NP-MRD: Showing NP-Card for (2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one (NP0289134)

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Record Information

Version

2.0

Created at

2022-09-09 19:10:59 UTC

Updated at

2022-09-09 19:10:59 UTC

NP-MRD ID

NP0289134

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one

Description

2',4',6'-TRIMETHOXYCHALCONE belongs to the class of organic compounds known as linear 1,3-diarylpropanoids. These are organic compounds with a structure based on a C6-C3-C6 skeleton, where the two benzene rings are not linked together. (2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one is found in Alpinia pricei. (2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one was first documented in 2020 (PMID: 32364107). Based on a literature review very few articles have been published on 2',4',6'-TRIMETHOXYCHALCONE.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
   -4.9402    1.7412    0.7594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2384    0.6466    1.2577 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8649    0.5902    1.3378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0997    1.6543    0.9124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7033    1.5937    0.9953 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1016    2.6449    0.5771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5395    3.7924    0.0586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0739    0.4753    1.5008 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3710    0.4437    1.5733 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9388    0.8576    2.5994 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1696   -0.0610    0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6444   -0.5148   -0.6421 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3739   -1.0350   -1.7854 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7140   -1.4907   -2.9186 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3869   -1.9870   -4.0119 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7646   -2.0485   -4.0165 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4446   -1.6029   -2.9049 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7432   -1.1056   -1.8122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8573   -0.6022    1.9312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2449   -1.7143    2.4334 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8792   -2.8617    2.9000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2320   -0.5268    1.8429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4942    2.1526   -0.1743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9771    2.5995    1.4736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0003    1.4675    0.5653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5324    2.5644    0.5043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2806    4.1484    0.8143 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1741    4.6083   -0.1646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0841    3.5851   -0.8789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2428   -0.0707    0.5591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401   -0.4745   -0.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6351   -1.4378   -2.9039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8202   -2.3329   -4.8788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3293   -2.4333   -4.8598 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5219   -1.6215   -2.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3169   -0.7698   -0.9683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703   -3.4791    3.5631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7604   -2.5261    3.5185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3479   -3.4766    2.0780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8127   -1.3927    2.1906 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  1  0
  5  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  8 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22  3  1  0
 18 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  7 27  1  0
  7 28  1  0
  7 29  1  0
 11 30  1  0
 12 31  1  0
 14 32  1  0
 15 33  1  0
 16 34  1  0
 17 35  1  0
 18 36  1  0
 21 37  1  0
 21 38  1  0
 21 39  1  0
 22 40  1  0
M  END


  Mrv1652309092221112D          

 22 23  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 O   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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    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   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    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  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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 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
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
  8 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
M  END
> <DATABASE_ID>
NP0289134

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C(C(=O)\C=C\C2=CC=CC=C2)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H18O4/c1-20-14-11-16(21-2)18(17(12-14)22-3)15(19)10-9-13-7-5-4-6-8-13/h4-12H,1-3H3/b10-9+

> <INCHI_KEY>
DRGVZVJDZOMQAI-MDZDMXLPSA-N

> <FORMULA>
C18H18O4

> <MOLECULAR_WEIGHT>
298.338

> <EXACT_MASS>
298.12050906

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
32.18739511691075

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one

> <JCHEM_LOGP>
3.4173115119999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.164535193957125

> <JCHEM_PKA_STRONGEST_BASIC>
-4.406596859420973

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
86.26660000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-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  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334 -14.630   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.000 -13.860   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334 -11.550   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
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9   19                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19    8   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19    3                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₈O₄

Average Mass

298.3380 Da

Monoisotopic Mass

298.12051 Da

IUPAC Name

(2E)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one

Traditional Name

(2E)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C(C(=O)\C=C\C2=CC=CC=C2)C(OC)=C1

InChI Identifier

InChI=1S/C18H18O4/c1-20-14-11-16(21-2)18(17(12-14)22-3)15(19)10-9-13-7-5-4-6-8-13/h4-12H,1-3H3/b10-9+

InChI Key

DRGVZVJDZOMQAI-MDZDMXLPSA-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
Alpinia pricei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear 1,3-diarylpropanoids. These are organic compounds with a structure based on a C6-C3-C6 skeleton, where the two benzene rings are not linked together.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Not Available

Direct Parent

Linear 1,3-diarylpropanoids

Alternative Parents

Substituents

Linear 1,3-diarylpropanoid
Cinnamic acid or derivatives
Anisole
Benzoyl
Phenoxy compound
Phenol ether
Styrene
Aryl ketone
Methoxybenzene
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Enone
Alpha,beta-unsaturated ketone
Acryloyl-group
Ketone
Ether
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
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
logP	3.42	ChemAxon
pKa (Strongest Acidic)	16.16	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	86.27 m³·mol⁻¹	ChemAxon
Polarizability	32.19 Å³	ChemAxon
Number of Rings	2	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

C00014431

Chemspider ID

4825605

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6154317

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Sousa-Batista AJ, Arruda-Costa N, Escrivani DO, Reynaud F, Steel PG, Rossi-Bergmann B: Single-dose treatment for cutaneous leishmaniasis with an easily synthesized chalcone entrapped in polymeric microparticles. Parasitology. 2020 Aug;147(9):1032-1037. doi: 10.1017/S0031182020000712. Epub 2020 May 4. [PubMed:32364107 ]
LOTUS database [Link]

Showing NP-Card for (2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one (NP0289134)

MOL for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

3D MOL for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

3D SDF for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

3D-SDF for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

PDB for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

3D PDB for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

SMILES for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

INCHI for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

Structure for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)

3D Structure for NP0289134 ((2e)-3-phenyl-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one)