NP-MRD: Showing NP-Card for 2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid (NP0156575)

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Record Information

Version

2.0

Created at

2022-09-02 13:48:03 UTC

Updated at

2022-09-02 13:48:03 UTC

NP-MRD ID

NP0156575

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid

Description

2-Hydroxy-5-[6-O-(2-hydroxybenzoyl)-beta-D-glucopyranosyloxy]benzoic acid belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. 2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid is found in Keiskea japonica. Based on a literature review very few articles have been published on 2-Hydroxy-5-[6-O-(2-hydroxybenzoyl)-beta-D-glucopyranosyloxy]benzoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022215482D          

 31 33  0  0  1  0            999 V2000
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1447   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    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  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  1  1  0  0  0
  6 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
  4 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    5.9266    4.3431   -0.6801 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4035    3.2280   -0.6569 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2636    2.1406   -0.3660 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0011    2.9104   -0.8958 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5582    1.5847   -0.8384 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2579    1.1950   -1.0540 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0095   -0.1378   -0.9576 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8031   -0.8337   -1.1355 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4241   -1.2794    0.1145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4305   -2.3571    0.1024 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9100   -2.5431    1.5201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5841   -1.4472    2.0560 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7876   -1.0234    1.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2249   -1.6554    0.5168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4962    0.1348    2.0477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9299    0.7927    3.1465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5599    1.8644    3.6760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7562    2.3163    3.1445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3242    1.6918    2.0773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6615    0.5681    1.5236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2849   -0.0173    0.4504 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1351   -3.6031   -0.4859 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9288   -4.4082   -0.8847 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0053   -3.2841   -1.6394 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3545   -3.5424   -1.2931 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8678   -1.9018   -2.1751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2750   -1.8476   -2.9703 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3298    2.1578   -1.3439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7099    3.4640   -1.4116 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0458    3.8578   -1.1893 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3746    5.1808   -1.2687 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7175    1.6182   -1.0971 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3366    0.8369   -0.6016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0364   -0.0916   -1.4290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2867   -2.0687   -0.5303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0113   -2.7005    2.1959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6018   -3.4098    1.6144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9898    0.4014    3.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1347    2.3865    4.5308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2308    3.1805    3.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2570    2.0168    1.6372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0800   -0.7755   -0.1176 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7241   -4.1057    0.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5204   -3.8692   -1.4756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8019   -4.0581   -2.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4029   -4.2382   -0.5963 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7261   -1.7425   -2.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4814   -2.7182   -3.3946 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2901    1.8908   -1.5202 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0036    4.2786   -1.6407 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2380    5.6197   -1.1446 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 22  1  0
 22 23  1  0
 22 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30  4  1  0
  4  5  2  0
  4  2  1  0
  2  3  1  0
  2  1  2  0
  8 26  1  0
 26 27  1  0
 26 24  1  0
 20 15  1  0
  5  6  1  0
 25 46  1  0
 24 45  1  6
 22 43  1  1
 23 44  1  0
 10 35  1  6
 11 36  1  0
 11 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 21 42  1  0
  8 34  1  6
 28 49  1  0
 29 50  1  0
 31 51  1  0
  5 33  1  0
  3 32  1  0
 26 47  1  6
 27 48  1  0
M  END


  Mrv1652309022215482D          

 31 33  0  0  1  0            999 V2000
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1447   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -9.0750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    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  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  1  1  0  0  0
  6 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
  4 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0156575

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@H]1[C@H](O)[C@@H](COC(=O)C2=CC=CC=C2O)O[C@@H](OC2=CC=C(O)C(=C2)C(O)=O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O11/c21-12-4-2-1-3-10(12)19(28)29-8-14-15(23)16(24)17(25)20(31-14)30-9-5-6-13(22)11(7-9)18(26)27/h1-7,14-17,20-25H,8H2,(H,26,27)/t14-,15-,16+,17-,20-/m1/s1

> <INCHI_KEY>
SPXLSUKGTNJSSN-ISIBIEBGSA-N

> <FORMULA>
C20H20O11

> <MOLECULAR_WEIGHT>
436.369

> <EXACT_MASS>
436.100561464

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
40.595284983707124

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-hydroxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid

