NP-MRD: Showing NP-Card for (1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol (NP0264591)

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Record Information

Version

2.0

Created at

2022-09-08 08:10:17 UTC

Updated at

2022-09-08 08:10:17 UTC

NP-MRD ID

NP0264591

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol

Description

(1R,8R,9S,16R)-9-[(1R,8R,9S,16R)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]Heptadeca-2,4,6,10(17),11,13-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]Heptadeca-2,4,6,10(17),11,13-hexaen-12-ol belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. (1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol is found in Hopea parviflora. Based on a literature review very few articles have been published on (1R,8R,9S,16R)-9-[(1R,8R,9S,16R)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]Heptadeca-2,4,6,10(17),11,13-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]Heptadeca-2,4,6,10(17),11,13-hexaen-12-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082210102D          

 64 75  0  0  1  0            999 V2000
    4.6920    1.0380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8905    1.2335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3204    0.6372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5189    0.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2875    1.6245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4860    1.8200    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3143    2.6269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0028    3.0815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9533    3.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2154    4.2740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5270    3.8194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5764    2.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1721    2.6490    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3676    1.8475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1903    1.7857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5481    1.0424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0833    0.3608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8372   -0.0741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2606    0.4226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1372    1.1949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9621    1.1827    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3090    0.4342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7851   -0.2032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0614   -0.0074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6403   -0.5952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5261   -0.7026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4207   -1.3904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3778   -1.5979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6946   -1.3790    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4431   -1.0322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0395   -1.6022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8314   -1.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0269   -0.5692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4305    0.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6386   -0.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1339    0.4219    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5028    1.1598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0482    1.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4172    2.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2407    2.6356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7856    3.3765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7691    1.7258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3263    1.2093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5718   -2.1948    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1595   -2.7738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9548   -2.5542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5426   -3.1331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3351   -3.9316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9077   -4.5596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399   -4.1511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9521   -3.5722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7579   -2.3301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5032    2.5491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8740    3.0826    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9357    3.9053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6791    4.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7408    5.0858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0592    5.5506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1210    6.3733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3159    5.1928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2541    4.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8575    2.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6590    2.0254    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
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 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
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
  6 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  1  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 23 29  1  0  0  0  0
 30 29  1  1  0  0  0
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 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
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 31 36  1  0  0  0  0
 36 37  1  0  0  0  0
 22 37  1  0  0  0  0
 37 38  1  6  0  0  0
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 28 53  1  0  0  0  0
 15 54  1  0  0  0  0
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 13 55  1  0  0  0  0
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 56 62  1  0  0  0  0
  5 63  1  0  0  0  0
 63 64  2  0  0  0  0
  2 64  1  0  0  0  0
M  END

     RDKit          3D

106117  0  0  0  0  0  0  0  0999 V2000
    2.3052    0.7956   -5.3910 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4166    0.4506   -4.4053 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8314   -0.8125   -4.3896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0481   -1.1075   -3.3843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4087   -0.2483   -2.3718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4118   -0.6031   -1.2976 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5779    0.3529   -1.4625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5378    0.8688   -2.7394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4502    1.8257   -3.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3999    2.2802   -2.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4399    1.7581   -0.9585 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8516    0.3770    0.7867 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0297   -0.7419    1.3338 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.2656   -2.4958    2.9540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9835   -2.9112    2.7354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4225   -3.9953    3.4195 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7023   -1.1292    1.0682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7862   -0.5127    0.1032 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6481   -0.6708    0.1797 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.2730   -2.7412   -1.6437 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.9268    1.9764    2.5038 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0463   -0.8128    2.2991 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.4660    0.8344    0.4824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4913    1.7216    0.7297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4074    2.6125    1.7865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4574    3.5135    2.0315 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2821    2.5818    2.5692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2644    1.6968    2.3187 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1963    1.0138   -2.4170 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.5826    0.1956   -6.1307 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1014   -1.5040   -5.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4926   -2.1164   -3.4028 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1267    3.0328   -2.5100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1684    2.1484   -0.2746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7854    1.2934    1.4383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9057   -2.9875    3.6665 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309082210102D          

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M  END
> <DATABASE_ID>
NP0264591

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)[C@@H]1OC2=C3[C@H]1C1=CC=CC=C1[C@H]([C@H]([C@H]1[C@H](C4=CC=C(O)C=C4)C4=CC=CC=C4[C@H]4[C@@H](OC5=C4C1=CC(O)=C5)C1=CC=C(O)C=C1)C3=CC(O)=C2)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C56H42O8/c57-33-17-9-29(10-18-33)47-39-5-1-3-7-41(39)53-49-43(25-37(61)27-45(49)63-55(53)31-13-21-35(59)22-14-31)51(47)52-44-26-38(62)28-46-50(44)54(56(64-46)32-15-23-36(60)24-16-32)42-8-4-2-6-40(42)48(52)30-11-19-34(58)20-12-30/h1-28,47-48,51-62H/t47-,48-,51-,52-,53-,54-,55+,56+/m1/s1

