NP-MRD: Showing NP-Card for (2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid (NP0195276)

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Record Information

Version

2.0

Created at

2022-09-04 13:06:22 UTC

Updated at

2022-09-04 13:06:22 UTC

NP-MRD ID

NP0195276

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid

Description

S-Mumefural belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. (2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid is found in Prunus mume. Based on a literature review very few articles have been published on S-Mumefural.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 33  0  0  0  0  0  0  0  0999 V2000
    6.7880   -1.4541   -1.7534 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5388   -1.3459   -1.7540 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8983   -0.5680   -0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5380    0.0901    0.3148 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5011    0.6857    1.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3184    0.3576    0.4227 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9736    0.7850    0.8704 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9491    0.2988    0.0476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3743    0.6016    0.3195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5850    1.3245    1.3301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5080    0.1106   -0.5234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8219    0.6114    0.0346 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8028    2.0157   -0.1524 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9395    0.1114   -0.8192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1652   -1.3299   -0.8084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4882   -2.1612   -0.1571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2082   -1.8304   -1.5755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9727    0.3654    1.4666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0668    1.3439    2.2513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0243   -0.8821    2.0704 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6026   -0.3758   -0.5983 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9596   -1.8325   -2.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6048    0.1480    0.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6561    1.2875    1.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9442    1.8952    0.9859 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7606    0.3931    1.9078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4672   -0.9719   -0.6367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4065    0.5645   -1.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2941    2.4713    0.5522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7883    0.4417   -1.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8836    0.6263   -0.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9835   -2.2884   -1.1073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2532   -1.4892    2.2195 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 15  1  0
 15 16  2  0
 15 14  1  0
 14 12  1  0
 12 13  1  1
 12 11  1  0
 11  9  1  0
  9 10  2  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3 21  1  0
  3  2  1  0
  2  1  2  0
 12 18  1  0
 18 20  1  0
 18 19  2  0
 21  6  1  0
 17 32  1  0
 14 30  1  0
 14 31  1  0
 13 29  1  0
 11 27  1  0
 11 28  1  0
  7 25  1  0
  7 26  1  0
  5 24  1  0
  4 23  1  0
  2 22  1  0
 20 33  1  0
M  END


  Mrv1652309042215062D          

 21 21  0  0  1  0            999 V2000
    1.2822    2.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3297   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1501   -0.7365    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6351   -1.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2995   -2.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4555   -1.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9405   -1.9851    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2730   -2.4700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6079   -1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5217   -0.6797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1891   -0.1948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7680   -0.3441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4254   -2.6525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0898   -3.4062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2459   -2.5663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  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
 12 11  1  6  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  6 21  1  0  0  0  0
  3 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195276

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)C[C@](O)(CC(=O)OCC1=CC=C(O1)C=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H12O9/c13-5-7-1-2-8(21-7)6-20-10(16)4-12(19,11(17)18)3-9(14)15/h1-2,5,19H,3-4,6H2,(H,14,15)(H,17,18)/t12-/m0/s1

> <INCHI_KEY>
FYDIRKLRXHXXHY-LBPRGKRZSA-N

> <FORMULA>
C12H12O9

> <MOLECULAR_WEIGHT>
300.219

> <EXACT_MASS>
300.048131966

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.630119125424052

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid

> <JCHEM_LOGP>
-0.7595701663333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.125522099220771

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.344571547434929

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0820936426064254

> <JCHEM_POLAR_SURFACE_AREA>
151.34000000000003

> <JCHEM_REFRACTIVITY>
63.858000000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  O   UNK     0       2.393   4.390   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.615  -1.536   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.147  -1.375   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -3.052  -2.621   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.426  -4.027   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -4.584  -2.460   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.489  -3.706   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -4.243  -4.611   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -6.735  -2.800   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.574  -1.269   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -7.820  -0.364   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -5.167  -0.642   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -6.394  -4.951   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -5.768  -6.358   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -7.926  -4.790   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -0.186   1.175   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   21                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14   18                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   12   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21    6    3                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₁₂O₉

Average Mass

300.2190 Da

Monoisotopic Mass

300.04813 Da

IUPAC Name

(2S)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid

Traditional Name

(2S)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid

CAS Registry Number

Not Available

SMILES

OC(=O)C[C@](O)(CC(=O)OCC1=CC=C(O1)C=O)C(O)=O

InChI Identifier

InChI=1S/C12H12O9/c13-5-7-1-2-8(21-7)6-20-10(16)4-12(19,11(17)18)3-9(14)15/h1-2,5,19H,3-4,6H2,(H,14,15)(H,17,18)/t12-/m0/s1

InChI Key

FYDIRKLRXHXXHY-LBPRGKRZSA-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
Prunus mume	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Fatty acid ester
Aryl-aldehyde
Alpha-hydroxy acid
Hydroxy acid
Fatty acyl
Furan
Heteroaromatic compound
Tertiary alcohol
Carboxylic acid ester
Oxacycle
Carboxylic acid
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Aldehyde
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	-0.76	ChemAxon
pKa (Strongest Acidic)	3.34	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	151.34 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	63.86 m³·mol⁻¹	ChemAxon
Polarizability	26.63 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

102124616

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid (NP0195276)

MOL for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

3D MOL for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

3D SDF for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

3D-SDF for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

PDB for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

3D PDB for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

SMILES for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

INCHI for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

Structure for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)

3D Structure for NP0195276 ((2s)-2-{2-[(5-formylfuran-2-yl)methoxy]-2-oxoethyl}-2-hydroxybutanedioic acid)