NP-MRD: Showing NP-Card for 2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate (NP0255588)

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Record Information

Version

2.0

Created at

2022-09-07 20:08:12 UTC

Updated at

2022-09-07 20:08:12 UTC

NP-MRD ID

NP0255588

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate

Description

2,3,4,6-Tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate belongs to the class of organic compounds known as cyclohexanols. Cyclohexanols are compounds containing an alcohol group attached to a cyclohexane ring. 2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate is found in Taraxacum linearisquameum. 2,3,4,6-Tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251506052D          

 32 34  0  0  0  0            999 V2000
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  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
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
  5 17  1  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
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 24 30  1  0  0  0  0
 19 31  1  0  0  0  0
  2 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
   -3.0974    0.4003   -1.1277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8409   -0.7620   -0.6370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8383   -1.7946   -0.9946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1587   -1.4542   -0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5878   -2.1012    0.7708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7899   -1.7476    1.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5897   -0.7511    0.8620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8002   -0.4043    1.4826 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1607   -0.1102   -0.2773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9536   -0.4633   -0.8882 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7210   -0.8992    0.1300 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9061    0.2044    0.3540 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5308    0.0459   -0.0804 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2588   -0.6056    0.9016 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0474    1.4816   -0.3252 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4519    1.5146   -0.0698 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4266    1.5936   -1.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0773    1.6247   -2.2346 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8911    1.6404   -0.6864 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5553    0.3526   -0.9188 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7878   -0.1520   -2.1616 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4309   -1.3839   -2.3411 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8398   -2.1074   -1.2532 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4714   -3.3192   -1.4519 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6093   -1.6025    0.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9770   -0.3949    0.1583 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3296    2.4791    0.4976 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6442    3.2223   -0.1523 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1119    1.9657    1.8516 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0065    1.9173    2.7001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8334    0.6562    1.8073 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0404    0.6238    2.4567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4833   -2.8008   -0.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9047   -1.7814   -2.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9422   -2.8842    1.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1056   -2.2675    2.2739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6913   -0.8153    1.2738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7667    0.6762   -0.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6459    0.0553   -1.7792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3370    1.0974   -0.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6210   -0.5569   -1.0094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4895   -1.5419    0.6637 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8220    1.6342   -1.4019 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0363    2.0268    0.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3363    2.4392   -1.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4862    0.3685   -3.0558 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5815   -1.7301   -3.3541 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7722   -3.8556   -0.6404 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9512   -2.1979    0.8383 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8149   -0.0260    1.1857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1175    3.2703    0.7707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1783    3.8656   -0.7464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7959    2.7232    2.2811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0111    1.1434    3.3055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1814   -0.1036    2.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6248    1.3942    2.3018 H   0  0  0  0  0  0  0  0  0  0  0  0
 30 29  1  0
 29 27  1  0
 27 28  1  0
 27 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 15 13  1  0
 13 14  1  0
 13 12  1  0
 12 11  1  0
 11  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 12 31  1  0
 31 32  1  0
 31 29  1  0
 26 20  1  0
 10  4  1  0
 30 54  1  0
 29 53  1  1
 27 51  1  1
 28 52  1  0
 15 43  1  6
 19 44  1  0
 19 45  1  0
 21 46  1  0
 22 47  1  0
 24 48  1  0
 25 49  1  0
 26 50  1  0
 13 41  1  6
 14 42  1  0
 12 40  1  6
  3 33  1  0
  3 34  1  0
  5 35  1  0
  6 36  1  0
  8 37  1  0
  9 38  1  0
 10 39  1  0
 31 55  1  1
 32 56  1  0
M  END


  Mrv1533004251506052D          

 32 34  0  0  0  0            999 V2000
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  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
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
  5 17  1  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
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 24 30  1  0  0  0  0
 19 31  1  0  0  0  0
  2 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0255588

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1C(O)C(OC(=O)CC2=CC=C(O)C=C2)C(O)C(OC(=O)CC2=CC=C(O)C=C2)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H24O10/c23-13-5-1-11(2-6-13)9-15(25)31-21-18(28)17(27)19(29)22(20(21)30)32-16(26)10-12-3-7-14(24)8-4-12/h1-8,17-24,27-30H,9-10H2

> <INCHI_KEY>
CNBAOMVSWGEEJJ-UHFFFAOYSA-N

> <FORMULA>
C22H24O10

> <MOLECULAR_WEIGHT>
448.424

> <EXACT_MASS>
448.136946973

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
44.68669426114574

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate

> <ALOGPS_LOGP>
0.85

> <JCHEM_LOGP>
0.16179016466666724

> <ALOGPS_LOGS>
-2.46

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.79668912624795

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.195138621276225

> <JCHEM_PKA_STRONGEST_BASIC>
-3.64719295718366

> <JCHEM_POLAR_SURFACE_AREA>
173.98

> <JCHEM_REFRACTIVITY>
107.48360000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.56e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      16.004  -4.620   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   10                                                       
CONECT   17    5   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   31                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   24                                                       
CONECT   31   19    2   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
2,3,4,6-Tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetic acid	Generator

Chemical Formula

C₂₂H₂₄O₁₀

Average Mass

448.4240 Da

Monoisotopic Mass

448.13695 Da

IUPAC Name

2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate

Traditional Name

2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate

CAS Registry Number

Not Available

SMILES

OC1C(O)C(OC(=O)CC2=CC=C(O)C=C2)C(O)C(OC(=O)CC2=CC=C(O)C=C2)C1O

InChI Identifier

InChI=1S/C22H24O10/c23-13-5-1-11(2-6-13)9-15(25)31-21-18(28)17(27)19(29)22(20(21)30)32-16(26)10-12-3-7-14(24)8-4-12/h1-8,17-24,27-30H,9-10H2

InChI Key

CNBAOMVSWGEEJJ-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
Taraxacum linearisquameum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclohexanols. Cyclohexanols are compounds containing an alcohol group attached to a cyclohexane ring.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Cyclohexanols

Alternative Parents

Substituents

1-hydroxy-2-unsubstituted benzenoid
Phenol
Cyclohexanol
Benzenoid
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Cyclitol or derivatives
Cyclic alcohol
Carboxylic acid ester
Polyol
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	0.85	ALOGPS
logP	0.16	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	9.2	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	173.98 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	107.48 m³·mol⁻¹	ChemAxon
Polarizability	44.69 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate (NP0255588)

MOL for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

3D MOL for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

3D SDF for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

3D-SDF for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

PDB for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

3D PDB for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

SMILES for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

INCHI for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

Structure for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)

3D Structure for NP0255588 (2,3,4,6-tetrahydroxy-5-{[2-(4-hydroxyphenyl)acetyl]oxy}cyclohexyl 2-(4-hydroxyphenyl)acetate)