NP-MRD: Showing NP-Card for Ethyl ferulate (NP0044149)

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Record Information

Version

1.0

Created at

2021-11-12 23:52:44 UTC

Updated at

2021-11-26 17:45:58 UTC

NP-MRD ID

NP0044149

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ethyl ferulate

Description

Ethyl ferulate belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. Ethyl ferulate is found in Coptis japonica, Glechoma longituba, Hedychium coronarium, Ipomoea nil, Micrandropsis scleroxylon, Murraya paniculata, Solanum melongena, Solanum nigrum, Spiraea formosana and Tocoyena formosa. It was first documented in 2017 (DHorbury, et al.). Ethyl ferulate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 30  0  0  0  0  0  0  0  0999 V2000
    5.4258   -1.3014    0.1893 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1707    0.1849    0.0044 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8678    0.5136    0.3833 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7143    0.0197   -0.1545 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8132   -0.8222   -1.0920 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3653    0.4213    0.3059 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2819   -0.0609   -0.2196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0671    0.2819    0.1753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3027    1.1844    1.1816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6224    1.4832    1.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6822    0.8931    0.8815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9903    1.1781    1.2117 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4266   -0.0101   -0.1259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5055   -0.5958   -0.7665 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3135   -1.5294   -1.8071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1337   -0.3358   -0.5012 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3182   -1.7853   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7325   -1.7120    0.9669 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4506   -1.4961    0.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3938    0.4604   -1.0459 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8903    0.7179    0.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3427    1.1325    1.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4286   -0.7883   -1.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4708    1.6409    1.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7686    2.1908    2.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1857    1.8407    1.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9922   -1.0565   -2.7597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5292   -2.2665   -1.5386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2822   -2.0625   -1.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9231   -1.0351   -1.2812 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  8 16  2  0
 16 13  1  0
 13 11  2  0
 11 10  1  0
 10  9  2  0
 11 12  1  0
 13 14  1  0
 14 15  1  0
  9  8  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  2 21  1  0
  6 22  1  0
  7 23  1  0
 16 30  1  0
 10 25  1  0
  9 24  1  0
 12 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
M  END


  Mrv1652311132100522D          

 16 16  0  0  0  0            999 V2000
   -1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   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    2.0625    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
    1.4289    0.8250    0.0000 C   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
    0.7145   -0.4125    0.0000 C   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
    0.0000    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
    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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 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
  8 13  1  0  0  0  0
 11 14  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0044149

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C12H14O4/c1-3-16-12(14)7-5-9-4-6-10(13)11(8-9)15-2/h4-8,13H,3H2,1-2H3/b7-5+

> <INCHI_KEY>
ATJVZXXHKSYELS-FNORWQNLSA-N

> <FORMULA>
C12H14O4

> <MOLECULAR_WEIGHT>
222.2372

> <EXACT_MASS>
222.089208936

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
23.58182448927126

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
ethyl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
2.60

> <JCHEM_LOGP>
2.410885016666666

> <ALOGPS_LOGS>
-2.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.867808617684545

> <JCHEM_PKA_STRONGEST_BASIC>
-4.888705648522334

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
61.02170000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.28e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ethyl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 13-NOV-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   13-NOV-21         0                                  
HETATM    1  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14   11                                                            
CONECT   15   10   16                                                       
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

View in JSmol

Synonyms

Value	Source
Ethyl ferulic acid	Generator
Ferulic acid, ethyl ester	MeSH

Chemical Formula

C₁₂H₁₄O₄

Average Mass

222.2372 Da

Monoisotopic Mass

222.08921 Da

IUPAC Name

ethyl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Traditional Name

ethyl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CCOC(=O)\C=C\C1=CC(OC)=C(O)C=C1

InChI Identifier

InChI=1S/C12H14O4/c1-3-16-12(14)7-5-9-4-6-10(13)11(8-9)15-2/h4-8,13H,3H2,1-2H3/b7-5+

InChI Key

ATJVZXXHKSYELS-FNORWQNLSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Chloroform-d, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Coptis japonica	LOTUS Database	35616633
Glechoma longituba	LOTUS Database	35616633
Hedychium coronarium	LOTUS Database	35616633
Ipomoea nil	LOTUS Database	35616633
Micrandropsis scleroxylon	LOTUS Database	35616633
Murraya paniculata	LOTUS Database	35616633
Solanum melongena	LOTUS Database	35616633
Solanum nigrum	LOTUS Database	35616633
Spiraea formosana	Plant	KNApSAcK
Tocoyena formosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids and derivatives

Alternative Parents

Substituents

Coumaric acid or derivatives
Cinnamic acid ester
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Styrene
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Fatty acid ester
Phenol
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Carbonyl group
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	2.6	ALOGPS
logP	2.41	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	9.87	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	61.02 m³·mol⁻¹	ChemAxon
Polarizability	23.58 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

DB11285

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

736681

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Michael D.Horbury, Lewis A.Baker, Natércia D.N. Rodrigues, Wen-Dong Quan, Vasilios G. Stavros (2017). Photoisomerization of ethyl ferulate: A solution phase transient absorption study. Chemical Physics Letters, Volume 673, April 2017, Pages 62-67. DOI: 10.1016/j.cplett.2017.02.004. Chemical Physics Letters.

Showing NP-Card for Ethyl ferulate (NP0044149)

MOL for NP0044149 (Ethyl ferulate)

3D MOL for NP0044149 (Ethyl ferulate)

3D SDF for NP0044149 (Ethyl ferulate)

3D-SDF for NP0044149 (Ethyl ferulate)

PDB for NP0044149 (Ethyl ferulate)

3D PDB for NP0044149 (Ethyl ferulate)

SMILES for NP0044149 (Ethyl ferulate)

INCHI for NP0044149 (Ethyl ferulate)

Structure for NP0044149 (Ethyl ferulate)

3D Structure for NP0044149 (Ethyl ferulate)