NP-MRD: Showing NP-Card for (1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate (NP0208108)

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Record Information

Version

2.0

Created at

2022-09-05 04:58:59 UTC

Updated at

2022-09-05 04:58:59 UTC

NP-MRD ID

NP0208108

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate

Description

(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]Dec-7-en-5-yl (2E)-3-(4-methoxyphenyl)prop-2-enoate belongs to the class of organic compounds known as cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid. (1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate is found in Catalpa ovata. Based on a literature review very few articles have been published on (1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]Dec-7-en-5-yl (2E)-3-(4-methoxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052206592D          

 36 40  0  0  1  0            999 V2000
    3.1816    7.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8636    7.0710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8027    6.2482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4847    5.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4237    4.9613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6807    4.6027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6197    3.7800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8767    3.4214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8157    2.5987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4978    2.1345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727    2.2401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  6 35  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309052206592D          

 36 40  0  0  1  0            999 V2000
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 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 21 29  1  0  0  0  0
 29 30  1  6  0  0  0
 19 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 34 33  1  1  0  0  0
 12 34  1  0  0  0  0
 18 34  1  0  0  0  0
  6 35  1  0  0  0  0
 35 36  2  0  0  0  0
  3 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0208108

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(\C=C\C(=O)O[C@@H]2[C@@H]3O[C@]3(CO)[C@@H]3[C@H]2C=CO[C@H]3O[C@@H]2OC(O)[C@H](O)C(O)[C@@H]2O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H28O12/c1-31-12-5-2-11(3-6-12)4-7-14(26)33-19-13-8-9-32-22(15(13)24(10-25)20(19)36-24)35-23-18(29)16(27)17(28)21(30)34-23/h2-9,13,15-23,25,27-30H,10H2,1H3/b7-4+/t13-,15-,16?,17-,18+,19+,20+,21?,22+,23+,24-/m1/s1

> <INCHI_KEY>
HXPCNWMFVBGRGF-NUAZGXGTSA-N

> <FORMULA>
C24H28O12

> <MOLECULAR_WEIGHT>
508.476

> <EXACT_MASS>
508.158076342

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
50.43113109682506

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl (2E)-3-(4-methoxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
-0.28947315700000054

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.288013224940597

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.22054064323562

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1218222708873125

> <JCHEM_POLAR_SURFACE_AREA>
176.9

> <JCHEM_REFRACTIVITY>
118.28980000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl (2E)-3-(4-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       5.939  14.066   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.212  13.199   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.098  11.663   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.371  10.797   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.258   9.261   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.871   8.592   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.757   7.056   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.370   6.387   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.256   4.851   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.529   3.984   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       3.869   4.182   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.755   2.646   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.931   1.651   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.874   0.433   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.348   0.226   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.395  -1.314   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.752  -2.042   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.812   0.339   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.700  -0.726   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.066  -2.222   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.954  -3.287   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.320  -4.783   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.208  -5.848   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.575  -7.343   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.270  -5.417   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.383  -6.482   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.637  -3.921   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -3.115  -3.491   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.524  -2.856   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.891  -1.360   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       0.221  -0.295   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.145   1.201   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.967   2.266   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.446   1.835   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.598   9.458   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.711  10.994   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   36                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   35                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   34                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13   15                                                       
CONECT   15   14   13   16   18                                             
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   34                                                  
CONECT   19   18   20   31                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   21   30                                                  
CONECT   30   29                                                            
CONECT   31   19   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   12   18                                                  
CONECT   35    6   36                                                       
CONECT   36   35    3                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,4S,5S,6R,10S)-2-(Hydroxymethyl)-10-{[(2S,3S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0,]dec-7-en-5-yl (2E)-3-(4-methoxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₄H₂₈O₁₂

Average Mass

508.4760 Da

Monoisotopic Mass

508.15808 Da

IUPAC Name

(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl (2E)-3-(4-methoxyphenyl)prop-2-enoate

Traditional Name

(1S,2S,4S,5S,6R,10S)-2-(hydroxymethyl)-10-{[(2S,3S,5R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-5-yl (2E)-3-(4-methoxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(\C=C\C(=O)O[C@@H]2[C@@H]3O[C@]3(CO)[C@@H]3[C@H]2C=CO[C@H]3O[C@@H]2OC(O)[C@H](O)C(O)[C@@H]2O)C=C1

InChI Identifier

InChI=1S/C24H28O12/c1-31-12-5-2-11(3-6-12)4-7-14(26)33-19-13-8-9-32-22(15(13)24(10-25)20(19)36-24)35-23-18(29)16(27)17(28)21(30)34-23/h2-9,13,15-23,25,27-30H,10H2,1H3/b7-4+/t13-,15-,16?,17-,18+,19+,20+,21?,22+,23+,24-/m1/s1

InChI Key

HXPCNWMFVBGRGF-NUAZGXGTSA-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
Catalpa ovata	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Cinnamic acid esters

Direct Parent

Cinnamic acid esters

Alternative Parents

Substituents

Cinnamic acid ester
O-glycosyl compound
Glycosyl compound
Phenoxy compound
Methoxybenzene
Styrene
Phenol ether
Anisole
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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	-0.29	ChemAxon
pKa (Strongest Acidic)	11.22	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	176.9 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	118.29 m³·mol⁻¹	ChemAxon
Polarizability	50.43 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

162818701

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate (NP0208108)

MOL for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

3D MOL for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

3D SDF for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

3D-SDF for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

PDB for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

3D PDB for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

SMILES for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

INCHI for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

Structure for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)

3D Structure for NP0208108 ((1s,2s,4s,5s,6r,10s)-2-(hydroxymethyl)-10-{[(2s,3s,5r)-3,4,5,6-tetrahydroxyoxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-5-yl (2e)-3-(4-methoxyphenyl)prop-2-enoate)