NP-MRD: Showing NP-Card for {3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate (NP0266709)

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Record Information

Version

1.0

Created at

2022-09-08 11:15:26 UTC

Updated at

2022-09-08 11:15:26 UTC

NP-MRD ID

NP0266709

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate

Description

{3,4,5-Trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]oxan-2-yl}methyl acetate belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings. {3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate is found in Aloe marlothii. {3,4,5-Trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]oxan-2-yl}methyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004271515322D          

 34 37  0  0  0  0            999 V2000
    0.0000    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    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
    1.4289    3.3000    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
    2.1434    2.0625    0.0000 C   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    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   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
    2.1434    3.7125    0.0000 C   0  0  0  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
    2.1434    1.2375    0.0000 C   0  0  0  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
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   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
    0.7145    2.0625    0.0000 O   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  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 15 34  1  0  0  0  0
 27 34  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
    6.8386    0.3094   -0.0356 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5292   -0.2241    0.4655 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3196   -1.4320    0.6227 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5346    0.6716    0.7568 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2570    0.3791    1.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5131   -0.4815    0.2520 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2357   -0.7859    0.6916 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2506   -0.0196    0.1259 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0243   -0.0115    0.9341 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0311    0.8352    0.2564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6759    2.1825    0.0622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5178    3.0049   -0.6294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1299    4.4446   -0.8324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6343    5.1646    0.2412 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7024    2.5730   -1.1468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0740    1.2229   -0.9589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2405    0.8078   -1.4724 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2116    0.3761   -0.2471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6047   -0.9942    0.0468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6692   -1.4397   -0.4037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7017   -1.8040    0.8817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1645   -3.0728    1.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3130   -3.6591    0.8062 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3988   -3.8562    2.1387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2507   -3.3588    2.6190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8029   -2.1081    2.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3828   -1.7014    2.8162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5204   -1.2911    1.3689 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0543   -0.2619   -1.3432 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8461   -1.2880   -1.6216 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4024   -0.5193   -1.9863 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4463    0.0840   -3.2386 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4717    0.1155   -1.1339 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6991   -0.1169   -1.7830 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6460   -0.4200    0.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0086    1.2727    0.4574 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7123    0.5289   -1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7321    1.3454    1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3210   -0.1870    2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0457   -1.4523    0.1828 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6497    1.0388    0.2001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7591    0.5634    1.8769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7497    2.4906    0.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5003    4.8429   -1.7801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0221    4.5340   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4359    6.1178    0.1881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3862    3.2094   -1.7009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7027   -0.0213   -1.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0003   -3.3935    0.2208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7461   -4.8390    2.4240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6681   -3.9844    3.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8912   -2.2824    3.4465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3500    0.6404   -1.8470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5629   -2.0912   -1.1319 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5810   -1.5983   -2.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9903   -0.4122   -3.8902 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2631    1.1856   -1.0377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6205   -0.8334   -2.4589 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  8  1  0
  8 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
 33  6  1  0
 28  9  1  0
 18 10  1  0
 28 21  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  6
  8 41  1  6
 29 53  1  6
 30 54  1  0
 31 55  1  6
 32 56  1  0
 33 57  1  1
 34 58  1  0
  9 42  1  1
 11 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 17 48  1  0
 23 49  1  0
 24 50  1  0
 25 51  1  0
 27 52  1  0
M  END


  Mrv1533004271515322D          

 34 37  0  0  0  0            999 V2000
    0.0000    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    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
    1.4289    3.3000    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
    2.1434    2.0625    0.0000 C   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    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   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
    2.1434    3.7125    0.0000 C   0  0  0  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
    2.1434    1.2375    0.0000 C   0  0  0  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
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   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
    0.7145    2.0625    0.0000 O   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  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
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 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
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 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 15 34  1  0  0  0  0
 27 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0266709

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1OC(C(O)C(O)C1O)C1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC(O)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O11/c1-8(25)33-7-14-19(29)21(31)22(32)23(34-14)16-10-4-9(6-24)5-13(28)15(10)20(30)18-12(27)3-2-11(26)17(16)18/h2-5,14,16,19,21-24,26-29,31-32H,6-7H2,1H3

> <INCHI_KEY>
YNTRKVVINRSNHR-UHFFFAOYSA-N

> <FORMULA>
C23H24O11

> <MOLECULAR_WEIGHT>
476.434

> <EXACT_MASS>
476.131861593

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
45.80448049947345

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]oxan-2-yl}methyl acetate

> <ALOGPS_LOGP>
0.05

> <JCHEM_LOGP>
0.5525498143333331

> <ALOGPS_LOGS>
-2.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.198415360572543

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.408038450395187

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8778380720611647

> <JCHEM_POLAR_SURFACE_AREA>
194.20999999999998

> <JCHEM_REFRACTIVITY>
114.92549999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.42e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-2-yl}methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-APR-15         0                                  
HETATM    1  C   UNK     0       0.000  10.780   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.334   8.470   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.668   6.930   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.001   8.470   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14                                                  
CONECT   14   13                                                            
CONECT   15    8   16   34                                                  
CONECT   16   15   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   16   25                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   34                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   15   27                                                  
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Value	Source
{3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]oxan-2-yl}methyl acetic acid	Generator

Chemical Formula

C₂₃H₂₄O₁₁

Average Mass

476.4340 Da

Monoisotopic Mass

476.13186 Da

IUPAC Name

{3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9,10-dihydroanthracen-9-yl]oxan-2-yl}methyl acetate

Traditional Name

{3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9H-anthracen-9-yl]oxan-2-yl}methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1OC(C(O)C(O)C1O)C1C2=CC(CO)=CC(O)=C2C(=O)C2=C(O)C=CC(O)=C12

InChI Identifier

InChI=1S/C23H24O11/c1-8(25)33-7-14-19(29)21(31)22(32)23(34-14)16-10-4-9(6-24)5-13(28)15(10)20(30)18-12(27)3-2-11(26)17(16)18/h2-5,14,16,19,21-24,26-29,31-32H,6-7H2,1H3

InChI Key

YNTRKVVINRSNHR-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
Aloe marlothii	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
C-glycosyl compound
Glycosyl compound
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monosaccharide
Oxane
Vinylogous acid
Carboxylic acid ester
Ketone
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Polyol
Organic oxygen compound
Organic oxide
Carbonyl group
Alcohol
Aromatic alcohol
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
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	0.05	ALOGPS
logP	0.55	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	8.41	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	194.21 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	114.93 m³·mol⁻¹	ChemAxon
Polarizability	45.8 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

73157761

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate (NP0266709)

MOL for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

3D MOL for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

3D SDF for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

3D-SDF for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

PDB for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

3D PDB for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

SMILES for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

INCHI for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

Structure for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)

3D Structure for NP0266709 ({3,4,5-trihydroxy-6-[1,4,5-trihydroxy-7-(hydroxymethyl)-10-oxo-9h-anthracen-9-yl]oxan-2-yl}methyl acetate)