NP-MRD: Showing NP-Card for [(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid (NP0305534)

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Record Information

Version

2.0

Created at

2022-09-10 21:26:45 UTC

Updated at

2022-09-10 21:26:45 UTC

NP-MRD ID

NP0305534

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid

Description

[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. [(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid is found in Diplospora dubia. Based on a literature review very few articles have been published on [(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102223262D          

 27 27  0  0  1  0            999 V2000
    5.5243    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8743    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  1  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  2  0  0  0  0
 20 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END

     RDKit          3D

 55 55  0  0  0  0  0  0  0  0999 V2000
    6.8260   -0.9324    0.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7969   -0.5874   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6771    0.8248   -0.9077 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3546    1.7241    0.1080 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1774    1.0096   -2.1929 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1902    1.1919   -0.9125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6873    0.9397    0.5086 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2532    1.2582    0.6385 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4088    0.3043    1.0036 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9063   -1.0759    1.2798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0504    0.5613    1.1528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7161   -0.2763    0.2682 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0983   -0.1165    0.3262 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6287   -1.3282    0.7552 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0066   -1.2889    0.9015 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5017   -2.7162    1.0183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1471   -3.4020   -0.1421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7065   -0.6549   -0.2568 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0515    0.6571    0.1416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6854    0.9344    0.0381 S   0  0  0  0  0  6  0  0  0  0  0  0
   -7.2984    0.8947    1.4308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3739   -0.0984   -0.8084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9778    2.4793   -0.5795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7805   -0.5031   -1.4380 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4188   -1.6972   -2.0147 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6143    0.3338   -0.9980 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0820    1.6634   -0.9076 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9133   -1.9532    0.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5886   -0.1915    0.6029 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0740   -1.3445   -0.7134 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8272    2.7147    0.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4318    1.8440   -0.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2329    1.2503    1.1044 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9965    0.4433   -2.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0493    2.2739   -1.0992 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6309    0.5387   -1.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661   -0.1178    0.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2292    1.6274    1.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371    2.2334    0.4529 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4051   -1.4834    0.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6064   -0.9873    2.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0926   -1.7391    1.5699 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2358    1.5990    0.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3338    0.3921    2.2028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2932    0.6782    1.1047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2522   -0.7996    1.8815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9447   -3.1792    1.8518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5923   -2.7631    1.2116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9655   -3.7259   -0.6346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6533   -1.1599   -0.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1119    2.9727   -0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3170    0.0945   -2.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5528   -1.6998   -2.4506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8542    0.3104   -1.8047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8137    2.0725   -0.0476 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9 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
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 23  1  0
 20 21  2  0
 20 22  2  0
 18 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  9  8  2  0
  8  7  1  0
  7  6  1  0
  6  3  1  0
  3  4  1  0
  3  5  1  6
  3  2  1  0
  2  1  2  3
 26 13  1  0
 10 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 13 45  1  1
 15 46  1  1
 16 47  1  0
 16 48  1  0
 17 49  1  0
 18 50  1  6
 23 51  1  0
 24 52  1  6
 25 53  1  0
 26 54  1  6
 27 55  1  0
  8 39  1  0
  7 37  1  0
  7 38  1  0
  6 35  1  0
  6 36  1  0
  4 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  2 30  1  0
  1 28  1  0
  1 29  1  0
M  END


  Mrv1652309102223262D          

 27 27  0  0  1  0            999 V2000
    5.5243    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993    1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8743    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.9355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  1  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  2  0  0  0  0
 20 23  1  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0305534

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CO[C@@H]1O[C@H](CO)[C@@H](OS(O)(=O)=O)[C@H](O)[C@H]1O)=C/CC[C@](C)(O)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C16H28O10S/c1-4-16(3,20)7-5-6-10(2)9-24-15-13(19)12(18)14(11(8-17)25-15)26-27(21,22)23/h4,6,11-15,17-20H,1,5,7-9H2,2-3H3,(H,21,22,23)/b10-6+/t11-,12-,13-,14-,15-,16-/m1/s1

> <INCHI_KEY>
CDAHNSRQLRCYBB-SGMCTCDHSA-N

> <FORMULA>
C16H28O10S

> <MOLECULAR_WEIGHT>
412.45

> <EXACT_MASS>
412.140318276

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
40.82452618498563

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid

> <JCHEM_LOGP>
-2.1641712763595202

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.266536686138243

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.006506126666218

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1942170655625968

> <JCHEM_POLAR_SURFACE_AREA>
162.98

> <JCHEM_REFRACTIVITY>
94.3864

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      10.312   2.874   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.772   2.874   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.232   0.206   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.336   0.770   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   20  S   UNK     0       2.667  -3.080   0.000  0.00  0.00           S+0
HETATM   21  O   UNK     0       3.437  -1.746   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.001  -3.850   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       1.897  -4.414   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20                                                            
CONECT   24   18   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   13   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Value	Source
[(2R,3S,4R,5R,6R)-4,5-Dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonate	Generator
[(2R,3S,4R,5R,6R)-4,5-Dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulphonate	Generator
[(2R,3S,4R,5R,6R)-4,5-Dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulphonic acid	Generator

Chemical Formula

C₁₆H₂₈O₁₀S

Average Mass

412.4500 Da

Monoisotopic Mass

412.14032 Da

IUPAC Name

[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid

Traditional Name

[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-{[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

C\C(CO[C@@H]1O[C@H](CO)[C@@H](OS(O)(=O)=O)[C@H](O)[C@H]1O)=C/CC[C@](C)(O)C=C

InChI Identifier

InChI=1S/C16H28O10S/c1-4-16(3,20)7-5-6-10(2)9-24-15-13(19)12(18)14(11(8-17)25-15)26-27(21,22)23/h4,6,11-15,17-20H,1,5,7-9H2,2-3H3,(H,21,22,23)/b10-6+/t11-,12-,13-,14-,15-,16-/m1/s1

InChI Key

CDAHNSRQLRCYBB-SGMCTCDHSA-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
Diplospora dubia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Monocyclic monoterpenoid
Monoterpenoid
Monosaccharide sulfate
Sulfate-ester
Sulfuric acid monoester
Sulfuric acid ester
Oxane
Alkyl sulfate
Monosaccharide
Tertiary alcohol
Organic sulfuric acid or derivatives
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
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	-2.2	ChemAxon
pKa (Strongest Acidic)	-2	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	162.98 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	94.39 m³·mol⁻¹	ChemAxon
Polarizability	40.82 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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

163186332

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid (NP0305534)

MOL for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D MOL for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D SDF for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D-SDF for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

PDB for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D PDB for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

SMILES for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

INCHI for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

Structure for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)

3D Structure for NP0305534 ([(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e,6s)-6-hydroxy-2,6-dimethylocta-2,7-dien-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl]oxidanesulfonic acid)