NP-MRD: Showing NP-Card for 1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione (NP0318996)

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Record Information

Version

2.0

Created at

2022-09-11 19:48:14 UTC

Updated at

2022-09-11 19:48:14 UTC

NP-MRD ID

NP0318996

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

Description

1,8-Dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone. 1,8-Dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, 1,8-Dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside has been detected, but not quantified in, green vegetables. 1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione is found in Rheum palmatum and Senna alexandrina. This could make 1,8-dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241209402D          

 31 34  0  0  0  0            999 V2000
    0.7150   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7150   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4287   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4287   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7150   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7150    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4287   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4287   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4287    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4287    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1437    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8573    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2874    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8573    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1437    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1437    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1437    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1437   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8573   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1437   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8573   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2874   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  7  1  0  0  0  0
  3  4  2  0  0  0  0
  3 28  1  0  0  0  0
  4  5  1  0  0  0  0
  4 26  1  0  0  0  0
  5  6  2  0  0  0  0
  5  8  1  0  0  0  0
  7  8  2  0  0  0  0
  7 12  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 13  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 17  1  0  0  0  0
 15 16  1  0  0  0  0
 15 23  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  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  2  0  0  0  0
 27 29  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
    4.4280    1.0499   -1.8258 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4217    0.6194   -1.2433 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5523   -0.5900   -0.4313 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7328   -1.2744   -0.2802 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8550   -2.4219    0.4908 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1531   -3.1466    0.6373 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1099   -2.4628   -0.1122 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7081   -2.8786    1.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5198   -2.1956    0.9828 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3761   -2.6516    1.6215 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4229   -1.0470    0.2041 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1420   -0.3431    0.0673 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1314   -0.7841    0.6583 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0211    0.8684   -0.7490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2210    1.5082   -0.8518 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2423    0.9237   -0.1572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5393    1.3921   -0.1255 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9762    1.7388    1.1539 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1809    0.6370    1.9696 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6493    1.1698    3.3154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7008    2.0156    3.8911 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2683   -0.2723    1.4573 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8231   -1.5982    1.4892 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6698    0.0665    0.0393 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6034    1.0984    0.0027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4406    0.3505   -0.7551 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8024    0.7360   -2.0425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2985    2.6392   -1.6238 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8434    3.1203   -2.2796 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0418    2.4643   -2.1532 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1563    1.3233   -1.3845 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6066   -0.8928   -0.7914 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6543   -1.8593    0.4520 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7797   -3.7708    1.7368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3505   -3.4688    2.2019 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.2603    0.0491    2.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5436    1.8259    3.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0003    0.3830    3.9875 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1895   -0.2428    2.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4743   -2.2228    1.1256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1631   -0.8196   -0.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1394    1.9377   -0.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8932   -0.6233   -0.8749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6947    0.0385   -2.7137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2370    3.1440   -1.7166 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7558    4.0127   -2.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9404    2.8090   -2.6454 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 14  2  0
 14 12  1  0
 12 13  2  0
 12 11  1  0
 11  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  2  0
  9 10  1  0
  3  2  1  0
  2  1  2  0
 17 26  1  0
 26 27  1  0
 26 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  1  0
 22 19  1  0
 14 15  1  0
  9 11  1  0
  2 31  1  0
 21 42  1  0
 20 40  1  0
 20 41  1  0
 19 39  1  1
 17 38  1  6
 28 49  1  0
 29 50  1  0
 30 51  1  0
  4 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  8 36  1  0
 10 37  1  0
 26 47  1  6
 27 48  1  0
 24 45  1  6
 25 46  1  0
 22 43  1  1
 23 44  1  0
M  END


