NP-MRD: Showing NP-Card for (2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol (NP0231647)

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Record Information

Version

2.0

Created at

2022-09-06 12:36:01 UTC

Updated at

2022-09-06 12:36:01 UTC

NP-MRD ID

NP0231647

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol

Description

2-Hydroxybenzyl-6-O-beta-D-xylopyranosyl beta-D-glucopyranoside belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Based on a literature review very few articles have been published on 2-Hydroxybenzyl-6-O-beta-D-xylopyranosyl beta-D-glucopyranoside.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062214362D          

 29 31  0  0  1  0            999 V2000
   -1.4289   -4.1250    0.0000 O   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
   -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
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1447   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.2881   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.2881   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    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
   -5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  1  0  0  0
 12 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    5.4927    2.1182    2.5279 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6143    1.7553    1.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4664    2.4534    0.3771 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5828    2.0956   -0.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8458    1.0476   -1.4443 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9744    0.3347   -0.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8540    0.6842    0.6866 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9983    0.0233    1.6539 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2143   -0.9956    1.2831 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2181   -0.7825    0.3532 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0128   -0.7657    1.1344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0680   -0.7406    0.2590 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3203   -0.3324    0.9659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3618   -0.3202    0.0666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5775    0.0527    0.6464 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4058   -1.0404    0.5448 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3398   -1.0197   -0.4558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3604    0.0996   -0.2492 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.2613   -0.3380    0.7090 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6382    1.3315    0.2902 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1885    2.4381   -0.3175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1627    1.2238   -0.0903 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5559    2.4273    0.2718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2390   -2.1513   -0.2672 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8039   -2.1762   -1.5211 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0905   -2.8822   -0.2064 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3834   -3.3149    1.0866 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1728   -1.9092   -0.6142 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0349   -1.5005   -1.9378 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0276    2.8821    2.8988 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0400    3.2797    0.7944 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2751    2.6705   -1.5740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9754    0.8072   -2.4938 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4417   -0.4726   -1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6426   -0.3511    2.5063 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3236    0.7796    2.1792 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2482    0.2346   -0.0809 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1473   -0.0099   -0.5252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1936    0.7267    1.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5212   -0.9325    1.8734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4568    0.2675    1.7336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8223   -0.7924   -1.4102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8548   -1.9774   -0.6083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8087    0.3431   -1.2190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1636   -0.0072    0.4536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7040    1.3079    1.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1730    3.2208    0.2761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0294    1.0653   -1.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9841    3.1406   -0.2789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9243   -2.6760    0.4326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9067   -1.2600   -1.8727 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0688   -3.7797   -0.8480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847   -3.2917    1.6739 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1341   -2.4708   -0.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9609   -0.5199   -2.0122 H   0  0  0  0  0  0  0  0  0  0  0  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 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
 10 28  1  0
 28 29  1  0
 28 26  1  0
 26 27  1  0
 26 24  1  0
 24 25  1  0
 15 22  1  0
 22 23  1  0
 22 20  1  0
 20 21  1  0
 20 18  1  0
 24 12  1  0
  2  7  1  0
 19 45  1  0
 18 44  1  6
 17 42  1  0
 17 43  1  0
 15 41  1  1
 13 39  1  0
 13 40  1  0
 12 38  1  6
 10 37  1  6
  8 35  1  0
  8 36  1  0
  6 34  1  0
  5 33  1  0
  4 32  1  0
  3 31  1  0
  1 30  1  0
 28 54  1  6
 29 55  1  0
 26 52  1  6
 27 53  1  0
 24 50  1  1
 25 51  1  0
 22 48  1  6
 23 49  1  0
 20 46  1  1
 21 47  1  0
M  END


  Mrv1652309062214362D          

 29 31  0  0  1  0            999 V2000
   -1.4289   -4.1250    0.0000 O   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
   -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
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.9500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1447   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.2881   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -6.6000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.2881   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    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
   -5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  1  0  0  0
 12 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0231647

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1CO[C@@H](OC[C@H]2O[C@@H](OCC3=CC=CC=C3O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O11/c19-9-4-2-1-3-8(9)5-26-18-16(25)14(23)13(22)11(29-18)7-28-17-15(24)12(21)10(20)6-27-17/h1-4,10-25H,5-7H2/t10-,11-,12+,13-,14+,15-,16-,17+,18-/m1/s1

> <INCHI_KEY>
JDCZPTGZKIDCQI-NWQIESHVSA-N

> <FORMULA>
C18H26O11

> <MOLECULAR_WEIGHT>
418.395

> <EXACT_MASS>
418.147511657

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
40.95857752335488

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5S,6R)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
-2.0090056223333335

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.928525532242636

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.116311429958117

> <JCHEM_PKA_STRONGEST_BASIC>
-3.526580404084756

> <JCHEM_POLAR_SURFACE_AREA>
178.53

> <JCHEM_REFRACTIVITY>
93.71890000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5S,6R)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol

> <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  -7.700   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -9.336 -10.010   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0     -10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0     -12.003 -11.550   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0     -13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0     -13.337 -13.860   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0     -14.670 -14.630   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -16.004 -13.860   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0     -17.338 -14.630   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0     -16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0     -17.338 -11.550   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0     -14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0     -14.670 -10.010   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0     -10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0     -12.003  -6.930   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.668  -6.930   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   24                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   15   23                                                  
CONECT   23   22                                                            
CONECT   24   12   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   10   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
2-Hydroxybenzyl-6-O-b-D-xylopyranosyl b-D-glucopyranoside	Generator
2-Hydroxybenzyl-6-O-β-D-xylopyranosyl β-D-glucopyranoside	Generator

Chemical Formula

C₁₈H₂₆O₁₁

Average Mass

418.3950 Da

Monoisotopic Mass

418.14751 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

O[C@@H]1CO[C@@H](OC[C@H]2O[C@@H](OCC3=CC=CC=C3O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C18H26O11/c19-9-4-2-1-3-8(9)5-26-18-16(25)14(23)13(22)11(29-18)7-28-17-15(24)12(21)10(20)6-27-17/h1-4,10-25H,5-7H2/t10-,11-,12+,13-,14+,15-,16-,17+,18-/m1/s1

InChI Key

JDCZPTGZKIDCQI-NWQIESHVSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Disaccharide
O-glycosyl compound
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Oxane
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Alcohol
Hydrocarbon derivative
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	-2	ChemAxon
pKa (Strongest Acidic)	9.12	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	178.53 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	93.72 m³·mol⁻¹	ChemAxon
Polarizability	40.96 Å³	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

102043286

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol (NP0231647)

MOL for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

3D MOL for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

3D SDF for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

3D-SDF for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

PDB for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

3D PDB for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

SMILES for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

INCHI for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

Structure for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)

3D Structure for NP0231647 ((2r,3r,4s,5s,6r)-2-[(2-hydroxyphenyl)methoxy]-6-({[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxane-3,4,5-triol)