> <INCHI_KEY>
ILRJFBHCTOHAPN-PSIZVQFASA-N

> <FORMULA>
C56H42O8

> <MOLECULAR_WEIGHT>
842.944

> <EXACT_MASS>
842.287968312

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
106

> <JCHEM_AVERAGE_POLARIZABILITY>
89.91300602062309

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
11.644623006000002

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
12

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.257652489904881

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.857995272206088

> <JCHEM_PKA_STRONGEST_BASIC>
-4.603154106650609

> <JCHEM_POLAR_SURFACE_AREA>
139.84

> <JCHEM_REFRACTIVITY>
245.18639999999988

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  O   UNK     0       8.758   1.938   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       7.262   2.303   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.198   1.189   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.702   1.554   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.270   3.032   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.774   3.397   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.453   4.904   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.739   5.752   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.646   7.289   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.269   7.978   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.984   7.130   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.076   5.592   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.321   4.945   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.686   3.449   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.222   3.333   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.890   1.946   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.022   0.673   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.429  -0.138   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.487   0.789   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.256   2.231   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.796   2.208   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.443   0.810   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.465  -0.379   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.115  -0.014   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.195  -1.111   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.849  -1.312   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.785  -2.595   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.705  -2.983   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.786  -1.886   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.163  -2.574   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.561  -1.927   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.674  -2.991   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.152  -2.559   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.517  -1.063   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.404   0.002   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.925  -0.431   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.983   0.788   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.672   2.165   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.823   3.450   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.512   4.828   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.049   4.920   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       7.066   6.303   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       7.036   3.222   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.209   2.257   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.934  -4.097   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.031  -5.178   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       5.516  -4.768   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       6.613  -5.848   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       6.226  -7.339   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       7.294  -8.511   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       4.741  -7.749   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       3.644  -6.668   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0       1.415  -4.350   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      -2.806   4.758   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      -1.631   5.754   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      -1.747   7.290   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      -3.134   7.958   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      -3.250   9.494   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      -1.977  10.361   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      -2.093  11.897   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      -0.590   9.693   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      -0.474   8.158   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0       5.334   4.146   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0       6.830   3.781   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   64                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   63                                                  
CONECT    6    5    7   21                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12   14   55                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16   54                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   14   21                                                  
CONECT   21   20    6   22                                                  
CONECT   22   21   23   37                                                  
CONECT   23   22   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   53                                                  
CONECT   29   28   23   30                                                  
CONECT   30   29   31   45                                                  
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31   37                                                  
CONECT   37   36   22   38                                                  
CONECT   38   37   39   44                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   38                                                       
CONECT   45   30   46   53                                                  
CONECT   46   45   47   52                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49   52                                                       
CONECT   52   51   46                                                       
CONECT   53   45   28                                                       
CONECT   54   15   55                                                       
CONECT   55   54   13   56                                                  
CONECT   56   55   57   62                                                  
CONECT   57   56   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58   60   61                                                  
CONECT   60   59                                                            
CONECT   61   59   62                                                       
CONECT   62   61   56                                                       
CONECT   63    5   64                                                       
CONECT   64   63    2                                                       
MASTER        0    0    0    0    0    0    0    0   64    0  150    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₅₆H₄₂O₈

Average Mass

842.9440 Da

Monoisotopic Mass

842.28797 Da

IUPAC Name

(1R,8R,9S,16R)-9-[(1R,8R,9S,16R)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol

Traditional Name

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)[C@@H]1OC2=C3[C@H]1C1=CC=CC=C1[C@H]([C@H]([C@H]1[C@H](C4=CC=C(O)C=C4)C4=CC=CC=C4[C@H]4[C@@H](OC5=C4C1=CC(O)=C5)C1=CC=C(O)C=C1)C3=CC(O)=C2)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C56H42O8/c57-33-17-9-29(10-18-33)47-39-5-1-3-7-41(39)53-49-43(25-37(61)27-45(49)63-55(53)31-13-21-35(59)22-14-31)51(47)52-44-26-38(62)28-46-50(44)54(56(64-46)32-15-23-36(60)24-16-32)42-8-4-2-6-40(42)48(52)30-11-19-34(58)20-12-30/h1-28,47-48,51-62H/t47-,48-,51-,52-,53-,54-,55+,56+/m1/s1

InChI Key

ILRJFBHCTOHAPN-PSIZVQFASA-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 parviflora	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
4-prenylated 2-arybenzofuran
Linear 1,7-diphenylheptane skeleton
Dibenzocycloheptene
Coumaran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Oxacycle
Ether
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
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	11.64	ChemAxon
pKa (Strongest Acidic)	8.86	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	139.84 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	245.19 m³·mol⁻¹	ChemAxon
Polarizability	89.91 Å³	ChemAxon
Number of Rings	12	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

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

163193091

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol (NP0264591)

MOL for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

3D MOL for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

3D SDF for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

3D-SDF for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

PDB for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

3D PDB for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

SMILES for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

INCHI for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

Structure for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)

3D Structure for NP0264591 ((1r,8r,9s,16r)-9-[(1r,8r,9s,16r)-12-hydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-9-yl]-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0²,⁷.0¹⁴,¹⁷]heptadeca-2,4,6,10,12,14(17)-hexaen-12-ol)