NP-MRD: Showing NP-Card for methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate (NP0308151)

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Record Information

Version

2.0

Created at

2022-09-11 01:45:02 UTC

Updated at

2022-09-11 01:45:02 UTC

NP-MRD ID

NP0308151

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate

Description

Methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]Henicosa-3(8),4,6,9,13,15,17,20-octaene-15-carbonyl}benzoate belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups. Based on a literature review very few articles have been published on methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]Henicosa-3(8),4,6,9,13,15,17,20-octaene-15-carbonyl}benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112203452D          

 42 47  0  0  0  0            999 V2000
   12.7216   -2.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4931   -1.2302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6923   -1.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1200   -1.6259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4639   -0.2389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0362    0.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8370    0.1568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8077    1.1480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0070    1.3466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4347    0.7523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6339    0.9509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6631   -0.0404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0908   -0.6346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3193   -1.4273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2901   -0.4361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0616    0.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1754    1.1738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2609    0.5552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6886   -0.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9170   -0.8318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7178   -1.0303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9462   -1.8230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4890   -1.6646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9901   -1.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8962   -0.3120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1291   -0.0953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9009    0.3915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9994   -1.0017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1660   -1.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0320   -2.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4533   -0.7529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6849   -1.0532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5607   -1.8688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0406   -0.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648    0.2778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5205    0.7931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9332    0.5780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5775    0.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3874    0.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4703    1.1560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5851   -1.6945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2503   -2.4485    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
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 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
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 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
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 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 19 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 26 39  1  0  0  0  0
 39 40  1  0  0  0  0
 28 41  1  0  0  0  0
 23 41  1  0  0  0  0
 41 42  2  0  0  0  0
M  END

     RDKit          3D

 66 71  0  0  0  0  0  0  0  0999 V2000
    3.1846    2.9964    0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7583    1.7523   -0.1491 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7198    1.1149    0.5779 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0880    1.7642    1.6163 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3339   -0.1645    0.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3319   -0.6547    1.1549 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6570   -0.0899    2.3287 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0335   -1.7960    0.7959 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7730   -2.4350   -0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7962   -1.9528   -1.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5704   -2.6384   -2.3506 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0438   -0.8038   -0.9029 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0948   -0.3748   -1.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5063   -0.2921   -3.1126 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6967   -0.0371   -1.6901 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9815    0.7263   -2.5669 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5211    1.3787   -3.6767 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0073    0.2693   -1.2705 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0621   -0.6639   -0.5769 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8466   -1.4126    0.2500 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1721   -1.2216    0.8385 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7931   -2.2390    0.3228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7646   -1.8115   -0.4777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2469   -0.3774   -0.3698 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4422    0.5551   -1.2212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0354   -0.0506    1.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9867    0.3455    1.9023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6543    0.6244    3.2362 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3627    0.4936    1.4637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3463    0.9504    2.3381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1425    1.2609    3.6400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6459    1.1014    1.8366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9062    0.8043    0.5381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2939    0.9706    0.0188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9298    0.3563   -0.3077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6346    0.1940    0.1513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6589   -0.3198   -0.8027 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0575   -1.5860   -1.2971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6787   -0.2215    1.5990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2192    0.3873    2.5812 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0607    2.9478    0.0905 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4254    3.3516    1.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4907    3.7729   -0.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.8045   -2.1862    1.4522 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3307   -3.3444   -0.6581 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8886   -2.4233   -3.0184 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0321    1.4840   -3.0426 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7345   -1.9374    1.0400 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.4188    1.2704    4.2641 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7544    0.3441   -1.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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  3  4  2  0
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 22 52  1  0
M  END


  Mrv1652309112203452D          

 42 47  0  0  0  0            999 V2000
   12.7216   -2.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4931   -1.2302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.6923   -1.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1200   -1.6259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4639   -0.2389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0362    0.3553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8370    0.1568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8077    1.1480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0070    1.3466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4347    0.7523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6339    0.9509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6631   -0.0404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0908   -0.6346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3193   -1.4273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2901   -0.4361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0616    0.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1754    1.1738    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4890   -1.6646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4533   -0.7529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6849   -1.0532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5607   -1.8688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0406   -0.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648    0.2778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5205    0.7931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9332    0.5780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5775    0.0627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3874    0.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4703    1.1560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5851   -1.6945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2503   -2.4485    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  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
 20 21  2  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 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  1  0  0  0  0
 19 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 26 39  1  0  0  0  0
 39 40  1  0  0  0  0
 28 41  1  0  0  0  0
 23 41  1  0  0  0  0
 41 42  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0308151

