NP-MRD: Showing NP-Card for glyceryl 1-linoleate (NP0289745)

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Record Information

Version

2.0

Created at

2022-09-09 20:04:56 UTC

Updated at

2022-09-09 20:04:56 UTC

NP-MRD ID

NP0289745

Secondary Accession Numbers

None

Natural Product Identification

Common Name

glyceryl 1-linoleate

Description

Glyceryl monolinoleate, also known as (+-)-1-monolinolein or DL-1-linoleoylglycerol, belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. Glyceryl monolinoleate is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. glyceryl 1-linoleate is found in Hyoscyamus niger, Nelumbo nucifera, Pseudostellaria heterophylla, Saposhnikovia divaricata and Streptomyces piomogenus. Based on a literature review a small amount of articles have been published on Glyceryl monolinoleate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 63 62  0  0  0  0  0  0  0  0999 V2000
    4.3309    2.0000    4.1069 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2884    1.7008    2.9581 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4484    1.7158    1.7104 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2305    1.4282    0.4466 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2249    1.4803   -0.7214 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8838    1.2031   -1.9777 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6322    0.2169   -2.7616 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6845   -0.8631   -2.6491 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8447   -1.0382   -1.4908 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5419   -1.0031   -1.4833 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7396   -0.7733   -2.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1799   -1.9670   -2.9800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1186   -2.2470   -1.8418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0585   -1.0892   -1.5189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9235   -0.7413   -2.6662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8617    0.3807   -2.3960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8313    0.1859   -1.2913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3185    0.0996    0.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3586    0.8652    0.3776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8372   -0.7655    0.9945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4932   -0.9506    2.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9554    0.0713    3.2650 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4911   -0.2340    4.5807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5680    1.4549    2.9733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1048    2.3593    3.9402 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8192    2.0740    5.0785 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6414    1.1085    4.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6854    2.8375    3.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0860    2.4545    2.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6593    0.6814    3.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8417    2.6363    1.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7104    0.8688    1.8010 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6163    0.3977    0.4616 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0505    2.1374    0.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3215    0.9907   -0.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0231    2.6352   -0.7583 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6932    1.9269   -2.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2711    0.1977   -3.7075 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3359   -1.8242   -2.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1187   -0.9972   -3.6331 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3374   -1.2578   -0.4996 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0551   -1.1574   -0.4919 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0143    0.0555   -2.4159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2482   -0.4073   -3.5685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7242   -1.7031   -3.9125 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4249   -2.8920   -3.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4867   -2.4061   -0.9295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7021   -3.1581   -1.9724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7087   -1.5027   -0.6973 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5048   -0.2260   -1.1424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2809   -0.4261   -3.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5623   -1.6147   -2.9790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3847    0.6668   -3.3495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2021    1.2639   -2.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5623    1.0543   -1.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4939   -0.7014   -1.5173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3411   -0.9733    2.3994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8399   -1.9846    2.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0883   -0.0102    3.3932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1422    0.0664    5.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5077    1.6208    2.8975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0862    1.7775    2.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0849    2.2705    3.8405 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  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  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  0
 15 52  1  0
 16 53  1  0
 16 54  1  0
 17 55  1  0
 17 56  1  0
 21 57  1  0
 21 58  1  0
 22 59  1  1
 23 60  1  0
 24 61  1  0
 24 62  1  0
 25 63  1  0
M  END


  Mrv1652309092222042D          

 25 24  0  0  0  0            999 V2000
    5.4730    8.9349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586    8.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586    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
    3.3296    6.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296    5.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    4.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0441    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586    3.5724    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 C   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
    9.7599    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  0  0  0  0  0  0  0  0  0  0
   10.4743    2.7474    0.0000 O   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
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    4.8099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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  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  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0289745

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(O)CO

> <INCHI_IDENTIFIER>
InChI=1S/C21H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(24)25-19-20(23)18-22/h6-7,9-10,20,22-23H,2-5,8,11-19H2,1H3/b7-6-,10-9-

> <INCHI_KEY>
WECGLUPZRHILCT-HZJYTTRNSA-N

> <FORMULA>
C21H38O4

> <MOLECULAR_WEIGHT>
354.531

> <EXACT_MASS>
354.277009704

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
43.4336563631112

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,3-dihydroxypropyl (9Z,12Z)-octadeca-9,12-dienoate

