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Showing metabocard for Ethyl trans-2-methyl-2-pentenoate (HMDB0032278)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:48:54 UTC
Update Date2023-02-21 17:21:51 UTC
HMDB IDHMDB0032278
Secondary Accession Numbers
  • HMDB32278
Metabolite Identification
Common NameEthyl trans-2-methyl-2-pentenoate
DescriptionEthyl trans-2-methyl-2-pentenoate belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. Based on a literature review a small amount of articles have been published on Ethyl trans-2-methyl-2-pentenoate.
Structure
Data?1677000111
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0032278 (Ethyl trans-2-methyl-2-pentenoate)


  Mrv0541 05061306262D          

 10  9  0  0  0  0            999 V2000
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.8579    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
   -0.4125   -2.1434    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  5  2  1  0  0  0  0
  6  4  1  0  0  0  0
  7  3  1  0  0  0  0
  7  6  2  0  0  0  0
  8  7  1  0  0  0  0
  9  8  2  0  0  0  0
 10  5  1  0  0  0  0
 10  8  1  0  0  0  0
M  END
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3D MOL for HMDB0032278 (Ethyl trans-2-methyl-2-pentenoate)

HMDB0032278
     RDKit          3D
Ethyl trans-2-methyl-2-pentenoate
 24 23  0  0  0  0  0  0  0  0999 V2000
   -3.8107   -0.5261    0.6838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9436   -0.0187   -0.4717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7205    0.6004    0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5350    0.1122   -0.1786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -1.0250   -1.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6907    0.7012    0.3966 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6657    1.6618    1.1782 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9168    0.1589    0.0493 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0997    0.7358    0.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3348    0.0184    0.1218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8275   -1.6384    0.6428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3698   -0.2562    1.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8263   -0.0933    0.6476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4928    0.7820   -1.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7028   -0.8241   -1.1687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8407    1.4247    0.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8507   -0.7555   -2.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9638   -1.9359   -0.7021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6030   -1.3051   -1.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0507    0.8093    1.7020 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1508    1.7724    0.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1980   -0.1456   -0.9674 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4271   -0.9293    0.6629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2083    0.6758    0.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  1 11  1  0
  1 12  1  0
  1 13  1  0
  2 14  1  0
  2 15  1  0
  3 16  1  0
  5 17  1  0
  5 18  1  0
  5 19  1  0
  9 20  1  0
  9 21  1  0
 10 22  1  0
 10 23  1  0
 10 24  1  0
M  END
Download

3D SDF for HMDB0032278 (Ethyl trans-2-methyl-2-pentenoate)


  Mrv0541 05061306262D          

 10  9  0  0  0  0            999 V2000
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.8579    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
   -0.4125   -2.1434    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  5  2  1  0  0  0  0
  6  4  1  0  0  0  0
  7  3  1  0  0  0  0
  7  6  2  0  0  0  0
  8  7  1  0  0  0  0
  9  8  2  0  0  0  0
 10  5  1  0  0  0  0
 10  8  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0032278

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C8H14O2/c1-4-6-7(3)8(9)10-5-2/h6H,4-5H2,1-3H3/b7-6+

> <INCHI_KEY>
HYQYCHQAUPHFKX-VOTSOKGWSA-N

> <FORMULA>
C8H14O2

> <MOLECULAR_WEIGHT>
142.1956

> <EXACT_MASS>
142.099379692

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
16.7308502898465

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
ethyl (2E)-2-methylpent-2-enoate

> <ALOGPS_LOGP>
2.86

> <JCHEM_LOGP>
2.495736785666667

> <ALOGPS_LOGS>
-1.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.843040682797944

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
41.44070000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.92e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ethyl (2E)-2-methylpent-2-enoate

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for HMDB0032278 (Ethyl trans-2-methyl-2-pentenoate)

HMDB0032278
     RDKit          3D
Ethyl trans-2-methyl-2-pentenoate
 24 23  0  0  0  0  0  0  0  0999 V2000
   -3.8107   -0.5261    0.6838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9436   -0.0187   -0.4717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7205    0.6004    0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5350    0.1122   -0.1786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4613   -1.0250   -1.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6907    0.7012    0.3966 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6657    1.6618    1.1782 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9168    0.1589    0.0493 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0997    0.7358    0.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3348    0.0184    0.1218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8275   -1.6384    0.6428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3698   -0.2562    1.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8263   -0.0933    0.6476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4928    0.7820   -1.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7028   -0.8241   -1.1687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8407    1.4247    0.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8507   -0.7555   -2.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9638   -1.9359   -0.7021 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6030   -1.3051   -1.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0507    0.8093    1.7020 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1508    1.7724    0.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1980   -0.1456   -0.9674 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4271   -0.9293    0.6629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2083    0.6758    0.3445 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  1 11  1  0
  1 12  1  0
  1 13  1  0
  2 14  1  0
  2 15  1  0
  3 16  1  0
  5 17  1  0
  5 18  1  0
  5 19  1  0
  9 20  1  0
  9 21  1  0
 10 22  1  0
 10 23  1  0
 10 24  1  0
M  END
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PDB for HMDB0032278 (Ethyl trans-2-methyl-2-pentenoate)

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -5.335   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.770  -4.001   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.310  -1.334   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       0.000  -2.667   0.000  0.00  0.00           O+0
CONECT    1    4                                                            
CONECT    2    5                                                            
CONECT    3    7                                                            
CONECT    4    1    6                                                       
CONECT    5    2   10                                                       
CONECT    6    4    7                                                       
CONECT    7    3    6    8                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    5    8                                                       
MASTER        0    0    0    0    0    0    0    0   10    0   18    0
END
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3D PDB for HMDB0032278 (Ethyl trans-2-methyl-2-pentenoate)

COMPND    HMDB0032278
HETATM    1  C1  UNL     1      -3.811  -0.526   0.684  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.944  -0.019  -0.472  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.721   0.600   0.128  1.00  0.00           C  
HETATM    4  C4  UNL     1      -0.535   0.112  -0.179  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.461  -1.025  -1.100  1.00  0.00           C  
HETATM    6  C6  UNL     1       0.691   0.701   0.397  1.00  0.00           C  
HETATM    7  O1  UNL     1       0.666   1.662   1.178  1.00  0.00           O  
HETATM    8  O2  UNL     1       1.917   0.159   0.049  1.00  0.00           O  
HETATM    9  C7  UNL     1       3.100   0.736   0.611  1.00  0.00           C  
HETATM   10  C8  UNL     1       4.335   0.018   0.122  1.00  0.00           C  
HETATM   11  H1  UNL     1      -3.828  -1.638   0.643  1.00  0.00           H  
HETATM   12  H2  UNL     1      -3.370  -0.256   1.665  1.00  0.00           H  
HETATM   13  H3  UNL     1      -4.826  -0.093   0.648  1.00  0.00           H  
HETATM   14  H4  UNL     1      -3.493   0.782  -1.028  1.00  0.00           H  
HETATM   15  H5  UNL     1      -2.703  -0.824  -1.169  1.00  0.00           H  
HETATM   16  H6  UNL     1      -1.841   1.425   0.791  1.00  0.00           H  
HETATM   17  H7  UNL     1      -0.851  -0.755  -2.108  1.00  0.00           H  
HETATM   18  H8  UNL     1      -0.964  -1.936  -0.702  1.00  0.00           H  
HETATM   19  H9  UNL     1       0.603  -1.305  -1.247  1.00  0.00           H  
HETATM   20  H10 UNL     1       3.051   0.809   1.702  1.00  0.00           H  
HETATM   21  H11 UNL     1       3.151   1.772   0.176  1.00  0.00           H  
HETATM   22  H12 UNL     1       4.198  -0.146  -0.967  1.00  0.00           H  
HETATM   23  H13 UNL     1       4.427  -0.929   0.663  1.00  0.00           H  
HETATM   24  H14 UNL     1       5.208   0.676   0.345  1.00  0.00           H  
CONECT    1    2   11   12   13
CONECT    2    3   14   15
CONECT    3    4    4   16
CONECT    4    5    6
CONECT    5   17   18   19
CONECT    6    7    7    8
CONECT    8    9
CONECT    9   10   20   21
CONECT   10   22   23   24
END
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SMILES for HMDB0032278 (Ethyl trans-2-methyl-2-pentenoate)

CCOC(=O)C(\C)=C\CC
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INCHI for HMDB0032278 (Ethyl trans-2-methyl-2-pentenoate)

InChI=1S/C8H14O2/c1-4-6-7(3)8(9)10-5-2/h6H,4-5H2,1-3H3/b7-6+
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
Ethyl trans-2-methyl-2-pentenoic acidGenerator
2-Pentenoic acid, 2-methyl-, ethyl esterHMDB
Ethyl (2E)-2-methyl-2-pentenoateHMDB
Ethyl (e)-2-methylpent-2-en-1-OateHMDB
Ethyl 2-methylpent-2-en-1-OateHMDB
Chemical FormulaC8H14O2
Average Molecular Weight142.1956
Monoisotopic Molecular Weight142.099379692
IUPAC Nameethyl (2E)-2-methylpent-2-enoate
Traditional Nameethyl (2E)-2-methylpent-2-enoate
CAS Registry Number1617-40-9
SMILES
CCOC(=O)C(\C)=C\CC
InChI Identifier
InChI=1S/C8H14O2/c1-4-6-7(3)8(9)10-5-2/h6H,4-5H2,1-3H3/b7-6+
InChI KeyHYQYCHQAUPHFKX-VOTSOKGWSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassFatty acid esters
Direct ParentFatty acid esters
Alternative Parents
Substituents
  • Fatty acid ester
  • Alpha,beta-unsaturated carboxylic ester
  • Enoate ester
  • Carboxylic acid ester
  • Monocarboxylic acid or derivatives
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effect
Organoleptic effect
Disposition
Biological locationRoute of exposureSource
Process
Naturally occurring process
Role
Biological roleIndustrial application
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility2.92 g/LALOGPS
logP2.86ALOGPS
logP2.5ChemAxon
logS-1.7ALOGPS
pKa (Strongest Basic)-6.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area26.3 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity41.44 m³·mol⁻¹ChemAxon
Polarizability16.73 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+132.71631661259
DarkChem[M-H]-129.78731661259
DeepCCS[M+H]+134.70230932474
DeepCCS[M-H]-132.15230932474
DeepCCS[M-2H]-168.67130932474
DeepCCS[M+Na]+143.77230932474
AllCCS[M+H]+134.432859911
AllCCS[M+H-H2O]+130.332859911
AllCCS[M+NH4]+138.232859911
AllCCS[M+Na]+139.332859911
AllCCS[M-H]-134.632859911
AllCCS[M+Na-2H]-137.032859911
AllCCS[M+HCOO]-139.832859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Ethyl trans-2-methyl-2-pentenoateCCOC(=O)C(\C)=C\CC1298.9Standard polar33892256
Ethyl trans-2-methyl-2-pentenoateCCOC(=O)C(\C)=C\CC979.5Standard non polar33892256
Ethyl trans-2-methyl-2-pentenoateCCOC(=O)C(\C)=C\CC1017.2Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Ethyl trans-2-methyl-2-pentenoate GC-MS (Non-derivatized) - 70eV, Positivesplash10-00kb-9000000000-824cf4b7fe7db79b0f1b2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Ethyl trans-2-methyl-2-pentenoate GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 10V, Positive-QTOFsplash10-0006-4900000000-7bb9052bfdfcce4ec1f42016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 20V, Positive-QTOFsplash10-0006-9200000000-6f9ff6e687e57d1ca8a62016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 40V, Positive-QTOFsplash10-00kf-9000000000-992e14f6af29e637a8242016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 10V, Negative-QTOFsplash10-0006-2900000000-8892f7f113eb026bea282016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 20V, Negative-QTOFsplash10-0007-9800000000-e34f3898274f765811f92016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 40V, Negative-QTOFsplash10-014i-9000000000-c289d2cd278e5d89e94e2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 10V, Positive-QTOFsplash10-014j-9000000000-8427ab9d484cfc482a822021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 20V, Positive-QTOFsplash10-014i-9000000000-d22266e12030cb3116d42021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 40V, Positive-QTOFsplash10-0gbc-9000000000-5bf622dd69b1306c9d412021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 10V, Negative-QTOFsplash10-03di-0900000000-d2d7e0e0a4bc977bee0f2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 20V, Negative-QTOFsplash10-01ba-9100000000-b9d16727776f7b313a9a2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Ethyl trans-2-methyl-2-pentenoate 40V, Negative-QTOFsplash10-014j-9000000000-e31214c77855bfe3ac672021-09-23Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-04FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-04FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB009410
KNApSAcK IDNot Available
Chemspider ID4940958
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound6436311
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  5. (). EAFUS: Everything Added to Food in the United States.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.