NP-MRD: Showing NP-Card for (2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one (NP0316175)

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Record Information

Version

2.0

Created at

2022-09-11 15:11:23 UTC

Updated at

2022-09-11 15:11:23 UTC

NP-MRD ID

NP0316175

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one is found in Acacia cyperophylla.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 35  0  0  0  0  0  0  0  0999 V2000
   -1.4922   -0.8861   -1.6976 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4709   -0.2522   -0.5943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1577   -0.0673    0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9391   -0.5480   -0.6033 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2594   -0.3946   -0.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5312    0.2490    1.1113 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8151    0.3920    1.6277 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8662   -0.1433    0.9193 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1405    0.0259    1.4791 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6363   -0.7938   -0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7108   -1.3346   -0.9696 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3365   -0.9281   -0.7611 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2350   -1.6024   -1.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7025    0.2164   -0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7573    0.9090    1.1500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6009    1.1920    1.8825 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9447    1.3781    1.7152 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1242    1.1511    1.0749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1288    0.4720   -0.1034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3282    0.2392   -0.7578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9333   -0.0075   -0.6848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0361   -0.6759   -1.8651 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0559    0.4383    0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7671   -1.0636   -1.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7429    0.6815    1.6965 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9966    0.9059    2.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9746   -0.3144    1.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6487   -1.2626   -0.6486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3631   -1.7590   -2.4051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5878    1.6891    2.7470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9415    1.9184    2.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0715    1.5125    1.5035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3453   -0.2625   -1.6310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3960   -1.0746   -2.4224 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  2  0
  2 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
  5 12  1  0
 12 13  1  0
 12 10  2  0
 10 11  1  0
 10  8  1  0
 21 14  1  0
  9 27  1  0
  7 26  1  0
  6 25  1  0
  4 24  1  0
  3 23  1  0
 16 30  1  0
 17 31  1  0
 18 32  1  0
 20 33  1  0
 22 34  1  0
 13 29  1  0
 11 28  1  0
M  END


  Mrv1652309112217112D          

 22 23  0  0  0  0            999 V2000
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    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
    4.2868   -1.6500    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
    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 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
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   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
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   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
    5.0013    2.0625    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
    5.7158    0.8250    0.0000 O   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
    4.2868    0.0000    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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 14 21  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0316175

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(\C=C\C(=O)C2=C(O)C=CC(O)=C2O)C(O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H12O7/c16-8(12-9(17)5-6-10(18)14(12)21)3-1-7-2-4-11(19)15(22)13(7)20/h1-6,17-22H/b3-1+

> <INCHI_KEY>
RTAZJHSWWRKIOX-HNQUOIGGSA-N

> <FORMULA>
C15H12O7

> <MOLECULAR_WEIGHT>
304.254

> <EXACT_MASS>
304.058302726

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
28.761225439149275

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <JCHEM_LOGP>
3.3689333789999996

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.349902255401437

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.306579040460263

> <JCHEM_PKA_STRONGEST_BASIC>
-6.2507829079494615

> <JCHEM_POLAR_SURFACE_AREA>
138.45000000000002

> <JCHEM_REFRACTIVITY>
78.7624

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    5   13                                                  
CONECT   13   12                                                            
CONECT   14    2   15   21                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₂O₇

Average Mass

304.2540 Da

Monoisotopic Mass

304.05830 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1=CC=C(\C=C\C(=O)C2=C(O)C=CC(O)=C2O)C(O)=C1O

InChI Identifier

InChI=1S/C15H12O7/c16-8(12-9(17)5-6-10(18)14(12)21)3-1-7-2-4-11(19)15(22)13(7)20/h1-6,17-22H/b3-1+

InChI Key

RTAZJHSWWRKIOX-HNQUOIGGSA-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
Acacia cyperophylla	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one (NP0316175)

MOL for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

3D MOL for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

3D SDF for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

3D-SDF for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

PDB for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

3D PDB for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

SMILES for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

INCHI for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

Structure for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)

3D Structure for NP0316175 ((2e)-3-(2,3,4-trihydroxyphenyl)-1-(2,3,6-trihydroxyphenyl)prop-2-en-1-one)