NP-MRD: Showing NP-Card for methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate (NP0010084)

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Record Information

Version

2.0

Created at

2021-01-05 19:43:05 UTC

Updated at

2021-07-15 17:05:06 UTC

NP-MRD ID

NP0010084

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate

Provided By

NPAtlas

Description

Methyl (4E)-6-(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate is found in Unknown-fungus sp. Based on a literature review very few articles have been published on methyl (4E)-6-(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106553D          

 32 31  0  0  0  0            999 V2000
   -6.0294   -0.9023   -0.5797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0831   -0.0667    0.0592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6988   -0.1914   -0.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4128   -1.0683   -1.0187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7604    0.6714    0.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4573    0.6402    0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8195   -0.2934   -0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4925   -0.3238   -0.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -1.2934   -1.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3039   -2.0768   -2.3296 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4350    0.5611   -0.1080 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3611   -0.1486    0.7008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    0.0855    2.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5202   -0.6987    2.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8694    0.9577    2.6157 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1856    1.3439   -1.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    1.2961   -1.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5185    2.0039   -1.9258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5410   -1.6108   -1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7702   -0.2611   -1.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5211   -1.4863    0.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1447    1.4416    1.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8726    1.3737    0.8747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3614   -1.0194   -1.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1051   -1.3507   -1.8846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9403    1.2759    0.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1959   -0.7460    3.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6725   -1.7189    2.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4831   -0.1166    2.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1423    2.2667   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0265    0.5131   -0.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9753    0.9425   -2.2524 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  8 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
 13 15  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  5 22  1  0  0  0  0
  6 23  1  0  0  0  0
  7 24  1  0  0  0  0
  9 25  1  0  0  0  0
 11 26  1  1  0  0  0
 14 27  1  0  0  0  0
 14 28  1  0  0  0  0
 14 29  1  0  0  0  0
 17 30  1  0  0  0  0
 17 31  1  0  0  0  0
 17 32  1  0  0  0  0
M  END

     RDKit          3D

 32 31  0  0  0  0  0  0  0  0999 V2000
   -6.0294   -0.9023   -0.5797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0831   -0.0667    0.0592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6988   -0.1914   -0.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4128   -1.0683   -1.0187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7604    0.6714    0.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4573    0.6402    0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8195   -0.2934   -0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4925   -0.3238   -0.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -1.2934   -1.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3039   -2.0768   -2.3296 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4350    0.5611   -0.1080 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3611   -0.1486    0.7008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    0.0855    2.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5202   -0.6987    2.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8694    0.9577    2.6157 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1856    1.3439   -1.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    1.2961   -1.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5185    2.0039   -1.9258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5410   -1.6108   -1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7702   -0.2611   -1.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5211   -1.4863    0.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1447    1.4416    1.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8726    1.3737    0.8747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3614   -1.0194   -1.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1051   -1.3507   -1.8846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9403    1.2759    0.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1959   -0.7460    3.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6725   -1.7189    2.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4831   -0.1166    2.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1423    2.2667   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0265    0.5131   -0.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9753    0.9425   -2.2524 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  8 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 11 16  1  0
 16 17  1  0
 16 18  2  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  6 23  1  0
  7 24  1  0
  9 25  1  0
 11 26  1  1
 14 27  1  0
 14 28  1  0
 14 29  1  0
 17 30  1  0
 17 31  1  0
 17 32  1  0
M  END


  Mrv1652306242106553D          

 32 31  0  0  0  0            999 V2000
   -6.0294   -0.9023   -0.5797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0831   -0.0667    0.0592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6988   -0.1914   -0.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4128   -1.0683   -1.0187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7604    0.6714    0.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4573    0.6402    0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8195   -0.2934   -0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4925   -0.3238   -0.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -1.2934   -1.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3039   -2.0768   -2.3296 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4350    0.5611   -0.1080 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3611   -0.1486    0.7008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    0.0855    2.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5202   -0.6987    2.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8694    0.9577    2.6157 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1856    1.3439   -1.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    1.2961   -1.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5185    2.0039   -1.9258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5410   -1.6108   -1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7702   -0.2611   -1.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5211   -1.4863    0.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1447    1.4416    1.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8726    1.3737    0.8747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3614   -1.0194   -1.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1051   -1.3507   -1.8846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9403    1.2759    0.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1959   -0.7460    3.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6725   -1.7189    2.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4831   -0.1166    2.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1423    2.2667   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0265    0.5131   -0.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9753    0.9425   -2.2524 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  8 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
 13 15  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  5 22  1  0  0  0  0
  6 23  1  0  0  0  0
  7 24  1  0  0  0  0
  9 25  1  0  0  0  0
 11 26  1  1  0  0  0
 14 27  1  0  0  0  0
 14 28  1  0  0  0  0
 14 29  1  0  0  0  0
 17 30  1  0  0  0  0
 17 31  1  0  0  0  0
 17 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010084

