NP-MRD: Showing NP-Card for (-)-phaseollin (NP0280673)

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Record Information

Version

2.0

Created at

2022-09-09 06:35:54 UTC

Updated at

2022-09-09 06:35:54 UTC

NP-MRD ID

NP0280673

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-phaseollin

Description

(-)-Phaseollin belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. (-)-phaseollin is found in Erythrina abyssinica, Erythrina addisoniae, Erythrina burttii, Erythrina lysistemon, Erythrina sigmoidea, Erythrina suberosa, Erythrina variegata, Glycyrrhiza inflata, Lespedeza cyrtobotrya, Phaseolus coccineus and Phaseolus vulgaris. Thus, (-)-phaseollin is considered to be a flavonoid lipid molecule (-)-phaseollin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

(-)-Phaseollin
  Mrv1652309271700112D          

 26 30  0  0  0  0            999 V2000
    2.7231   -0.1690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458    2.2444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3167   -1.5381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3410    2.2310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2443    1.0014    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5584    0.6055    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8329    0.4716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2571    1.8264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5108   -0.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8378    1.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9853   -0.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8313    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6520    0.5704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8064   -0.8467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9674   -2.3230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1419   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1037    0.5603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6178   -1.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1120   -2.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0906    2.2672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6895   -2.6480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0471   -3.1111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3529    0.9784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3463    1.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0006    1.3313    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8947    0.1155    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  6  1  0  0  0  0
  1  9  1  0  0  0  0
  2  8  1  0  0  0  0
  2 12  1  0  0  0  0
  3 14  1  0  0  0  0
  3 15  1  0  0  0  0
  4 24  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  5  8  1  0  0  0  0
  6 10  1  0  0  0  0
  7  9  2  0  0  0  0
  7 13  1  0  0  0  0
  9 11  1  0  0  0  0
 10 12  2  0  0  0  0
 10 17  1  0  0  0  0
 11 14  2  0  0  0  0
 11 18  1  0  0  0  0
 12 20  1  0  0  0  0
 13 16  2  0  0  0  0
 14 16  1  0  0  0  0
 15 19  1  0  0  0  0
 15 21  1  1  0  0  0
 15 22  1  6  0  0  0
 17 23  2  0  0  0  0
 18 19  2  0  0  0  0
 20 24  2  0  0  0  0
 23 24  1  0  0  0  0
  5 25  1  6  0  0  0
  6 26  1  6  0  0  0
M  END

     RDKit          3D

 42 46  0  0  0  0  0  0  0  0999 V2000
   -3.6242    2.5733   -0.2138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6224    1.0569   -0.1077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0330    0.5212    0.0452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0504    0.5588   -1.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9642   -0.1817   -1.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2904   -0.5379   -0.1212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7923   -0.0916    1.1026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1587   -0.4253    2.2795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0225   -1.2012    2.2883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4948   -1.6558    1.0915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1542   -1.3105   -0.0739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5335   -1.8723   -1.1700 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8938   -2.0294   -0.7287 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5488   -0.6964   -0.7884 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2238    0.2593   -1.7290 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8777    1.5001   -1.7347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8473    1.7682   -0.8000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4799    2.9915   -0.8193 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1513    0.7995    0.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5226   -0.4298    0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8076   -1.4200    1.0679 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8441   -2.3197    1.5790 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6527   -2.4848    0.6900 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9219    0.6756    1.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5694    2.8602   -0.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8489    3.0694    0.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3071    2.8568   -1.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6325    1.1508    0.7323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9423   -0.4916    0.5048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5352    0.3665   -0.9313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5158    0.7957   -2.3380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5229   -0.5623   -2.2919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5710   -0.0632    3.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4979   -1.4815    3.1805 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4153   -2.7739   -1.3415 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4561    0.0343   -2.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.1935   -2.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2763    3.7085   -1.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9115    0.9814    0.8744 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4869   -1.8692    2.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2975   -3.2904    1.8349 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2950   -3.5330    0.6374 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 21  1  0
 21 20  1  0
 20 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  2  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  2  1  0
  2  1  1  0
  2  3  1  0
  2 24  1  0
 13 23  1  0
  6 11  1  0
 10 23  1  0
 24  7  1  0
 19 20  1  0
 23 42  1  6
 22 40  1  0
 22 41  1  0
 15 36  1  0
 16 37  1  0
 18 38  1  0
 19 39  1  0
 13 35  1  6
  9 34  1  0
  8 33  1  0
  5 32  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
M  END

