NP-MRD: Showing NP-Card for (8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol (NP0250770)

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Record Information

Version

2.0

Created at

2022-09-07 13:43:20 UTC

Updated at

2022-09-07 13:43:21 UTC

NP-MRD ID

NP0250770

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol

Description

Malibatol A belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. (8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol is found in Hopea utilis and Vitis vinifera. Based on a literature review very few articles have been published on malibatol A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072215432D          

 35 40  0  0  1  0            999 V2000
    3.9362   -2.0798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3484   -1.5008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5532   -1.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9654   -1.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1729   -0.3430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5851    0.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7712    0.1006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3911    0.8328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4074    1.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6270    1.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4255    2.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0481    2.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984    2.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9700    1.4206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    1.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4565    1.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0528    0.8285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8447    1.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4411    0.4899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0402    1.8615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    2.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6393    3.2330    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6519    2.2001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1472    2.8526    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5161    3.5905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0615    4.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4305    5.0169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2540    5.0664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6229    5.8043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7086    4.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3396    3.6400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3223    2.8649    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9754    3.6134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5559   -0.7024    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
  3  4  1  0  0  0  0
  4  5  2  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  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 15  2  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
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 26 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
 25 31  1  0  0  0  0
 24 32  1  0  0  0  0
 13 32  1  0  0  0  0
 32 33  1  6  0  0  0
  5 34  1  0  0  0  0
 34 35  2  0  0  0  0
  2 35  1  0  0  0  0
M  END

     RDKit          3D

 55 60  0  0  0  0  0  0  0  0999 V2000
   -5.7838   -3.5068    1.8911 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8445   -2.5343    1.5735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5013   -2.8689    1.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6104   -1.8777    1.3066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9525   -0.6070    0.9416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0652    0.4634    0.5381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3647    1.7330    0.8901 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4467    2.5714    0.4648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2426    3.9458    0.5507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1286    4.5238   -0.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0914    5.9037    0.0710 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8300    3.7503   -0.6701 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6590    2.3622   -0.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4805    1.8838   -0.2055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9062    0.5476   -0.1528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3096   -0.5605   -0.8842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2683   -1.4747   -1.2251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8489   -2.6294   -1.8959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7993   -3.5536   -2.2378 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4843   -2.7774   -2.1759 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4198   -1.8296   -1.8225 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7408   -2.0600   -2.1473 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0433   -0.6599   -1.1507 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1504    0.3135   -0.9964 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8691    0.2584    0.2561 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1442   -0.3154    0.2562 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8947   -0.4196    1.3896 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4025    0.0497    2.5905 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1987   -0.0778    3.7102 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1504    0.6164    2.6053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3897    0.7210    1.4525 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8076    1.7141   -1.4272 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4620    1.6064   -2.7981 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3233   -0.3243    0.9042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2483   -1.2666    1.2131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7724   -3.3054    1.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2105   -3.8683    1.9134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5424   -2.1456    1.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9783    4.5349    1.0614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5609    6.5030    0.5342 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6941    4.2093   -1.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3130   -1.3235   -1.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5813   -4.4114   -2.7220 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7701   -3.6923   -2.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9957   -2.9052   -2.6301 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8800   -0.0267   -1.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5559   -0.6867   -0.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8793   -0.8759    1.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1387   -0.9145    4.2886 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7574    0.9896    3.5567 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4196    1.1772    1.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7185    2.3515   -1.4274 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5470    1.1816   -2.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6785    0.6644    0.6245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3324   -1.0772    1.1935 H   0  0  0  0  0  0  0  0  0  0  0  0
 33 32  1  0
 32 24  1  0
 24 25  1  0
 25 26  2  0
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 27 28  2  0
 28 29  1  0
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 30 31  2  0
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 18 17  1  0
 17 16  2  0
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 15  6  2  0
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 12 13  1  0
 13 14  2  0
  6  5  1  0
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  4  3  1  0
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  2  1  1  0
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 35 34  2  0
 13 32  1  0
 34  5  1  0
 31 25  1  0
 16 23  1  0
 14 15  1  0
 14  8  1  0
 33 53  1  0
 32 52  1  6
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 27 48  1  0
 29 49  1  0
 30 50  1  0
 31 51  1  0
 22 45  1  0
 20 44  1  0
 19 43  1  0
 17 42  1  0
  9 39  1  0
 11 40  1  0
 12 41  1  0
  4 38  1  0
  3 37  1  0
  1 36  1  0
 35 55  1  0
 34 54  1  0
M  END


  Mrv1652309072215432D          

 35 40  0  0  1  0            999 V2000
    3.9362   -2.0798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3484   -1.5008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5532   -1.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9654   -1.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1729   -0.3430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5851    0.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7712    0.1006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3911    0.8328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4074    1.0403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6270    1.8355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4255    2.0430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0481    2.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7984    2.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9700    1.4206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7079    1.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4565    1.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0528    0.8285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8447    1.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4411    0.4899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0402    1.8615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438    2.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6393    3.2330    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6519    2.2001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1472    2.8526    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5161    3.5905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0615    4.2790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4305    5.0169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2540    5.0664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6229    5.8043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7086    4.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3396    3.6400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3223    2.8649    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9754    3.6134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5559   -0.7024    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
  3  4  1  0  0  0  0
  4  5  2  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  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
 12 13  1  0  0  0  0
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  8 14  1  0  0  0  0
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  6 15  2  0  0  0  0
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 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
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 25 26  2  0  0  0  0
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 25 31  1  0  0  0  0
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 13 32  1  0  0  0  0
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  5 34  1  0  0  0  0
 34 35  2  0  0  0  0
  2 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0250770

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1[C@@H](C2=CC=C(O)C=C2)C2=C(O)C=C(O)C=C2C2=C(OC3=CC(O)=CC1=C23)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H20O7/c29-15-5-1-13(2-6-15)23-24-19(9-17(31)11-21(24)33)26-25-20(27(23)34)10-18(32)12-22(25)35-28(26)14-3-7-16(30)8-4-14/h1-12,23,27,29-34H/t23-,27-/m0/s1

> <INCHI_KEY>
GCOPXRXOORFRHV-HOFKKMOUSA-N

> <FORMULA>
C28H20O7

> <MOLECULAR_WEIGHT>
468.461

> <EXACT_MASS>
468.120902984

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
48.13393743162797

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(8S,9R)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol

> <JCHEM_LOGP>
4.660077063999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.975755117906804

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.32163884359192

> <JCHEM_PKA_STRONGEST_BASIC>
-2.834139536376006

> <JCHEM_POLAR_SURFACE_AREA>
134.52

> <JCHEM_REFRACTIVITY>
129.3158

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(8S,9R)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  O   UNK     0       7.348  -3.882   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.250  -2.802   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.766  -3.211   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.669  -2.131   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.056  -0.640   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.959   0.440   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.440   0.188   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.730   1.555   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.760   1.942   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.170   3.426   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.661   3.814   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.090   4.524   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.490   4.158   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.811   2.652   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.188   1.963   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.585   2.611   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.699   1.547   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.177   1.979   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.290   0.915   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.542   3.475   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.428   4.539   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.793   6.035   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.950   4.107   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.008   5.325   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.697   6.702   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.848   7.987   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.537   9.365   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.074   9.457   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.763  10.835   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.923   8.172   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.234   6.795   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.468   5.348   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       1.821   6.745   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.540  -0.230   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.638  -1.311   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   35                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   34                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   32                                                  
CONECT   14   13    8   15                                                  
CONECT   15   14    6   16                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   16   24                                                  
CONECT   24   23   25   32                                                  
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   25                                                       
CONECT   32   24   13   33                                                  
CONECT   33   32                                                            
CONECT   34    5   35                                                       
CONECT   35   34    2                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₂₀O₇

Average Mass

468.4610 Da

Monoisotopic Mass

468.12090 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

O[C@@H]1[C@@H](C2=CC=C(O)C=C2)C2=C(O)C=C(O)C=C2C2=C(OC3=CC(O)=CC1=C23)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C28H20O7/c29-15-5-1-13(2-6-15)23-24-19(9-17(31)11-21(24)33)26-25-20(27(23)34)10-18(32)12-22(25)35-28(26)14-3-7-16(30)8-4-14/h1-12,23,27,29-34H/t23-,27-/m0/s1

InChI Key

GCOPXRXOORFRHV-HOFKKMOUSA-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
Hopea utilis	LOTUS Database	35616633
Vitis vinifera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
2-phenylbenzofuran
Phenylbenzofuran
Benzofuran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Furan
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Polyol
Organooxygen compound
Alcohol
Organic oxygen compound
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	4.66	ChemAxon
pKa (Strongest Acidic)	8.32	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	134.52 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00033157

Chemspider ID

24697752

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44575508

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol (NP0250770)

MOL for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

3D MOL for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

3D SDF for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

3D-SDF for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

PDB for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

3D PDB for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

SMILES for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

INCHI for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

Structure for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)

3D Structure for NP0250770 ((8s,9r)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-1(16),2,4,6,10(17),11,13-heptaene-4,6,9,12-tetrol)