NP-MRD: Showing NP-Card for 3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran (NP0062564)

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Record Information

Version

2.0

Created at

2022-04-28 07:11:35 UTC

Updated at

2022-04-28 07:11:36 UTC

NP-MRD ID

NP0062564

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran

Description

3-[3-(Hydroxymethyl)-4,6-dimethoxy-1-benzofuran-2-yl]-2,6-dimethoxyphenol belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. 3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran is found in Andira inermis . Based on a literature review very few articles have been published on 3-[3-(hydroxymethyl)-4,6-dimethoxy-1-benzofuran-2-yl]-2,6-dimethoxyphenol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282209112D          

 26 28  0  0  0  0            999 V2000
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.0940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.0940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -0.6205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768    3.1465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
    5.8233    1.4741   -2.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8580    0.3830   -1.2542 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4789    0.0298   -1.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3169   -0.5069    0.1301 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0788   -0.7377    0.6907 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9736   -1.1939    1.9677 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8938   -1.6293    3.1844 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9162   -0.4638    0.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6218   -0.4089    0.4144 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0842   -0.6609    1.7675 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1542    0.5570    2.5830 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0099    0.0309   -0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4338    0.2336   -0.7521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559    1.5725   -0.8143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2205    1.9697   -0.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2062    0.9877   -0.7984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5532    1.3038   -0.7346 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2036    2.4820   -0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7691   -0.3141   -0.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7610   -1.3065   -0.7159 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4262   -0.6916   -0.7139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1966   -2.0271   -0.5910 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3902   -2.7909    0.6066 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8814    0.2343   -1.7279 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1200    0.0460   -1.3333 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3957    0.2745   -1.8393 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8297    1.4917   -2.7089 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9061    2.3353   -1.5996 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7361    1.3070   -2.8919 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1636   -0.8550    0.7852 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2649   -0.7941    3.9638 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6339   -2.5144    3.4474 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9467   -1.8807    3.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3640   -1.5117    2.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0870   -0.6110    1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0542    0.9087    2.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1040    2.3093   -0.8375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5545    2.9525   -1.0276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3764    2.9387   -1.5840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5895    3.2415    0.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2157    2.4406   -0.0307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6336   -2.2522   -0.8861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2829   -3.4536    0.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4975   -3.5036    0.7150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4628   -2.1562    1.4818 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4337    0.7599   -2.7755 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
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  9 12  2  0
 12 24  1  0
 24 25  1  0
 25 26  2  0
 12 13  1  0
 13 21  2  0
 21 22  1  0
 22 23  1  0
 21 19  1  0
 19 20  1  0
 19 16  2  0
 16 17  1  0
 17 18  1  0
 16 15  1  0
 15 14  2  0
 26  3  1  0
 14 13  1  0
 25  8  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 26 46  1  0
 23 43  1  0
 23 44  1  0
 23 45  1  0
 20 42  1  0
 18 39  1  0
 18 40  1  0
 18 41  1  0
 15 38  1  0
 14 37  1  0
M  END


  Mrv1652304282209112D          

 26 28  0  0  0  0            999 V2000
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0587    2.2374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.0940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.0940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -0.6205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    2.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768    3.1465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0062564

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C2C(CO)=C(OC2=C1)C1=C(OC)C(O)=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H20O7/c1-22-10-7-14(24-3)16-12(9-20)18(26-15(16)8-10)11-5-6-13(23-2)17(21)19(11)25-4/h5-8,20-21H,9H2,1-4H3

> <INCHI_KEY>
SQHIQBUKBJSGPO-UHFFFAOYSA-N

> <FORMULA>
C19H20O7

> <MOLECULAR_WEIGHT>
360.362

> <EXACT_MASS>
360.120902984

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
37.39091428469525

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[3-(hydroxymethyl)-4,6-dimethoxy-1-benzofuran-2-yl]-2,6-dimethoxyphenol

> <ALOGPS_LOGP>
2.50

> <JCHEM_LOGP>
1.9979955506666665

> <ALOGPS_LOGS>
-3.32

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.025355487798034

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.998975582310614

> <JCHEM_PKA_STRONGEST_BASIC>
-2.789269091698033

> <JCHEM_POLAR_SURFACE_AREA>
90.52000000000001

> <JCHEM_REFRACTIVITY>
94.56240000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.74e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[3-(hydroxymethyl)-4,6-dimethoxy-1-benzofuran-2-yl]-2,6-dimethoxyphenol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.924   5.923   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.258   6.693   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.126   4.089   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.320   2.843   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.090   1.509   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.630   1.509   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.400   2.843   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.630   4.177   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.090   4.177   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.940   2.843   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -5.710   4.177   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.400   0.175   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -0.320   0.175   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.090  -1.158   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.650   5.553   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.143   5.874   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       7.591   1.303   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.925   2.073   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    5   10   23                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10    4                                                       
CONECT   12   10   13   17                                                  
CONECT   13   12   14   21                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15   19                                                       
CONECT   19   18                                                            
CONECT   20   14                                                            
CONECT   21   13   22                                                       
CONECT   22   21                                                            
CONECT   23    9   24                                                       
CONECT   24   23                                                            
CONECT   25    2   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

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Synonyms

Not Available

Chemical Formula

C₁₉H₂₀O₇

Average Mass

360.3620 Da

Monoisotopic Mass

360.12090 Da

IUPAC Name

3-[3-(hydroxymethyl)-4,6-dimethoxy-1-benzofuran-2-yl]-2,6-dimethoxyphenol

Traditional Name

3-[3-(hydroxymethyl)-4,6-dimethoxy-1-benzofuran-2-yl]-2,6-dimethoxyphenol

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C2C(CO)=C(OC2=C1)C1=C(OC)C(O)=C(OC)C=C1

InChI Identifier

InChI=1S/C19H20O7/c1-22-10-7-14(24-3)16-12(9-20)18(26-15(16)8-10)11-5-6-13(23-2)17(21)19(11)25-4/h5-8,20-21H,9H2,1-4H3

InChI Key

SQHIQBUKBJSGPO-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Andira inermis	Plant	KNApSAcK

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
Pterofuran
2-phenylbenzofuran
Phenylbenzofuran
Benzopyran
Methoxyphenol
Dimethoxybenzene
M-dimethoxybenzene
Benzofuran
Methoxybenzene
Anisole
Phenol ether
Phenoxy compound
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Heteroaromatic compound
Furan
Organoheterocyclic compound
Oxacycle
Ether
Hydrocarbon derivative
Alcohol
Organooxygen compound
Primary alcohol
Organic oxygen compound
Aromatic alcohol
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	2.5	ALOGPS
logP	2	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	9	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	90.52 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	94.56 m³·mol⁻¹	ChemAxon
Polarizability	37.39 Å³	ChemAxon
Number of Rings	3	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

C00019190

Chemspider ID

8536597

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10361148

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran (NP0062564)

MOL for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

3D MOL for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

3D SDF for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

3D-SDF for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

PDB for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

3D PDB for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

SMILES for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

INCHI for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

Structure for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)

3D Structure for NP0062564 (3'-Hydroxy-4,6,2',4'-tetramethoxy-3-hydroxymethyl-2-arylbenzofuran)