NP-MRD: Showing NP-Card for 5-methyl-2-(phenylmethylidene)hex-4-enoic acid (NP0315654)

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Record Information

Version

2.0

Created at

2022-09-11 14:23:29 UTC

Updated at

2022-09-11 14:23:29 UTC

NP-MRD ID

NP0315654

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-methyl-2-(phenylmethylidene)hex-4-enoic acid

Description

SCHEMBL3123187 belongs to the class of organic compounds known as cinnamic acids. These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. 5-methyl-2-(phenylmethylidene)hex-4-enoic acid is found in Pandanus tectorius. Based on a literature review very few articles have been published on SCHEMBL3123187.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
   -3.9161   -0.4166    0.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3442    0.7920   -0.2051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1592    1.6416   -1.1096 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0973    1.1330    0.0342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2719    0.2947    0.9323 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0068   -0.1647    0.2790 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1361    0.1586    0.8556 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4822   -0.1580    0.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9707   -1.4183    0.2249 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2816   -1.6285   -0.1992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1421   -0.5770   -0.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6568    0.6940   -0.1894 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3609    0.9089    0.2297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0284   -0.8632   -0.9734 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9946   -1.1785   -1.5861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2787   -1.1985   -1.5264 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9939   -0.5410    0.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8049   -0.3673    1.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4234   -1.3473    0.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6555    2.5965   -1.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2844    1.0985   -2.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1453    1.9069   -0.6890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6486    2.0304   -0.4183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8135   -0.6314    1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0691    0.8464    1.8597 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0252    0.7627    1.7915 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3140   -2.2712    0.4087 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6152   -2.6403   -0.3598 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1694   -0.7496   -0.7451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3333    1.5316   -0.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9926    1.9131    0.4009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5469   -2.1575   -1.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
  6 14  1  0
 14 16  1  0
 14 15  2  0
 13  8  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  7 26  1  0
  9 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 13 31  1  0
 16 32  1  0
M  END


  Mrv1652309112216232D          

 16 16  0  0  0  0            999 V2000
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    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
    0.0000    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
    0.0000    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
   -0.7145    3.7125    0.0000 O   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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  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
  6 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0315654

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC(=CC1=CC=CC=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H16O2/c1-11(2)8-9-13(14(15)16)10-12-6-4-3-5-7-12/h3-8,10H,9H2,1-2H3,(H,15,16)

> <INCHI_KEY>
ZKVOPDUGWCSBPC-UHFFFAOYSA-N

> <FORMULA>
C14H16O2

> <MOLECULAR_WEIGHT>
216.28

> <EXACT_MASS>
216.115029755

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
23.77779255456571

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-methyl-2-(phenylmethylidene)hex-4-enoic acid

> <JCHEM_LOGP>
3.7467823593333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.898763060274854

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
66.61860000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-methyl-2-(phenylmethylidene)hex-4-enoic acid

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+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  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14    6   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₆O₂

Average Mass

216.2800 Da

Monoisotopic Mass

216.11503 Da

IUPAC Name

5-methyl-2-(phenylmethylidene)hex-4-enoic acid

Traditional Name

5-methyl-2-(phenylmethylidene)hex-4-enoic acid

CAS Registry Number

Not Available

SMILES

CC(C)=CCC(=CC1=CC=CC=C1)C(O)=O

InChI Identifier

InChI=1S/C14H16O2/c1-11(2)8-9-13(14(15)16)10-12-6-4-3-5-7-12/h3-8,10H,9H2,1-2H3,(H,15,16)

InChI Key

ZKVOPDUGWCSBPC-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
Pandanus tectorius	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Cinnamic acids

Direct Parent

Cinnamic acids

Alternative Parents

Substituents

Cinnamic acid
Medium-chain fatty acid
Branched fatty acid
Fatty acyl
Fatty acid
Benzenoid
Unsaturated fatty acid
Monocyclic benzene moiety
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.75	ChemAxon
pKa (Strongest Acidic)	4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	66.62 m³·mol⁻¹	ChemAxon
Polarizability	23.78 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

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

68520111

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-methyl-2-(phenylmethylidene)hex-4-enoic acid (NP0315654)

MOL for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

3D MOL for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

3D SDF for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

3D-SDF for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

PDB for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

3D PDB for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

SMILES for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

INCHI for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

Structure for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)

3D Structure for NP0315654 (5-methyl-2-(phenylmethylidene)hex-4-enoic acid)