NP-MRD: Showing NP-Card for (2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate (NP0142675)

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Record Information

Version

2.0

Created at

2022-09-01 21:15:59 UTC

Updated at

2022-09-01 21:15:59 UTC

NP-MRD ID

NP0142675

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate

Description

Umbraculumin C belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. (2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate is found in Umbraculum mediterraneum. Based on a literature review very few articles have been published on Umbraculumin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 52  0  0  0  0  0  0  0  0999 V2000
   -9.1703   -0.3727   -1.2221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7788    0.0164   -0.8321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0128   -0.8711   -0.2578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5772   -0.5703    0.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5556   -0.7982    1.6306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3549   -0.5802    2.4272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1100   -1.3173    2.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4323   -1.1896    0.9024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1184    0.2171    0.5731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8692    0.6681    0.3496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7101    2.0575    0.0397 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4464    2.6197   -0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7021    1.9118   -0.1772 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8213    0.6999    0.0659 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9105    2.5708   -0.4396 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1459    1.8825   -0.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2449    0.7731   -1.4278 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2246    1.2630   -2.7410 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5509    0.2010   -1.2648 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093   -1.1548   -1.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6934   -1.8691   -0.9455 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0444   -1.7391   -0.8542 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1294   -1.0029   -0.9299 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7698   -1.6755   -0.7331 S   0  0  0  0  0  0  0  0  0  0  0  0
   10.8596   -0.3615   -0.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8459    0.5136   -1.2705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1242   -0.8937   -2.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6106   -1.0812   -0.5068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4057    1.0063   -1.0166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3884   -1.8627   -0.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9875   -1.2054   -0.4707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4056    0.4825   -0.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0306   -1.8219    1.8143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3632   -0.1130    2.0659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6719   -0.7204    3.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0846    0.5347    2.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1502   -2.3902    2.5700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3540   -0.8810    2.9773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9238   -1.7681    0.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3921   -1.6813    0.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9440    0.9040    0.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0807   -0.0538    0.4211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6222    2.7000   -0.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4090    3.7040   -0.4228 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9970    2.5648   -0.5830 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2644    1.4973    0.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5239   -0.0345   -1.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1250    1.5093   -3.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1434   -2.7887   -0.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0240    0.0431   -1.1173 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3654    0.2096    0.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7984   -0.8533    0.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1722    0.3285   -0.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 23  1  0
 23 22  2  0
 22 20  1  0
 20 21  2  0
 20 19  1  0
 19 17  1  0
 17 18  1  0
 17 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  2  0
 13 12  1  0
 12 11  2  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 23 50  1  0
 22 49  1  0
 17 47  1  6
 18 48  1  0
 16 45  1  0
 16 46  1  0
 12 44  1  0
 11 43  1  0
 10 42  1  0
  9 41  1  0
  8 39  1  0
  8 40  1  0
  7 37  1  0
  7 38  1  0
  6 35  1  0
  6 36  1  0
  5 33  1  0
  5 34  1  0
  4 31  1  0
  4 32  1  0
  3 30  1  0
  2 29  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
M  END


  Mrv1652309012223162D          

 25 24  0  0  1  0            999 V2000
   -3.2408    8.0289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5263    7.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5263    6.7914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8118    6.3789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8118    5.5539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    5.1414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829    3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316    2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    2.6664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039    1.4289    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9039    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4763    1.8414    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908    1.4289    0.0000 C   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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  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  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0142675

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CS\C=C\C(=O)O[C@H](O)COC(=O)\C=C/C=C/CCCCC\C=C\C

> <INCHI_IDENTIFIER>
InChI=1S/C19H28O5S/c1-3-4-5-6-7-8-9-10-11-12-13-17(20)23-16-19(22)24-18(21)14-15-25-2/h3-4,10-15,19,22H,5-9,16H2,1-2H3/b4-3+,11-10+,13-12-,15-14+/t19-/m0/s1

> <INCHI_KEY>
BNSKWDBAKDEEGE-UQISZPTISA-N

> <FORMULA>
C19H28O5S

> <MOLECULAR_WEIGHT>
368.49

> <EXACT_MASS>
368.165745176

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
42.186847256357254

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-hydroxy-2-{[(2E)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2Z,4E,11E)-trideca-2,4,11-trienoate

> <ALOGPS_LOGP>
5.06

> <JCHEM_LOGP>
5.1859162743333345

> <ALOGPS_LOGS>
-5.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.513145996666495

> <JCHEM_PKA_STRONGEST_BASIC>
-4.323949941058076

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
105.34669999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.85e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-hydroxy-2-{[(2E)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2Z,4E,11E)-trideca-2,4,11-trienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.049  14.987   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.716  14.217   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.716  12.677   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.382  11.907   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.382  10.367   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.048   9.597   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.048   8.057   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.715   7.287   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.715   5.747   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.619   4.977   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.619   3.437   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.953   2.667   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.286   3.437   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.286   4.977   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       4.620   2.667   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.287   2.667   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.287   1.127   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       8.621   3.437   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.955   2.667   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.955   1.127   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.288   3.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.622   2.667   0.000  0.00  0.00           C+0
HETATM   24  S   UNK     0      13.956   3.437   0.000  0.00  0.00           S+0
HETATM   25  C   UNK     0      15.289   2.667   0.000  0.00  0.00           C+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   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₈O₅S

Average Mass

368.4900 Da

Monoisotopic Mass

368.16575 Da

IUPAC Name

(2S)-2-hydroxy-2-{[(2E)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2Z,4E,11E)-trideca-2,4,11-trienoate

Traditional Name

(2S)-2-hydroxy-2-{[(2E)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2Z,4E,11E)-trideca-2,4,11-trienoate

CAS Registry Number

Not Available

SMILES

CS\C=C\C(=O)O[C@H](O)COC(=O)\C=C/C=C/CCCCC\C=C\C

InChI Identifier

InChI=1S/C19H28O5S/c1-3-4-5-6-7-8-9-10-11-12-13-17(20)23-16-19(22)24-18(21)14-15-25-2/h3-4,10-15,19,22H,5-9,16H2,1-2H3/b4-3+,11-10+,13-12-,15-14+/t19-/m0/s1

InChI Key

BNSKWDBAKDEEGE-UQISZPTISA-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 mediterraneum	LOTUS Database	35616633

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

Fatty acid ester
Dicarboxylic acid or derivatives
Vinylogous thioester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Acrylic acid or derivatives
Thioenolether
Hemiacetal
Carboxylic acid ester
Sulfenyl compound
Carboxylic acid derivative
Hydrocarbon derivative
Carbonyl group
Organosulfur compound
Organooxygen compound
Organic oxygen compound
Organic oxide
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	5.06	ALOGPS
logP	5.19	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	11.51	ChemAxon
pKa (Strongest Basic)	-4.3	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	105.35 m³·mol⁻¹	ChemAxon
Polarizability	42.19 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

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

101613865

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate (NP0142675)

MOL for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

3D MOL for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

3D SDF for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

3D-SDF for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

PDB for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

3D PDB for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

SMILES for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

INCHI for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

Structure for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)

3D Structure for NP0142675 ((2s)-2-hydroxy-2-{[(2e)-3-(methylsulfanyl)prop-2-enoyl]oxy}ethyl (2z,4e,11e)-trideca-2,4,11-trienoate)