NP-MRD: Showing NP-Card for [(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid (NP0224534)

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Record Information

Version

2.0

Created at

2022-09-06 02:54:59 UTC

Updated at

2022-09-06 02:54:59 UTC

NP-MRD ID

NP0224534

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid

Description

[(2S,3S,4S,5R,6S)-6-[(2S)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid belongs to the class of organic compounds known as sulfoquinovosyldiacylglycerols. These are glycerolipids made up of a sulfonic acid linked to the C6 atom of glucose, which in turn is bound to the O3 atom of the a 1,2-diacylglycerol moiety. [(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid is found in Lobophora variegata. Based on a literature review very few articles have been published on [(2S,3S,4S,5R,6S)-6-[(2S)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid.

Structure

MOL SDF PDB SMILES InChI

  Mrv1652309062204552D          

 52 52  0  0  1  0            999 V2000
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   24.2920   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   25.7210   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   26.4354   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -7.0125    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   25.6104   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.2604   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   25.0065   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   23.5775   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.5775   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.2946   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.0091   -2.0625    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  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  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  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  2  0  0  0  0
 27 30  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 23 35  1  0  0  0  0
 35 36  1  1  0  0  0
 20 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 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  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END

  Mrv1652309062204552D          

 52 52  0  0  1  0            999 V2000
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   24.2920   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   25.7210   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   26.4354   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -7.0125    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   25.6104   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.2604   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   25.0065   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   23.5775   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.5775   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.2946   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.0091   -2.0625    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  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  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  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  2  0  0  0  0
 27 30  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 23 35  1  0  0  0  0
 35 36  1  1  0  0  0
 20 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 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  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0224534

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)OC[C@H](CO[C@H]1O[C@H](CS(O)(=O)=O)[C@@H](O)[C@H](O)[C@H]1O)OC(=O)CCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C39H74O12S/c1-3-5-7-9-11-13-15-16-18-19-21-23-25-27-34(40)48-29-32(50-35(41)28-26-24-22-20-17-14-12-10-8-6-4-2)30-49-39-38(44)37(43)36(42)33(51-39)31-52(45,46)47/h32-33,36-39,42-44H,3-31H2,1-2H3,(H,45,46,47)/t32-,33-,36-,37+,38-,39+/m1/s1

> <INCHI_KEY>
GQKFRHKBEFDUTG-MRZVKHCOSA-N

> <FORMULA>
C39H74O12S

> <MOLECULAR_WEIGHT>
767.07

> <EXACT_MASS>
766.490098997

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
126

> <JCHEM_AVERAGE_POLARIZABILITY>
90.89791059383158

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2S,3S,4S,5R,6S)-6-[(2S)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid

> <JCHEM_LOGP>
9.053513523666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.220718690426109

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.2174811752618364

> <JCHEM_PKA_STRONGEST_BASIC>
-3.63738687072283

> <JCHEM_POLAR_SURFACE_AREA>
186.11999999999998

> <JCHEM_REFRACTIVITY>
199.30420000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
36

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(2S,3S,4S,5R,6S)-6-[(2S)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid

> <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      21.339  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      22.673  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      24.006  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      25.340  -3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      26.674  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      28.007  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      29.341  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      30.675  -3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      32.008  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      33.342  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      34.676  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      36.009  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      37.343  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      38.677  -3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      40.010  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      41.344  -3.850   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      41.344  -2.310   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      42.678  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      44.011  -3.850   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      45.345  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      45.345  -6.160   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      46.679  -6.930   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      46.679  -8.470   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      48.012  -9.240   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      48.012 -10.780   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      49.346 -11.550   0.000  0.00  0.00           C+0
HETATM   27  S   UNK     0      49.346 -13.090   0.000  0.00  0.00           S+0
HETATM   28  O   UNK     0      47.806 -13.090   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      50.886 -13.090   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      49.346 -14.630   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      46.679 -11.550   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      46.679 -13.090   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      45.345 -10.780   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      44.011 -11.550   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      45.345  -9.240   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      44.011  -8.470   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      46.679  -3.850   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      48.012  -4.620   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      48.012  -6.160   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      49.346  -3.850   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      50.680  -4.620   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      52.013  -3.850   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      53.347  -4.620   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      54.681  -3.850   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      56.015  -4.620   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      57.348  -3.850   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      58.682  -4.620   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      60.016  -3.850   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      61.349  -4.620   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      62.683  -3.850   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      64.017  -4.620   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      65.350  -3.850   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   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   37                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   35                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27                                                            
CONECT   31   25   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   23   36                                                  
CONECT   36   35                                                            
CONECT   37   20   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   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                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  104    0
END

View in JSmol

Synonyms

Value	Source
[(2S,3S,4S,5R,6S)-6-[(2S)-3-(Hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonate	Generator
[(2S,3S,4S,5R,6S)-6-[(2S)-3-(Hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulphonate	Generator
[(2S,3S,4S,5R,6S)-6-[(2S)-3-(Hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulphonic acid	Generator

Chemical Formula

C₃₉H₇₄O₁₂S

Average Mass

767.0700 Da

Monoisotopic Mass

766.49010 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)OC[C@H](CO[C@H]1O[C@H](CS(O)(=O)=O)[C@@H](O)[C@H](O)[C@H]1O)OC(=O)CCCCCCCCCCCCC

InChI Identifier

InChI=1S/C39H74O12S/c1-3-5-7-9-11-13-15-16-18-19-21-23-25-27-34(40)48-29-32(50-35(41)28-26-24-22-20-17-14-12-10-8-6-4-2)30-49-39-38(44)37(43)36(42)33(51-39)31-52(45,46)47/h32-33,36-39,42-44H,3-31H2,1-2H3,(H,45,46,47)/t32-,33-,36-,37+,38-,39+/m1/s1

InChI Key

GQKFRHKBEFDUTG-MRZVKHCOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Lobophora variegata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sulfoquinovosyldiacylglycerols. These are glycerolipids made up of a sulfonic acid linked to the C6 atom of glucose, which in turn is bound to the O3 atom of the a 1,2-diacylglycerol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Glycosylglycerols

Direct Parent

Sulfoquinovosyldiacylglycerols

Alternative Parents

Substituents

Sulfoquinovosyldiacylglycerol
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Monosaccharide
Oxane
Alkanesulfonic acid
Sulfonyl
Organosulfonic acid
Organosulfonic acid or derivatives
Organic sulfonic acid or derivatives
Carboxylic acid ester
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Polyol
Carboxylic acid derivative
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organosulfur compound
Carbonyl group
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

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

162860966

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid (NP0224534)

MOL for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

3D MOL for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

3D SDF for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

3D-SDF for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

PDB for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

3D PDB for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

SMILES for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

INCHI for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

Structure for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)

3D Structure for NP0224534 ([(2s,3s,4s,5r,6s)-6-[(2s)-3-(hexadecanoyloxy)-2-(tetradecanoyloxy)propoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid)