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Showing NP-Card for methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate (NP0156328)

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Record Information
Version2.0
Created at2022-09-02 13:31:09 UTC
Updated at2022-09-02 13:31:09 UTC
NP-MRD IDNP0156328
Secondary Accession NumbersNone
Natural Product Identification
Common Namemethyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate
Description2-Methoxy-5-hydroxy-trans-cinnamic acid methyl ester 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. methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate is found in Murraya paniculata. Based on a literature review very few articles have been published on 2-Methoxy-5-hydroxy-trans-cinnamic acid methyl ester.
Structure
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MOL3D MOLSDFPDBSMILESInChI

MOL for NP0156328 (methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate)


  Mrv1652309022215312D          

 15 15  0  0  0  0            999 V2000
   -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
    2.1434   -0.4125    0.0000 O   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
   -0.7145    2.0625    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
  3  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
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
Download

3D MOL for NP0156328 (methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate)

     RDKit          3D

 27 27  0  0  0  0  0  0  0  0999 V2000
    5.0387    0.5714    0.2503 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6412    0.5270    0.1287 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9556   -0.6674   -0.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6724   -1.7147   -0.0482 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4965   -0.7412   -0.1540 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8148    0.3670   -0.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6299    0.5097   -0.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1744    1.7978   -0.1762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5176    2.0620   -0.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9846    3.3664   -0.2034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4114    1.0260   -0.4269 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8964   -0.2423   -0.4850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5268   -0.5113   -0.3910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0889   -1.8084   -0.4579 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9141   -2.9246   -0.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4070    0.4575    1.2722 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5624   -0.1233   -0.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3521    1.6040   -0.0792 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0257   -1.6784   -0.2689 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4168    1.2820    0.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4683    2.6345   -0.0495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2105    3.7083    0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4753    1.2014   -0.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6031   -1.0606   -0.6101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3549   -3.8398   -0.8991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4447   -3.1042    0.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6825   -2.6987   -1.3982 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 13  7  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  5 19  1  0
  6 20  1  0
  8 21  1  0
 10 22  1  0
 11 23  1  0
 12 24  1  0
 15 25  1  0
 15 26  1  0
 15 27  1  0
M  END
Download

3D SDF for NP0156328 (methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate)


  Mrv1652309022215312D          

 15 15  0  0  0  0            999 V2000
   -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
    2.1434   -0.4125    0.0000 O   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
   -0.7145    2.0625    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
  3  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
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0156328

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)\C=C\C1=CC(O)=CC=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C11H12O4/c1-14-10-5-4-9(12)7-8(10)3-6-11(13)15-2/h3-7,12H,1-2H3/b6-3+

> <INCHI_KEY>
YYCNSXSWKOQWFN-ZZXKWVIFSA-N

> <FORMULA>
C11H12O4

> <MOLECULAR_WEIGHT>
208.213

> <EXACT_MASS>
208.073558866

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
27

> <JCHEM_AVERAGE_POLARIZABILITY>
21.36183318025704

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2E)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
1.79

> <JCHEM_LOGP>
2.054077062

> <ALOGPS_LOGS>
-2.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.860227878173648

> <JCHEM_PKA_STRONGEST_BASIC>
-4.822529226145047

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
56.273100000000014

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.67e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2E)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for NP0156328 (methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate)

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PDB for NP0156328 (methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate)
HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+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  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    7   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

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3D PDB for NP0156328 (methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate)
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SMILES for NP0156328 (methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate)
COC(=O)\C=C\C1=CC(O)=CC=C1OC
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INCHI for NP0156328 (methyl (2e)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate)
InChI=1S/C11H12O4/c1-14-10-5-4-9(12)7-8(10)3-6-11(13)15-2/h3-7,12H,1-2H3/b6-3+
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Synonyms
ValueSource
2-Methoxy-5-hydroxy-trans-cinnamate methyl esterGenerator
Chemical FormulaC11H12O4
Average Mass208.2130 Da
Monoisotopic Mass208.07356 Da
IUPAC Namemethyl (2E)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate
Traditional Namemethyl (2E)-3-(5-hydroxy-2-methoxyphenyl)prop-2-enoate
CAS Registry NumberNot Available
SMILES
COC(=O)\C=C\C1=CC(O)=CC=C1OC
InChI Identifier
InChI=1S/C11H12O4/c1-14-10-5-4-9(12)7-8(10)3-6-11(13)15-2/h3-7,12H,1-2H3/b6-3+
InChI KeyYYCNSXSWKOQWFN-ZZXKWVIFSA-N
Experimental Spectra
Not Available
Predicted Spectra
Spectrum TypeDescriptionDepositor IDDepositor OrganizationDepositorDeposition DateView
1D NMR13C NMR Spectrum (1D, 25 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 100 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 252 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 1000 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 50 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 200 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 75 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 300 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 101 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 400 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 126 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 500 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 151 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 600 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 176 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 700 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 201 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 800 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 226 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 900 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
Chemical Shift Submissions
Not Available
Species
Species of Origin
Species NameSourceReference
Murraya paniculataLOTUS Database
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.
KingdomOrganic compounds  
Super ClassPhenylpropanoids and polyketides  
ClassCinnamic acids and derivatives  
Sub ClassHydroxycinnamic acids and derivatives  
Direct ParentCoumaric acids and derivatives  
Alternative Parents
Substituents
  • Coumaric acid or derivatives
    • 

  • Cinnamic acid ester
    • 

  • Methoxyphenol
    • 

  • 4-alkoxyphenol
    • 

  • Phenoxy compound
    • 

  • Anisole
    • 

  • Phenol ether
    • 

  • Methoxybenzene
    • 

  • Styrene
    • 

  • Alkyl aryl ether
    • 

  • 1-hydroxy-2-unsubstituted benzenoid
    • 

  • Fatty acid ester
    • 

  • Phenol
    • 

  • Fatty acyl
    • 

  • Monocyclic benzene moiety
    • 

  • Benzenoid
    • 

  • Methyl ester
    • 

  • Enoate ester
    • 

  • Alpha,beta-unsaturated carboxylic ester
    • 

  • Carboxylic acid ester
    • 

  • Monocarboxylic acid or derivatives
    • 

  • Ether
    • 

  • Carboxylic acid derivative
    • 

  • Hydrocarbon derivative
    • 

  • Organooxygen compound
    • 

  • Organic oxide
    • 

  • Organic oxygen compound
    • 

  • Carbonyl group
    • 

  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP1.79ALOGPS
logP2.05ChemAxon
logS-2.6ALOGPS
pKa (Strongest Acidic)9.86ChemAxon
pKa (Strongest Basic)-4.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area55.76 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity56.27 m³·mol⁻¹ChemAxon
Polarizability21.36 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID9439262  
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound11264250  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References
  1. LOTUS database [Link]