NP-MRD: Showing NP-Card for 1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one (NP0150058)

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Record Information

Version

2.0

Created at

2022-09-02 06:04:11 UTC

Updated at

2022-09-02 06:04:11 UTC

NP-MRD ID

NP0150058

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one

Description

Tetramethoxychalcone belongs to the class of organic compounds known as retrochalcones. These are a form of normal chalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions. 1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one is found in Murraya paniculata. 1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one was first documented in 2019 (PMID: 31160179). Based on a literature review a small amount of articles have been published on tetramethoxychalcone (PMID: 34116328) (PMID: 33529859) (PMID: 32937168) (PMID: 32296334).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 45  0  0  0  0  0  0  0  0999 V2000
   -3.7854    3.4673   -1.1211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0719    2.3120   -0.3883 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0458    1.4187   -0.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7567    1.6818   -0.3933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7129    0.7914   -0.0356 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6105    1.1516   -0.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7277    0.5971   -0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0089    1.1065   -0.6786 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9193    2.1096   -1.4749 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2920    0.5449   -0.3636 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4231    1.0940   -0.9230 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6783    0.5704   -0.6360 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7921   -0.5145    0.2212 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6756   -1.0670    0.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4444   -0.5176    0.4715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0159   -0.3329    0.6784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0771   -1.2502    1.0546 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2187   -2.4104    0.2713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3576   -0.5489    1.0281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7010   -1.6897    1.7619 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0482   -2.8821    1.0846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3767    0.2939    0.6962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6914    0.0506    1.0578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4961   -0.6878    0.1648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6488    3.2504   -2.2157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9516    4.0249   -0.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6784    4.1436   -1.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5370    2.5794   -0.9612 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6925    2.0132   -1.1668 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8181   -0.2127    0.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3586    1.9446   -1.5978 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5331    1.0362   -1.0996 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7795   -0.8978    0.4241 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7681   -1.9041    1.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5888   -0.9757    0.9286 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3203   -2.5399    0.3071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1996   -3.3000    0.7859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0909   -2.3047   -0.7743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4713   -3.7007    1.6007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1279   -3.1025    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7071   -2.8419    0.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9990    0.0754   -0.4956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2545   -1.3039    0.6870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8471   -1.2721   -0.5143 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  5 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22 23  1  0
 23 24  1  0
 22  3  1  0
 15 10  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  6 29  1  0
  7 30  1  0
 11 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 15 35  1  0
 18 36  1  0
 18 37  1  0
 18 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
M  END


  Mrv1652309022208042D          

 24 25  0  0  0  0            999 V2000
    2.1434   -1.2375    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
    2.8579   -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
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    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
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    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
    1.4289   -4.1250    0.0000 O   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
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   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  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 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
 10 15  1  0  0  0  0
  5 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0150058

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C=CC(=O)C2=CC=CC=C2)=C(OC)C(OC)=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C19H20O5/c1-21-16-12-14(17(22-2)19(24-4)18(16)23-3)10-11-15(20)13-8-6-5-7-9-13/h5-12H,1-4H3

> <INCHI_KEY>
FALFKLOXQUVHQP-UHFFFAOYSA-N

> <FORMULA>
C19H20O5

> <MOLECULAR_WEIGHT>
328.364

> <EXACT_MASS>
328.131073744

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
35.53299394607586

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one

> <ALOGPS_LOGP>
3.59

> <JCHEM_LOGP>
3.259640246333334

> <ALOGPS_LOGS>
-4.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.272358555404168

> <JCHEM_PKA_STRONGEST_BASIC>
-4.331694464228032

> <JCHEM_POLAR_SURFACE_AREA>
53.99000000000001

> <JCHEM_REFRACTIVITY>
92.72979999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.24e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   16                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16    5   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19    3   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀O₅

Average Mass

328.3640 Da

Monoisotopic Mass

328.13107 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC(C=CC(=O)C2=CC=CC=C2)=C(OC)C(OC)=C1OC

InChI Identifier

InChI=1S/C19H20O5/c1-21-16-12-14(17(22-2)19(24-4)18(16)23-3)10-11-15(20)13-8-6-5-7-9-13/h5-12H,1-4H3

InChI Key

FALFKLOXQUVHQP-UHFFFAOYSA-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
Murraya paniculata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as retrochalcones. These are a form of normal chalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

Retrochalcones

Alternative Parents

Substituents

Retrochalcone
Phenoxy compound
Methoxybenzene
Aryl ketone
Styrene
Phenol ether
Benzoyl
Anisole
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Alpha,beta-unsaturated ketone
Enone
Acryloyl-group
Ketone
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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

C00006964

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

145786676

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Rioux B, Pinon A, Gamond A, Martin F, Laurent A, Champavier Y, Barette C, Liagre B, Fagnere C, Sol V, Pouget C: Synthesis and biological evaluation of chalcone-polyamine conjugates as novel vectorized agents in colorectal and prostate cancer chemotherapy. Eur J Med Chem. 2021 Oct 15;222:113586. doi: 10.1016/j.ejmech.2021.113586. Epub 2021 May 28. [PubMed:34116328 ]
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Siima AA, Stephano F, Munissi JJE, Nyandoro SS: Ameliorative effects of flavonoids and polyketides on the rotenone induced Drosophila model of Parkinson's disease. Neurotoxicology. 2020 Dec;81:209-215. doi: 10.1016/j.neuro.2020.09.004. Epub 2020 Sep 13. [PubMed:32937168 ]
Peng F, Xiong L, Xie X, Tang H, Huang R, Peng C: Isoliquiritigenin Derivative Regulates miR-374a/BAX Axis to Suppress Triple-Negative Breast Cancer Tumorigenesis and Development. Front Pharmacol. 2020 Mar 31;11:378. doi: 10.3389/fphar.2020.00378. eCollection 2020. [PubMed:32296334 ]
Rioux B, Pouget C, Ndong-Ntoutoume GMA, Granet R, Gamond A, Laurent A, Pinon A, Champavier Y, Liagre B, Fagnere C, Sol V: Enhancement of hydrosolubility and in vitro antiproliferative properties of chalcones following encapsulation into beta-cyclodextrin/cellulose-nanocrystal complexes. Bioorg Med Chem Lett. 2019 Aug 1;29(15):1895-1898. doi: 10.1016/j.bmcl.2019.05.056. Epub 2019 May 28. [PubMed:31160179 ]
LOTUS database [Link]

Showing NP-Card for 1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one (NP0150058)

MOL for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

3D MOL for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

3D SDF for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

3D-SDF for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

PDB for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

3D PDB for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

SMILES for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

INCHI for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

Structure for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)

3D Structure for NP0150058 (1-phenyl-3-(2,3,4,5-tetramethoxyphenyl)prop-2-en-1-one)