NP-MRD: Showing NP-Card for (2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide (NP0190917)

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Record Information

Version

2.0

Created at

2022-09-04 07:41:09 UTC

Updated at

2022-09-04 07:41:09 UTC

NP-MRD ID

NP0190917

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide

Description

(2E)-N-methyl-N-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide 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. Based on a literature review very few articles have been published on (2E)-N-methyl-N-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 33  0  0  0  0  0  0  0  0999 V2000
    4.4676   -2.0413    0.7126 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3826   -0.9283   -0.2078 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.8895    0.7866    0.0123 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9522    1.6898   -0.7774 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5995    1.4979   -0.2759 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1828    2.3590    0.8116 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7228    0.5227   -0.8138 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1107   -0.2214   -1.7690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6128    0.4023   -0.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4182   -0.4990   -0.7470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7651   -0.6836   -0.2399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3269    0.0404    0.7848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6329   -0.1687    1.2460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3764   -1.1455    0.6377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8731   -1.9090   -0.3969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5872   -1.6621   -0.8093 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4806   -1.9673    0.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4310   -1.7957    1.8012 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0350   -3.0756    0.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9337    0.9585   -0.3723 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9053    1.0582    1.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3047    2.7338   -0.6174 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9841    1.4505   -1.8511 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8602    3.1964    0.9691 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9974    1.7424    1.7223 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1638    2.7447    0.5146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9368    1.0282    0.5552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0780   -1.1283   -1.5612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509    0.8186    1.2779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0041    0.4415    2.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3944   -1.3162    0.9895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4914   -2.6840   -0.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1551   -2.2457   -1.6247 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  1  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  6 24  1  0
  6 25  1  0
  6 26  1  0
  9 27  1  0
 10 28  1  0
 12 29  1  0
 13 30  1  0
 14 31  1  0
 15 32  1  0
 16 33  1  0
M  END


  Mrv1652309042209412D          

 16 16  0  0  0  0            999 V2000
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    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  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190917

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CSCCN(C)C(=O)\C=C\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H17NOS/c1-14(10-11-16-2)13(15)9-8-12-6-4-3-5-7-12/h3-9H,10-11H2,1-2H3/b9-8+

> <INCHI_KEY>
XFYGGQGDUBKTFT-CMDGGOBGSA-N

> <FORMULA>
C13H17NOS

> <MOLECULAR_WEIGHT>
235.35

> <EXACT_MASS>
235.103085345

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.692887951130977

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-N-methyl-N-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide

> <JCHEM_LOGP>
2.568864911666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.4452978874033281

> <JCHEM_POLAR_SURFACE_AREA>
20.310000000000002

> <JCHEM_REFRACTIVITY>
71.80140000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-N-methyl-N-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0       5.335  -9.240   0.000  0.00  0.00           S+0
HETATM    3  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       9.336 -10.010   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.670 -10.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

View in JSmol

Synonyms

Value	Source
(2E)-N-Methyl-N-[2-(methylsulphanyl)ethyl]-3-phenylprop-2-enamide	Generator

Chemical Formula

C₁₃H₁₇NOS

Average Mass

235.3500 Da

Monoisotopic Mass

235.10309 Da

IUPAC Name

(2E)-N-methyl-N-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide

Traditional Name

(2E)-N-methyl-N-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide

CAS Registry Number

Not Available

SMILES

CSCCN(C)C(=O)\C=C\C1=CC=CC=C1

InChI Identifier

InChI=1S/C13H17NOS/c1-14(10-11-16-2)13(15)9-8-12-6-4-3-5-7-12/h3-9H,10-11H2,1-2H3/b9-8+

InChI Key

XFYGGQGDUBKTFT-CMDGGOBGSA-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

Not Available

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
Styrene
Monocyclic benzene moiety
Benzenoid
Tertiary carboxylic acid amide
Carboxamide group
Dialkylthioether
Sulfenyl compound
Thioether
Carboxylic acid derivative
Organic oxygen compound
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Carbonyl group
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	2.57	ChemAxon
pKa (Strongest Basic)	-0.45	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	20.31 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	71.8 m³·mol⁻¹	ChemAxon
Polarizability	26.69 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

10376706

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21762182

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide (NP0190917)

MOL for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

3D MOL for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

3D SDF for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

3D-SDF for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

PDB for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

3D PDB for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

SMILES for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

INCHI for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

Structure for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)

3D Structure for NP0190917 ((2e)-n-methyl-n-[2-(methylsulfanyl)ethyl]-3-phenylprop-2-enamide)