NP-MRD: Showing NP-Card for (3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate (NP0213857)

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Record Information

Version

2.0

Created at

2022-09-05 12:58:08 UTC

Updated at

2022-09-05 12:58:09 UTC

NP-MRD ID

NP0213857

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate

Description

Prasanthaline belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed. (3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate is found in Jatropha gossypiifolia. Based on a literature review very few articles have been published on Prasanthaline.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052214582D          

 33 35  0  0  0  0            999 V2000
    1.7605   -5.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9355   -5.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -5.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5230   -2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9355   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1730   -2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1730   -3.6020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -0.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5395   -0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4595    2.1839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5395   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9520   -0.7441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7770   -0.7441    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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   -4.8534   -1.2532   -2.7095 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309052214582D          

 33 35  0  0  0  0            999 V2000
    1.7605   -5.7454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0213857

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(CC(COC(C)=O)C(\COC(C)=O)=C\C2=CC=C3OCOC3=C2)C=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O8/c1-16(26)30-13-20(9-18-5-7-22(28-3)24(11-18)29-4)21(14-31-17(2)27)10-19-6-8-23-25(12-19)33-15-32-23/h5-8,10-12,20H,9,13-15H2,1-4H3/b21-10+

> <INCHI_KEY>
QBKCYLIJKLGCQD-UFFVCSGVSA-N

> <FORMULA>
C25H28O8

> <MOLECULAR_WEIGHT>
456.491

> <EXACT_MASS>
456.178417862

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
47.96968699477359

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3Z)-3-[(acetyloxy)methyl]-4-(2H-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate

> <JCHEM_LOGP>
3.2005502630000007

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.357462266640536

> <JCHEM_POLAR_SURFACE_AREA>
89.52000000000002

> <JCHEM_REFRACTIVITY>
120.16810000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3Z)-3-[(acetyloxy)methyl]-4-(2H-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate

> <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       3.286 -10.725   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.746 -10.725   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.976  -9.391   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.564  -9.391   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -8.057   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.564  -6.724   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.564  -4.056   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.976  -4.056   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.746  -5.390   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.286  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.056  -4.056   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.056  -6.724   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.334  -2.723   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.564  -1.389   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334  -0.055   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.874  -0.055   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.644   1.278   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.874   2.612   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334   2.612   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.564   1.278   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.858   4.077   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -2.104   4.982   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.350   4.077   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.874  -2.723   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.644  -1.389   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.184  -1.389   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.954  -2.723   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -5.954  -0.055   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       0.976  -6.724   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.746  -8.057   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.286  -8.057   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.056  -9.391   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   31                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   30                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    8   15   25                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20   16                                                       
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   14   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30    6   31                                                       
CONECT   31   30    3   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₈O₈

Average Mass

456.4910 Da

Monoisotopic Mass

456.17842 Da

IUPAC Name

(3Z)-3-[(acetyloxy)methyl]-4-(2H-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate

Traditional Name

(3Z)-3-[(acetyloxy)methyl]-4-(2H-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(CC(COC(C)=O)C(\COC(C)=O)=C\C2=CC=C3OCOC3=C2)C=C1OC

InChI Identifier

InChI=1S/C25H28O8/c1-16(26)30-13-20(9-18-5-7-22(28-3)24(11-18)29-4)21(14-31-17(2)27)10-19-6-8-23-25(12-19)33-15-32-23/h5-8,10-12,20H,9,13-15H2,1-4H3/b21-10+

InChI Key

QBKCYLIJKLGCQD-UFFVCSGVSA-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
Jatropha gossypifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Not Available

Sub Class

Not Available

Direct Parent

Lignans, neolignans and related compounds

Alternative Parents

Substituents

Norlignan skeleton
O-dimethoxybenzene
Dimethoxybenzene
Benzodioxole
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
Alkyl aryl ether
Benzenoid
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.2	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	89.52 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	120.17 m³·mol⁻¹	ChemAxon
Polarizability	47.97 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

14213835

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate (NP0213857)

MOL for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

3D MOL for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

3D SDF for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

3D-SDF for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

PDB for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

3D PDB for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

SMILES for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

INCHI for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

Structure for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)

3D Structure for NP0213857 ((3z)-3-[(acetyloxy)methyl]-4-(2h-1,3-benzodioxol-5-yl)-2-[(3,4-dimethoxyphenyl)methyl]but-3-en-1-yl acetate)