NP-MRD: Showing NP-Card for (2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol (NP0156734)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 13:59:05 UTC

Updated at

2022-09-02 13:59:06 UTC

NP-MRD ID

NP0156734

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol

Description

Cassigarol D belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. (2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol is found in Maackia amurensis and Senna garrettiana. Based on a literature review very few articles have been published on Cassigarol D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022215592D          

 36 41  0  0  1  0            999 V2000
    5.6817   -2.8090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9811   -2.3735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2536   -2.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5529   -2.3271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8254   -2.7162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5797   -1.5025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3072   -1.1135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0872    2.1096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.1221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492    1.6739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7927   -0.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4235    0.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1994    0.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3446   -0.6668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1205   -0.9471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7139   -1.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8591   -2.0108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9380   -0.9184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0079   -1.5490    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  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
  9 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  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 18 25  1  0  0  0  0
 14 25  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 28 35  1  0  0  0  0
  7 36  2  0  0  0  0
  2 36  1  0  0  0  0
M  END

     RDKit          3D

 56 61  0  0  0  0  0  0  0  0999 V2000
   -2.8496   -3.2681    3.8077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4490   -3.2462    2.4970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3003   -4.4433    1.8002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8986   -4.4402    0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7502   -5.6357   -0.2136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6551   -3.2073   -0.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7908   -2.0088    0.5535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5160   -0.7452   -0.1660 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2636   -0.0809    0.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5462    0.8750    1.1872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5023    1.6326    1.7355 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8056    1.4239    1.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7493    2.2032    1.9290 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0869    0.4716    0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0458   -0.2816   -0.1314 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3110   -1.2291   -1.0600 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5763   -1.4852   -1.4942 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6030   -0.7536   -0.9664 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9055   -1.0044   -1.4009 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9816   -0.3112   -0.9166 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2873   -0.5744   -1.3632 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7274    0.6499    0.0227 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7913    1.3641    0.5286 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4472    0.9490    0.4991 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3854    0.2426    0.0001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9141    0.8987    1.4138 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5469    0.2490    0.2885 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8805    1.3164   -0.6665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7317    1.2601   -2.0179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0845    2.3505   -2.7903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5879    3.5116   -2.2556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9358    4.6014   -3.0777 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7351    3.5587   -0.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2506    4.7532   -0.3616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3949    2.4987   -0.1036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1904   -2.0411    1.8589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9599   -2.4001    4.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5037   -5.3646    2.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4556   -5.6161   -1.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3501   -3.2326   -1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5438   -0.8882   -1.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2507    2.3832    2.4731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5764    2.9180    2.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4835   -1.7990   -1.4731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8059   -2.2366   -2.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0782   -1.7717   -2.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0491   -0.0341   -0.9739 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6339    2.0739    1.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3240    1.7047    1.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4902   -0.2206    0.6252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3438    0.3654   -2.4817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9558    2.2834   -3.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3010    5.4419   -2.6817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3935    4.8802    0.6299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5304    2.5884    0.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3080   -1.1297    2.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2 36  2  0
 36  7  1  0
  7  6  2  0
  6  4  1  0
  4  5  1  0
  4  3  2  0
  7  8  1  0
  8 27  1  0
 27 26  1  0
 26 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 15  9  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 33 35  2  0
  3  2  1  0
  9  8  1  0
 35 28  1  0
  9 10  1  0
 25 14  1  0
 25 18  1  0
  1 37  1  0
 36 56  1  0
  6 40  1  0
  5 39  1  0
  3 38  1  0
  8 41  1  6
 27 50  1  1
 11 42  1  0
 13 43  1  0
 16 44  1  0
 17 45  1  0
 19 46  1  0
 21 47  1  0
 23 48  1  0
 24 49  1  0
 29 51  1  0
 30 52  1  0
 32 53  1  0
 34 54  1  0
 35 55  1  0
M  END


  Mrv1652309022215592D          

 36 41  0  0  1  0            999 V2000
    5.6817   -2.8090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9811   -2.3735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2536   -2.7626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5529   -2.3271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8254   -2.7162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5797   -1.5025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3072   -1.1135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0872    2.1096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098    0.1221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492    1.6739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7927   -0.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4235    0.4256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1994    0.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3446   -0.6668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1205   -0.9471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7139   -1.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8591   -2.0108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9380   -0.9184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0079   -1.5490    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  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
  9 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  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 18 25  1  0  0  0  0
 14 25  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
 28 35  1  0  0  0  0
  7 36  2  0  0  0  0
  2 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0156734

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC(=CC(O)=C1)[C@H]1[C@@H](OC2=CC(O)=C3C(C=CC4=CC(O)=C(O)C=C34)=C12)C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H20O8/c29-15-5-14(6-16(30)9-15)25-27-17-3-1-12-7-21(33)22(34)10-18(12)26(17)23(35)11-24(27)36-28(25)13-2-4-19(31)20(32)8-13/h1-11,25,28-35H/t25-,28+/m1/s1

> <INCHI_KEY>
HJVFPIFXFXQWKU-NAKRPHOHSA-N

> <FORMULA>
C28H20O8

> <MOLECULAR_WEIGHT>
484.46

> <EXACT_MASS>
484.115817604

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
49.662913503231806

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(12R,13R)-13-(3,4-dihydroxyphenyl)-12-(3,5-dihydroxyphenyl)-14-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),2,4,6,8,10,15-heptaene-4,5,17-triol

> <ALOGPS_LOGP>
3.78

> <JCHEM_LOGP>
4.992476304666666

> <ALOGPS_LOGS>
-4.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.93732119799298

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.502334324567345

> <JCHEM_PKA_STRONGEST_BASIC>
-4.907133849547187

> <JCHEM_POLAR_SURFACE_AREA>
150.84

> <JCHEM_REFRACTIVITY>
131.44689999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.83e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(12R,13R)-13-(3,4-dihydroxyphenyl)-12-(3,5-dihydroxyphenyl)-14-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),2,4,6,8,10,15-heptaene-4,5,17-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0      10.606  -5.244   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       9.298  -4.431   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.940  -5.157   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.632  -4.344   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.274  -5.070   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.682  -2.805   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.040  -2.078   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.874   0.406   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.896   3.938   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.366   1.312   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.358   0.135   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.182   0.499   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.698   0.228   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.652   3.125   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.850   1.041   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.937   1.804   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.365   0.325   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.813  -0.198   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.990   0.794   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.439   0.271   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      13.710  -1.245   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      15.158  -1.768   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      12.533  -2.237   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      12.804  -3.753   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      11.084  -1.714   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.348  -2.891   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   36                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   36                                                  
CONECT    8    7    9   27                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11   26                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   25                                                  
CONECT   15   14    9   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   25                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   18   14                                                  
CONECT   26   10   27                                                       
CONECT   27   26    8   28                                                  
CONECT   28   27   29   35                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   28                                                       
CONECT   36    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₂₀O₈

Average Mass

484.4600 Da

Monoisotopic Mass

484.11582 Da

IUPAC Name

(12R,13R)-13-(3,4-dihydroxyphenyl)-12-(3,5-dihydroxyphenyl)-14-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),2,4,6,8,10,15-heptaene-4,5,17-triol

Traditional Name

(12R,13R)-13-(3,4-dihydroxyphenyl)-12-(3,5-dihydroxyphenyl)-14-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),2,4,6,8,10,15-heptaene-4,5,17-triol

CAS Registry Number

Not Available

SMILES

OC1=CC(=CC(O)=C1)[C@H]1[C@@H](OC2=CC(O)=C3C(C=CC4=CC(O)=C(O)C=C34)=C12)C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C28H20O8/c29-15-5-14(6-16(30)9-15)25-27-17-3-1-12-7-21(33)22(34)10-18(12)26(17)23(35)11-24(27)36-28(25)13-2-4-19(31)20(32)8-13/h1-11,25,28-35H/t25-,28+/m1/s1

InChI Key

HJVFPIFXFXQWKU-NAKRPHOHSA-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
Maackia amurensis	LOTUS Database	35616633
Senna garrettiana	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
1-phenylcoumaran
Phenanthrol
Phenanthrene
Stilbene
Naphthofuran
1-naphthol
2-naphthol
Naphthalene
Coumaran
Catechol
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Oxacycle
Ether
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
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	3.78	ALOGPS
logP	4.99	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	8.5	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	150.84 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	131.45 m³·mol⁻¹	ChemAxon
Polarizability	49.66 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	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

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

101631691

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol (NP0156734)

MOL for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

3D MOL for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

3D SDF for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

3D-SDF for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

PDB for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

3D PDB for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

SMILES for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

INCHI for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

Structure for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)

3D Structure for NP0156734 ((2r,3r)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2h,3h-phenanthro[2,1-b]furan-7,8,10-triol)