> <JCHEM_LOGP>
5.247333896333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.561713304317518

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.619245765321082

> <JCHEM_PKA_STRONGEST_BASIC>
-2.968684336972288

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
105.54269999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2,3-dihydroxypropyl (9Z,12Z)-octadeca-9,12-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      10.216  16.678   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.883  15.908   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.883  14.368   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.549  13.598   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.549  12.058   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.215  11.288   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.215   9.748   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.549   8.978   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.549   7.438   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.883   6.668   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.216   7.438   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.884   7.438   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.217   6.668   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.551   7.438   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.885   6.668   0.000  0.00  0.00           C+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  O   UNK     0      19.552   5.128   0.000  0.00  0.00           O+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  C   UNK     0      23.553   7.438   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      23.553   8.978   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      24.887   6.668   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      26.220   7.438   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                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

View in JSmol

Synonyms

Value	Source
(+-)-1-Monolinolein	ChEBI
(+-)-2,3-Dihydroxypropyl (9Z,12Z)-9,12-octadecadienoate	ChEBI
(+-)-Glycerol 1-monolinolate	ChEBI
1-(9Z,12Z-Octadecadienoyl)-rac-glycerol	ChEBI
1-Monolinoleoyl-rac-glycerol	ChEBI
DL-1-Linoleoylglycerol	ChEBI
Linoleoyl monoglyceride racemic mixture	ChEBI
MG(18:2(9Z,12Z)/0:0/0:0)[rac]	ChEBI
rac-(9Z,12Z)-Octadecadienoylglycerol	ChEBI
(+-)-2,3-Dihydroxypropyl (9Z,12Z)-9,12-octadecadienoic acid	Generator
(+-)-Glycerol 1-monolinolic acid	Generator
Glyceryl monolinoleic acid	Generator
Glyceryl linoleic acid monoester	HMDB
Monolinolein	HMDB
MLG CPD	HMDB

Chemical Formula

C₂₁H₃₈O₄

Average Mass

354.5310 Da

Monoisotopic Mass

354.27701 Da

IUPAC Name

2,3-dihydroxypropyl (9Z,12Z)-octadeca-9,12-dienoate

Traditional Name

2,3-dihydroxypropyl (9Z,12Z)-octadeca-9,12-dienoate

CAS Registry Number

Not Available

SMILES

CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(O)CO

InChI Identifier

InChI=1S/C21H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-21(24)25-19-20(23)18-22/h6-7,9-10,20,22-23H,2-5,8,11-19H2,1H3/b7-6-,10-9-

InChI Key

WECGLUPZRHILCT-HZJYTTRNSA-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
Hyoscyamus niger	LOTUS Database	35616633
Nelumbo nucifera	LOTUS Database	35616633
Pseudostellaria heterophylla	LOTUS Database	35616633
Saposhnikovia divaricata	LOTUS Database	35616633
Streptomyces piomogenus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
1-acyl-sn-glycerol
Monoradylglycerol
Monoacylglycerol
Fatty acid ester
Glycerolipid
1,2-diol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Primary alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

1-monoglyceride (CHEBI:75568 )
monoacylglycerol 18:2 (CHEBI:75568 )
Monoacylglycerols (LMGL01010006 )

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	5.25	ChemAxon
pKa (Strongest Acidic)	13.62	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	105.54 m³·mol⁻¹	ChemAxon
Polarizability	43.43 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

HMDB0242115

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00040789

Chemspider ID

4446589

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5283469

PDB ID

Not Available

ChEBI ID

75565

Good Scents ID

rw1365851

References

General References

LOTUS database [Link]

Showing NP-Card for glyceryl 1-linoleate (NP0289745)

MOL for NP0289745 (glyceryl 1-linoleate)

3D MOL for NP0289745 (glyceryl 1-linoleate)

3D SDF for NP0289745 (glyceryl 1-linoleate)

3D-SDF for NP0289745 (glyceryl 1-linoleate)

PDB for NP0289745 (glyceryl 1-linoleate)

3D PDB for NP0289745 (glyceryl 1-linoleate)

SMILES for NP0289745 (glyceryl 1-linoleate)

INCHI for NP0289745 (glyceryl 1-linoleate)

Structure for NP0289745 (glyceryl 1-linoleate)

3D Structure for NP0289745 (glyceryl 1-linoleate)