NP-MRD: Showing NP-Card for 3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal (NP0184970)

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Record Information

Version

1.0

Created at

2022-09-04 00:14:29 UTC

Updated at

2022-09-04 00:14:29 UTC

NP-MRD ID

NP0184970

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal

Description

3-(3-Hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. 3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal is found in Cordia americana. 3-(3-Hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 35  0  0  0  0  0  0  0  0999 V2000
    2.1602   -2.7250   -0.9589 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6627   -1.6075   -1.6729 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6345   -0.8734   -1.0988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6508   -1.2486   -1.3826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9159   -2.3411   -2.2278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6865   -0.5289   -0.8194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9839   -0.9125   -1.1081 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7184   -1.8360   -0.3620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3841    0.5314   -0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4000    1.2661    0.5738 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9073    0.8806    1.8428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0591    0.9088    0.2829 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1243    2.0022    1.1147 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1143    3.2679    0.4085 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9773    0.2057   -0.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3703    0.5204   -0.0248 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8964    1.3741    0.7943 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3780    1.4791    0.8165 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0905    0.7784    0.0807 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9726   -2.4434   -0.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5121   -3.5148   -1.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3745   -3.2193   -0.3434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1090   -2.8171   -2.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4173   -1.8360    0.6917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5750   -2.8855   -0.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8020   -1.5931   -0.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8435    0.2922    1.7259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1572    0.2675    2.3901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1033    1.7979    2.4618 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8509    3.2357   -0.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8794    3.3954   -0.0679 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2833    4.1054    1.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0750   -0.0772   -0.6623 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3109    1.9687    1.4459 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8046    2.1820    1.4914 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6  4  2  0
  4  5  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 15 12  1  0
 12 13  1  0
 13 14  1  0
 12  9  2  0
  9 10  1  0
 10 11  1  0
  9  6  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
  5 23  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
 16 33  1  0
 17 34  1  0
 18 35  1  0
 14 30  1  0
 14 31  1  0
 14 32  1  0
 11 27  1  0
 11 28  1  0
 11 29  1  0
M  END


  Mrv1533004231515202D          

 19 19  0  0  0  0            999 V2000
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    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
    1.4289    0.8250    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
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    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
    0.7145   -0.4125    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
   -0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  2  0  0  0  0
 10  9  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  2  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0184970

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C13H16O6/c1-16-10-8(6-5-7-14)11(17-2)13(19-4)12(18-3)9(10)15/h5-7,15H,1-4H3

> <INCHI_KEY>
NYZCSOGYWISDAF-UHFFFAOYSA-N

> <FORMULA>
C13H16O6

> <MOLECULAR_WEIGHT>
268.265

> <EXACT_MASS>
268.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
26.884731185005933

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal

> <ALOGPS_LOGP>
1.48

> <JCHEM_LOGP>
1.0432196233333335

> <ALOGPS_LOGS>
-2.86

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.788954711410629

> <JCHEM_PKA_STRONGEST_BASIC>
-4.272220606408788

> <JCHEM_POLAR_SURFACE_AREA>
74.22

> <JCHEM_REFRACTIVITY>
69.9682

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.70e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.001  -0.770   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       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14    9   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14    3   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₁₆O₆

Average Mass

268.2650 Da

Monoisotopic Mass

268.09469 Da

IUPAC Name

3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal

Traditional Name

3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C13H16O6/c1-16-10-8(6-5-7-14)11(17-2)13(19-4)12(18-3)9(10)15/h5-7,15H,1-4H3

InChI Key

NYZCSOGYWISDAF-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
Cordia americana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Cinnamaldehyde
Methoxyphenol
4-alkoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Styrene
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Enal
Alpha,beta-unsaturated aldehyde
Ether
Hydrocarbon derivative
Carbonyl group
Aldehyde
Organic oxide
Organic oxygen compound
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
logP	1.48	ALOGPS
logP	1.04	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	9.79	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	74.22 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	69.97 m³·mol⁻¹	ChemAxon
Polarizability	26.88 Å³	ChemAxon
Number of Rings	1	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal (NP0184970)

MOL for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

3D MOL for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

3D SDF for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

3D-SDF for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

PDB for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

3D PDB for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

SMILES for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

INCHI for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

Structure for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)

3D Structure for NP0184970 (3-(3-hydroxy-2,4,5,6-tetramethoxyphenyl)prop-2-enal)