NP-MRD: Showing NP-Card for 6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid (NP0314198)

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Record Information

Version

2.0

Created at

2022-09-11 12:10:38 UTC

Updated at

2022-09-11 12:10:38 UTC

NP-MRD ID

NP0314198

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid

Description

Parmentin A 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. 6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid is found in Parmentiera cereifera. Based on a literature review very few articles have been published on Parmentin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112214102D          

 31 33  0  0  1  0            999 V2000
    0.0000   -1.6500    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
    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  1  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   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    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 11 23  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  6  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
    2.7355   -1.5266    0.9757 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0342   -0.5384    0.2563 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0430    0.3778    0.0648 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7673    0.2446    0.6249 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5134    1.3519    1.6157 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0216    0.8194    2.7884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3821    2.4398    1.1627 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4595    3.6166    0.7085 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3679    3.9605    1.7083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2594    2.1292    0.1573 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5583    0.7461    0.1991 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6301    0.4418   -0.6187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6810   -0.1955    0.0679 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8114    0.7188    0.0022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9817    0.3649   -0.4484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2682   -0.9776   -0.9285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3047   -1.8575   -0.9028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5805   -3.1692   -1.3704 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9684   -1.5436   -0.4158 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6131   -2.5383    0.6620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1597   -2.1129    1.7302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7986   -3.8722    0.4353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3287    0.0848   -0.4004 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5349   -1.2596   -0.6508 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3746   -0.4381   -0.3079 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7251    0.6346   -1.0984 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9717    0.7922   -1.6631 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9225   -0.1744   -1.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2056   -0.0796   -1.9659 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6146   -1.2650   -0.6406 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3401   -1.3937   -0.0832 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7730   -0.7033    1.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5051    1.7632    1.9059 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4117   -0.0191    3.0630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0031    2.8372    2.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0073    3.4312   -0.2263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1766    4.5219    0.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2925    3.9243    1.3837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7170    0.4364    1.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3179   -0.2723    1.1361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6954    1.7605    0.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7950    1.1074   -0.4707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2551   -1.2684   -1.3061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8110   -3.6762   -1.7882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2674   -1.8651   -1.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3690   -4.6217    0.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1220    0.6558   -1.3318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7424   -1.4249   -1.5954 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9368    1.3866   -1.2643 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2152    1.6445   -2.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4311    0.7274   -2.5464 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3790   -2.0171   -0.4657 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1276   -2.2507    0.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 22  1  0
 20 21  2  0
 11 23  1  0
 23 24  1  0
 23  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  2  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
 19 13  1  0
 31 25  1  0
  9 38  1  0
  8 36  1  0
  8 37  1  0
  7 35  1  1
 11 39  1  1
 13 40  1  1
 14 41  1  0
 15 42  1  0
 16 43  1  0
 18 44  1  0
 19 45  1  6
 22 46  1  0
 23 47  1  6
 24 48  1  0
  4 32  1  1
 26 49  1  0
 27 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
  5 33  1  1
  6 34  1  0
M  END


  Mrv1652309112214102D          

 31 33  0  0  1  0            999 V2000
    0.0000   -1.6500    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
    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  1  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   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    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 11 23  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  6  0  0  0
  2 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0314198

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@H](OC2C=CC=C(O)C2C(O)=O)[C@H](O)[C@@H](OC(=O)C2=CC=C(O)C=C2)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O11/c21-8-13-15(24)17(31-19(28)9-4-6-10(22)7-5-9)16(25)20(30-13)29-12-3-1-2-11(23)14(12)18(26)27/h1-7,12-17,20-25H,8H2,(H,26,27)/t12?,13-,14?,15-,16-,17+,20-/m1/s1

> <INCHI_KEY>
LFYZEEIUGCPAGW-TUPSLAKHSA-N

> <FORMULA>
C20H22O11

> <MOLECULAR_WEIGHT>
438.385

> <EXACT_MASS>
438.116211528

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
41.54233355386206

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-{[(2R,3R,4S,5R,6R)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid

> <JCHEM_LOGP>
-0.1585384346666659

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.933215618988435

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.613219611689906

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9811031690541254

> <JCHEM_POLAR_SURFACE_AREA>
183.20999999999998

> <JCHEM_REFRACTIVITY>
103.5491

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
6-{[(2R,3R,4S,5R,6R)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.667 -12.320   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   23                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12   23                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   13   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   11    4   24                                                  
CONECT   24   23                                                            
CONECT   25    2   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   25                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₂O₁₁

Average Mass

438.3850 Da

Monoisotopic Mass

438.11621 Da

IUPAC Name

6-{[(2R,3R,4S,5R,6R)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid

Traditional Name

6-{[(2R,3R,4S,5R,6R)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@H](OC2C=CC=C(O)C2C(O)=O)[C@H](O)[C@@H](OC(=O)C2=CC=C(O)C=C2)[C@@H]1O

InChI Identifier

InChI=1S/C20H22O11/c21-8-13-15(24)17(31-19(28)9-4-6-10(22)7-5-9)16(25)20(30-13)29-12-3-1-2-11(23)14(12)18(26)27/h1-7,12-17,20-25H,8H2,(H,26,27)/t12?,13-,14?,15-,16-,17+,20-/m1/s1

InChI Key

LFYZEEIUGCPAGW-TUPSLAKHSA-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
Parmentiera cereifera	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
Hexose monosaccharide
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
O-glycosyl compound
Glycosyl compound
Benzoate ester
Benzoic acid or derivatives
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Oxane
Monosaccharide
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Enol
Carboxylic acid
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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	-0.16	ChemAxon
pKa (Strongest Acidic)	3.61	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	183.21 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	103.55 m³·mol⁻¹	ChemAxon
Polarizability	41.54 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

102138460

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid (NP0314198)

MOL for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

3D MOL for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

3D SDF for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

3D-SDF for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

PDB for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

3D PDB for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

SMILES for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

INCHI for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

Structure for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)

3D Structure for NP0314198 (6-{[(2r,3r,4s,5r,6r)-3,5-dihydroxy-4-(4-hydroxybenzoyloxy)-6-(hydroxymethyl)oxan-2-yl]oxy}-2-hydroxycyclohexa-2,4-diene-1-carboxylic acid)