NP-MRD: Showing NP-Card for 2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol (NP0198805)

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Record Information

Version

2.0

Created at

2022-09-04 17:19:11 UTC

Updated at

2022-09-04 17:19:11 UTC

NP-MRD ID

NP0198805

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol

Description

Ptelatoside A 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. Ptelatoside A is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Ptelatoside A has been detected, but not quantified in, green vegetables and root vegetables. 2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol is found in Pteridium aquilinum and Pteridium esculentum. This could make ptelatoside a a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241215412D          

 29 31  0  0  0  0            999 V2000
   -5.3249   -2.1616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3249   -1.2011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4439   -0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4439    0.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6432    0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7622    0.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7622   -0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6432   -1.2011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812    0.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4402    0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0397    1.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4402    2.1616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0397    0.1597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7603    0.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1607   -0.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9615   -0.5601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9226   -0.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3230    0.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1237    0.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4439    0.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3230   -1.2011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1237   -1.2011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4439   -0.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3249   -0.5601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9615    0.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1607    0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7603    1.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1607    2.1616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9226    0.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  8  2  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
  6  9  1  0  0  0  0
  7  8  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 13  1  0  0  0  0
 11 12  1  0  0  0  0
 11 27  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 26  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 21  1  0  0  0  0
 18 19  1  0  0  0  0
 18 29  1  0  0  0  0
 19 20  1  0  0  0  0
 19 23  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    7.9448    2.3721    0.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2423    2.0288   -0.8155 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9321    1.3958   -0.7751 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2715    1.0750   -1.9538 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0375    0.4783   -1.9448 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3661    0.1551   -0.7576 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1228   -0.4462   -0.8384 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3232   -0.8318    0.2306 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0936   -0.1439    0.2517 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5977   -0.6009    1.3852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5515    0.3672    1.9652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5659    0.8589    1.2421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5640    0.0865    0.7711 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7771    0.4996    1.3356 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8528    0.3663    0.4774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7535    1.2838   -0.7220 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2075    2.5629   -0.4410 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3453    1.3363   -1.2721 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6894    2.4750   -0.8266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6256    0.1199   -0.7398 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1592   -1.0577   -1.2541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0380   -1.9840    1.1123 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4407   -2.1783   -0.2204 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2489   -2.8513    1.2291 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9117   -2.5617    2.4021 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1097   -2.3435    0.0753 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5138   -2.5504   -1.1477 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0181    0.4717    0.4098 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2792    1.0815    0.3941 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9124    2.8395    0.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5644    2.1920    1.2337 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6853    2.2394   -1.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7900    1.3246   -2.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5362    0.2348   -2.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7810   -0.6106    1.2091 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2507   -0.6853    2.1643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9235    1.2693    2.2873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8617   -0.0489    2.9677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4267   -0.9635    1.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7511    0.6854    1.0457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0317   -0.6680    0.1557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4107    0.8611   -1.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4749    3.0982   -0.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3235    1.2914   -2.3601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8417    3.2186   -1.4729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5739    0.1848   -1.0951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7332   -0.8819   -2.0501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7357   -2.4496    1.7963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5941   -3.1549   -0.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0302   -3.9090    1.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3358   -3.3902    2.7450 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1132   -2.7874    0.0865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1090   -2.9243   -1.8271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5667    0.2546    1.3456 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7605    1.3154    1.3478 H   0  0  0  0  0  0  0  0  0  0  0  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  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  2  3
  3 29  1  0
 29 28  2  0
  8 26  1  0
 26 27  1  0
 26 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  1  0
 13 20  1  0
 20 21  1  0
 20 18  1  0
 18 19  1  0
 18 16  1  0
 22 10  1  0
 28  6  1  0
 17 43  1  0
 16 42  1  6
 15 40  1  0
 15 41  1  0
 13 39  1  6
 11 37  1  0
 11 38  1  0
 10 36  1  1
  8 35  1  1
  5 34  1  0
  4 33  1  0
  2 32  1  0
  1 30  1  0
  1 31  1  0
 29 55  1  0
 28 54  1  0
 26 52  1  6
 27 53  1  0
 24 50  1  6
 25 51  1  0
 22 48  1  1
 23 49  1  0
 20 46  1  6
 21 47  1  0
 18 44  1  6
 19 45  1  0
M  END


