NP-MRD: Showing NP-Card for L-Malic acid caffeate (NP0045336)

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Record Information

Version

2.0

Created at

2022-03-17 19:18:09 UTC

Updated at

2022-03-17 19:18:09 UTC

NP-MRD ID

NP0045336

Secondary Accession Numbers

None

Natural Product Identification

Common Name

L-Malic acid caffeate

Description

Caffeoylmalic acid, also known as caffeoylmalate or (S)-phaselic acid, belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. Caffeoylmalic acid is an extremely weak basic (essentially neutral) compound (based on its pKa). Caffeoylmalic acid is a hydroxycinnamic acid ester found in the leaves and flowers of Parietaria officinalis. Outside of the human body, Caffeoylmalic acid has been detected, but not quantified in, several different foods, such as yellow wax beans, herbs and spices, tea, pulses, and radish. L-Malic acid caffeate is found in Marrubium velutinum, Phaseolus sp., Trifolium pratense and Trifolium subterraneum. This could make caffeoylmalic acid a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 33  0  0  0  0  0  0  0  0999 V2000
   -5.9687    1.0076    0.9819 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1950    0.0512    1.2399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7327   -1.1913    1.5059 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7301    0.2635    1.2531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1464   -0.4001    0.0225 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7475   -0.2392   -0.0372 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8978   -1.3026    0.0594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3608   -2.4588    0.1947 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5704   -1.1274    0.0096 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0561    0.0772   -0.1312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4864    0.3180   -0.1853 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9482    1.6347   -0.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2842    1.9321   -0.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2278    0.9376   -0.2702 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5863    1.2906   -0.3144 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8218   -0.3654   -0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7391   -1.3685   -0.0082 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4592   -0.6442   -0.0794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7986    0.0390   -1.2210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0838    0.5150   -2.1692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1851   -0.0592   -1.3786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4349   -1.9618    0.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4874    1.3615    1.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2650   -0.1289    2.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3424   -1.5031    0.1715 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2066   -1.9658    0.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3424    0.9198   -0.2120 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1775    2.3990   -0.4280 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6204    2.9627   -0.5024 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8401    2.2691   -0.4223 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5547   -2.3424    0.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684   -1.6740    0.0412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7134    0.7541   -1.7178 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
  5 19  1  0
 19 21  1  0
 19 20  2  0
 18 11  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  1
  9 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 15 30  1  0
 17 31  1  0
 18 32  1  0
 21 33  1  0
M  END


  Mrv0541 02241219542D          

 21 21  0  0  0  0            999 V2000
   -0.7143    3.5077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143    2.6827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279    2.2702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4294    1.4452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4294    2.2702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1444    2.6827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7143    2.6827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0007    2.2702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0007    1.4452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143    1.0326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279    1.4452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143    0.2077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279   -0.2048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279   -1.0298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1444   -1.4438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1444   -2.2702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279   -2.6827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143   -2.2702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143   -1.4438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4279   -3.5077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0007   -2.6827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  8  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  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  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 19  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 20  1  0  0  0  0
 18 19  2  0  0  0  0
 18 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0045336

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C13H12O8/c14-8-3-1-7(5-9(8)15)2-4-12(18)21-10(13(19)20)6-11(16)17/h1-5,10,14-15H,6H2,(H,16,17)(H,19,20)/b4-2+

> <INCHI_KEY>
PMKQSEYPLQIEAY-DUXPYHPUSA-N

> <FORMULA>
C13H12O8

> <MOLECULAR_WEIGHT>
296.2296

> <EXACT_MASS>
296.05321736

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
26.853398909837985

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}butanedioic acid

> <ALOGPS_LOGP>
1.87

> <JCHEM_LOGP>
1.3131186466666667

> <ALOGPS_LOGS>
-2.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.010506366272061

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.070120323000287

> <JCHEM_PKA_STRONGEST_BASIC>
-6.283762288194251

> <JCHEM_POLAR_SURFACE_AREA>
141.36

> <JCHEM_REFRACTIVITY>
68.40470000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.32e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}butanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0      -1.333   6.548   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.333   5.008   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -2.665   4.238   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.668   2.698   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.668   4.238   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.003   5.008   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.333   5.008   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.001   4.238   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.001   2.698   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.333   1.928   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.665   2.698   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.333   0.388   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.665  -0.382   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.665  -1.922   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.003  -2.695   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.003  -4.238   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.665  -5.008   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.333  -4.238   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.333  -2.695   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -2.665  -6.548   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.001  -5.008   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2                                                            
CONECT    4    5                                                            
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    2    7    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19   21                                                  
CONECT   19   14   18                                                       
CONECT   20   17                                                            
CONECT   21   18                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
Caffeoylmalate	Generator
(S)-Phaselic acid	HMDB
Phaseolic acid?	HMDB
2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}butanedioate	Generator
Caffeoylmalic acid	MeSH
L-Malate caffeate	Generator
L-Malic acid caffeic acid	Generator

Chemical Formula

C₁₃H₁₂O₈

Average Mass

296.2296 Da

Monoisotopic Mass

296.05322 Da

IUPAC Name

2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}butanedioic acid

Traditional Name

2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}butanedioic acid

CAS Registry Number

53755-04-7

SMILES

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

InChI Identifier

InChI=1S/C13H12O8/c14-8-3-1-7(5-9(8)15)2-4-12(18)21-10(13(19)20)6-11(16)17/h1-5,10,14-15H,6H2,(H,16,17)(H,19,20)/b4-2+

InChI Key

PMKQSEYPLQIEAY-DUXPYHPUSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Marrubium velutinum	LOTUS Database	35616633
Phaseolus sp.	Plant	KNApSAcK
Phaseolus vulgaris	FooDB	Dr. Duke's Phytochemical and Ethnobotanical Databases
Pyrus communis	FooDB	18778075
Raphanus sativus	FooDB	KNAPSACK
Trifolium pratense	Plant	KNApSAcK
Trifolium subterraneum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids and derivatives

Alternative Parents

Substituents

Coumaric acid or derivatives
Cinnamic acid ester
Tricarboxylic acid or derivatives
Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Phenol
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	1.87	ALOGPS
logP	1.31	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	3.07	ChemAxon
pKa (Strongest Basic)	-6.3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	141.36 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	68.4 m³·mol⁻¹	ChemAxon
Polarizability	26.85 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon