NP-MRD: Showing NP-Card for docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0156260)

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Record Information

Version

2.0

Created at

2022-09-02 13:26:44 UTC

Updated at

2022-09-02 13:26:44 UTC

NP-MRD ID

NP0156260

Secondary Accession Numbers

None

Natural Product Identification

Common Name

docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

Description

(E)-3-(4-Hydroxyphenyl)acrylic acid docosylester belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid. docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate is found in Artemisia igniaria, Schefflera taiwaniana, Myoschilos oblongum and Psiadia punctulata. Based on a literature review very few articles have been published on (E)-3-(4-Hydroxyphenyl)acrylic acid docosylester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022215262D          

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M  END

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M  END


  Mrv1652309022215262D          

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   29.2933  -17.7375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -17.3250    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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 28 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0156260

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C31H52O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-28-34-31(33)27-24-29-22-25-30(32)26-23-29/h22-27,32H,2-21,28H2,1H3/b27-24+

> <INCHI_KEY>
PHDAMXFKBIUHBU-SOYKGTTHSA-N

> <FORMULA>
C31H52O3

> <MOLECULAR_WEIGHT>
472.754

> <EXACT_MASS>
472.391645534

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
62.79750922254451

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
docosyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
10.24

> <JCHEM_LOGP>
11.537883312333332

> <ALOGPS_LOGS>
-7.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.398661260312757

> <JCHEM_PKA_STRONGEST_BASIC>
-5.9547309780583015

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
146.50149999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.95e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
docosyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

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      16.004 -30.800   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.338 -30.030   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.672 -30.800   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.005 -30.030   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      21.339 -30.800   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.673 -30.030   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      24.006 -30.800   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      25.340 -30.030   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      26.674 -30.800   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      28.007 -30.030   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      29.341 -30.800   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      30.675 -30.030   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      32.008 -30.800   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      33.342 -30.030   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      34.676 -30.800   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      36.009 -30.030   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      37.343 -30.800   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      38.677 -30.030   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      40.010 -30.800   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      41.344 -30.030   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      42.678 -30.800   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      44.011 -30.030   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      45.345 -30.800   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      46.679 -30.030   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      46.679 -28.490   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      48.012 -30.800   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      49.346 -30.030   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      50.680 -30.800   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      52.013 -30.030   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      53.347 -30.800   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      53.347 -32.340   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      54.681 -33.110   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      52.013 -33.110   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      50.680 -32.340   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                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   28                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   68    0
END

View in JSmol

Synonyms

Value	Source
(e)-3-(4-Hydroxyphenyl)acrylate docosylester	Generator

Chemical Formula

C₃₁H₅₂O₃

Average Mass

472.7540 Da

Monoisotopic Mass

472.39165 Da

IUPAC Name

docosyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

docosyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C31H52O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-28-34-31(33)27-24-29-22-25-30(32)26-23-29/h22-27,32H,2-21,28H2,1H3/b27-24+

InChI Key

PHDAMXFKBIUHBU-SOYKGTTHSA-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
Artemisia igniaria	LOTUS Database	35616633
Heptapleurum taiwanianum	LOTUS Database	35616633
Myoschilos oblongum	LOTUS Database	35616633
Psiadia punctulata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acid esters

Alternative Parents

Substituents

Coumaric acid ester
Coumaric acid or derivatives
Fatty alcohol ester
Cinnamic acid ester
Styrene
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Phenol
Fatty acyl
Monocyclic benzene moiety
Benzenoid
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxide
Organic oxygen compound
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	10.24	ALOGPS
logP	11.54	ChemAxon
logS	-7.4	ALOGPS
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	24	ChemAxon
Refractivity	146.5 m³·mol⁻¹	ChemAxon
Polarizability	62.8 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

8180616

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10005036

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0156260)

MOL for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0156260 (docosyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)