NP-MRD: Showing NP-Card for 3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid (NP0151338)

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Record Information

Version

2.0

Created at

2022-09-02 07:38:29 UTC

Updated at

2022-09-02 07:38:29 UTC

NP-MRD ID

NP0151338

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid

Description

Sulfuric acid 3-[(2S)-2alpha-(3-methoxy-4-hydroxyphenyl)-3beta-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. 3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid is found in Glochidion zeylanicum. Based on a literature review very few articles have been published on Sulfuric acid 3-[(2S)-2alpha-(3-methoxy-4-hydroxyphenyl)-3beta-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022209382D          

 30 32  0  0  1  0            999 V2000
   -2.6462    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    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
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -3.9979    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0832   -4.7124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9082   -3.2835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    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
    1.1387   -1.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  3 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -7.9155   -1.3031    0.5074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9172   -0.5325    0.0759 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4172    0.1967   -0.5025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0122   -0.0292   -0.2075 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5908   -1.3611   -0.2716 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4265   -3.1709    1.2653 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3633    1.0755    0.0744 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.4353    2.1460    1.3574 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8147    0.9789   -0.7703 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5642    3.2813   -0.7962 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5708    0.2798   -0.5216 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2342   -0.0653   -0.6287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512    0.6598   -1.1236 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5966    2.0673   -0.7358 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0653    2.0400    0.5335 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5586    1.6795   -1.0743 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0248    1.3097   -0.8009 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8932    1.2163   -1.1149 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1129    3.0343   -1.5909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2152    3.0261   -1.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309022209382D          

 30 32  0  0  1  0            999 V2000
   -2.6462    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8212    0.7310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4087    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5837    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    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
    4.0668   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957   -3.9979    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    6.2102   -4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0832   -4.7124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9082   -3.2835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    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
    1.1387   -1.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.0768   -2.3215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  8  9  2  0  0  0  0
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 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0151338

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2O[C@@H]([C@@H](CO)C2=CC(CCCOS(O)(=O)=O)=C1)C1=CC=C(O)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O9S/c1-26-17-10-13(5-6-16(17)22)19-15(11-21)14-8-12(4-3-7-28-30(23,24)25)9-18(27-2)20(14)29-19/h5-6,8-10,15,19,21-22H,3-4,7,11H2,1-2H3,(H,23,24,25)/t15-,19+/m0/s1

> <INCHI_KEY>
KXNUUGLBJAAEGW-HNAYVOBHSA-N

> <FORMULA>
C20H24O9S

> <MOLECULAR_WEIGHT>
440.46

> <EXACT_MASS>
440.114103527

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
44.287693950248624

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxy}sulfonic acid

> <ALOGPS_LOGP>
0.65

> <JCHEM_LOGP>
0.11401801250096395

> <ALOGPS_LOGS>
-3.26

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.909972272858758

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.0643113833712894

> <JCHEM_PKA_STRONGEST_BASIC>
-2.71365077806448

> <JCHEM_POLAR_SURFACE_AREA>
131.75

> <JCHEM_REFRACTIVITY>
107.4861

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.40e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.940   1.365   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.400   1.365   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.630   0.031   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.090   0.031   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.320  -1.303   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.126  -0.057   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.924   1.777   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.258   2.547   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.591  -2.843   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.591  -4.383   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.925  -5.153   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.925  -6.693   0.000  0.00  0.00           O+0
HETATM   18  S   UNK     0      10.259  -7.463   0.000  0.00  0.00           S+0
HETATM   19  O   UNK     0      11.592  -8.233   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       9.489  -8.797   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      11.029  -6.129   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.143  -4.334   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.090  -2.637   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.630  -2.637   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.400  -1.303   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.940  -1.303   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7   24                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   23                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   13   23                                                       
CONECT   23   22    8   24                                                  
CONECT   24   23    6   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27    5   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28    3   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
Sulfate 3-[(2S)-2a-(3-methoxy-4-hydroxyphenyl)-3b-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulfate 3-[(2S)-2alpha-(3-methoxy-4-hydroxyphenyl)-3beta-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulfate 3-[(2S)-2α-(3-methoxy-4-hydroxyphenyl)-3β-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulfuric acid 3-[(2S)-2a-(3-methoxy-4-hydroxyphenyl)-3b-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulfuric acid 3-[(2S)-2α-(3-methoxy-4-hydroxyphenyl)-3β-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulphate 3-[(2S)-2a-(3-methoxy-4-hydroxyphenyl)-3b-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulphate 3-[(2S)-2alpha-(3-methoxy-4-hydroxyphenyl)-3beta-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulphate 3-[(2S)-2α-(3-methoxy-4-hydroxyphenyl)-3β-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulphuric acid 3-[(2S)-2a-(3-methoxy-4-hydroxyphenyl)-3b-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulphuric acid 3-[(2S)-2alpha-(3-methoxy-4-hydroxyphenyl)-3beta-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator
Sulphuric acid 3-[(2S)-2α-(3-methoxy-4-hydroxyphenyl)-3β-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl]propyl ester	Generator

Chemical Formula

C₂₀H₂₄O₉S

Average Mass

440.4600 Da

Monoisotopic Mass

440.11410 Da

IUPAC Name

{3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxy}sulfonic acid

Traditional Name

3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid

CAS Registry Number

Not Available

SMILES

COC1=C2O[C@@H]([C@@H](CO)C2=CC(CCCOS(O)(=O)=O)=C1)C1=CC=C(O)C(OC)=C1

InChI Identifier

InChI=1S/C20H24O9S/c1-26-17-10-13(5-6-16(17)22)19-15(11-21)14-8-12(4-3-7-28-30(23,24)25)9-18(27-2)20(14)29-19/h5-6,8-10,15,19,21-22H,3-4,7,11H2,1-2H3,(H,23,24,25)/t15-,19+/m0/s1

InChI Key

KXNUUGLBJAAEGW-HNAYVOBHSA-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
Glochidion zeylanicum	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
Norlignan skeleton
Neolignan skeleton
Methoxyphenol
Benzofuran
Coumaran
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Sulfuric acid ester
Alkyl sulfate
Sulfuric acid monoester
Sulfate-ester
Organic sulfuric acid or derivatives
Oxacycle
Ether
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Organooxygen compound
Alcohol
Hydrocarbon derivative
Primary 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	0.65	ALOGPS
logP	0.11	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	-2.1	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	131.75 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	107.49 m³·mol⁻¹	ChemAxon
Polarizability	44.29 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

Not Available

Chemspider ID

8750490

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10575104

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid (NP0151338)

MOL for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

3D MOL for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

3D SDF for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

3D-SDF for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

PDB for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

3D PDB for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

SMILES for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

INCHI for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

Structure for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)

3D Structure for NP0151338 (3-[(2s,3r)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxysulfonic acid)