NP-MRD: Showing NP-Card for (2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid (NP0280216)

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Record Information

Version

2.0

Created at

2022-09-09 05:52:49 UTC

Updated at

2022-09-09 05:52:49 UTC

NP-MRD ID

NP0280216

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid

Description

Caffeic Acid Phenethyl Amide, also known as caffeate phenethyl amide, belongs to the class of organic compounds known as hydroxycinnamic acids and derivatives. Hydroxycinnamic acids and derivatives are compounds containing an cinnamic acid (or a derivative thereof) where the benzene ring is hydroxylated. (2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid is found in Annona cherimola. Based on a literature review very few articles have been published on Caffeic Acid Phenethyl Amide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
   -0.4002    0.5620    0.8115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0015   -0.1285   -0.3161 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4241   -0.2578   -0.5719 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3472    0.2518    0.2201 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7841    0.1449   -0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3528   -0.4948   -1.0517 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7247   -0.5634   -1.2075 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5436    0.0256   -0.2834 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9133   -0.0368   -0.4293 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0066    0.6820    0.7941 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8670    1.2671    1.7106 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6345    0.7342    0.9235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8378   -0.6314   -1.1000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2494   -0.6570   -1.0947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8175    0.0417    0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3027    0.0297    0.1192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0860    1.0137   -0.4597 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4662    0.9674   -0.4095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1062   -0.0739    0.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3505   -1.0643    0.8101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9713   -0.9985    0.7482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.2483    1.7570 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7476   -0.7896   -1.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9481    0.7865    1.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7273   -0.9648   -1.7899 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1545   -1.0785   -2.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3464   -0.5171   -1.2189 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4466    1.7496    2.5035 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2366    1.2554    1.7782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6704   -0.1838   -2.0293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5752   -1.7259   -1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5257    1.1058    0.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4711   -0.4820    1.0043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5674    1.8223   -0.9542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0823    1.7306   -0.8583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1882   -0.1314    0.2790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8862   -1.8701    1.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3869   -1.7685    1.2017 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  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
  2 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 12  5  1  0
 21 16  1  0
  1 22  1  0
  3 23  1  0
  4 24  1  0
  6 25  1  0
  7 26  1  0
  9 27  1  0
 11 28  1  0
 12 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  0
 15 33  1  0
 17 34  1  0
 18 35  1  0
 19 36  1  0
 20 37  1  0
 21 38  1  0
M  END


  Mrv1652309092207522D          

 21 22  0  0  0  0            999 V2000
    0.0000   -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
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   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 O   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
    0.0000   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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
    0.7145   -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 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
  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  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
  2 13  2  0  0  0  0
 13 14  1  4  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0280216

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(\C=C\C1=CC=C(O)C(O)=C1)=NCCC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H17NO3/c19-15-8-6-14(12-16(15)20)7-9-17(21)18-11-10-13-4-2-1-3-5-13/h1-9,12,19-20H,10-11H2,(H,18,21)/b9-7+

> <INCHI_KEY>
QOWABIXYAFJMQE-VQHVLOKHSA-N

> <FORMULA>
C17H17NO3

> <MOLECULAR_WEIGHT>
283.327

> <EXACT_MASS>
283.120843411

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
31.328481652801504

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-(3,4-dihydroxyphenyl)-N-(2-phenylethyl)prop-2-enimidic acid

> <JCHEM_LOGP>
3.1882918393987687

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.277780583195678

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.572820421118441

> <JCHEM_PKA_STRONGEST_BASIC>
6.536839190932879

> <JCHEM_POLAR_SURFACE_AREA>
73.05

> <JCHEM_REFRACTIVITY>
83.62990000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-(3,4-dihydroxyphenyl)-N-(2-phenylethyl)prop-2-enimidic acid

> <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  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.667 -13.860   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.000 -12.320   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       2.667  -4.620   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
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                                                       
CONECT   13    2   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Value	Source
Caffeate phenethyl amide	Generator

Chemical Formula

C₁₇H₁₇NO₃

Average Mass

283.3270 Da

Monoisotopic Mass

283.12084 Da

IUPAC Name

(2E)-3-(3,4-dihydroxyphenyl)-N-(2-phenylethyl)prop-2-enimidic acid

Traditional Name

(2E)-3-(3,4-dihydroxyphenyl)-N-(2-phenylethyl)prop-2-enimidic acid

CAS Registry Number

Not Available

SMILES

OC(\C=C\C1=CC=C(O)C(O)=C1)=NCCC1=CC=CC=C1

InChI Identifier

InChI=1S/C17H17NO3/c19-15-8-6-14(12-16(15)20)7-9-17(21)18-11-10-13-4-2-1-3-5-13/h1-9,12,19-20H,10-11H2,(H,18,21)/b9-7+

InChI Key

QOWABIXYAFJMQE-VQHVLOKHSA-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
Annona cherimola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxycinnamic acids and derivatives. Hydroxycinnamic acids and derivatives are compounds containing an cinnamic acid (or a derivative thereof) where the benzene ring is hydroxylated.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Hydroxycinnamic acids and derivatives

Alternative Parents

Substituents

Cinnamic acid amide
Hydroxycinnamic acid or derivatives
Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid derivative
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organonitrogen compound
Organic nitrogen 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	3.19	ChemAxon
pKa (Strongest Acidic)	4.57	ChemAxon
pKa (Strongest Basic)	6.54	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	73.05 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	83.63 m³·mol⁻¹	ChemAxon
Polarizability	31.33 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

Not Available

Chemspider ID

9566839

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11391937

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid (NP0280216)

MOL for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

3D MOL for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

3D SDF for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

3D-SDF for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

PDB for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

3D PDB for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

SMILES for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

INCHI for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

Structure for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)

3D Structure for NP0280216 ((2e)-3-(3,4-dihydroxyphenyl)-n-(2-phenylethyl)prop-2-enimidic acid)