> <ALOGPS_LOGP>
0.57

> <JCHEM_LOGP>
2.2473645143333325

> <ALOGPS_LOGS>
-2.43

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.716053631928654

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.512085249189858

> <JCHEM_PKA_STRONGEST_BASIC>
-3.649110487330473

> <JCHEM_POLAR_SURFACE_AREA>
183.20999999999998

> <JCHEM_REFRACTIVITY>
101.22330000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.63e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      10.669 -12.320   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.003 -14.630   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      12.003 -16.170   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.337 -16.940   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      13.337 -18.480   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      14.670 -19.250   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      16.004 -18.480   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      14.670 -20.790   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.004 -21.560   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.004 -23.100   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.670 -23.870   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.337 -23.100   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.337 -21.560   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.003 -20.790   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.669 -16.940   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.669 -18.480   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.336 -16.170   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.002 -16.940   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.002 -13.860   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   30                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   26                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   22                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15   21                                                  
CONECT   21   20                                                            
CONECT   22   10   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    8   27                                                  
CONECT   27   26                                                            
CONECT   28    6   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    4   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
2-Hydroxy-5-[6-O-(2-hydroxybenzoyl)-b-D-glucopyranosyloxy]benzoate	Generator
2-Hydroxy-5-[6-O-(2-hydroxybenzoyl)-b-D-glucopyranosyloxy]benzoic acid	Generator
2-Hydroxy-5-[6-O-(2-hydroxybenzoyl)-beta-D-glucopyranosyloxy]benzoate	Generator
2-Hydroxy-5-[6-O-(2-hydroxybenzoyl)-β-D-glucopyranosyloxy]benzoate	Generator
2-Hydroxy-5-[6-O-(2-hydroxybenzoyl)-β-D-glucopyranosyloxy]benzoic acid	Generator

Chemical Formula

C₂₀H₂₀O₁₁

Average Mass

436.3690 Da

Monoisotopic Mass

436.10056 Da

IUPAC Name

2-hydroxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid

Traditional Name

2-hydroxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid

CAS Registry Number

Not Available

SMILES

O[C@H]1[C@H](O)[C@@H](COC(=O)C2=CC=CC=C2O)O[C@@H](OC2=CC=C(O)C(=C2)C(O)=O)[C@@H]1O

InChI Identifier

InChI=1S/C20H20O11/c21-12-4-2-1-3-10(12)19(28)29-8-14-15(23)16(24)17(25)20(31-14)30-9-5-6-13(22)11(7-9)18(26)27/h1-7,14-17,20-25H,8H2,(H,26,27)/t14-,15-,16+,17-,20-/m1/s1

InChI Key

SPXLSUKGTNJSSN-ISIBIEBGSA-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
Keiskea japonica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Hexose monosaccharide
O-hydroxybenzoic acid ester
O-glycosyl compound
Salicylic acid or derivatives
Salicylic acid
Hydroxybenzoic acid
Benzoate ester
4-alkoxyphenol
Benzoic acid
Benzoic acid or derivatives
Benzoyl
Phenol ether
Phenoxy compound
1-hydroxy-2-unsubstituted benzenoid
Sugar acid
1-hydroxy-4-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Oxane
Benzenoid
Monosaccharide
Vinylogous acid
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Oxacycle
Carboxylic acid
Polyol
Alcohol
Hydrocarbon derivative
Organic oxide
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	0.57	ALOGPS
logP	2.25	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	2.51	ChemAxon
pKa (Strongest Basic)	-3.6	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	101.22 m³·mol⁻¹	ChemAxon
Polarizability	40.6 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

56926746

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid (NP0156575)

MOL for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

3D MOL for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

3D SDF for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

3D-SDF for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

PDB for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

3D PDB for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

SMILES for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

INCHI for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

Structure for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)

3D Structure for NP0156575 (2-hydroxy-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[(2-hydroxybenzoyloxy)methyl]oxan-2-yl]oxy}benzoic acid)