NP-MRD: Showing NP-Card for (2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene (NP0195299)

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Record Information

Version

2.0

Created at

2022-09-04 13:07:55 UTC

Updated at

2022-09-04 13:07:55 UTC

NP-MRD ID

NP0195299

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene

Description

3,5,7-Trimethyl-2e,4e,6e,8e-decatetraene belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. (2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene is found in Aspergillus candidus. Based on a literature review very few articles have been published on 3,5,7-trimethyl-2e,4e,6e,8e-decatetraene.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 32  0  0  0  0  0  0  0  0999 V2000
    5.7130   -0.4512   -1.1041 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5018   -0.0196   -0.3131 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2942   -0.3146   -0.7037 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0673    0.0756    0.0244 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2021    0.7330    1.3335 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8875   -0.2453   -0.4365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3994    0.0721    0.1507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6631    0.9990    1.2582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4506   -0.4193   -0.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8521   -0.3264   -0.1841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5370    0.2557    0.9870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7039   -0.9190   -1.0706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1560   -0.8586   -0.8326 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4894   -1.3416   -1.6859 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5611   -0.6732   -0.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9946    0.3716   -1.7912 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6500    0.5531    0.5845 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2122   -0.8911   -1.6375 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3175    1.8098    1.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5077    0.3866    2.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2138    0.3697    1.7968 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9480   -0.8238   -1.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7848    0.5576    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6001    1.6226    1.0431 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0812    1.8676    1.2851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2200   -1.0261   -1.4055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9526    0.1002    1.8968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7949    1.3030    0.8401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5163   -0.3378    1.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3142   -1.4221   -1.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4938   -1.6077   -0.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4865    0.1834   -0.5481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7162   -1.0696   -1.7902 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  5 19  1  0
  5 20  1  0
  5 21  1  0
  6 22  1  0
  8 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
 11 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 13 32  1  0
 13 33  1  0
M  END

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       9.240   5.335   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.470   4.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.930   1.334   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.620   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+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    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12                                                            
MASTER        0    0    0    0    0    0    0    0   13    0   24    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₂₀

Average Mass

176.3030 Da

Monoisotopic Mass

176.15650 Da

IUPAC Name

(2E,4E,6E,8E)-3,5,7-trimethyldeca-2,4,6,8-tetraene

Traditional Name

(2E,4E,6E,8E)-3,5,7-trimethyldeca-2,4,6,8-tetraene

CAS Registry Number

Not Available

SMILES

C\C=C\C(\C)=C\C(\C)=C\C(\C)=C\C

InChI Identifier

InChI=1S/C13H20/c1-6-8-12(4)10-13(5)9-11(3)7-2/h6-10H,1-5H3/b8-6+,11-7+,12-10+,13-9+

InChI Key

RRPFGKUHEMWGSW-RYNMLCPOSA-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
Aspergillus candidus	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
Alkatetraene
Branched unsaturated hydrocarbon
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Acyclic olefin
Hydrocarbon
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Hydrocarbons (LMFA11000054 )

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	4.19	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	65.12 m³·mol⁻¹	ChemAxon
Polarizability	23.19 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

Not Available

Chemspider ID

14449931

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14656044

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene (NP0195299)

MOL for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

3D MOL for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

3D SDF for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

3D-SDF for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

PDB for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

3D PDB for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

SMILES for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

INCHI for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

Structure for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)

3D Structure for NP0195299 ((2e,4e,6e,8e)-3,5,7-trimethyldeca-2,4,6,8-tetraene)