NP-MRD: Showing NP-Card for trans-Dodec-2-enoic acid (NP0091119)

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Record Information

Version

2.0

Created at

2022-05-11 18:31:13 UTC

Updated at

2022-05-11 18:31:13 UTC

NP-MRD ID

NP0091119

Secondary Accession Numbers

None

Natural Product Identification

Common Name

trans-Dodec-2-enoic acid

Description

Trans-Dodec-2-enoic acid belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms. Trans-Dodec-2-enoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Trans-Dodec-2-enoic acid exists in all eukaryotes, ranging from yeast to humans. Within humans, trans-dodec-2-enoic acid participates in a number of enzymatic reactions. In particular, trans-dodec-2-enoic acid can be biosynthesized from (R)-3-hydroxydodecanoic acid; which is mediated by the enzyme fatty acid synthase. Dyhydrase domain. In addition, trans-dodec-2-enoic acid can be converted into dodecanoic acid; which is mediated by the enzyme fatty acid synthase. Enoyl reductase domain. trans-Dodec-2-enoic acid is found in Lumbricus terrestris. In humans, trans-dodec-2-enoic acid is involved in fatty acid biosynthesis.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 35  0  0  0  0  0  0  0  0999 V2000
    5.1685    0.4282    1.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5685   -0.3744    0.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0819   -0.1209    0.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5170   -0.9477   -0.7932 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0383   -0.7382   -0.9832 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7209    0.6818   -1.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7569    0.9262   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5611    0.5728   -0.2722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0255    0.8696   -0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8573    0.5388    0.5503 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8282   -0.3635    0.5463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6293   -0.6680    1.7163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4228   -0.0724    2.7933 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6167   -1.6228    1.6135 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9435    0.0306    2.6050 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2855    0.3518    1.4910 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9418    1.5158    1.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7946   -1.4339    0.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0575   -0.0930   -0.4659 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5548   -0.3408    1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9953    0.9617    0.0996 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7130   -2.0283   -0.6032 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0218   -0.6478   -1.7437 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5567   -1.0594   -0.0135 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6883   -1.4555   -1.7475 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2336    0.9852   -2.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0816    1.3083   -0.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8866    2.0104   -1.6869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1066    0.3403   -2.3472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4415   -0.5074   -0.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2804    1.1656    0.6105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1356    1.9149   -0.9650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2474    0.2135   -1.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6719    1.0577    1.4754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9942   -0.8699   -0.3931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5010   -2.5296    1.1782 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
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 14  1  0
 12 13  2  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 11 35  1  0
 14 36  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      17.344 -11.839   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.677 -12.609   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.011 -11.839   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.345 -12.609   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.678 -11.839   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      24.012 -12.609   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      25.346 -11.839   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      26.680 -12.609   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      28.013 -11.839   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      29.347 -12.609   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      28.013 -10.299   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      16.010 -12.609   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.676 -11.839   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.343 -12.609   0.000  0.00  0.00           C+0
CONECT    1    2   12                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    1   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

View in JSmol

Synonyms

Value	Source
trans-Dodec-2-enoate	Generator
(e)-2-Dodecenoic acid	ChEBI
12:1, N-10 trans	ChEBI
2-Lauroleic acid	ChEBI
2t-Dodecensaeure	ChEBI
C12:1, N-10 trans	ChEBI
Dodecen-(2t)-saeure	ChEBI
trans-2-Lauroleic acid	ChEBI
(e)-2-Dodecenoate	Generator
2-Lauroleate	Generator
trans-2-Lauroleate	Generator
2-Dodecenoic acid	MeSH, HMDB
cis-2-Dodecenoic acid	MeSH, HMDB

Chemical Formula

C₁₂H₂₂O₂

Average Mass

198.3019 Da

Monoisotopic Mass

198.16198 Da

IUPAC Name

(2E)-dodec-2-enoic acid

Traditional Name

trans-2-dodecenoic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCC\C=C\C(O)=O

InChI Identifier

InChI=1S/C12H22O2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h10-11H,2-9H2,1H3,(H,13,14)/b11-10+

InChI Key

PAWGRNGPMLVJQH-ZHACJKMWSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Lumbricus terrestris	LOTUS Database	35616633
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
Unsaturated fatty acid
Straight chain fatty acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

2-dodecenoic acid (CHEBI:37162 )
Unsaturated fatty acids (LMFA01030788 )

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	5.02	ALOGPS
logP	4.48	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	5.03	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	9	ChemAxon
Refractivity	59.77 m³·mol⁻¹	ChemAxon
Polarizability	25.21 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

HMDB0010729

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB027876

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for trans-Dodec-2-enoic acid (NP0091119)

MOL for NP0091119 (trans-Dodec-2-enoic acid)

3D MOL for NP0091119 (trans-Dodec-2-enoic acid)

3D SDF for NP0091119 (trans-Dodec-2-enoic acid)

3D-SDF for NP0091119 (trans-Dodec-2-enoic acid)

PDB for NP0091119 (trans-Dodec-2-enoic acid)

3D PDB for NP0091119 (trans-Dodec-2-enoic acid)

SMILES for NP0091119 (trans-Dodec-2-enoic acid)

INCHI for NP0091119 (trans-Dodec-2-enoic acid)

Structure for NP0091119 (trans-Dodec-2-enoic acid)

3D Structure for NP0091119 (trans-Dodec-2-enoic acid)