NP-MRD: Showing NP-Card for (2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate (NP0206593)

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Record Information

Version

2.0

Created at

2022-09-05 02:53:50 UTC

Updated at

2022-09-05 02:53:50 UTC

NP-MRD ID

NP0206593

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate

Description

(2S,3R,4S,5S,6R)-6-[(9S)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings. (2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate is found in Picramnia antidesma. Based on a literature review very few articles have been published on (2S,3R,4S,5S,6R)-6-[(9S)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052204532D          

 32 35  0  0  1  0            999 V2000
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    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
    3.5724    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  2  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
    2.1434    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 18 26  1  0  0  0  0
  8 26  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
    5.5250    2.1252   -1.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6382    0.9876   -1.2391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8153   -0.1852   -1.6709 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5780    1.2343   -0.3713 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6938    0.2383    0.0480 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3817    0.5288   -0.3428 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6622   -0.6518   -0.2426 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6548   -0.5720   -0.9853 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3025   -1.8920   -0.7916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6087   -2.9863   -1.2247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0986   -4.2627   -1.0730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3055   -4.4535   -0.4770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0572   -3.3511   -0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2510   -3.5614    0.5735 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5215   -2.0705   -0.1900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2592   -0.8896    0.2317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3801   -0.9846    0.7907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6947    0.4303    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4420    1.5561    0.3844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6580    1.5449    0.9899 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9204    2.8392    0.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7104    2.9494   -0.4690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1729    4.3345   -0.7289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5755    4.8065   -1.9722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9815    1.8415   -0.8380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4668    0.5740   -0.6031 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4736   -0.9442    1.2255 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2751   -2.1106    1.4264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8420   -1.2073    1.8210 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6911   -1.4113    3.1935 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6776    0.0449    1.5501 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9402   -0.0480    2.0962 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4753    1.7704   -2.0659 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7691    2.6570   -0.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0010    2.8695   -2.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0005   -0.7365   -0.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3178   -1.4481   -0.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4095   -0.5028   -2.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3533   -2.8706   -1.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5217   -5.1374   -1.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7344   -5.4445   -0.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9215   -2.9967    0.9560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2172    0.8267    1.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5112    3.7286    0.4324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0741    4.3514   -0.6062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5982    5.0134    0.0379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4131    4.4146   -2.2851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0115    2.0298   -1.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0514   -0.0795    1.7768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8723   -1.9157    2.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3516   -2.0679    1.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1526   -0.6619    3.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1001    0.9212    1.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1297    0.8257    2.5628 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  2  0
 31  5  1  0
 26  8  1  0
 15  9  1  0
 26 18  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  6
  7 37  1  6
 27 49  1  1
 28 50  1  0
 29 51  1  6
 30 52  1  0
 31 53  1  1
 32 54  1  0
  8 38  1  6
 10 39  1  0
 11 40  1  0
 12 41  1  0
 14 42  1  0
 20 43  1  0
 21 44  1  0
 23 45  1  0
 23 46  1  0
 24 47  1  0
 25 48  1  0
M  END


  Mrv1652309052204532D          

 32 35  0  0  1  0            999 V2000
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    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
    3.5724    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  2  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
    2.1434    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    4.5375    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 18 26  1  0  0  0  0
  8 26  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0206593

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)[C@H]1C2=CC=CC(O)=C2C(=O)C2=C(O)C=C(CO)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H22O10/c1-8(24)31-22-20(30)18(28)19(29)21(32-22)14-10-3-2-4-12(25)15(10)17(27)16-11(14)5-9(7-23)6-13(16)26/h2-6,14,18-23,25-26,28-30H,7H2,1H3/t14-,18-,19-,20+,21+,22+/m0/s1

> <INCHI_KEY>
WLMRFFFLFIPZEO-SFXGZIOESA-N

> <FORMULA>
C22H22O10

> <MOLECULAR_WEIGHT>
446.408

> <EXACT_MASS>
446.121296908

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
42.93466093856182

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-6-[(9S)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate

> <JCHEM_LOGP>
1.122226136333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.96737897372803

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.305656211935863

> <JCHEM_PKA_STRONGEST_BASIC>
-2.87611621829664

> <JCHEM_POLAR_SURFACE_AREA>
173.98

> <JCHEM_REFRACTIVITY>
108.01200000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-6-[(9S)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668   8.470   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.335   9.240   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.668   6.930   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.667   1.540   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.001   8.470   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   27                                                  
CONECT    8    7    9   26                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    9   16                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   26                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25   18    8                                                  
CONECT   27    7   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    5   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Value	Source
(2S,3R,4S,5S,6R)-6-[(9S)-4,5-Dihydroxy-2-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetic acid	Generator

Chemical Formula

C₂₂H₂₂O₁₀

Average Mass

446.4080 Da

Monoisotopic Mass

446.12130 Da

IUPAC Name

(2S,3R,4S,5S,6R)-6-[(9S)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate

Traditional Name

(2S,3R,4S,5S,6R)-6-[(9S)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)[C@H]1C2=CC=CC(O)=C2C(=O)C2=C(O)C=C(CO)C=C12

InChI Identifier

InChI=1S/C22H22O10/c1-8(24)31-22-20(30)18(28)19(29)21(32-22)14-10-3-2-4-12(25)15(10)17(27)16-11(14)5-9(7-23)6-13(16)26/h2-6,14,18-23,25-26,28-30H,7H2,1H3/t14-,18-,19-,20+,21+,22+/m0/s1

InChI Key

WLMRFFFLFIPZEO-SFXGZIOESA-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
Picramnia antidesma	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Not Available

Direct Parent

Anthracenes

Alternative Parents

Substituents

Anthracene
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monosaccharide
Oxane
Vinylogous acid
Carboxylic acid ester
Ketone
Secondary alcohol
Acetal
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Carbonyl group
Alcohol
Primary alcohol
Aromatic alcohol
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	1.12	ChemAxon
pKa (Strongest Acidic)	8.31	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	173.98 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	108.01 m³·mol⁻¹	ChemAxon
Polarizability	42.93 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

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

162917329

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate (NP0206593)

MOL for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

3D MOL for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

3D SDF for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

3D-SDF for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

PDB for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

3D PDB for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

SMILES for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

INCHI for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

Structure for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)

3D Structure for NP0206593 ((2s,3r,4s,5s,6r)-6-[(9s)-4,5-dihydroxy-2-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl acetate)