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C(O)C=CC(O)=C1C(=O)C1=C(O)C=C2CC34C=CC(C(=O)C3=C(O)C3=C(O)C=C(C)C=C3C4O)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C31H24O11/c1-11-7-14-20(17(34)8-11)28(39)24-25(36)13-5-6-31(24,29(14)40)10-12-9-18(35)23(26(37)19(12)13)27(38)21-15(32)3-4-16(33)22(21)30(41)42-2/h3-9,13,29,32-35,37,39-40H,10H2,1-2H3

> <INCHI_KEY>
HIABMWDNEAHXTD-UHFFFAOYSA-N

> <FORMULA>
C31H24O11

> <MOLECULAR_WEIGHT>
572.522

> <EXACT_MASS>
572.131861593

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
56.81777618634525

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0^{1,10}.0^{3,8}.0^{13,18}]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate

> <JCHEM_LOGP>
5.8848036116666655

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.763762162397203

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.305827058214587

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3610610031338926

> <JCHEM_POLAR_SURFACE_AREA>
202.04999999999998

> <JCHEM_REFRACTIVITY>
151.27989999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0^{1,10}.0^{3,8}.0^{13,18}]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      23.747  -3.776   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      23.320  -2.296   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      21.826  -1.926   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      20.757  -3.035   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      21.399  -0.446   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.468   0.663   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      23.962   0.293   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      22.041   2.143   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.546   2.514   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.478   1.404   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      17.983   1.775   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      19.905  -0.075   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.836  -1.185   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      19.263  -2.664   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      17.341  -0.814   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.915   0.666   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      17.127   2.191   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      15.420   1.036   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.352  -0.073   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.778  -1.553   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.273  -1.923   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      16.700  -3.403   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      13.980  -3.107   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.048  -2.011   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.873  -0.582   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.441  -0.178   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.882   0.731   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.199  -1.870   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.643  -2.244   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.393  -3.764   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.313  -1.405   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.878  -1.966   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.647  -3.488   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.676  -1.004   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.908   0.518   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.705   1.480   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.342   1.079   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.545   0.117   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.056   0.626   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      10.211   2.158   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      12.292  -3.163   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      11.667  -4.570   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   12                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    5   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   21                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21   23                                                  
CONECT   21   20   15   22                                                  
CONECT   22   21                                                            
CONECT   23   20   24   41                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28   39                                             
CONECT   27   26   19                                                       
CONECT   28   26   29   41                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   38                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   31   39                                                  
CONECT   39   38   26   40                                                  
CONECT   40   39                                                            
CONECT   41   28   23   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Value	Source
Methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0,.0,.0,]henicosa-3(8),4,6,9,13,15,17,20-octaene-15-carbonyl}benzoic acid	Generator

Chemical Formula

C₃₁H₂₄O₁₁

Average Mass

572.5220 Da

Monoisotopic Mass

572.13186 Da

IUPAC Name

methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0^{1,10}.0^{3,8}.0^{13,18}]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate

Traditional Name

methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0^{1,10}.0^{3,8}.0^{13,18}]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C(O)C=CC(O)=C1C(=O)C1=C(O)C=C2CC34C=CC(C(=O)C3=C(O)C3=C(O)C=C(C)C=C3C4O)C2=C1O

InChI Identifier

InChI=1S/C31H24O11/c1-11-7-14-20(17(34)8-11)28(39)24-25(36)13-5-6-31(24,29(14)40)10-12-9-18(35)23(26(37)19(12)13)27(38)21-15(32)3-4-16(33)22(21)30(41)42-2/h3-9,13,29,32-35,37,39-40H,10H2,1-2H3

InChI Key

HIABMWDNEAHXTD-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzophenones

Direct Parent

Benzophenones

Alternative Parents

Substituents

Benzophenone
Aryl-phenylketone
M-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Dihydroxybenzoic acid
1-naphthol
Benzoate ester
Naphthalene
Salicylic acid or derivatives
Benzoic acid or derivatives
Benzoyl
Hydroquinone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Cyclohexenone
Phenol
Methyl ester
Vinylogous acid
Ketone
Carboxylic acid ester
Secondary alcohol
Enol
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Organic oxygen compound
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	5.88	ChemAxon
pKa (Strongest Acidic)	5.31	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	202.05 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	151.28 m³·mol⁻¹	ChemAxon
Polarizability	56.82 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

19741929

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21022496

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate (NP0308151)

MOL for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

3D MOL for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

3D SDF for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

3D-SDF for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

PDB for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

3D PDB for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

SMILES for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

INCHI for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

Structure for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)

3D Structure for NP0308151 (methyl 3,6-dihydroxy-2-{2,7,9,14,16-pentahydroxy-5-methyl-11-oxopentacyclo[10.7.2.0¹,¹⁰.0³,⁸.0¹³,¹⁸]henicosa-3,5,7,9,13,15,17,20-octaene-15-carbonyl}benzoate)