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C(=O)C(=C(/[H])\C(\[H])=C(\[H])C(=O)OC([H])([H])[H])\[C@@]([H])(OC(=O)C([H])([H])[H])C(=O)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C12H14O6/c1-8(14)12(18-9(2)15)10(7-13)5-4-6-11(16)17-3/h4-7,12H,1-3H3/b6-4-,10-5-/t12-/m0/s1

> <INCHI_KEY>
ZDTIBPQJDROEEG-TYASGOSFSA-N

> <FORMULA>
C12H14O6

> <MOLECULAR_WEIGHT>
254.238

> <EXACT_MASS>
254.079038171

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
25.145990569019222

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2Z,4E,6R)-6-(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate

> <ALOGPS_LOGP>
1.14

> <JCHEM_LOGP>
0.28238234066666656

> <ALOGPS_LOGS>
-2.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.755685242288294

> <JCHEM_PKA_STRONGEST_BASIC>
-6.1752947831582405

> <JCHEM_POLAR_SURFACE_AREA>
86.74000000000001

> <JCHEM_REFRACTIVITY>
63.43360000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.01e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2Z,4E,6R)-6-(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 32 31  0  0  0  0  0  0  0  0999 V2000
   -6.0294   -0.9023   -0.5797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0831   -0.0667    0.0592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6988   -0.1914   -0.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4128   -1.0683   -1.0187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7604    0.6714    0.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4573    0.6402    0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8195   -0.2934   -0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4925   -0.3238   -0.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -1.2934   -1.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3039   -2.0768   -2.3296 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4350    0.5611   -0.1080 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3611   -0.1486    0.7008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    0.0855    2.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5202   -0.6987    2.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8694    0.9577    2.6157 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1856    1.3439   -1.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    1.2961   -1.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5185    2.0039   -1.9258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5410   -1.6108   -1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7702   -0.2611   -1.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5211   -1.4863    0.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1447    1.4416    1.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8726    1.3737    0.8747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3614   -1.0194   -1.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1051   -1.3507   -1.8846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9403    1.2759    0.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1959   -0.7460    3.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6725   -1.7189    2.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4831   -0.1166    2.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1423    2.2667   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0265    0.5131   -0.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9753    0.9425   -2.2524 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  8 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 11 16  1  0
 16 17  1  0
 16 18  2  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  6 23  1  0
  7 24  1  0
  9 25  1  0
 11 26  1  1
 14 27  1  0
 14 28  1  0
 14 29  1  0
 17 30  1  0
 17 31  1  0
 17 32  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -6.029  -0.902  -0.580  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.083  -0.067   0.059  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.699  -0.191  -0.206  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.413  -1.068  -1.019  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.760   0.671   0.458  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.457   0.640   0.285  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.820  -0.293  -0.617  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.493  -0.324  -0.791  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.048  -1.293  -1.716  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.304  -2.077  -2.330  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.435   0.561  -0.108  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.361  -0.149   0.701  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.537   0.086   2.040  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.520  -0.699   2.799  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.869   0.958   2.616  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.186   1.344  -1.157  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.660   1.296  -1.227  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.519   2.004  -1.926  0.00  0.00           O+0
HETATM   19  H   UNK     0      -5.541  -1.611  -1.270  0.00  0.00           H+0
HETATM   20  H   UNK     0      -6.770  -0.261  -1.109  0.00  0.00           H+0
HETATM   21  H   UNK     0      -6.521  -1.486   0.249  0.00  0.00           H+0
HETATM   22  H   UNK     0      -3.145   1.442   1.187  0.00  0.00           H+0
HETATM   23  H   UNK     0      -0.873   1.374   0.875  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.361  -1.019  -1.203  0.00  0.00           H+0
HETATM   25  H   UNK     0       2.105  -1.351  -1.885  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.940   1.276   0.538  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.196  -0.746   3.872  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.672  -1.719   2.394  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.483  -0.117   2.829  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.142   2.267  -0.974  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.027   0.513  -0.533  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.975   0.943  -2.252  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   22                                                  
CONECT    6    5    7   23                                                  
CONECT    7    6    8   24                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10   25                                                  
CONECT   10    9                                                            
CONECT   11    8   12   16   26                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13   27   28   29                                             
CONECT   15   13                                                            
CONECT   16   11   17   18                                                  
CONECT   17   16   30   31   32                                             
CONECT   18   16                                                            
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    5                                                            
CONECT   23    6                                                            
CONECT   24    7                                                            
CONECT   25    9                                                            
CONECT   26   11                                                            
CONECT   27   14                                                            
CONECT   28   14                                                            
CONECT   29   14                                                            
CONECT   30   17                                                            
CONECT   31   17                                                            
CONECT   32   17                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   62    0
END

RDKit          3D

32 31  0  0  0  0  0  0  0  0999 V2000
   -6.0294   -0.9023   -0.5797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0831   -0.0667    0.0592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6988   -0.1914   -0.2059 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4128   -1.0683   -1.0187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7604    0.6714    0.4581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4573    0.6402    0.2853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8195   -0.2934   -0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4925   -0.3238   -0.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0482   -1.2934   -1.7156 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3039   -2.0768   -2.3296 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4350    0.5611   -0.1080 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3611   -0.1486    0.7008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    0.0855    2.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5202   -0.6987    2.7993 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8694    0.9577    2.6157 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1856    1.3439   -1.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    1.2961   -1.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5185    2.0039   -1.9258 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5410   -1.6108   -1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7702   -0.2611   -1.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5211   -1.4863    0.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1447    1.4416    1.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8726    1.3737    0.8747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3614   -1.0194   -1.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1051   -1.3507   -1.8846 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9403    1.2759    0.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1959   -0.7460    3.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6725   -1.7189    2.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4831   -0.1166    2.8285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1423    2.2667   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0265    0.5131   -0.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9753    0.9425   -2.2524 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  8 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 11 16  1  0
 16 17  1  0
 16 18  2  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  6 23  1  0
  7 24  1  0
  9 25  1  0
 11 26  1  1
 14 27  1  0
 14 28  1  0
 14 29  1  0
 17 30  1  0
 17 31  1  0
 17 32  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Methyl (4E)-6-(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoic acid	Generator

Chemical Formula

C₁₂H₁₄O₆

Average Mass

254.2380 Da

Monoisotopic Mass

254.07904 Da

IUPAC Name

methyl (2Z,4E,6R)-6-(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate

Traditional Name

methyl (2Z,4E,6R)-6-(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate

CAS Registry Number

Not Available

SMILES

COC(=O)\C=C/C=C(/C=O)C(OC(C)=O)C(C)=O

InChI Identifier

InChI=1S/C12H14O6/c1-8(14)12(18-9(2)15)10(7-13)5-4-6-11(16)17-3/h4-7,12H,1-3H3/b6-4-,10-5-

InChI Key

ZDTIBPQJDROEEG-TYASGOSFSA-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
Unknown-fungus sp.	NPAtlas	21632082

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid esters

Alternative Parents

Substituents

Alpha-acyloxy ketone
Fatty acid ester
Medium-chain aldehyde
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated aldehyde
Enal
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Aldehyde
Carbonyl group
Organic oxygen compound
Organooxygen compound
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	1.14	ALOGPS
logP	0.28	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	9.76	ChemAxon
pKa (Strongest Basic)	-6.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	86.74 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	63.43 m³·mol⁻¹	ChemAxon
Polarizability	25.15 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA014839

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435996

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54589667

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate (NP0010084)

MOL for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

3D MOL for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

3D SDF for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

3D-SDF for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

PDB for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

3D PDB for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

SMILES for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

INCHI for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

Structure for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)

3D Structure for NP0010084 (methyl (2Z,4E)-6(acetyloxy)-5-formyl-7-oxoocta-2,4-dienoate)