NP-MRD: Showing NP-Card for 3-Prenyl-4,2',4'-trihydroxychalcone (NP0060656)

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Record Information

Version

2.0

Created at

2022-04-28 05:40:17 UTC

Updated at

2022-04-28 05:40:17 UTC

NP-MRD ID

NP0060656

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-Prenyl-4,2',4'-trihydroxychalcone

Description

(E)-2',4,4'-Trihydroxy-3-prenylchalcone, also known as 3-prenyl-4,2',4'-trihydroxychalcone or licoagrochalcone a, belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position. Thus, (e)-2',4,4'-trihydroxy-3-prenylchalcone is considered to be a flavonoid lipid molecule (E)-2',4,4'-Trihydroxy-3-prenylchalcone is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, (E)-2',4,4'-Trihydroxy-3-prenylchalcone has been detected, but not quantified in, herbs and spices and tea. 3-Prenyl-4,2',4'-trihydroxychalcone is found in Dorstenia elliptica, Erythrina abussinica, Erythrina abyssinica , Glycyrrhiza glabra , Glycyrrhiza inflata and Lespedeza cyrtobotrya. This could make (e)-2',4,4'-trihydroxy-3-prenylchalcone a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 45  0  0  0  0  0  0  0  0999 V2000
   -6.1115   -1.7015    0.6993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3265   -0.4690    1.0899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1085    0.7132    1.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0118   -0.5044    1.0150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1323    0.6388    1.3697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2500    1.0294    0.2404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9380    0.6274    0.2525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0179    0.9175   -0.7547 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3650    0.4197   -0.6435 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2459    0.6370   -1.5559 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6213    0.2714   -1.6847 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1973    0.6859   -2.8012 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5183   -0.4662   -0.8362 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2003   -0.9963    0.3903 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1237   -1.7021    1.1829 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4033   -1.8935    0.7561 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2869   -2.6029    1.5801 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7539   -1.3875   -0.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8450   -0.6725   -1.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3156   -0.2239   -2.4286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4762    1.6518   -1.8115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8158    2.0669   -1.8314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6961    1.7625   -0.8213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0220    2.2148   -0.9149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9414   -1.3361    0.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4684   -2.3410    0.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4576   -2.2611    1.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7639    1.6561    1.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9594    0.7957    2.6608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1906    0.5923    1.3444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5560   -1.4495    0.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5160    0.3494    2.2582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7485    1.4977    1.7247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6038    0.0454    1.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5756   -0.1237    0.2266 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8807    1.2468   -2.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2117   -0.8794    0.7877 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7756   -2.0825    2.1416 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2489   -2.7774    1.3153 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7770   -1.5295   -0.8106 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1422    0.2323   -3.2065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1456    1.9412   -2.6543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1967    2.6591   -2.6764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3250    2.7477   -1.6949 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6 23  2  0
 23 24  1  0
 23 22  1  0
 22 21  2  0
 21  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 19  2  0
 19 20  1  0
 19 18  1  0
 18 16  2  0
 16 17  1  0
 16 15  1  0
 15 14  2  0
  8  7  2  0
  7  6  1  0
 14 13  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
  4 31  1  0
  5 32  1  0
  5 33  1  0
 24 44  1  0
 22 43  1  0
 21 42  1  0
  9 35  1  0
 10 36  1  0
 20 41  1  0
 18 40  1  0
 17 39  1  0
 15 38  1  0
 14 37  1  0
  7 34  1  0
M  END


  Mrv0541 05061306372D          

 24 25  0  0  0  0            999 V2000
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   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
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    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
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    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
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    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
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    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
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   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
  6  3  1  0  0  0  0
  8  7  2  0  0  0  0
  9  4  2  0  0  0  0
 10  5  2  0  0  0  0
 13  1  1  0  0  0  0
 13  2  1  0  0  0  0
 13  3  2  0  0  0  0
 14  4  1  0  0  0  0
 14  5  1  0  0  0  0
 14 11  2  0  0  0  0
 15  6  1  0  0  0  0
 15 11  1  0  0  0  0
 16  7  1  0  0  0  0
 16 12  2  0  0  0  0
 17  8  1  0  0  0  0
 18  9  1  0  0  0  0
 18 15  2  0  0  0  0
 19 10  1  0  0  0  0
 19 17  1  0  0  0  0
 20 12  1  0  0  0  0
 20 17  2  0  0  0  0
 21 16  1  0  0  0  0
 22 18  1  0  0  0  0
 23 19  2  0  0  0  0
 24 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0060656

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C(O)C=CC(\C=C\C(=O)C2=C(O)C=C(O)C=C2)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O4/c1-13(2)3-6-15-11-14(4-9-18(15)22)5-10-19(23)17-8-7-16(21)12-20(17)24/h3-5,7-12,21-22,24H,6H2,1-2H3/b10-5+

> <INCHI_KEY>
TVUGLERLRIQATC-BJMVGYQFSA-N

> <FORMULA>
C20H20O4

> <MOLECULAR_WEIGHT>
324.3704

> <EXACT_MASS>
324.136159128

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
35.93519451776794

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-1-(2,4-dihydroxyphenyl)-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-en-1-one

> <ALOGPS_LOGP>
4.09

> <JCHEM_LOGP>
5.358196343333335

> <ALOGPS_LOGS>
-4.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.680302387735027

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.739927907253223

> <JCHEM_PKA_STRONGEST_BASIC>
-5.917849611544182

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
97.06249999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.73e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
licoagrochalcone A

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336   2.310   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  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
CONECT    1   13                                                            
CONECT    2   13                                                            
CONECT    3    6   13                                                       
CONECT    4    9   14                                                       
CONECT    5   10   14                                                       
CONECT    6    3   15                                                       
CONECT    7    8   16                                                       
CONECT    8    7   17                                                       
CONECT    9    4   18                                                       
CONECT   10    5   19                                                       
CONECT   11   14   15                                                       
CONECT   12   16   20                                                       
CONECT   13    1    2    3                                                  
CONECT   14    4    5   11                                                  
CONECT   15    6   11   18                                                  
CONECT   16    7   12   21                                                  
CONECT   17    8   19   20                                                  
CONECT   18    9   15   22                                                  
CONECT   19   10   17   23                                                  
CONECT   20   12   17   24                                                  
CONECT   21   16                                                            
CONECT   22   18                                                            
CONECT   23   19                                                            
CONECT   24   20                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
3-Prenyl-4,2',4'-trihydroxychalcone	HMDB
Licoagrochalcone a	HMDB

Chemical Formula

C₂₀H₂₀O₄

Average Mass

324.3704 Da

Monoisotopic Mass

324.13616 Da

IUPAC Name

(2E)-1-(2,4-dihydroxyphenyl)-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-en-1-one

Traditional Name

licoagrochalcone A

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(O)C=CC(\C=C\C(=O)C2=C(O)C=C(O)C=C2)=C1

InChI Identifier

InChI=1S/C20H20O4/c1-13(2)3-6-15-11-14(4-9-18(15)22)5-10-19(23)17-8-7-16(21)12-20(17)24/h3-5,7-12,21-22,24H,6H2,1-2H3/b10-5+

InChI Key

TVUGLERLRIQATC-BJMVGYQFSA-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
Dorstenia elliptica	LOTUS Database	35616633
Erythrina abussinica	Plant	KNApSAcK
Erythrina abyssinica	Plant	KNApSAcK
Glycyrrhiza glabra	Plant	KNApSAcK
Glycyrrhiza inflata	LOTUS Database	35616633
Lespedeza cyrtobotrya	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

2'-Hydroxychalcones

Alternative Parents

Substituents

2'-hydroxychalcone
Cinnamylphenol
Hydroxycinnamic acid or derivatives
Benzoyl
Resorcinol
Styrene
Aryl ketone
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Acryloyl-group
Enone
Alpha,beta-unsaturated ketone
Ketone
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120068 )

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	4.09	ALOGPS
logP	5.36	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	7.74	ChemAxon
pKa (Strongest Basic)	-5.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	77.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	97.06 m³·mol⁻¹	ChemAxon
Polarizability	35.94 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0032671

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB010625

KNApSAcK ID

C00014456

Chemspider ID

9274517

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11099375

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3-Prenyl-4,2',4'-trihydroxychalcone (NP0060656)

MOL for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

3D MOL for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

3D SDF for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

3D-SDF for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

PDB for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

3D PDB for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

SMILES for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

INCHI for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

Structure for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)

3D Structure for NP0060656 (3-Prenyl-4,2',4'-trihydroxychalcone)