NP-MRD: Showing NP-Card for (2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one (NP0240879)

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Record Information

Version

2.0

Created at

2022-09-07 00:48:06 UTC

Updated at

2022-09-07 00:48:06 UTC

NP-MRD ID

NP0240879

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one

Description

(2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one belongs to the class of organic compounds known as 6-prenylated isoflavanones. These are isoflavanones featuring a C5-isoprenoid unit at the 6-position. (2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one is found in Cajanus cajan, Lupinus albus and Lupinus luteus. Based on a literature review very few articles have been published on (2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202482D          

 26 29  0  0  1  0            999 V2000
    5.3649   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3649    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    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
   -1.4289    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
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 O   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
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  2  0  0  0  0
  6 24  1  0  0  0  0
 24 25  1  0  0  0  0
  7 26  1  0  0  0  0
  4 26  1  0  0  0  0
M  END

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
    6.6484   -0.4009   -1.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7493   -0.3528   -0.4506 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1940   -0.1474    0.9445 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3285   -0.5013   -0.7597 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5059    0.7039   -0.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1568    0.1113   -0.2052 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3208   -1.2462   -0.0342 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2047   -2.0429    0.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0915   -1.5495    0.1270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1342   -2.3237    0.2818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3785   -1.8490    0.2815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6420   -0.5090    0.1170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9614    0.0930    0.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2152    1.1716    0.9527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4202    1.7916    1.0567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4449    1.2966    0.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6981    1.8860    0.3374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2468    0.2371   -0.5562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9928   -0.3837   -0.6444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8487   -1.4520   -1.5093 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5236    0.3170   -0.0480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6828    1.5473   -0.2025 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2400   -0.1873   -0.0454 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8732    0.6113   -0.2068 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6511    1.9779   -0.3762 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6996   -1.5444   -0.0638 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4031   -0.5490   -2.4674 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7246   -0.2933   -1.2191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7442   -0.8692    1.6573 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9074    0.8995    1.2231 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3138   -0.1794    1.0207 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1615   -0.6089   -1.8694 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8079    1.0791    0.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5282    1.5156   -1.1050 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3168   -3.1133    0.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2008   -2.5431    0.4167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3723    1.5375    1.5600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5505    2.6440    1.7357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9018    2.6796    0.9412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0793   -0.1351   -1.1654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0188   -1.9674   -1.6839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4044    2.6490   -0.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7 26  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 26  4  1  0
 23  9  1  0
 19 13  1  0
 24  6  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  1 27  1  0
  1 28  1  0
  4 32  1  6
  5 33  1  0
  5 34  1  0
  8 35  1  0
 11 36  1  0
 25 42  1  0
 14 37  1  0
 15 38  1  0
 17 39  1  0
 18 40  1  0
 20 41  1  0
M  END


  Mrv1652309072202482D          

 26 29  0  0  1  0            999 V2000
    5.3649   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3649    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    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
   -1.4289    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
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 O   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
  4  2  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  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
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  2  0  0  0  0
  6 24  1  0  0  0  0
 24 25  1  0  0  0  0
  7 26  1  0  0  0  0
  4 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240879

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)[C@@H]1CC2=C(O1)C=C1OC=C(C(=O)C1=C2O)C1=CC=C(O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O6/c1-9(2)15-6-12-16(26-15)7-17-18(19(12)23)20(24)13(8-25-17)11-4-3-10(21)5-14(11)22/h3-5,7-8,15,21-23H,1,6H2,2H3/t15-/m0/s1

> <INCHI_KEY>
DOGAHANJPKBCGB-HNNXBMFYSA-N

> <FORMULA>
C20H16O6

> <MOLECULAR_WEIGHT>
352.342

> <EXACT_MASS>
352.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
36.2909529050944

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one

> <JCHEM_LOGP>
3.9934677953333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.558101517754627

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.447917249321063

> <JCHEM_PKA_STRONGEST_BASIC>
-4.777137475370766

> <JCHEM_POLAR_SURFACE_AREA>
96.22

> <JCHEM_REFRACTIVITY>
94.57059999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2H,3H-furo[3,2-g]chromen-5-one

> <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      10.015  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.245   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.015   2.104   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.705   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.799   2.016   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001   2.310   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      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       6.799  -0.476   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   26                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   24                                                  
CONECT    7    6    8   26                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   23                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   13   20                                                  
CONECT   20   19                                                            
CONECT   21   12   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    9   24                                                  
CONECT   24   23    6   25                                                  
CONECT   25   24                                                            
CONECT   26    7    4                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₆O₆

Average Mass

352.3420 Da

Monoisotopic Mass

352.09469 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=C)[C@@H]1CC2=C(O1)C=C1OC=C(C(=O)C1=C2O)C1=CC=C(O)C=C1O

InChI Identifier

InChI=1S/C20H16O6/c1-9(2)15-6-12-16(26-15)7-17-18(19(12)23)20(24)13(8-25-17)11-4-3-10(21)5-14(11)22/h3-5,7-8,15,21-23H,1,6H2,2H3/t15-/m0/s1

InChI Key

DOGAHANJPKBCGB-HNNXBMFYSA-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
Cajanus cajan	LOTUS Database	35616633
Lupinus albus	LOTUS Database	35616633
Lupinus luteus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 6-prenylated isoflavanones. These are isoflavanones featuring a C5-isoprenoid unit at the 6-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflavans

Direct Parent

6-prenylated isoflavanones

Alternative Parents

Substituents

6-prenylated isoflavanone
Furanoisoflavonoid skeleton
Isoflavone
Hydroxyisoflavonoid
Furanochromone
Chromone
Benzopyran
1-benzopyran
Coumaran
Resorcinol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Pyran
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Vinylogous acid
Ether
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen 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

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

162968450

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one (NP0240879)

MOL for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D MOL for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D SDF for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D-SDF for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

PDB for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D PDB for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

SMILES for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

INCHI for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

Structure for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)

3D Structure for NP0240879 ((2s)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one)