NP-MRD: Showing NP-Card for (2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate (NP0230036)

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Record Information

Version

2.0

Created at

2022-09-06 10:21:25 UTC

Updated at

2022-09-06 10:21:25 UTC

NP-MRD ID

NP0230036

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate

Description

1,2-Di-(9Z,12Z-octadecadienoyl)-3-(beta-D-galactosyl)-sn-glycerol, also known as 1-18:2-2-18:2-Monogalactosyldiacylglycerol or 18:2-18:2-MGDG, belongs to the class of organic compounds known as 1,2-diacyl-3-o-beta-d-galactosyl-sn-glycerols. These are glycosyldiacylglycerols carrying a beta-D-galactose at the 3-position of the glycerol moiety. Thus, 1,2-di-(9Z,12Z-octadecadienoyl)-3-(beta-D-galactosyl)-sn-glycerol is considered to be a glycosyldiradylglycerol. (2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate is found in Arisaema amurense and Ipomoea batatas. Based on a literature review very few articles have been published on 1,2-di-(9Z,12Z-octadecadienoyl)-3-(beta-D-galactosyl)-sn-glycerol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062212212D          

 55 55  0  0  1  0            999 V2000
    6.6885    1.5542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7721    0.7335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5247    0.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6083   -0.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3609   -0.7632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4445   -1.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7756   -2.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0230   -1.7288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3540   -2.2116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4376   -3.0323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1902   -3.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6118   -3.2255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2808   -2.7427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0334   -3.0806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7023   -2.5978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4549   -2.9358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1239   -2.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0403   -1.6322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8765   -2.7909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5455   -2.3081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2981   -2.6461    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.3817   -3.4669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1343   -3.8048    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2180   -4.6256    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.9706   -4.9635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0542   -5.7843    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.8068   -6.1222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8904   -6.9430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3852   -6.2671    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.4688   -7.0878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.6326   -5.9291    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.9636   -6.4119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.5490   -5.1084    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.7964   -4.7704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.9671   -2.1633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7197   -2.5013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8033   -3.3220    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.3887   -2.0185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1413   -2.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8103   -1.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5629   -2.2116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2318   -1.7288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9844   -2.0667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0681   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3991   -3.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4827   -4.1910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.2353   -4.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3189   -5.3498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0715   -5.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7405   -5.2049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4931   -5.5429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1621   -5.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.9147   -5.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.5837   -4.9152    0.0000 C   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
 23 24  1  0  0  0  0
 25 24  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 25 34  1  0  0  0  0
 34 35  1  1  0  0  0
 22 36  1  1  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END

     RDKit          3D

133133  0  0  0  0  0  0  0  0999 V2000
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   -7.2282    5.6472   -1.4914 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8435   -0.5614    2.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3844   -1.6168    1.7312 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9642   -0.8906    1.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4869   -1.3710    1.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8115   -2.1027    3.1347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2122   -2.5362    3.3255 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8644   -3.3974    2.2909 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1164   -2.7747    0.9941 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8940   -2.1900   -1.3178 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9812   -2.1883   -2.5022 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8508   -3.4092   -3.2930 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4286   -4.5382   -2.8009 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2718   -7.2700   -1.8634 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.5504    2.7971   -3.6845 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2946    4.2301   -3.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1864    4.4656   -3.0860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5536    5.8301   -2.6389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0831    6.2310   -1.2684 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6295    5.3506   -0.2234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9408    4.6731    0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
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 55131  1  0
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 55133  1  0
M  END


  Mrv1652309062212212D          

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   16.8068   -6.1222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   24.5837   -4.9152    0.0000 C   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
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  6  7  2  0  0  0  0
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  9 10  2  0  0  0  0
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 17 18  1  0  0  0  0
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 25 26  1  0  0  0  0
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 32 33  1  6  0  0  0
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 25 34  1  0  0  0  0
 34 35  1  1  0  0  0
 22 36  1  1  0  0  0
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 49 50  2  0  0  0  0
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 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0230036

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC[C@H](CO[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C45H78O10/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-40(47)52-36-38(37-53-45-44(51)43(50)42(49)39(35-46)55-45)54-41(48)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h11-14,17-20,38-39,42-46,49-51H,3-10,15-16,21-37H2,1-2H3/b13-11-,14-12-,19-17-,20-18-/t38-,39-,42+,43+,44-,45-/m1/s1

> <INCHI_KEY>
BROOMPUVDPTGEG-RHNBIRJRSA-N

> <FORMULA>
C45H78O10

> <MOLECULAR_WEIGHT>
779.109

> <EXACT_MASS>
778.559498712

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
133

> <JCHEM_AVERAGE_POLARIZABILITY>
94.18930091983061

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-1-[(9Z,12Z)-octadeca-9,12-dienoyloxy]-3-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9Z,12Z)-octadeca-9,12-dienoate

> <JCHEM_LOGP>
10.562846169666669

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.200206016280394

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.21085705828492

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810834223250415

> <JCHEM_POLAR_SURFACE_AREA>
151.98

> <JCHEM_REFRACTIVITY>
222.98260000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
37

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-1-[(9Z,12Z)-octadeca-9,12-dienoyloxy]-3-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9Z,12Z)-octadeca-9,12-dienoate

> <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      12.485   2.901   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.641   1.369   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.046   0.738   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.202  -0.794   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.607  -1.425   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.763  -2.957   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.514  -3.858   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.110  -3.227   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.861  -4.128   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.017  -5.660   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.422  -6.291   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.075  -6.021   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.324  -5.120   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.729  -5.750   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      19.978  -4.849   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.383  -5.480   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      22.631  -4.579   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      22.475  -3.047   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      24.036  -5.210   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      25.285  -4.309   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      26.690  -4.939   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      26.846  -6.471   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      28.251  -7.102   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      28.407  -8.634   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      29.812  -9.265   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      29.968 -10.797   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      31.373 -11.428   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      31.529 -12.960   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      28.719 -11.699   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      28.875 -13.231   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      27.314 -11.068   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      26.065 -11.969   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      27.158  -9.536   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      25.753  -8.905   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      27.939  -4.038   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      29.343  -4.669   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      29.500  -6.201   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      30.592  -3.768   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      31.997  -4.399   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      33.246  -3.497   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      34.651  -4.128   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      35.899  -3.227   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      37.304  -3.858   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      37.460  -5.390   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      36.212  -6.291   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      36.368  -7.823   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      37.773  -8.454   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      37.929  -9.986   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      39.334 -10.617   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      40.582  -9.716   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      41.987 -10.347   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      43.236  -9.445   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      44.641 -10.076   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      45.890  -9.175   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                                                       
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   36                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   34                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   25   35                                                  
CONECT   35   34                                                            
CONECT   36   22   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  110    0
END

View in JSmol

Synonyms

Value	Source
1,2-(9Z,12Z-Octadecadienoyl)-3-O-beta-D-galactosyl-sn-glycerol	ChEBI
1,2-Di-(9Z,12Z-octadecadienoyl)-3-beta-D-galactosyl-sn-glycerol	ChEBI
1,2-Dilinoleoyl-3-(beta-D-galactosyl)-sn-glycerol	ChEBI
1-18:2-2-18:2-Monogalactosyldiacylglycerol	ChEBI
18:2-18:2-MGDG	ChEBI
1,2-(9Z,12Z-Octadecadienoyl)-3-O-b-D-galactosyl-sn-glycerol	Generator
1,2-(9Z,12Z-Octadecadienoyl)-3-O-β-D-galactosyl-sn-glycerol	Generator
1,2-Di-(9Z,12Z-octadecadienoyl)-3-b-D-galactosyl-sn-glycerol	Generator
1,2-Di-(9Z,12Z-octadecadienoyl)-3-β-D-galactosyl-sn-glycerol	Generator
1,2-Dilinoleoyl-3-(b-D-galactosyl)-sn-glycerol	Generator
1,2-Dilinoleoyl-3-(β-D-galactosyl)-sn-glycerol	Generator
1,2-Di-(9Z,12Z-octadecadienoyl)-3-(b-D-galactosyl)-sn-glycerol	Generator
1,2-Di-(9Z,12Z-octadecadienoyl)-3-(β-D-galactosyl)-sn-glycerol	Generator

Chemical Formula

C₄₅H₇₈O₁₀

Average Mass

779.1090 Da

Monoisotopic Mass

778.55950 Da

IUPAC Name

(2S)-1-[(9Z,12Z)-octadeca-9,12-dienoyloxy]-3-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9Z,12Z)-octadeca-9,12-dienoate

Traditional Name

(2S)-1-[(9Z,12Z)-octadeca-9,12-dienoyloxy]-3-{[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9Z,12Z)-octadeca-9,12-dienoate

CAS Registry Number

Not Available

SMILES

CCCCC\C=C/C\C=C/CCCCCCCC(=O)OC[C@H](CO[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC

InChI Identifier

InChI=1S/C45H78O10/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-40(47)52-36-38(37-53-45-44(51)43(50)42(49)39(35-46)55-45)54-41(48)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h11-14,17-20,38-39,42-46,49-51H,3-10,15-16,21-37H2,1-2H3/b13-11-,14-12-,19-17-,20-18-/t38-,39-,42+,43+,44-,45-/m1/s1

InChI Key

BROOMPUVDPTGEG-RHNBIRJRSA-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
Arisaema amurense	LOTUS Database	35616633
Ipomoea batatas	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,2-diacyl-3-o-beta-d-galactosyl-sn-glycerols. These are glycosyldiacylglycerols carrying a beta-D-galactose at the 3-position of the glycerol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Glycosylglycerols

Direct Parent

1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols

Alternative Parents

Substituents

1,2-diacyl-3-o-beta-d-galactosyl-sn-glycerol
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Octadecanoid
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Monosaccharide
Oxane
Secondary alcohol
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Polyol
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Carbonyl group
Primary alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	10.56	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	151.98 Å²	ChemAxon
Rotatable Bond Count	37	ChemAxon
Refractivity	222.98 m³·mol⁻¹	ChemAxon
Polarizability	94.19 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

58145803

KEGG Compound ID

Not Available

BioCyc ID

CPD-8165

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90657255

PDB ID

Not Available

ChEBI ID

90506

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate (NP0230036)

MOL for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

3D MOL for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

3D SDF for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

3D-SDF for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

PDB for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

3D PDB for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

SMILES for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

INCHI for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

Structure for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)

3D Structure for NP0230036 ((2s)-1-[(9z,12z)-octadeca-9,12-dienoyloxy]-3-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}propan-2-yl (9z,12z)-octadeca-9,12-dienoate)