NP-MRD: Showing NP-Card for 3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate (NP0247825)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 09:48:38 UTC

Updated at

2022-09-07 09:48:38 UTC

NP-MRD ID

NP0247825

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

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

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072211482D          

 29 31  0  0  1  0            999 V2000
   -5.9985    4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1735    4.3164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7610    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9360    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5235    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6985    2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2136    3.5549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136    2.2201    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4685    1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2755    1.2639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9360    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7610    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1735    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9985    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  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
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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
 13 21  1  0  0  0  0
 21 22  2  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
  5 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
   -5.3173   -0.3033    3.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1210    0.3816    2.0965 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5481    0.6724    0.8635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2483    0.3197    0.5420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7153    0.6201   -0.6783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3670    0.2911   -1.1019 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9871   -1.0559   -0.7702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5931   -1.0613   -0.9371 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3259   -2.0638   -1.2540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2085   -3.3508   -1.4562 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7165   -4.3710   -1.7773 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6787   -1.8142   -1.3639 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1716   -0.5435   -1.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6374   -0.2500   -1.2743 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3248   -0.4306    0.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7962   -0.1149   -0.1430 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5006   -0.2607    1.0537 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2620    0.4482    2.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0688    0.2232    3.4500 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3394    1.3005    2.2157 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2604    0.4421   -0.8472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0985    0.2083   -0.7333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2785    1.0523   -0.4135 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1386    2.4623   -0.9136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1425    3.1603   -0.2842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5423    1.2958   -1.5776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8272    1.6515   -1.2770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3412    1.3394   -0.0453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6560    1.6917    0.2907 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1609   -1.3402    2.6540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3389    0.2034    3.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8294   -0.4140    4.0169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6403   -0.2010    1.2617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2496    0.3654   -2.1973 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4557   -4.3931   -0.9257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3245   -4.0287   -2.6641 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2437   -5.3373   -1.9570 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3669   -2.6245   -1.6136 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7752    0.7896   -1.6350 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1358   -0.9126   -1.9963 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8362    0.2847    0.7565 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1771   -1.4586    0.4269 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9514    0.8408   -0.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1739   -0.9063   -0.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0851    0.6637    3.3504 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1535   -0.8617    3.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5708    0.7044    4.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6497    1.4332   -0.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4643    1.0174    0.6697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1026    2.9749   -0.7139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0231    2.4342   -2.0241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1767    2.9215    0.6863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1524    1.5516   -2.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4784    2.1803   -1.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2346    2.1725   -0.3581 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  7  6  1  0
  6 23  1  0
 23 24  1  0
 24 25  1  0
 23 22  1  0
 22 21  2  0
 21 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 13 12  2  0
  6  5  1  0
  5 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 28  3  1  0
  3  2  1  0
  2  1  1  0
  3  4  2  0
 12  9  1  0
  4  5  1  0
 22  8  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
  6 34  1  6
 23 49  1  1
 24 50  1  0
 24 51  1  0
 25 52  1  0
 21 48  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 12 38  1  0
 26 53  1  0
 27 54  1  0
 29 55  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
M  END


  Mrv1652309072211482D          

 29 31  0  0  1  0            999 V2000
   -5.9985    4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1735    4.3164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7610    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9360    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5235    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6985    2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2136    3.5549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136    2.2201    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4685    1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2755    1.2639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9360    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7610    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1735    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9985    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  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
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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
 13 21  1  0  0  0  0
 21 22  2  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
  5 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
  3 28  1  0  0  0  0
 28 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0247825

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O7/c1-13(24)28-8-4-5-14-9-16-17(12-23)21(29-22(16)20(10-14)27-3)15-6-7-18(25)19(11-15)26-2/h6-7,9-11,17,21,23,25H,4-5,8,12H2,1-3H3/t17-,21+/m1/s1

> <INCHI_KEY>
CITIYUITOLVCJJ-UTKZUKDTSA-N

> <FORMULA>
C22H26O7

> <MOLECULAR_WEIGHT>
402.443

> <EXACT_MASS>
402.167853177

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
43.86367990307093

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate

> <JCHEM_LOGP>
2.397651840666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.194673667900037

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.909972272858406

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7136507375064873

> <JCHEM_POLAR_SURFACE_AREA>
94.45

> <JCHEM_REFRACTIVITY>
106.64580000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0     -11.197   8.057   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -9.657   8.057   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -8.887   6.724   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.347   6.724   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.577   5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.037   5.390   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.132   6.636   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.334   8.470   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000   9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.132   4.144   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.608   2.679   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -6.114   2.359   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -7.347   4.056   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -8.887   4.056   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -9.657   5.390   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0     -11.197   5.390   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   26                                                  
CONECT    6    5    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   22                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   13   22                                                       
CONECT   22   21    8   23                                                  
CONECT   23   22    6   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26    5   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    3   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
2b-(3-Methoxy-4-hydroxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3a-methanol 5-acetate	Generator
2b-(3-Methoxy-4-hydroxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3a-methanol 5-acetic acid	Generator
2beta-(3-Methoxy-4-hydroxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3alpha-methanol 5-acetic acid	Generator
2Β-(3-methoxy-4-hydroxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3α-methanol 5-acetate	Generator
2Β-(3-methoxy-4-hydroxyphenyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-3α-methanol 5-acetic acid	Generator

Chemical Formula

C₂₂H₂₆O₇

Average Mass

402.4430 Da

Monoisotopic Mass

402.16785 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C22H26O7/c1-13(24)28-8-4-5-14-9-16-17(12-23)21(29-22(16)20(10-14)27-3)15-6-7-18(25)19(11-15)26-2/h6-7,9-11,17,21,23,25H,4-5,8,12H2,1-3H3/t17-,21+/m1/s1

InChI Key

CITIYUITOLVCJJ-UTKZUKDTSA-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
Sambucus nigra	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
Coumaran
Benzofuran
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Ether
Monocarboxylic acid or derivatives
Organic oxygen compound
Carbonyl group
Alcohol
Organic oxide
Primary alcohol
Organooxygen compound
Hydrocarbon derivative
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

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

101117933

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate (NP0247825)

MOL for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

3D MOL for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

3D SDF for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

3D-SDF for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

PDB for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

3D PDB for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

SMILES for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

INCHI for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

Structure for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)

3D Structure for NP0247825 (3-[(2r,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate)