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Showing NP-Card for 2-C-Methyl-aldotetronolactone (NP0044977)

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Record Information
Version2.0
Created at2022-03-10 18:52:08 UTC
Updated at2022-03-10 22:16:55 UTC
NP-MRD IDNP0044977
Secondary Accession NumbersNone
Natural Product Identification
Common Name2-C-Methyl-aldotetronolactone
Description2-C-Methyl-1,4-erythrono-D-lactone, 2-C-methyl-D-erythrono-1,4-lactone (MDEL) or 2-C-Methyl-Aldotetronolactone belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-membered ring with four carbon atoms, one oxygen atom, forming part of a carboxyl functional group. 2-C-Methyl-1,4-erythrono-D-lactone is a neutral, hydrophobic molecule that is not soluble in water. 2-C-Methyl-1,4-erythrono-D-lactone is a known constituent of Trifolium incarnatum (crimson clover) and Phaseolus vulgaris (kidney bean). It has also been detected, but not quantified in several different foods, such as green beans, pulses, tea, and yellow wax beans. It has been identified as an insect pheromone that acts as an oviposition stimulant for the Swallowtail butterfly (PMID: 11055405 ). 2-C-Methyl-1,4-erythrono-D-lactone is synthesized in plants via the terpenoid precursor 1‚Äêdeoxy‚ÄêD‚Äêxylulose, which is phosphorylated to 1‚Äêdeoxy‚ÄêD‚Äêxylulose‚Äê5‚Äêphosphate, which is then transformed by the enzyme 1‚Äêdeoxy‚ÄêD‚Äêxylulose‚Äê5‚Äêphosphate reducto isomerase to 2C‚ÄêMethyl‚ÄêD‚Äêerythritol‚Äê4‚Äêphosphate. This compound is then oxidized at the alcoholic group at C‚Äê1 to 2-Methyl-2,3,4-trihydroxybutanoic acid-4-phosphate by an uncharacterized dehydrogenase. Dephosphorylation yields the free acid which spontaneously forms the lactone. 2-C-Methyl-1,4-erythrono-D-lactone is one of a small number of lactones found in cannabis plants (PMID: 6991645 ).
Structure
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MOL3D MOLSDFPDBSMILESInChI

MOL for NP0044977 (2-C-Methyl-aldotetronolactone)


  Mrv1652303192001283D          

  9  9  0  0  0  0            999 V2000
    1.4483    0.4304    0.8721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5426    0.6318    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7806   -0.6408    0.4371 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1912    0.6498   -1.2304 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5828   -0.2917   -0.1326 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3206   -1.6100   -0.4353 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0275    1.1506   -2.0434 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1982   -1.4171   -0.6344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1825    0.8580   -1.1910 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  5  1  0  0  0  0
  2  3  1  0  0  0  0
  2  9  1  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  2  0  0  0  0
  4  9  1  0  0  0  0
  5  8  1  0  0  0  0
M  END
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3D MOL for NP0044977 (2-C-Methyl-aldotetronolactone)

     RDKit          3D

 17 17  0  0  0  0  0  0  0  0999 V2000
    1.5220    0.3202   -0.5942 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4766    0.1018    0.4557 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8709    0.5592    1.6878 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1623   -1.3651    0.4723 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5562   -2.1870    1.3277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6394   -1.5610   -0.6530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2371   -0.3596   -1.0639 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8849    0.6444    0.0313 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7522    0.4230    1.0884 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2695   -0.5137   -0.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1483    0.2759   -1.6181 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0544    1.2565   -0.4295 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8782    1.5410    1.6632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3174   -0.4548   -1.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8282   -0.0251   -2.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8474    1.6698   -0.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4317   -0.3254    1.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  1
  2  8  1  0
  8  9  1  0
  8  7  1  0
  7  6  1  0
  6  4  1  0
  4  5  2  0
  4  2  1  0
  1 10  1  0
  1 11  1  0
  1 12  1  0
  3 13  1  0
  8 16  1  6
  9 17  1  0
  7 14  1  0
  7 15  1  0
M  END
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3D SDF for NP0044977 (2-C-Methyl-aldotetronolactone)


  Mrv1652303192001283D          

  9  9  0  0  0  0            999 V2000
    1.4483    0.4304    0.8721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5426    0.6318    0.1835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7806   -0.6408    0.4371 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1912    0.6498   -1.2304 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5828   -0.2917   -0.1326 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3206   -1.6100   -0.4353 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0275    1.1506   -2.0434 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1982   -1.4171   -0.6344 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1825    0.8580   -1.1910 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  5  1  0  0  0  0
  2  3  1  0  0  0  0
  2  9  1  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  4  5  1  0  0  0  0
  4  7  2  0  0  0  0
  4  9  1  0  0  0  0
  5  8  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0044977

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]1(O)[C@H](O)COC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C5H8O4/c1-5(8)3(6)2-9-4(5)7/h3,6,8H,2H2,1H3/t3-,5-/m1/s1

