NP-MRD: Showing NP-Card for Psoralenol (NP0056534)

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Record Information

Version

2.0

Created at

2022-04-28 02:17:03 UTC

Updated at

2022-04-28 02:17:03 UTC

NP-MRD ID

NP0056534

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Psoralenol

Description

7-Hydroxy-3-[(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl]-4H-chromen-4-one belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton. Psoralenol is found in Psoralea corylifolia and Psoralea coryfolia. Based on a literature review very few articles have been published on 7-hydroxy-3-[(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl]-4H-chromen-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
   -5.3614    0.8605    1.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5012    0.6180    0.0543 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3275    0.7920   -1.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4273    1.5191   -0.0176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1177    1.1147   -0.0905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1154    1.8826   -0.6583 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1728    1.3991   -0.6892 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5332    0.1770   -0.1812 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9191   -0.2758   -0.2464 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -1.5526   -0.6334 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5328   -1.9148   -0.6770 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5305   -1.1280   -0.3688 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8311   -1.5447   -0.4272 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8853   -0.6991   -0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1815   -1.1394   -0.1632 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5833    0.5784    0.2934 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2771    0.9992    0.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2606    0.1526    0.0244 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9631    0.5925    0.0905 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6425    1.7576    0.4439 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4772   -0.5854    0.3856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7793   -0.1174    0.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8559   -0.9498    1.0403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0599   -0.8257    0.1039 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0863   -1.5688    0.6593 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7359   -0.0966    1.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7834    1.4086    2.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2090    1.5101    1.0079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3147    1.8421   -1.5751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3902    0.4962   -1.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9359    0.1705   -2.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3717    2.8506   -1.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9404    2.0248   -1.1420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4695   -2.2315   -0.8962 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0944   -2.5416   -0.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7136   -1.0446   -1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3958    1.2611    0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0897    2.0248    0.6693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2367   -1.5475    0.7943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5836   -2.0122    1.0483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1036   -0.6304    2.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7573   -1.1700   -0.8966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7609   -2.4563    0.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 22 21  1  0
 21  8  2  0
  8  7  1  0
  7  6  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 24  2  1  0
 19  9  1  0
  6  5  1  0
 18 12  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
 23 40  1  0
 23 41  1  0
 24 42  1  6
 25 43  1  0
 21 39  1  0
  7 33  1  0
  6 32  1  0
 10 34  1  0
 13 35  1  0
 15 36  1  0
 16 37  1  0
 17 38  1  0
M  END


  Mrv1652304282204172D          

 25 28  0  0  1  0            999 V2000
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 O   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
   -1.4289   -1.6500    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
   -0.7145   -2.8875    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
    0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   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
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   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
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5806    0.2871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9679   -0.3837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  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
  4 10  1  0  0  0  0
 10 11  2  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  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 14 21  1  0  0  0  0
 20 22  1  6  0  0  0
 19 23  1  0  0  0  0
 19 24  1  0  0  0  0
  1 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0056534

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=C(C[C@H]1O)C=C(C=C2)C1=COC2=CC(O)=CC=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O5/c1-20(2)18(22)8-12-7-11(3-6-16(12)25-20)15-10-24-17-9-13(21)4-5-14(17)19(15)23/h3-7,9-10,18,21-22H,8H2,1-2H3/t18-/m1/s1

> <INCHI_KEY>
IPXXMSXJVCGTCG-GOSISDBHSA-N

> <FORMULA>
C20H18O5

> <MOLECULAR_WEIGHT>
338.359

> <EXACT_MASS>
338.11542368

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
36.00747434039254

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-hydroxy-3-[(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl]-4H-chromen-4-one

> <ALOGPS_LOGP>
3.56

> <JCHEM_LOGP>
2.9830370246666664

> <ALOGPS_LOGS>
-4.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.813809662374851

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.4782048014437

> <JCHEM_PKA_STRONGEST_BASIC>
-3.317639792722127

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
92.5134

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxy-3-[(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.817   0.536   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.540  -0.716   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -8.002  -7.700   0.000  0.00  0.00           O+0
CONECT    1    2    6   25                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15   19                                                       
CONECT   19   18   20   23   24                                             
CONECT   20   19   21   22                                                  
CONECT   21   20   14                                                       
CONECT   22   20                                                            
CONECT   23   19                                                            
CONECT   24   19                                                            
CONECT   25    1                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₈O₅

Average Mass

338.3590 Da

Monoisotopic Mass

338.11542 Da

IUPAC Name

7-hydroxy-3-[(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-6-yl]-4H-chromen-4-one

Traditional Name

7-hydroxy-3-[(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]chromen-4-one

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=C(C[C@H]1O)C=C(C=C2)C1=COC2=CC(O)=CC=C2C1=O

InChI Identifier

InChI=1S/C20H18O5/c1-20(2)18(22)8-12-7-11(3-6-16(12)25-20)15-10-24-17-9-13(21)4-5-14(17)19(15)23/h3-7,9-10,18,21-22H,8H2,1-2H3/t18-/m1/s1

InChI Key

IPXXMSXJVCGTCG-GOSISDBHSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cullen corylifolium	Plant	KNApSAcK
Psoralea coryfolia	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Pyranoisoflavonoids

Direct Parent

Pyranoisoflavonoids

Alternative Parents

Substituents

Pyranoisoflavonoid
Hydroxyisoflavonoid
Isoflavone
2,2-dimethyl-1-benzopyran
Chromone
Chromane
Benzopyran
1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Alcohol
Hydrocarbon derivative
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
logP	3.56	ALOGPS
logP	2.98	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	6.48	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.51 m³·mol⁻¹	ChemAxon
Polarizability	36.01 Å³	ChemAxon
Number of Rings	4	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

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

154497306

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Psoralenol (NP0056534)

MOL for NP0056534 (Psoralenol)

3D MOL for NP0056534 (Psoralenol)

3D SDF for NP0056534 (Psoralenol)

3D-SDF for NP0056534 (Psoralenol)

PDB for NP0056534 (Psoralenol)

3D PDB for NP0056534 (Psoralenol)

SMILES for NP0056534 (Psoralenol)

INCHI for NP0056534 (Psoralenol)

Structure for NP0056534 (Psoralenol)

3D Structure for NP0056534 (Psoralenol)