NP-MRD: Showing NP-Card for (4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate (NP0224143)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 02:26:04 UTC

Updated at

2022-09-06 02:26:05 UTC

NP-MRD ID

NP0224143

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate

Description

(4E,6E,8E,11E)-trideca-4,6,8,11-tetraen-1-yl (3R)-3-{[(3R)-3-hydroxybutanoyl]oxy}butanoate belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. (4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate is found in Umbraculum umbraculum. Based on a literature review very few articles have been published on (4E,6E,8E,11E)-trideca-4,6,8,11-tetraen-1-yl (3R)-3-{[(3R)-3-hydroxybutanoyl]oxy}butanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062204262D          

 26 25  0  0  1  0            999 V2000
    4.0441    9.7599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296    8.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296    7.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    7.2849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    6.4599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586    6.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586    5.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    4.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6164    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3309    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4743    3.5724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4743    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  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
 10 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  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  1  0  0  0
M  END

     RDKit          3D

 58 57  0  0  0  0  0  0  0  0999 V2000
   -9.8044    2.6751    1.3122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6851    1.8012    0.1351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2826    0.5490    0.2498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1790   -0.2911   -0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7702   -0.7362   -1.0961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8257   -0.3997   -0.2322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4675   -0.8706   -0.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5351   -0.5320    0.4425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1528   -1.0070    0.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1921   -0.6992    1.0850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7538   -1.1609    0.9402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6827   -2.0004   -0.2857 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6085   -2.6208   -0.6156 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6548   -1.7520   -0.7910 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3706   -0.9965    0.0726 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1287   -1.0365    1.2927 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4532   -0.1083   -0.4086 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7584   -0.8375   -0.2128 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7386   -2.1440   -1.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8776   -0.1230   -0.6692 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9883    0.1690    0.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9928   -0.2259    1.2933 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0834    0.9349   -0.5294 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2340    1.1660    0.4474 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3454    1.9387   -0.1904 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7204    1.9143    1.5056 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7772    2.5973    1.8314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6372    3.7489    1.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0129    2.4887    2.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9320    2.1817   -0.8672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0278    0.1202    1.2025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5097    0.2478   -1.8775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8004   -1.2142   -0.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5310   -1.3664   -1.9484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0597    0.2167    0.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2137   -1.5005   -1.2684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8081    0.0920    1.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9352   -1.6282   -0.5970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4543   -0.0659    1.9361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4508   -1.6787    1.8510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2081   -0.1897    0.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0291   -1.4459   -1.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4236   -2.8664   -0.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8521   -3.4015    0.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5036   -3.2953   -1.5252 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2732    0.1258   -1.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4318    0.8026    0.2002 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8231   -1.1562    0.8429 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5677   -1.9298   -2.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7634   -2.5958   -0.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505   -2.8813   -0.5866 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7312    1.9055   -0.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4620    0.2977   -1.3572 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5585    0.1985    0.8706 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2882    1.7608   -1.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3096    1.5687    0.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2537    2.9971    0.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3186    1.9516    2.2905 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
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  1
 19 49  1  0
 19 50  1  0
 19 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  1
 25 55  1  0
 25 56  1  0
 25 57  1  0
 26 58  1  0
M  END


  Mrv1652309062204262D          

 26 25  0  0  1  0            999 V2000
    4.0441    9.7599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296    8.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296    7.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    7.2849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    6.4599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586    6.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586    5.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    4.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6164    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3309    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4743    3.5724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4743    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  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
 10 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  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0224143

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C21H32O5/c1-4-5-6-7-8-9-10-11-12-13-14-15-25-20(23)17-19(3)26-21(24)16-18(2)22/h4-5,7-12,18-19,22H,6,13-17H2,1-3H3/b5-4+,8-7+,10-9+,12-11+/t18-,19-/m1/s1

> <INCHI_KEY>
XKXAEQCZZGRRAV-BXQDGFAKSA-N

> <FORMULA>
C21H32O5

> <MOLECULAR_WEIGHT>
364.482

> <EXACT_MASS>
364.22497413

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
42.038869650551405

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4E,6E,8E,11E)-trideca-4,6,8,11-tetraen-1-yl (3R)-3-{[(3R)-3-hydroxybutanoyl]oxy}butanoate

> <JCHEM_LOGP>
3.913683554999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.407216648531552

> <JCHEM_PKA_STRONGEST_BASIC>
-2.620683437932299

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
107.95410000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4E,6E,8E,11E)-trideca-4,6,8,11-tetraen-1-yl (3R)-3-{[(3R)-3-hydroxybutanoyl]oxy}butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       7.549  18.218   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.549  16.678   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.215  15.908   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.215  14.368   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.549  13.598   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.549  12.058   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.883  11.288   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.883   9.748   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.216   8.978   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.216   7.438   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.884   7.438   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.217   6.668   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      15.551   7.438   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      16.885   6.668   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      16.885   5.128   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      18.218   7.438   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.552   6.668   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      19.552   5.128   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      20.886   7.438   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      22.219   6.668   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      22.219   5.128   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      23.553   7.438   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      24.887   6.668   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.220   7.438   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      24.887   5.128   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
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                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   50    0
END

View in JSmol

Synonyms

Value	Source
(4E,6E,8E,11E)-Trideca-4,6,8,11-tetraen-1-yl (3R)-3-{[(3R)-3-hydroxybutanoyl]oxy}butanoic acid	Generator

Chemical Formula

C₂₁H₃₂O₅

Average Mass

364.4820 Da

Monoisotopic Mass

364.22497 Da

IUPAC Name

(4E,6E,8E,11E)-trideca-4,6,8,11-tetraen-1-yl (3R)-3-{[(3R)-3-hydroxybutanoyl]oxy}butanoate

Traditional Name

(4E,6E,8E,11E)-trideca-4,6,8,11-tetraen-1-yl (3R)-3-{[(3R)-3-hydroxybutanoyl]oxy}butanoate

CAS Registry Number

Not Available

SMILES

C\C=C\C\C=C\C=C\C=C\CCCOC(=O)C[C@@H](C)OC(=O)C[C@@H](C)O

InChI Identifier

InChI=1S/C21H32O5/c1-4-5-6-7-8-9-10-11-12-13-14-15-25-20(23)17-19(3)26-21(24)16-18(2)22/h4-5,7-12,18-19,22H,6,13-17H2,1-3H3/b5-4+,8-7+,10-9+,12-11+/t18-,19-/m1/s1

InChI Key

XKXAEQCZZGRRAV-BXQDGFAKSA-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
Umbraculum umbraculum	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohol esters

Direct Parent

Fatty alcohol esters

Alternative Parents

Substituents

Fatty alcohol ester
Fatty acid ester
Beta-hydroxy acid
Hydroxy acid
Dicarboxylic acid or derivatives
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.91	ChemAxon
pKa (Strongest Acidic)	15.41	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	107.95 m³·mol⁻¹	ChemAxon
Polarizability	42.04 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

10471815

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14258872

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate (NP0224143)

MOL for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

3D MOL for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

3D SDF for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

3D-SDF for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

PDB for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

3D PDB for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

SMILES for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

INCHI for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

Structure for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)

3D Structure for NP0224143 ((4e,6e,8e,11e)-trideca-4,6,8,11-tetraen-1-yl (3r)-3-{[(3r)-3-hydroxybutanoyl]oxy}butanoate)