(-)-Phaseollin
  Mrv1652309271700112D          

 26 30  0  0  0  0            999 V2000
    2.7231   -0.1690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458    2.2444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3167   -1.5381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3410    2.2310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2443    1.0014    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5584    0.6055    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8329    0.4716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2571    1.8264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5108   -0.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8378    1.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9853   -0.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8313    1.8319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6520    0.5704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8064   -0.8467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9674   -2.3230    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1419   -0.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1037    0.5603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6178   -1.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1120   -2.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0906    2.2672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6895   -2.6480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0471   -3.1111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3529    0.9784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3463    1.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0006    1.3313    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8947    0.1155    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  6  1  0  0  0  0
  1  9  1  0  0  0  0
  2  8  1  0  0  0  0
  2 12  1  0  0  0  0
  3 14  1  0  0  0  0
  3 15  1  0  0  0  0
  4 24  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  5  8  1  0  0  0  0
  6 10  1  0  0  0  0
  7  9  2  0  0  0  0
  7 13  1  0  0  0  0
  9 11  1  0  0  0  0
 10 12  2  0  0  0  0
 10 17  1  0  0  0  0
 11 14  2  0  0  0  0
 11 18  1  0  0  0  0
 12 20  1  0  0  0  0
 13 16  2  0  0  0  0
 14 16  1  0  0  0  0
 15 19  1  0  0  0  0
 15 21  1  1  0  0  0
 15 22  1  6  0  0  0
 17 23  2  0  0  0  0
 18 19  2  0  0  0  0
 20 24  2  0  0  0  0
 23 24  1  0  0  0  0
  5 25  1  6  0  0  0
  6 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0280673

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12COC3=C(C=CC(O)=C3)[C@]1([H])OC1=C2C=CC2=C1C=CC(C)(C)O2

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O4/c1-20(2)8-7-14-16(24-20)6-5-12-15-10-22-17-9-11(21)3-4-13(17)19(15)23-18(12)14/h3-9,15,19,21H,10H2,1-2H3/t15-,19-/m0/s1

> <INCHI_KEY>
LWTDZKXXJRRKDG-KXBFYZLASA-N

> <FORMULA>
C20H18O4

> <MOLECULAR_WEIGHT>
322.36

> <EXACT_MASS>
322.12050906

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.65919066005638

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,11R)-17,17-dimethyl-4,12,18-trioxapentacyclo[11.8.0.0^{2,11}.0^{5,10}.0^{14,19}]henicosa-1(13),5(10),6,8,14(19),15,20-heptaen-7-ol

> <ALOGPS_LOGP>
4.14

> <JCHEM_LOGP>
3.5675180639999997

> <ALOGPS_LOGS>
-4.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.420753775266402

> <JCHEM_PKA_STRONGEST_BASIC>
-4.422821909752098

> <JCHEM_POLAR_SURFACE_AREA>
47.92

> <JCHEM_REFRACTIVITY>
90.99130000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.00e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,11R)-17,17-dimethyl-4,12,18-trioxapentacyclo[11.8.0.0^{2,11}.0^{5,10}.0^{14,19}]henicosa-1(13),5(10),6,8,14(19),15,20-heptaen-7-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-SEP-17   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: (-)-Phaseollin                                    
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-SEP-17         0                                  
HETATM    1  O   UNK     0       5.083  -0.316   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0       4.752   4.190   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0       9.924  -2.871   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.637   4.164   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.056   1.869   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.776   1.130   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.155   0.880   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.080   3.409   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.553  -0.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.431   1.880   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.439  -1.730   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.418   3.420   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.684   1.065   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.972  -1.581   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.272  -4.336   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.598  -0.174   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.060   1.046   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.753  -3.180   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.676  -4.492   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.036   4.232   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.620  -4.943   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.421  -5.807   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.659   1.826   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.646   3.430   0.000  0.00  0.00           C+0
HETATM   25  H   UNK     0       7.468   2.485   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.537   0.216   0.000  0.00  0.00           H+0
CONECT    1    6    9                                                       
CONECT    2    8   12                                                       
CONECT    3   14   15                                                       
CONECT    4   24                                                            
CONECT    5    6    7    8   25                                             
CONECT    6    1    5   10   26                                             
CONECT    7    5    9   13                                                  
CONECT    8    2    5                                                       
CONECT    9    1    7   11                                                  
CONECT   10    6   12   17                                                  
CONECT   11    9   14   18                                                  
CONECT   12    2   10   20                                                  
CONECT   13    7   16                                                       
CONECT   14    3   11   16                                                  
CONECT   15    3   19   21   22                                             
CONECT   16   13   14                                                       
CONECT   17   10   23                                                       
CONECT   18   11   19                                                       
CONECT   19   15   18                                                       
CONECT   20   12   24                                                       
CONECT   21   15                                                            
CONECT   22   15                                                            
CONECT   23   17   24                                                       
CONECT   24    4   20   23                                                  
CONECT   25    5                                                            
CONECT   26    6                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

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Synonyms

Value	Source
Phaseolin	Kegg

Chemical Formula

C₂₀H₁₈O₄

Average Mass

322.3600 Da

Monoisotopic Mass

322.12051 Da

IUPAC Name

(2R,11R)-17,17-dimethyl-4,12,18-trioxapentacyclo[11.8.0.0^{2,11}.0^{5,10}.0^{14,19}]henicosa-1(13),5(10),6,8,14(19),15,20-heptaen-7-ol

Traditional Name

(2R,11R)-17,17-dimethyl-4,12,18-trioxapentacyclo[11.8.0.0^{2,11}.0^{5,10}.0^{14,19}]henicosa-1(13),5(10),6,8,14(19),15,20-heptaen-7-ol

CAS Registry Number

Not Available

SMILES

[H][C@@]12COC3=C(C=CC(O)=C3)[C@]1([H])OC1=C2C=CC2=C1C=CC(C)(C)O2

InChI Identifier

InChI=1S/C20H18O4/c1-20(2)8-7-14-16(24-20)6-5-12-15-10-22-17-9-11(21)3-4-13(17)19(15)23-18(12)14/h3-9,15,19,21H,10H2,1-2H3/t15-,19-/m0/s1

InChI Key

LWTDZKXXJRRKDG-KXBFYZLASA-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
Erythrina abyssinica	LOTUS Database	35616633
Erythrina addisoniae	LOTUS Database	35616633
Erythrina burttii	LOTUS Database	35616633
Erythrina lysistemon	LOTUS Database	35616633
Erythrina sigmoidea	LOTUS Database	35616633
Erythrina suberosa	LOTUS Database	35616633
Erythrina variegata	LOTUS Database	35616633
Glycyrrhiza inflata	LOTUS Database	35616633
Lespedeza cyrtobotrya	LOTUS Database	35616633
Phaseolus coccineus	LOTUS Database	35616633
Phaseolus vulgaris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Furanoisoflavonoids

Direct Parent

Pterocarpans

Alternative Parents

Substituents

Isoflavanol
Pterocarpan
Isoflavan
2,2-dimethyl-1-benzopyran
Chromane
Benzopyran
1-benzopyran
Benzofuran
Coumaran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Ether
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

pterocarpans (C10514 )
Pterocarpanes (C10514 )
Pterocarpans (LMPK12070020 )

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	4.14	ALOGPS
logP	3.57	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	9.42	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	47.92 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	90.99 m³·mol⁻¹	ChemAxon
Polarizability	34.66 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00002559

Chemspider ID

Not Available

KEGG Compound ID

C10514

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

91572

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (-)-phaseollin (NP0280673)

MOL for NP0280673 ((-)-phaseollin)

3D MOL for NP0280673 ((-)-phaseollin)

3D SDF for NP0280673 ((-)-phaseollin)

3D-SDF for NP0280673 ((-)-phaseollin)

PDB for NP0280673 ((-)-phaseollin)

3D PDB for NP0280673 ((-)-phaseollin)

SMILES for NP0280673 ((-)-phaseollin)

INCHI for NP0280673 ((-)-phaseollin)

Structure for NP0280673 ((-)-phaseollin)

3D Structure for NP0280673 ((-)-phaseollin)