NP-MRD: Showing NP-Card for [(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0235984)

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Record Information

Version

2.0

Created at

2022-09-06 18:46:23 UTC

Updated at

2022-09-06 18:46:23 UTC

NP-MRD ID

NP0235984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

Description

Juncusyl ester A belongs to the class of organic compounds known as coumaric acid esters. These are aromatic compounds containing an ester derivative of coumaric acid. [(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate is found in Juncus effusus. Based on a literature review very few articles have been published on Juncusyl ester A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
   -5.8759   -0.4450    0.5085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5190    0.1009    0.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7600    1.2060   -0.9037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8222   -0.9886   -0.4639 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9390   -1.3707    0.5567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5439   -0.0745    1.1458 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7189    0.8149    0.3178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4149    0.4877    0.0814 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1531   -0.4489   -0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5636   -1.1882   -1.3967 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6359   -0.6044   -0.7451 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3480    0.1939   -0.0002 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7949    0.1273    0.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4942   -0.7776   -0.7149 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8858   -0.7691   -0.6189 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5345    0.1255    0.2062 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9329    0.1017    0.2744 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8079    1.0240    0.9473 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4481    1.0310    0.8669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8605    0.5074    1.2398 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3415    0.2842    1.2120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5429   -0.4741   -0.3797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7942   -1.4530    0.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2739    2.1643   -0.6207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3312    0.8652   -1.8842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8290    1.4197   -0.9829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1424   -2.0268    0.2975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5488   -1.9525    1.3373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1394   -0.1848    2.1745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2425    0.9055   -0.7139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8132    1.8624    0.7734 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0555   -1.3477   -1.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8493    0.9495    0.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9929   -1.4746   -1.3576 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4104   -1.4973   -1.2236 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4548   -0.5614   -0.2734 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3265    1.7204    1.5905 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8925    1.7480    1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
  6 20  1  0
 20  2  1  0
 19 13  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  1
  7 30  1  0
  7 31  1  0
 11 32  1  0
 12 33  1  0
 14 34  1  0
 15 35  1  0
 17 36  1  0
 18 37  1  0
 19 38  1  0
M  END


  Mrv1652309062220462D          

 20 21  0  0  1  0            999 V2000
    4.0177   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -3.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9136   -3.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331   -4.2590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8781   -5.0437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0531   -5.0437    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5682   -5.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7477   -5.6249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2628   -6.2923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -7.0460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4423   -6.2061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0426   -6.8735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8631   -6.7873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -7.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1685   -7.3685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5040   -6.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3245   -6.5286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0191   -5.9473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1986   -6.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7982   -4.2590    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 13 19  1  0  0  0  0
  6 20  1  0  0  0  0
  2 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0235984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC[C@@H](COC(=O)\C=C\C2=CC=C(O)C=C2)O1

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O5/c1-15(2)19-10-13(20-15)9-18-14(17)8-5-11-3-6-12(16)7-4-11/h3-8,13,16H,9-10H2,1-2H3/b8-5+/t13-/m1/s1

> <INCHI_KEY>
FUKGNSLDUOSYKO-OQHXTRMZSA-N

> <FORMULA>
C15H18O5

> <MOLECULAR_WEIGHT>
278.304

> <EXACT_MASS>
278.11542368

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
29.496247375231892

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_LOGP>
2.5937359893333327

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.398644304002975

> <JCHEM_PKA_STRONGEST_BASIC>
-4.065847396608662

> <JCHEM_POLAR_SURFACE_AREA>
64.99000000000001

> <JCHEM_REFRACTIVITY>
74.27170000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       7.500  -5.901   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.469  -7.045   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.439  -5.901   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.715  -7.950   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.239  -9.415   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.699  -9.415   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.794 -10.661   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.262 -10.500   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.357 -11.746   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.984 -13.152   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.826 -11.585   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.079 -12.831   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.611 -12.670   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.516 -13.915   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.048 -13.754   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.674 -12.348   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -6.206 -12.187   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.769 -11.102   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.237 -11.263   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.223  -7.950   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   20                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   20                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   13                                                       
CONECT   20    6    2                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₈O₅

Average Mass

278.3040 Da

Monoisotopic Mass

278.11542 Da

IUPAC Name

[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CC1(C)OC[C@@H](COC(=O)\C=C\C2=CC=C(O)C=C2)O1

InChI Identifier

InChI=1S/C15H18O5/c1-15(2)19-10-13(20-15)9-18-14(17)8-5-11-3-6-12(16)7-4-11/h3-8,13,16H,9-10H2,1-2H3/b8-5+/t13-/m1/s1

InChI Key

FUKGNSLDUOSYKO-OQHXTRMZSA-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
Juncus effusus	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
Cinnamic acid ester
Styrene
1-hydroxy-2-unsubstituted benzenoid
Ketal
Fatty acid ester
Phenol
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Meta-dioxolane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Organoheterocyclic compound
Acetal
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	2.59	ChemAxon
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.99 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	74.27 m³·mol⁻¹	ChemAxon
Polarizability	29.5 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

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

101688441

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate (NP0235984)

MOL for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0235984 ([(4s)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl (2e)-3-(4-hydroxyphenyl)prop-2-enoate)