> <INCHI_KEY>
OHTGZAWPVDWARE-NQXXGFSBSA-N

> <FORMULA>
C5H8O4

> <MOLECULAR_WEIGHT>
132.115

> <EXACT_MASS>
132.042258738

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
17

> <JCHEM_AVERAGE_POLARIZABILITY>
11.699144016837439

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,4R)-3,4-dihydroxy-3-methyloxolan-2-one

> <ALOGPS_LOGP>
-1.46

> <JCHEM_LOGP>
-1.0518374160000001

> <ALOGPS_LOGS>
0.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.772566814924513

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.572919327231176

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6878977110596667

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
27.5671

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.36e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4R)-3,4-dihydroxy-3-methyloxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for NP0044977 (2-C-Methyl-aldotetronolactone)

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PDB for NP0044977 (2-C-Methyl-aldotetronolactone)
HEADER    PROTEIN                                 19-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-MAR-20         0                                  
HETATM    1  C   UNK     0       1.448   0.430   0.872  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.543   0.632   0.184  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.781  -0.641   0.437  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.191   0.650  -1.230  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.583  -0.292  -0.133  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.321  -1.610  -0.435  0.00  0.00           O+0
HETATM    7  O   UNK     0       1.028   1.151  -2.043  0.00  0.00           O+0
HETATM    8  O   UNK     0       1.198  -1.417  -0.634  0.00  0.00           O+0
HETATM    9  O   UNK     0      -1.183   0.858  -1.191  0.00  0.00           O+0
CONECT    1    5                                                            
CONECT    2    3    9                                                       
CONECT    3    2    5    6                                                  
CONECT    4    5    7    9                                                  
CONECT    5    1    3    4    8                                             
CONECT    6    3                                                            
CONECT    7    4                                                            
CONECT    8    5                                                            
CONECT    9    2    4                                                       
MASTER        0    0    0    0    0    0    0    0    9    0   18    0
END

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3D PDB for NP0044977 (2-C-Methyl-aldotetronolactone)
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SMILES for NP0044977 (2-C-Methyl-aldotetronolactone)
C[C@@]1(O)[C@H](O)COC1=O
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INCHI for NP0044977 (2-C-Methyl-aldotetronolactone)
InChI=1S/C5H8O4/c1-5(8)3(6)2-9-4(5)7/h3,6,8H,2H2,1H3/t3-,5-/m1/s1
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View in JSmol
SynonymsNot Available
Chemical FormulaC5H8O4
Average Mass132.1150 Da
Monoisotopic Mass132.04226 Da
IUPAC Name(3R,4R)-3,4-dihydroxy-3-methyloxolan-2-one
Traditional Name(3R,4R)-3,4-dihydroxy-3-methyloxolan-2-one
CAS Registry Number18465-71-9
SMILES
C[C@@]1(O)[C@H](O)COC1=O
InChI Identifier
InChI=1S/C5H8O4/c1-5(8)3(6)2-9-4(5)7/h3,6,8H,2H2,1H3/t3-,5-/m1/s1
InChI KeyOHTGZAWPVDWARE-NQXXGFSBSA-N
Experimental Spectra
Not Available
Predicted Spectra
Spectrum TypeDescriptionDepositor IDDepositor OrganizationDepositorDeposition DateView
1D NMR13C NMR Spectrum (1D, 25 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 252 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 50 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 75 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 101 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 126 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 151 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 176 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 201 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 226 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
Chemical Shift Submissions
Not Available
Species
Species of Origin
Species NameSourceReference
Anaphalis margaritaceaLOTUS Database
Cannabis sativaNULL
      Not Available
Erophaca baeticaLOTUS Database
Hymenoxys richardsoniiLOTUS Database
Leucaena glaucaLOTUS Database
Orixa japonicaLOTUS Database
Chemical Taxonomy
Description Belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.
KingdomOrganic compounds  
Super ClassOrganoheterocyclic compounds  
ClassLactones  
Sub ClassGamma butyrolactones  
Direct ParentGamma butyrolactones  
Alternative Parents
Substituents
  • Gamma butyrolactone
    • 

  • Oxolane
    • 

  • Tertiary alcohol
    • 

  • 1,2-diol
    • 

  • Carboxylic acid ester
    • 

  • Secondary alcohol
    • 

  • Carboxylic acid derivative
    • 

  • Monocarboxylic acid or derivatives
    • 

  • Oxacycle
    • 

  • Hydrocarbon derivative
    • 

  • Organic oxide
    • 

  • Organic oxygen compound
    • 

  • Carbonyl group
    • 

  • Alcohol
    • 

  • Organooxygen compound
    • 

  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP-1.5ALOGPS
logP-1.1ChemAxon
logS0.8ALOGPS
pKa (Strongest Acidic)11.57ChemAxon
pKa (Strongest Basic)-3.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area66.76 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity27.57 m³·mol⁻¹ChemAxon
Polarizability11.7 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound11126294  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References