NP-MRD: Showing NP-Card for [(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate (NP0234394)

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Record Information

Version

2.0

Created at

2022-09-06 16:24:32 UTC

Updated at

2022-09-06 16:24:33 UTC

NP-MRD ID

NP0234394

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

Description

Hymenoside L 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)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate is found in Hymenophyllum barbatum. Based on a literature review very few articles have been published on Hymenoside L.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062218242D          

 30 31  0  0  1  0            999 V2000
    1.4289   -1.6500    0.0000 O   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   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  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   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   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
    3.5724   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    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
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    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  0  0  0  0
  4  5  2  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  4 11  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
    3.2713   -0.8868    0.0761 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0608   -0.2750    1.1436 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1201    0.7009    1.5897 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2424    0.7289    0.6186 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2491    1.6019   -0.4529 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2809    1.6449   -1.3668 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3634    0.8007   -1.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4182    0.8353   -2.1629 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3682   -0.0753   -0.1746 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4680   -0.9220   -0.0591 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3332   -0.1138    0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9275   -0.5143    1.8210 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8348   -1.3012    1.6516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1285   -1.0760    0.5557 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7152    0.1611    0.5352 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0465    0.0072    0.0203 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4965    1.2089   -0.4109 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4617    1.9253    0.1131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8959    1.4516    0.0528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7685    2.2123   -0.5705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2000    2.0043   -0.7265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8198    0.9319   -0.2099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2715    0.2072    0.7204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9579    0.2470    2.1002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1482   -1.0461   -1.0265 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7327   -2.2116   -0.5831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8834   -1.3594   -1.7773 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0100   -2.6439   -2.3001 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3194   -1.3972   -0.8256 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9487   -2.6205   -0.8705 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4458    0.3490    2.5911 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6731    1.7081    1.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3915    2.2688   -0.5509 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2859    2.3296   -2.2069 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2016    0.2058   -2.0485 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5792   -1.5986    0.6740 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3422   -0.8049    1.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1207   -2.4173    1.5903 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2572   -1.2868    2.6328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9989   -1.8024    0.7943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5996   -0.3230    0.9232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4179    2.9671   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2431    2.1245    1.2310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3565    3.1513   -1.0515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4164    1.9941   -1.8540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7746    2.9178   -0.3280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4342    0.4417   -0.8073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7306   -0.6662    0.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3403   -0.0593    0.7151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9617   -0.6826    2.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8543   -0.6384   -1.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3489   -2.6049   -1.2498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6843   -0.6699   -2.6172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3214   -3.2874   -1.6065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.6100   -1.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4998   -3.2328   -0.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 20  1  0
 20 19  2  0
 19 23  1  0
 23 24  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  2  0
 14 29  1  0
 29 30  1  0
 29 27  1  0
 27 28  1  0
 27 25  1  0
 25 26  1  0
 25 16  1  0
 11  4  1  0
 22 47  1  0
 21 45  1  0
 21 46  1  0
 20 44  1  0
 23 48  1  0
 23 49  1  0
 24 50  1  0
 18 42  1  0
 18 43  1  0
 16 41  1  1
 14 40  1  1
 13 38  1  0
 13 39  1  0
  3 31  1  0
  3 32  1  0
  5 33  1  0
  6 34  1  0
  8 35  1  0
 10 36  1  0
 11 37  1  0
 29 55  1  6
 30 56  1  0
 27 53  1  6
 28 54  1  0
 25 51  1  6
 26 52  1  0
M  END


  Mrv1652309062218242D          

 30 31  0  0  1  0            999 V2000
    1.4289   -1.6500    0.0000 O   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   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    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
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  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   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   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
    3.5724   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    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
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    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  0  0  0  0
  4  5  2  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  4 11  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0234394

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC\C=C(/CO)CO[C@@H]1O[C@H](COC(=O)CC2=CC=C(O)C(O)=C2)[C@@H](O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O11/c20-4-3-11(7-21)8-29-19-18(27)17(26)16(25)14(30-19)9-28-15(24)6-10-1-2-12(22)13(23)5-10/h1-3,5,14,16-23,25-27H,4,6-9H2/b11-3+/t14-,16-,17-,18-,19-/m1/s1

> <INCHI_KEY>
SPEAUKMMJNSLEL-TZUBGXFXSA-N

> <FORMULA>
C19H26O11

> <MOLECULAR_WEIGHT>
430.406

> <EXACT_MASS>
430.147511657

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.17923886642752

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,3S,4R,5R,6R)-3,4,5-trihydroxy-6-{[(2E)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

> <JCHEM_LOGP>
-1.8213743513333331

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.093828478832732

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.266607174860924

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5330740485992314

> <JCHEM_POLAR_SURFACE_AREA>
186.37

> <JCHEM_REFRACTIVITY>
101.17740000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4R,5R,6R)-3,4,5-trihydroxy-6-{[(2E)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl (3,4-dihydroxyphenyl)acetate

> <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  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      16.004  -3.080   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      14.670  -2.310   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    4                                                       
CONECT   12    2   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   29                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   19   24                                                       
CONECT   24   23                                                            
CONECT   25   16   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   14   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₁₁

Average Mass

430.4060 Da

Monoisotopic Mass

430.14751 Da

IUPAC Name

[(2R,3S,4R,5R,6R)-3,4,5-trihydroxy-6-{[(2E)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

Traditional Name

[(2R,3S,4R,5R,6R)-3,4,5-trihydroxy-6-{[(2E)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl (3,4-dihydroxyphenyl)acetate

CAS Registry Number

Not Available

SMILES

OC\C=C(/CO)CO[C@@H]1O[C@H](COC(=O)CC2=CC=C(O)C(O)=C2)[C@@H](O)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C19H26O11/c20-4-3-11(7-21)8-29-19-18(27)17(26)16(25)14(30-19)9-28-15(24)6-10-1-2-12(22)13(23)5-10/h1-3,5,14,16-23,25-27H,4,6-9H2/b11-3+/t14-,16-,17-,18-,19-/m1/s1

InChI Key

SPEAUKMMJNSLEL-TZUBGXFXSA-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
Hymenophyllum barbatum	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
Glycosyl compound
O-glycosyl compound
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Monosaccharide
Oxane
Carboxylic acid ester
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Polyol
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Primary alcohol
Organic oxide
Carbonyl group
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	-1.8	ChemAxon
pKa (Strongest Acidic)	9.27	ChemAxon
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	186.37 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	101.18 m³·mol⁻¹	ChemAxon
Polarizability	42.18 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	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

C00033038

Chemspider ID

9223431

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11048264

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)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate (NP0234394)

MOL for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

3D MOL for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

3D SDF for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

3D-SDF for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

PDB for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

3D PDB for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

SMILES for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

INCHI for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

Structure for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)

3D Structure for NP0234394 ([(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate)