NP-MRD: Showing NP-Card for [(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate (NP0153683)

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Record Information

Version

2.0

Created at

2022-09-02 10:23:10 UTC

Updated at

2022-09-02 10:23:10 UTC

NP-MRD ID

NP0153683

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

Description

[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 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. [(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate is found in Pyrola incarnata. Based on a literature review very few articles have been published on [(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022212232D          

 31 33  0  0  1  0            999 V2000
    4.2868   -4.1250    0.0000 C   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
    9.2881  -12.7875    0.0000 O   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
    7.8592  -13.6125    0.0000 O   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
    6.4302  -12.7875    0.0000 O   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
    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  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 13 21  1  0  0  0  0
  8 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
  6 26  1  0  0  0  0
 26 27  1  1  0  0  0
  4 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -6.4914    1.2916   -2.4275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4673    1.2438   -1.3531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3962    0.3955   -1.3702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4173    0.3277   -0.3771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3896   -0.5827   -0.5309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3375   -0.7917    0.3370 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1378   -0.4885   -0.2815 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6171   -1.5642   -0.6397 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7218   -1.2568   -1.6032 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6519   -0.3172   -1.1170 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4227   -0.4879    0.0151 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3038   -1.5483    0.6733 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3671    0.5109    0.4766 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5262    1.6871   -0.2253 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4154    2.6565    0.1894 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5550    3.8284   -0.5347 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1715    2.4515    1.3386 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0487    3.4441    1.7200 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0202    1.2886    2.0405 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7745    1.0622    3.2042 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1223    0.3236    1.6109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2975   -2.6697   -1.1798 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5627   -3.6641   -1.6449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0919   -3.2735   -0.0395 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2523   -3.8924   -0.4859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3508   -2.1797    0.9408 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4782   -2.3057    2.0035 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5689    1.1878    0.6806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6502    2.0748    0.7417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5837    2.1022   -0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6447    2.9723   -0.1990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0838    0.3543   -2.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1337    2.1798   -2.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9915    1.3039   -3.4157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3023   -0.2729   -2.2190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4176   -0.1052    1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0687   -1.9995    0.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3268   -0.8263   -2.5668 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3140   -2.1776   -1.8303 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9416    1.8646   -1.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0026    3.9728   -1.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6005    3.2896    2.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6554    0.2010    3.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0292   -0.5720    2.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9567   -2.2912   -1.9852 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5621   -4.4718   -1.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756   -4.0659    0.4292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4301   -3.7017   -1.4552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3823   -2.3287    1.3503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7176   -1.6960    2.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8512    1.1851    1.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7116    2.7238    1.5983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7719    3.6079    0.5658 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  2  0
  8 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
  4 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 30  2  1  0
 26  6  1  0
 21 13  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  6 36  1  1
  8 37  1  1
  9 38  1  0
  9 39  1  0
 14 40  1  0
 16 41  1  0
 18 42  1  0
 20 43  1  0
 21 44  1  0
 22 45  1  6
 23 46  1  0
 24 47  1  1
 25 48  1  0
 26 49  1  1
 27 50  1  0
 28 51  1  0
 29 52  1  0
 31 53  1  0
M  END


  Mrv1652309022212232D          

 31 33  0  0  1  0            999 V2000
    4.2868   -4.1250    0.0000 C   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
    9.2881  -12.7875    0.0000 O   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
    7.8592  -13.6125    0.0000 O   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
    6.4302  -12.7875    0.0000 O   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
    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  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 13 21  1  0  0  0  0
  8 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
  6 26  1  0  0  0  0
 26 27  1  1  0  0  0
  4 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
  2 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0153683

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(O[C@@H]2O[C@H](COC(=O)C3=CC(O)=C(O)C(O)=C3)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O11/c1-8-4-10(2-3-11(8)21)30-20-18(27)17(26)16(25)14(31-20)7-29-19(28)9-5-12(22)15(24)13(23)6-9/h2-6,14,16-18,20-27H,7H2,1H3/t14-,16-,17+,18-,20-/m1/s1

> <INCHI_KEY>
SRAPOXOXKGUIKG-UVNCQSPWSA-N

> <FORMULA>
C20H22O11

> <MOLECULAR_WEIGHT>
438.385

> <EXACT_MASS>
438.116211528

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
41.730688059305265

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

> <ALOGPS_LOGP>
0.58

> <JCHEM_LOGP>
1.196072352333333

> <ALOGPS_LOGS>
-2.43

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.15622166429523

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.104286325191902

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6491104813415864

> <JCHEM_POLAR_SURFACE_AREA>
186.37

> <JCHEM_REFRACTIVITY>
102.97010000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.63e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

> <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  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.669 -12.320   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      12.003 -14.630   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      12.003 -16.170   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.337 -16.940   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      13.337 -18.480   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      14.670 -19.250   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      16.004 -18.480   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      14.670 -20.790   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.004 -21.560   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.004 -23.100   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      17.338 -23.870   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      14.670 -23.870   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      14.670 -25.410   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      13.337 -23.100   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.003 -23.870   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      13.337 -21.560   0.000  0.00  0.00           C+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   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   28                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   22                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   13                                                       
CONECT   22    8   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    6   27                                                  
CONECT   27   26                                                            
CONECT   28    4   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    2   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
[(2R,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoic acid	Generator

Chemical Formula

C₂₀H₂₂O₁₁

Average Mass

438.3850 Da

Monoisotopic Mass

438.11621 Da

IUPAC Name

[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

Traditional Name

[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

CAS Registry Number

Not Available

SMILES

CC1=CC(O[C@@H]2O[C@H](COC(=O)C3=CC(O)=C(O)C(O)=C3)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1O

InChI Identifier

InChI=1S/C20H22O11/c1-8-4-10(2-3-11(8)21)30-20-18(27)17(26)16(25)14(31-20)7-29-19(28)9-5-12(22)15(24)13(23)6-9/h2-6,14,16-18,20-27H,7H2,1H3/t14-,16-,17+,18-,20-/m1/s1

InChI Key

SRAPOXOXKGUIKG-UVNCQSPWSA-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
Pyrola incarnata	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
Galloyl ester
Gallic acid or derivatives
O-glycosyl compound
P-hydroxybenzoic acid alkyl ester
M-hydroxybenzoic acid ester
P-hydroxybenzoic acid ester
Benzoate ester
4-alkoxyphenol
Benzenetriol
Benzoic acid or derivatives
Pyrogallol derivative
Benzoyl
Phenol ether
O-cresol
Phenoxy compound
1-hydroxy-2-unsubstituted benzenoid
Toluene
1-hydroxy-4-unsubstituted benzenoid
Phenol
Monosaccharide
Benzenoid
Oxane
Monocyclic benzene moiety
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Oxacycle
Polyol
Monocarboxylic acid or derivatives
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	0.58	ALOGPS
logP	1.2	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	8.1	ChemAxon
pKa (Strongest Basic)	-3.6	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	6	ChemAxon
Refractivity	102.97 m³·mol⁻¹	ChemAxon
Polarizability	41.73 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

14259010

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,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate (NP0153683)

MOL for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D MOL for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D SDF for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D-SDF for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

PDB for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D PDB for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

SMILES for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

INCHI for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

Structure for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)

3D Structure for NP0153683 ([(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(4-hydroxy-3-methylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate)