NP-MRD: Showing NP-Card for 3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol (NP0211470)

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Record Information

Version

2.0

Created at

2022-09-05 09:45:43 UTC

Updated at

2022-09-05 09:45:43 UTC

NP-MRD ID

NP0211470

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol

Description

11-(3-Hydroxyphenyl)-3,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]Heptacosa-1(25),2,5,7,9(27),13,15,17(26),21,23-decaene-7,15,23-triol belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. 3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol is found in Caragana sinica. Based on a literature review very few articles have been published on 11-(3-hydroxyphenyl)-3,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]Heptacosa-1(25),2,5,7,9(27),13,15,17(26),21,23-decaene-7,15,23-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052211452D          

 51 60  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309052211452D          

 51 60  0  0  0  0            999 V2000
    8.2902   -3.7067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8932   -2.9835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0684   -2.9656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6715   -2.2424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0993   -1.5370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7024   -0.8138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0542   -0.0676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5014    0.3931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6338    1.2074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9949    1.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1273    2.5436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2234    1.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0910    0.6225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7299    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8840   -0.7098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4810   -1.4297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1199   -1.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9875   -2.7659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6264   -3.2877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2160   -3.0583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5771   -2.5364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7095   -1.7221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9306   -1.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5087   -0.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7372   -1.0338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0983   -0.5119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3268   -0.8043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2307    0.3024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0022    0.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6411    0.0729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2660    0.6116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9469    1.3723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3747    2.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1995    2.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6274    2.7653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2304    3.4885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4056    3.5063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0087    4.2296    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9778    2.8009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1247    1.3039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4314   -2.1071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6066   -2.0892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1787   -2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3539   -2.7768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9569   -2.0535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1321   -2.0357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3848   -1.3482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2096   -1.3660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9017   -2.7849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9241   -1.5549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3211   -2.2781    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  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 13 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  2  0  0  0  0
 33 39  1  0  0  0  0
 32 40  1  0  0  0  0
 29 40  1  0  0  0  0
 23 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  2  0  0  0  0
 42 48  1  0  0  0  0
 41 49  1  0  0  0  0
 21 49  1  0  0  0  0
  5 50  1  0  0  0  0
 50 51  2  0  0  0  0
  2 51  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0211470

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)C1OC2=C3C1C1=CC(O)=CC4=C1C(C(O4)C1=CC=CC(O)=C1)C1=C4C(OC(=C4C3=CC(O)=C2)C2=CC=C(O)C=C2)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C42H28O9/c43-22-8-4-19(5-9-22)40-37-28-13-25(46)16-31-34(28)38(41(49-31)20-6-10-23(44)11-7-20)29-14-26(47)18-33-36(29)39(30-15-27(48)17-32(50-40)35(30)37)42(51-33)21-2-1-3-24(45)12-21/h1-18,38-39,41-48H

> <INCHI_KEY>
ARMLOXGBRBHILM-UHFFFAOYSA-N

> <FORMULA>
C42H28O9

> <MOLECULAR_WEIGHT>
676.677

> <EXACT_MASS>
676.173332482

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
69.85761995094933

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1^{2,5}.1^{10,13}.0^{21,25}.0^{9,27}.0^{17,26}]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol

> <JCHEM_LOGP>
7.8826517723333325

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
10

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.922149926289432

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.527081462120753

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8217538874148342

> <JCHEM_POLAR_SURFACE_AREA>
152.98000000000002

> <JCHEM_REFRACTIVITY>
188.12079999999992

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1^{2,5}.1^{10,13}.0^{21,25}.0^{9,27}.0^{17,26}]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol

> <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  O   UNK     0      15.475  -6.919   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      14.734  -5.569   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.194  -5.536   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.453  -4.186   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.252  -2.869   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.511  -1.519   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      13.168  -0.126   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      12.136   0.734   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.383   2.254   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.190   3.228   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.438   4.748   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.750   2.682   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.503   1.162   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.696   0.188   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.983  -1.325   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.231  -2.669   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.424  -3.643   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.177  -5.163   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      12.369  -6.137   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.737  -5.709   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.544  -4.735   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.791  -3.215   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.337  -2.707   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.550  -1.384   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.110  -1.930   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.917  -0.956   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.477  -1.501   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.164   0.564   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.604   1.110   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.797   0.136   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.963   1.142   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.367   2.562   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.166   3.878   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.706   3.845   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.504   5.162   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.763   6.512   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.224   6.545   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       7.483   7.895   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       7.425   5.228   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       5.833   2.434   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       6.405  -3.933   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.866  -3.900   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.067  -5.217   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.527  -5.183   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.786  -3.833   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       0.247  -3.800   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       2.585  -2.517   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       4.125  -2.550   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       7.283  -5.198   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      14.792  -2.902   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      15.533  -4.252   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   51                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   50                                                  
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   31                                                  
CONECT   14   13    8   15                                                  
CONECT   15   14    6   16                                                  
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   49                                                  
CONECT   22   21   16   23                                                  
CONECT   23   22   24   41                                                  
CONECT   24   23   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   40                                                  
CONECT   30   29   24   31                                                  
CONECT   31   30   13   32                                                  
CONECT   32   31   33   40                                                  
CONECT   33   32   34   39                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   33                                                       
CONECT   40   32   29                                                       
CONECT   41   23   42   49                                                  
CONECT   42   41   43   48                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47   42                                                       
CONECT   49   41   21                                                       
CONECT   50    5   51                                                       
CONECT   51   50    2                                                       
MASTER        0    0    0    0    0    0    0    0   51    0  120    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₂₈O₉

Average Mass

676.6770 Da

Monoisotopic Mass

676.17333 Da

IUPAC Name

3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1^{2,5}.1^{10,13}.0^{21,25}.0^{9,27}.0^{17,26}]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol

Traditional Name

3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1^{2,5}.1^{10,13}.0^{21,25}.0^{9,27}.0^{17,26}]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)C1OC2=C3C1C1=CC(O)=CC4=C1C(C(O4)C1=CC=CC(O)=C1)C1=C4C(OC(=C4C3=CC(O)=C2)C2=CC=C(O)C=C2)=CC(O)=C1

InChI Identifier

InChI=1S/C42H28O9/c43-22-8-4-19(5-9-22)40-37-28-13-25(46)16-31-34(28)38(41(49-31)20-6-10-23(44)11-7-20)29-14-26(47)18-33-36(29)39(30-15-27(48)17-32(50-40)35(30)37)42(51-33)21-2-1-3-24(45)12-21/h1-18,38-39,41-48H

InChI Key

ARMLOXGBRBHILM-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Caragana sinica	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
Coumaran
Benzofuran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Furan
Oxacycle
Organoheterocyclic compound
Ether
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	7.88	ChemAxon
pKa (Strongest Acidic)	8.53	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	152.98 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	188.12 m³·mol⁻¹	ChemAxon
Polarizability	69.86 Å³	ChemAxon
Number of Rings	10	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

162899999

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol (NP0211470)

MOL for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

3D MOL for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

3D SDF for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

3D-SDF for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

PDB for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

3D PDB for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

SMILES for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

INCHI for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

Structure for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)

3D Structure for NP0211470 (3-(3-hydroxyphenyl)-11,19-bis(4-hydroxyphenyl)-4,12,20-trioxaheptacyclo[16.6.1.1²,⁵.1¹⁰,¹³.0²¹,²⁵.0⁹,²⁷.0¹⁷,²⁶]heptacosa-1(25),5(27),6,8,13(26),14,16,18,21,23-decaene-7,15,23-triol)