.539

> <EXACT_MASS>
296.307915908

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
40.30403550961883

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
7.038550290000001

> <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>
96.23729999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       8.883   5.128   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.883   6.668   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.549   7.438   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.215   6.668   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.882   7.438   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.216   7.438   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.884   7.438   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.217   6.668   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.217   5.128   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.551   7.438   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.885   6.668   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.218   7.438   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      19.552   6.668   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.552   5.128   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      20.886   7.438   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      22.219   6.668   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.553   7.438   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      24.887   6.668   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      26.220   7.438   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      24.887   5.128   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    2    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                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₄₀O

Average Mass

296.5390 Da

Monoisotopic Mass

296.30792 Da

IUPAC Name

(2E,7S,11S)-3,7,11,15-tetramethylhexadec-2-en-1-ol

Traditional Name

(2E,7S,11S)-3,7,11,15-tetramethylhexadec-2-en-1-ol

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C20H40O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h15,17-19,21H,6-14,16H2,1-5H3/b20-15+/t18-,19-/m0/s1

InChI Key

BOTWFXYSPFMFNR-PFIWFTBQSA-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
Artemisia gmelinii	LOTUS Database	35616633
Bidens pilosa	LOTUS Database	35616633
Cacalia auriculata	LOTUS Database	35616633
Caesalpinia pulcherrima	LOTUS Database	35616633
Carthamus tinctorius	LOTUS Database	35616633
Caulerpa racemosa	LOTUS Database	35616633
Chrysanthemum coronarium	LOTUS Database	35616633
Cinnamomum kotoense	LOTUS Database	35616633
Desmarestia aculeata	LOTUS Database	35616633
Elodea canadensis	LOTUS Database	35616633
Farfugium japonicum	LOTUS Database	35616633
Fossombronia alaskana	LOTUS Database	35616633
Goniophlebium mengtzeense	LOTUS Database	35616633
Grangea maderaspatana	LOTUS Database	35616633
Hydrocotyle sibthorpioides	LOTUS Database	35616633
Laurencia nipponica	LOTUS Database	35616633
Lavandula latifolia	LOTUS Database	35616633
Lemna minor	LOTUS Database	35616633
Lindera glauca	LOTUS Database	35616633
Myriophyllum verticillatum	LOTUS Database	35616633
Paronychia kapela	LOTUS Database	35616633
Peperomia leptostachya	LOTUS Database	35616633
Picea abies	LOTUS Database	35616633
Piper aduncum	LOTUS Database	35616633
Piper auritum	LOTUS Database	35616633
Plagiochasma rupestre	LOTUS Database	35616633
Porella platyphylla	LOTUS Database	35616633
Pteris wallichiana	LOTUS Database	35616633
Pyrus communis	LOTUS Database	35616633
Schefflera arboricola	LOTUS Database	35616633
Tetragonia tetragonioides	LOTUS Database	35616633
Tetragonotheca repanda	LOTUS Database	35616633
Trichocolea tomentella	LOTUS Database	35616633
Xanthium strumarium	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	7.04	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	13	ChemAxon
Refractivity	96.24 m³·mol⁻¹	ChemAxon
Polarizability	40.3 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

32787421

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

40467768

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol (NP0283615)

MOL for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

3D MOL for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

3D SDF for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

3D-SDF for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

PDB for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

3D PDB for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

SMILES for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

INCHI for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

Structure for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)

3D Structure for NP0283615 ((2e,7s,11s)-3,7,11,15-tetramethylhexadec-2-en-1-ol)