  Mrv0541 02241215412D          

 29 31  0  0  0  0            999 V2000
   -5.3249   -2.1616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3249   -1.2011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4439   -0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4439    0.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6432    0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7622    0.3201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7622   -0.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6432   -1.2011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812    0.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4402    0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0397    1.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4402    2.1616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0397    0.1597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7603    0.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1607   -0.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9615   -0.5601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9226   -0.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3230    0.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1237    0.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4439    0.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3230   -1.2011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1237   -1.2011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4439   -0.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3249   -0.5601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9615    0.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1607    0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7603    1.5213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1607    2.1616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9226    0.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  8  2  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
  6  9  1  0  0  0  0
  7  8  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 13  1  0  0  0  0
 11 12  1  0  0  0  0
 11 27  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 26  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 21  1  0  0  0  0
 18 19  1  0  0  0  0
 18 29  1  0  0  0  0
 19 20  1  0  0  0  0
 19 23  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198805

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1COC(OCC2OC(OC3=CC=C(C=C)C=C3)C(O)C(O)C2O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O10/c1-2-9-3-5-10(6-4-9)28-19-17(25)15(23)14(22)12(29-19)8-27-18-16(24)13(21)11(20)7-26-18/h2-6,11-25H,1,7-8H2

> <INCHI_KEY>
DZMYOBBWRZTUTA-UHFFFAOYSA-N

> <FORMULA>
C19H26O10

> <MOLECULAR_WEIGHT>
414.4037

> <EXACT_MASS>
414.152597052

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
41.138679889123814

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-0.93

> <JCHEM_LOGP>
-1.0021862346666661

> <ALOGPS_LOGS>
-1.42

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.457148443528592

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.922616789462726

> <JCHEM_PKA_STRONGEST_BASIC>
-3.526580404084756

> <JCHEM_POLAR_SURFACE_AREA>
158.3

> <JCHEM_REFRACTIVITY>
96.3204

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.57e+01 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -9.940  -4.035   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -9.940  -2.242   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.295  -1.195   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.295   0.598   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.801   1.493   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.156   0.598   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.156  -1.195   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.801  -2.242   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.512   1.493   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.822   1.493   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.074   2.840   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.822   4.035   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -0.074   0.298   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.419   0.298   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.167  -1.046   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.661  -1.046   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.456  -1.046   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.203   0.298   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.698   0.298   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.295   1.493   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       6.203  -2.242   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.698  -2.242   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.295  -1.046   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.940  -1.046   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.661   1.493   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.167   1.493   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.419   2.840   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.167   4.035   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       5.456   1.493   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    3    7                                                       
CONECT    9    6   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12   27                                                  
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17   19   29                                                  
CONECT   19   18   20   23                                                  
CONECT   20   19                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23                                                       
CONECT   23   19   22   24                                                  
CONECT   24   23                                                            
CONECT   25   26                                                            
CONECT   26   14   25   27                                                  
CONECT   27   11   26   28                                                  
CONECT   28   27                                                            
CONECT   29   18                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
Ptelatoside a	MeSH

Chemical Formula

C₁₉H₂₆O₁₀

Average Mass

414.4037 Da

Monoisotopic Mass

414.15260 Da

IUPAC Name

2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol

Traditional Name

2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

OC1COC(OCC2OC(OC3=CC=C(C=C)C=C3)C(O)C(O)C2O)C(O)C1O

InChI Identifier

InChI=1S/C19H26O10/c1-2-9-3-5-10(6-4-9)28-19-17(25)15(23)14(22)12(29-19)8-27-18-16(24)13(21)11(20)7-26-18/h2-6,11-25H,1,7-8H2

InChI Key

DZMYOBBWRZTUTA-UHFFFAOYSA-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
Pteridium aquilinum	LOTUS Database	35616633
Pteridium esculentum	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
Disaccharide
O-glycosyl compound
Phenoxy compound
Styrene
Phenol ether
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	-0.93	ALOGPS
logP	-1	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	11.92	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	158.3 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	96.32 m³·mol⁻¹	ChemAxon
Polarizability	41.14 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0032600

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB010538

KNApSAcK ID

Not Available

Chemspider ID

26503885

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13964506

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol (NP0198805)

MOL for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

3D MOL for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

3D SDF for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

3D-SDF for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

PDB for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

3D PDB for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

SMILES for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

INCHI for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

Structure for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)

3D Structure for NP0198805 (2-(4-ethenylphenoxy)-6-{[(3,4,5-trihydroxyoxan-2-yl)oxy]methyl}oxane-3,4,5-triol)