NP-MRD: Showing NP-Card for (2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0318659)

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Record Information

Version

2.0

Created at

2022-09-11 19:16:52 UTC

Updated at

2022-09-11 19:16:52 UTC

NP-MRD ID

NP0318659

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

Description

Specicoside belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid. (2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate is found in Radermachera sinica. (2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate was first documented in 2011 (PMID: 21487780). Based on a literature review very few articles have been published on specicoside (PMID: 21814840).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112221162D          

 36 40  0  0  1  0            999 V2000
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    7.0000    1.1187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309112221162D          

 36 40  0  0  1  0            999 V2000
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 18 31  1  0  0  0  0
 14 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  0  0  0  0
 32 35  1  0  0  0  0
 36 35  1  6  0  0  0
 13 36  1  0  0  0  0
 32 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0318659

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@@H]1O[C@@H](O[C@H]2OC=CC3[C@@H](OC(=O)\C=C\C4=CC=C(O)C=C4)[C@H]4O[C@@]4(CO)C23)[C@@H](O)[C@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O12/c25-9-14-17(29)18(30)19(31)23(33-14)35-22-16-13(7-8-32-22)20(21-24(16,10-26)36-21)34-15(28)6-3-11-1-4-12(27)5-2-11/h1-8,13-14,16-23,25-27,29-31H,9-10H2/b6-3+/t13?,14-,16?,17+,18+,19-,20+,21+,22+,23-,24-/m0/s1

> <INCHI_KEY>
SKNVKBJSSSJNCI-SAACDNBZSA-N

> <FORMULA>
C24H28O12

> <MOLECULAR_WEIGHT>
508.476

> <EXACT_MASS>
508.158076342

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
49.50122711171637

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,4R,5R,10R)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
-0.7014782133333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.203821839665082

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.397916404846361

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601929344

> <JCHEM_POLAR_SURFACE_AREA>
187.9

> <JCHEM_REFRACTIVITY>
118.74010000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4R,5R,10R)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

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  O   UNK     0       6.246   3.899   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.360   2.363   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.747   1.694   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.020   2.560   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.407   1.891   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.680   2.758   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.067   2.088   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.181   0.553   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      14.568  -0.117   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.907  -0.314   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.521   0.355   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.087   1.497   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.200  -0.039   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.510  -0.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.988  -0.419   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.101  -1.484   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.734  -2.980   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.256  -3.411   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.889  -4.906   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.002  -5.971   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.480  -5.541   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.592  -6.606   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.071  -6.175   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.437  -4.680   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.226  -8.102   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      11.338  -9.167   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.747  -8.532   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.381 -10.028   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.635  -7.467   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.157  -7.898   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.143  -2.345   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.608  -2.459   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.560  -3.998   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.204  -4.727   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       3.082  -2.251   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       4.025  -1.034   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    5                                                       
CONECT   12    2   13                                                       
CONECT   13   12   14   36                                                  
CONECT   14   13   15   31                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   31                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   20   30                                                  
CONECT   30   29                                                            
CONECT   31   18   14   32                                                  
CONECT   32   31   33   35   36                                             
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   32   36                                                       
CONECT   36   35   13   32                                                  
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₈O₁₂

Average Mass

508.4760 Da

Monoisotopic Mass

508.15808 Da

IUPAC Name

(2R,4R,5R,10R)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

(2R,4R,5R,10R)-2-(hydroxymethyl)-10-{[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

OC[C@@H]1O[C@@H](O[C@H]2OC=CC3[C@@H](OC(=O)\C=C\C4=CC=C(O)C=C4)[C@H]4O[C@@]4(CO)C23)[C@@H](O)[C@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C24H28O12/c25-9-14-17(29)18(30)19(31)23(33-14)35-22-16-13(7-8-32-22)20(21-24(16,10-26)36-21)34-15(28)6-3-11-1-4-12(27)5-2-11/h1-8,13-14,16-23,25-27,29-31H,9-10H2/b6-3+/t13?,14-,16?,17+,18+,19-,20+,21+,22+,23-,24-/m0/s1

InChI Key

SKNVKBJSSSJNCI-SAACDNBZSA-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
Radermachera sinica	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
Hexose monosaccharide
Cinnamic acid ester
O-glycosyl compound
Glycosyl compound
Styrene
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acid ester
Monocyclic benzene moiety
Monosaccharide
Oxane
Fatty acyl
Benzenoid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Dialkyl ether
Oxirane
Ether
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Organic oxygen compound
Carbonyl group
Alcohol
Organic oxide
Primary alcohol
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	-0.7	ChemAxon
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	187.9 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	118.74 m³·mol⁻¹	ChemAxon
Polarizability	49.5 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

71591712

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zofou D, Tene M, Tane P, Titanji VP: Antimalarial drug interactions of compounds isolated from Kigelia africana (Bignoniaceae) and their synergism with artemether, against the multidrug-resistant W2mef Plasmodium falciparum strain. Parasitol Res. 2012 Feb;110(2):539-44. doi: 10.1007/s00436-011-2519-9. Epub 2011 Aug 4. [PubMed:21814840 ]
Zofou D, Kengne AB, Tene M, Ngemenya MN, Tane P, Titanji VP: In vitro antiplasmodial activity and cytotoxicity of crude extracts and compounds from the stem bark of Kigelia africana (Lam.) Benth (Bignoniaceae). Parasitol Res. 2011 Jun;108(6):1383-90. doi: 10.1007/s00436-011-2363-y. Epub 2011 Apr 13. [PubMed:21487780 ]
LOTUS database [Link]

Showing NP-Card for (2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0318659)

MOL for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0318659 ((2r,4r,5r,10r)-2-(hydroxymethyl)-10-{[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)