NP-MRD: Showing NP-Card for (6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol (NP0295657)

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Record Information

Version

2.0

Created at

2022-09-10 04:46:12 UTC

Updated at

2022-09-10 04:46:12 UTC

NP-MRD ID

NP0295657

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol

Description

Fokienol belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. (6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol is found in Dittrichia viscosa and Lentinellus cochleatus. (6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol was first documented in 2019 (PMID: 30654130). Based on a literature review very few articles have been published on Fokienol (PMID: 34946654).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 45  0  0  0  0  0  0  0  0999 V2000
   -5.3550    1.5874   -1.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9361    0.4020   -1.2396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0902   -0.1447    0.1198 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3330    0.9408    1.1462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2097   -0.9735    0.1326 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8674   -0.9542    0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6276   -0.0846    0.5436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253   -0.8755    0.8988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -0.9374    0.0458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4458   -0.2523   -1.2625 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -1.7397    0.4600 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0609   -1.0125    0.6221 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6228   -0.3015   -0.5542 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9478    0.3434   -0.2147 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0180   -0.0021   -0.8684 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3406    0.5469   -0.6310 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3489    0.1248   -1.3504 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5580    1.5732    0.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8511    2.2186   -0.8953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2214    1.9478   -2.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4353   -0.2346   -1.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9962    0.5916    2.1250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3781    1.2994    1.1299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7112    1.8197    0.8092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7019   -0.9243   -0.7081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7008   -1.7117   -0.3047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0414   -1.4922    1.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8496    0.6978    1.3188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4851    0.4702   -0.3980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4091   -1.3969    1.8504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3566    0.8318   -1.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4037   -0.5062   -1.8022 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3423   -0.6285   -1.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5505   -2.2276    1.4473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8884   -2.6321   -0.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8871   -0.2154    1.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8560   -1.6584    1.0676 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7771   -0.9127   -1.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9330    0.5850   -0.7391 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0072    1.0783    0.5568 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9029   -0.7618   -1.6514 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3300    0.5335   -1.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2524   -0.6227   -2.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5542    1.1300    1.4414 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7470    2.3591    0.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5003    2.1216    0.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 16  1  0
 16 17  2  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  1  0
  9  8  2  0
  8  7  1  0
  7  6  1  0
  6  3  1  0
  3  4  1  0
  3  5  1  6
  3  2  1  0
  2  1  2  3
 18 44  1  0
 18 45  1  0
 18 46  1  0
 17 42  1  0
 17 43  1  0
 15 41  1  0
 14 40  1  0
 13 38  1  0
 13 39  1  0
 12 36  1  0
 12 37  1  0
 11 34  1  0
 11 35  1  0
 10 31  1  0
 10 32  1  0
 10 33  1  0
  8 30  1  0
  7 28  1  0
  7 29  1  0
  6 26  1  0
  6 27  1  0
  4 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  2 21  1  0
  1 19  1  0
  1 20  1  0
M  END


  Mrv1652309102206462D          

 18 17  0  0  0  0            999 V2000
    7.0125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.7145    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
    3.3000    1.4289    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
    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
    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
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  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  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0295657

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H28O/c1-6-17(5,18)14-10-13-16(4)12-9-7-8-11-15(2)3/h6,8,11,13,18H,1-2,7,9-10,12,14H2,3-5H3/b11-8+,16-13+

> <INCHI_KEY>
XCTSDLUOCRRDLZ-YZLWMTBJSA-N

> <FORMULA>
C17H28O

> <MOLECULAR_WEIGHT>
248.41

> <EXACT_MASS>
248.214015522

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
31.770677006819533

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6E,11E)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol

> <JCHEM_LOGP>
4.892356071333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.459388332284092

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2856635434589379

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
83.25529999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(6E,11E)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      13.090  -1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.320  -0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.780  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.780   1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.780  -1.540   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.240  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.470   1.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.930   1.334   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000  -2.667   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    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                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₂₈O

Average Mass

248.4100 Da

Monoisotopic Mass

248.21402 Da

IUPAC Name

(6E,11E)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol

Traditional Name

(6E,11E)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C17H28O/c1-6-17(5,18)14-10-13-16(4)12-9-7-8-11-15(2)3/h6,8,11,13,18H,1-2,7,9-10,12,14H2,3-5H3/b11-8+,16-13+

InChI Key

XCTSDLUOCRRDLZ-YZLWMTBJSA-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
Dittrichia viscosa	LOTUS Database	35616633
Lentinellus cochleatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Acyclic monoterpenoids

Alternative Parents

Substituents

Acyclic monoterpenoid
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
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	4.89	ChemAxon
pKa (Strongest Acidic)	18.46	ChemAxon
pKa (Strongest Basic)	-1.3	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	9	ChemAxon
Refractivity	83.26 m³·mol⁻¹	ChemAxon
Polarizability	31.77 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00011421

Chemspider ID

4509331

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5352449

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Khoury M, El Beyrouthy M, Ouaini N, Eparvier V, Stien D: Hirtellina lobelii DC. essential oil, its constituents, its combination with antimicrobial drugs and its mode of action. Fitoterapia. 2019 Mar;133:130-136. doi: 10.1016/j.fitote.2019.01.001. Epub 2019 Jan 14. [PubMed:30654130 ]
Narangerel T, Bonikowski R, Jastrzabek K, Kunicka-Styczynska A, Plucinska A, Smigielski K, Majak I, Bartos A, Leszczynska J: Chemical and Biological Characteristics of Oxytropis pseudoglandulosa Plant of Mongolian Origin. Molecules. 2021 Dec 14;26(24):7573. doi: 10.3390/molecules26247573. [PubMed:34946654 ]
LOTUS database [Link]

Showing NP-Card for (6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol (NP0295657)

MOL for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

3D MOL for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

3D SDF for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

3D-SDF for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

PDB for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

3D PDB for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

SMILES for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

INCHI for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

Structure for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)

3D Structure for NP0295657 ((6e,11e)-3,7,13-trimethyltetradeca-1,6,11,13-tetraen-3-ol)