NP-MRD: Showing NP-Card for [(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate (NP0213809)

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Record Information

Version

2.0

Created at

2022-09-05 12:54:29 UTC

Updated at

2022-09-05 12:54:30 UTC

NP-MRD ID

NP0213809

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate

Description

Pleionesin C belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. Based on a literature review very few articles have been published on Pleionesin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052214542D          

 34 38  0  0  1  0            999 V2000
    8.6060    0.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8301    0.6771    0.0000 O   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
    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
    5.7927   -0.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  2  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
    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
    2.3387    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
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  1  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
    5.0079   -1.5490    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
    5.6817   -2.8090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2536   -2.7626    0.0000 O   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
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0872    2.1096    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
    6.4235    0.4256    0.0000 C   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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  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
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  2  0  0  0  0
 25 33  1  0  0  0  0
 14 33  1  0  0  0  0
  8 34  2  0  0  0  0
  3 34  1  0  0  0  0
M  END

     RDKit          3D

 60 64  0  0  0  0  0  0  0  0999 V2000
    6.1532   -2.9456    0.3658 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5427   -1.6850   -0.0848 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6811   -0.7161   -0.5735 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2045    0.4880   -0.9853 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3607    1.4775   -1.4800 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9189    2.6877   -1.8900 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0054    1.2855   -1.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4722    0.0960   -1.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0600   -0.1839   -1.2285 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3902    0.1584   -2.3744 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0321    0.0546   -2.0569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0783   -0.2870   -2.7999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3471   -0.3172   -2.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4685    0.0133   -0.9274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3488    0.3659   -0.1807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0985    0.3915   -0.6955 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2606    0.6442   -0.1588 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6528   -0.0559    1.0903 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2582    0.3294    2.3240 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6230    1.5735    2.8746 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1861    1.9917    4.2315 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3382    2.2785    2.1218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6253    0.9671    1.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4574    0.0443    1.9525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7511   -0.0952    1.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9311   -0.1909    1.8665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1095   -0.4097    1.1793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2677   -0.4982    1.9149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0862   -0.5293   -0.1872 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8769   -0.4310   -0.9070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9174   -0.5565   -2.2725 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1254   -0.7810   -2.9650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7375   -0.2146   -0.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3233   -0.9009   -0.6671 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2803   -3.3680   -0.1690 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0034   -3.6545    0.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0032   -2.9162    1.4630 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2522    0.6624   -0.9257 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1963    2.7207   -2.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3824    2.0569   -1.9518 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7970   -1.2422   -0.9799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9790   -0.5432   -3.8505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1545   -0.5912   -2.8605 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4781    1.7003   -0.2378 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7897   -0.1790    1.1210 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3318   -1.1408    0.9419 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4587    1.1661    4.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0796    2.1815    4.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6675    2.9456    4.4559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8526    1.5323    1.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3907    1.8329    0.8840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6387    0.3599    2.9774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9911   -0.9817    1.8898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9358   -0.0938    2.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6366   -1.3662    2.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9943   -0.6997   -0.7221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4967   -1.8237   -2.8273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9118   -0.0625   -2.7092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9002   -0.6924   -4.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9257   -1.8522   -0.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
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  7  8  1  0
  8 34  2  0
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 34  3  1  0
 17  9  1  0
 16 11  1  0
 33 14  1  0
 33 25  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  4 38  1  0
  6 39  1  0
  7 40  1  0
 34 60  1  0
  9 41  1  1
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 23 50  1  0
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 32 59  1  0
 17 44  1  1
 18 45  1  0
 18 46  1  0
 21 47  1  0
 21 48  1  0
 21 49  1  0
M  END


  Mrv1652309052214542D          

 34 38  0  0  1  0            999 V2000
    8.6060    0.3968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8301    0.6771    0.0000 O   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
    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
    5.7927   -0.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  2  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
    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
    2.3387    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
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  1  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
    5.0079   -1.5490    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
    5.6817   -2.8090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2536   -2.7626    0.0000 O   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
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0872    2.1096    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
    6.4235    0.4256    0.0000 C   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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
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 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  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
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
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 29 30  1  0  0  0  0
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 30 33  2  0  0  0  0
 25 33  1  0  0  0  0
 14 33  1  0  0  0  0
  8 34  2  0  0  0  0
  3 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213809

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=CC(=C1)[C@@H]1OC2=CC=C3C(CCC4=CC(O)=CC(OC)=C34)=C2[C@H]1COC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H26O7/c1-14(28)33-13-22-26-21-5-4-15-8-18(30)12-24(32-3)25(15)20(21)6-7-23(26)34-27(22)16-9-17(29)11-19(10-16)31-2/h6-12,22,27,29-30H,4-5,13H2,1-3H3/t22-,27+/m1/s1

> <INCHI_KEY>
WXWSVLIALIBTJH-AMGIVPHBSA-N

> <FORMULA>
C27H26O7

> <MOLECULAR_WEIGHT>
462.498

> <EXACT_MASS>
462.167853177

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
50.22298663803301

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(12S,13R)-5-hydroxy-13-(3-hydroxy-5-methoxyphenyl)-3-methoxy-14-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),2,4,6,10,15-hexaen-12-yl]methyl acetate

> <JCHEM_LOGP>
4.338548654333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.81998160807852

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.15353435396968

> <JCHEM_PKA_STRONGEST_BASIC>
-4.385362169424418

> <JCHEM_POLAR_SURFACE_AREA>
94.45000000000002

> <JCHEM_REFRACTIVITY>
125.87119999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(12S,13R)-5-hydroxy-13-(3-hydroxy-5-methoxyphenyl)-3-methoxy-14-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),2,4,6,10,15-hexaen-12-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      16.065   0.741   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      14.616   1.264   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      13.439   0.271   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.710  -1.245   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.533  -2.237   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      12.804  -3.753   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      11.084  -1.714   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.813  -0.198   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.365   0.325   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.937   1.804   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+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       6.874   0.406   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.040  -2.078   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.348  -2.891   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.298  -4.431   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.606  -5.244   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.940  -5.157   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.182   0.499   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.698   0.228   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       2.380   3.667   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       3.896   3.938   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.850   1.041   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.990   0.794   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   34                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   34                                                  
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   33                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15   11   17                                                  
CONECT   17   16    9   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   15   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   33                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   33                                                  
CONECT   31   30   32                                                       
CONECT   32   31                                                            
CONECT   33   30   25   14                                                  
CONECT   34    8    3                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₂₆O₇

Average Mass

462.4980 Da

Monoisotopic Mass

462.16785 Da

IUPAC Name

[(12S,13R)-5-hydroxy-13-(3-hydroxy-5-methoxyphenyl)-3-methoxy-14-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),2,4,6,10,15-hexaen-12-yl]methyl acetate

Traditional Name

[(12S,13R)-5-hydroxy-13-(3-hydroxy-5-methoxyphenyl)-3-methoxy-14-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(17),2,4,6,10,15-hexaen-12-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=CC(=C1)[C@@H]1OC2=CC=C3C(CCC4=CC(O)=CC(OC)=C34)=C2[C@H]1COC(C)=O

InChI Identifier

InChI=1S/C27H26O7/c1-14(28)33-13-22-26-21-5-4-15-8-18(30)12-24(32-3)25(15)20(21)6-7-23(26)34-27(22)16-9-17(29)11-19(10-16)31-2/h6-12,22,27,29-30H,4-5,13H2,1-3H3/t22-,27+/m1/s1

InChI Key

WXWSVLIALIBTJH-AMGIVPHBSA-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 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
Phenanthrene
Naphthofuran
Naphthalene
Methoxyphenol
Coumaran
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	4.34	ChemAxon
pKa (Strongest Acidic)	9.15	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	94.45 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	125.87 m³·mol⁻¹	ChemAxon
Polarizability	50.22 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

102097659

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate (NP0213809)

MOL for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

3D MOL for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

3D SDF for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

3D-SDF for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

PDB for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

3D PDB for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

SMILES for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

INCHI for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

Structure for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)

3D Structure for NP0213809 ([(2r,3s)-7-hydroxy-2-(3-hydroxy-5-methoxyphenyl)-9-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-3-yl]methyl acetate)