NP-MRD: Showing NP-Card for 1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one (NP0212319)

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Record Information

Version

2.0

Created at

2022-09-05 10:56:52 UTC

Updated at

2022-09-05 10:56:52 UTC

NP-MRD ID

NP0212319

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one

Description

1-[3-(4-Methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid. 1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one is found in Piper sarmentosum. 1-[3-(4-Methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
    6.5068    0.2750    0.6104 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3180    1.0198    0.7523 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0767    0.5539    0.3894 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9218   -0.7027   -0.1487 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6912   -1.1710   -0.5099 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5086   -0.3922   -0.3518 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2757   -0.9372   -0.8261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9476   -0.6708   -0.5957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6799    0.2406    0.2072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1891    1.0689    0.9810 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1449    0.1912    0.1059 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9116   -0.7034   -0.7292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3069   -0.5802   -0.1551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3557    0.8756    0.2526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0056    1.0465    0.8323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6825    1.7926    1.7725 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7331    0.8437    0.1849 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9730    1.3486    0.5637 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3229    0.6891    1.2129 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3770   -0.7923    0.9100 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7747    0.2850   -0.4792 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8106   -1.3248   -0.2827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5754   -2.1685   -0.9305 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4435   -1.7913   -1.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6544   -1.3748   -1.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5549   -1.7570   -0.7021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8803   -0.2890   -1.7646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0862   -0.8328   -0.9018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3689   -1.2096    0.7525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1717    1.0921    0.9557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3920    1.5144   -0.6632 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9341    1.5298    0.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0890    2.3304    0.9833 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
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
  6 17  1  0
 17 18  2  0
 18  3  1  0
 15 11  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  4 22  1  0
  5 23  1  0
  7 24  1  0
  8 25  1  0
 12 26  1  0
 12 27  1  0
 13 28  1  0
 13 29  1  0
 14 30  1  0
 14 31  1  0
 17 32  1  0
 18 33  1  0
M  END


  Mrv1533004241503092D          

 18 19  0  0  0  0            999 V2000
   -1.5356    8.0652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8212    8.4777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    8.0652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6078    8.4777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222    8.0652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222    7.2402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    6.8277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    6.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512    5.5902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    6.0027    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512    4.7652    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4186    4.2803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1637    3.4956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    3.4956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0837    4.2803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2991    4.5352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6078    6.8277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    7.2402    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
  7  6  1  4  0  0  0
  7  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  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  2  0  0  0  0
  6 17  1  0  0  0  0
 17 18  2  0  0  0  0
  3 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0212319

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=CC(=O)N2CCCC2=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C14H15NO3/c1-18-12-7-4-11(5-8-12)6-9-14(17)15-10-2-3-13(15)16/h4-9H,2-3,10H2,1H3

> <INCHI_KEY>
ZOZBLVYNAYBARF-UHFFFAOYSA-N

> <FORMULA>
C14H15NO3

> <MOLECULAR_WEIGHT>
245.278

> <EXACT_MASS>
245.105193347

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.343066886554567

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one

> <ALOGPS_LOGP>
1.83

> <JCHEM_LOGP>
1.610759716

> <ALOGPS_LOGS>
-2.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.87367094608128

> <JCHEM_POLAR_SURFACE_AREA>
46.61

> <JCHEM_REFRACTIVITY>
68.70320000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.75e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -2.867  15.055   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.533  15.825   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.199  15.055   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.134  15.825   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.468  15.055   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.468  13.515   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.802  12.745   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.802  11.205   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.136  10.435   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.469  11.205   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       5.136   8.895   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       6.381   7.990   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.906   6.525   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.366   6.525   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.890   7.990   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.425   8.466   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.134  12.745   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.199  13.515   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   11   16                                                  
CONECT   16   15                                                            
CONECT   17    6   18                                                       
CONECT   18   17    3                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₅NO₃

Average Mass

245.2780 Da

Monoisotopic Mass

245.10519 Da

IUPAC Name

1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one

Traditional Name

1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=CC(=O)N2CCCC2=O)C=C1

InChI Identifier

InChI=1S/C14H15NO3/c1-18-12-7-4-11(5-8-12)6-9-14(17)15-10-2-3-13(15)16/h4-9H,2-3,10H2,1H3

InChI Key

ZOZBLVYNAYBARF-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
Piper sarmentosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cinnamic acids and derivatives. These are organic aromatic compounds containing a benzene and a carboxylic acid group (or a derivative thereof) forming 3-phenylprop-2-enoic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Not Available

Direct Parent

Cinnamic acids and derivatives

Alternative Parents

Substituents

Cinnamic acid or derivatives
Anisole
N-acylpyrrolidine
Phenol ether
Styrene
Methoxybenzene
Phenoxy compound
Alkyl aryl ether
Carboxylic acid imide, n-substituted
Benzenoid
Monocyclic benzene moiety
2-pyrrolidone
Pyrrolidone
Carboxylic acid imide
Dicarboximide
Pyrrolidine
Lactam
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Azacycle
Organonitrogen compound
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organopnictogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	1.83	ALOGPS
logP	1.61	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	46.61 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	68.7 m³·mol⁻¹	ChemAxon
Polarizability	26.34 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

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 1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one (NP0212319)

MOL for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

3D MOL for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

3D SDF for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

3D-SDF for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

PDB for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

3D PDB for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

SMILES for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

INCHI for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

Structure for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)

3D Structure for NP0212319 (1-[3-(4-methoxyphenyl)prop-2-enoyl]pyrrolidin-2-one)