  Mrv0541 02241209402D          

 31 34  0  0  0  0            999 V2000
    0.7150   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7150   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4287   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4287   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7150   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7150    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4287   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4287   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4287    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4287    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7150    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1437    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8573    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2874    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8573    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1437    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1437    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1437    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1437   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8573   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1437   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8573   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2874   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  7  1  0  0  0  0
  3  4  2  0  0  0  0
  3 28  1  0  0  0  0
  4  5  1  0  0  0  0
  4 26  1  0  0  0  0
  5  6  2  0  0  0  0
  5  8  1  0  0  0  0
  7  8  2  0  0  0  0
  7 12  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 13  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 17  1  0  0  0  0
 15 16  1  0  0  0  0
 15 23  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 22  1  0  0  0  0
 19 20  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  2  0  0  0  0
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 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0318996

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC1OC(OC2=CC=CC3=C2C(=O)C2=C(C=C(CO)C=C2O)C3=O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O10/c22-6-8-4-10-14(11(24)5-8)18(27)15-9(16(10)25)2-1-3-12(15)30-21-20(29)19(28)17(26)13(7-23)31-21/h1-5,13,17,19-24,26,28-29H,6-7H2

> <INCHI_KEY>
KIZBWUUJNJEYCM-UHFFFAOYSA-N

> <FORMULA>
C21H20O10

> <MOLECULAR_WEIGHT>
432.3775

> <EXACT_MASS>
432.10564686

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
41.78424463586711

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

> <ALOGPS_LOGP>
-0.04

> <JCHEM_LOGP>
-0.07384242933333349

> <ALOGPS_LOGS>
-2.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.19962804160011

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.225710655567365

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9453149455851575

> <JCHEM_POLAR_SURFACE_AREA>
173.98

> <JCHEM_REFRACTIVITY>
104.07309999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.22e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

> <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  O   UNK     0       1.335  -5.390   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.335  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.335  -0.770   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.335   0.770   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.335  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  -1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.335  -3.850   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.335   0.770   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.335   3.850   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -4.002   0.770   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -5.334   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.668   0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -8.003   1.540   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -6.668   3.850   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -5.334   3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.002   3.850   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.002   5.390   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       4.002   0.770   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.002  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.334  -1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.002  -3.850   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.334  -3.080   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.003  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4   28                                                  
CONECT    4    3    5   26                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5                                                            
CONECT    7    2    8   12                                                  
CONECT    8    5    7    9                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12    7   11                                                       
CONECT   13    9   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   22                                                            
CONECT   22   18   21   23                                                  
CONECT   23   15   22   24                                                  
CONECT   24   23                                                            
CONECT   25   26                                                            
CONECT   26    4   25   27                                                  
CONECT   27   26   29                                                       
CONECT   28    3   29                                                       
CONECT   29   27   28   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀O₁₀

Average Mass

432.3775 Da

Monoisotopic Mass

432.10565 Da

IUPAC Name

1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

Traditional Name

1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

CAS Registry Number

Not Available

SMILES

OCC1OC(OC2=CC=CC3=C2C(=O)C2=C(C=C(CO)C=C2O)C3=O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C21H20O10/c22-6-8-4-10-14(11(24)5-8)18(27)15-9(16(10)25)2-1-3-12(15)30-21-20(29)19(28)17(26)13(7-23)31-21/h1-5,13,17,19-24,26,28-29H,6-7H2

InChI Key

KIZBWUUJNJEYCM-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
Rheum palmatum	LOTUS Database	35616633
Senna alexandrina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

9,10-anthraquinone
Anthraquinone
Phenolic glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monosaccharide
Oxane
Vinylogous acid
Ketone
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Aromatic alcohol
Primary alcohol
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	-0.04	ALOGPS
logP	-0.074	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	9.23	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	173.98 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	104.07 m³·mol⁻¹	ChemAxon
Polarizability	41.78 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0029679

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB000864

KNApSAcK ID

Not Available

Chemspider ID

12944950

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14077415

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione (NP0318996)

MOL for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

3D MOL for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

3D SDF for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

3D-SDF for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

PDB for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

3D PDB for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

SMILES for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

INCHI for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

Structure for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)

3D Structure for NP0318996 (1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione)