NP-MRD: Showing NP-Card for WF 3681 (NP0019921)

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Record Information

Version

2.0

Created at

2021-01-06 05:26:39 UTC

Updated at

2021-07-15 17:32:16 UTC

NP-MRD ID

NP0019921

Secondary Accession Numbers

None

Natural Product Identification

Common Name

WF 3681

Provided By

NPAtlas

Description

WF 3681 is found in Chaetomella raphigera. Based on a literature review very few articles have been published on 3-(4-hydroxy-5-oxo-3-phenyl-2,5-dihydrofuran-2-yl)propanoic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242120253D          

 30 31  0  0  0  0            999 V2000
    3.2617    0.1455   -2.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4341    0.9295   -1.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9999    2.1801   -1.3859 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0793    0.6053    0.3451 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6278    0.3435    0.5344 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0885   -0.8260   -0.2651 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7359   -2.0074    0.0813 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065   -2.9053    0.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0119   -4.0992    0.9863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4998   -2.2682    0.5172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6987   -2.8756    0.9274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3507   -1.0511    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4561   -0.1205   -0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4531   -0.0358    0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5199    0.8264    0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5826    1.6125   -0.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6158    1.5613   -1.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610    0.6843   -1.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0085    2.8785   -0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3499    1.4702    0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7143   -0.2395    0.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0567    1.2482    0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4551    0.1194    1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1804   -0.6117   -1.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4928   -2.9421    0.2819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3924   -0.6626    1.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3094    0.9024    1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4075    2.3129   -0.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6762    2.1913   -2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7945    0.6337   -2.0465 H   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  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 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
 17 18  2  0  0  0  0
 12  6  1  0  0  0  0
 18 13  1  0  0  0  0
  3 19  1  0  0  0  0
  4 20  1  0  0  0  0
  4 21  1  0  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  6 24  1  6  0  0  0
 11 25  1  0  0  0  0
 14 26  1  0  0  0  0
 15 27  1  0  0  0  0
 16 28  1  0  0  0  0
 17 29  1  0  0  0  0
 18 30  1  0  0  0  0
M  END

     RDKit          3D

 30 31  0  0  0  0  0  0  0  0999 V2000
    3.2617    0.1455   -2.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4341    0.9295   -1.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9999    2.1801   -1.3859 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0793    0.6053    0.3451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6278    0.3435    0.5344 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0885   -0.8260   -0.2651 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7359   -2.0074    0.0813 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065   -2.9053    0.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0119   -4.0992    0.9863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4998   -2.2682    0.5172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6987   -2.8756    0.9274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3507   -1.0511    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4561   -0.1205   -0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4531   -0.0358    0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5199    0.8264    0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5826    1.6125   -0.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6158    1.5613   -1.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610    0.6843   -1.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0085    2.8785   -0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3499    1.4702    0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7143   -0.2395    0.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0567    1.2482    0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4551    0.1194    1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1804   -0.6117   -1.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4928   -2.9421    0.2819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3924   -0.6626    1.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3094    0.9024    1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4075    2.3129   -0.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6762    2.1913   -2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7945    0.6337   -2.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 12  6  1  0
 18 13  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  6
 11 25  1  0
 14 26  1  0
 15 27  1  0
 16 28  1  0
 17 29  1  0
 18 30  1  0
M  END


  Mrv1652306242120253D          

 30 31  0  0  0  0            999 V2000
    3.2617    0.1455   -2.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4341    0.9295   -1.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9999    2.1801   -1.3859 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0793    0.6053    0.3451 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6278    0.3435    0.5344 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0885   -0.8260   -0.2651 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7359   -2.0074    0.0813 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065   -2.9053    0.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0119   -4.0992    0.9863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4998   -2.2682    0.5172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6987   -2.8756    0.9274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3507   -1.0511    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4561   -0.1205   -0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4531   -0.0358    0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5199    0.8264    0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5826    1.6125   -0.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6158    1.5613   -1.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610    0.6843   -1.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0085    2.8785   -0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3499    1.4702    0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7143   -0.2395    0.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0567    1.2482    0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4551    0.1194    1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1804   -0.6117   -1.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4928   -2.9421    0.2819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3924   -0.6626    1.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3094    0.9024    1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4075    2.3129   -0.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6762    2.1913   -2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7945    0.6337   -2.0465 H   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  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 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
 17 18  2  0  0  0  0
 12  6  1  0  0  0  0
 18 13  1  0  0  0  0
  3 19  1  0  0  0  0
  4 20  1  0  0  0  0
  4 21  1  0  0  0  0
  5 22  1  0  0  0  0
  5 23  1  0  0  0  0
  6 24  1  6  0  0  0
 11 25  1  0  0  0  0
 14 26  1  0  0  0  0
 15 27  1  0  0  0  0
 16 28  1  0  0  0  0
 17 29  1  0  0  0  0
 18 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0019921

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C([H])([H])C([H])([H])[C@@]1([H])OC(=O)C(O[H])=C1C1=C([H])C([H])=C([H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H12O5/c14-10(15)7-6-9-11(12(16)13(17)18-9)8-4-2-1-3-5-8/h1-5,9,16H,6-7H2,(H,14,15)/t9-/m1/s1

> <INCHI_KEY>
PPZVSYXNLXFYAD-UHFFFAOYSA-N

> <FORMULA>
C13H12O5

> <MOLECULAR_WEIGHT>
248.234

> <EXACT_MASS>
248.068473486

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
24.263205797383506

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(2R)-4-hydroxy-5-oxo-3-phenyl-2,5-dihydrofuran-2-yl]propanoic acid

> <ALOGPS_LOGP>
1.31

> <JCHEM_LOGP>
1.5972808046666664

> <ALOGPS_LOGS>
-2.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.104297238293896

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.064177110923771

> <JCHEM_PKA_STRONGEST_BASIC>
-3.161973031141736

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
62.801000000000016

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.14e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(2R)-4-hydroxy-5-oxo-3-phenyl-2H-furan-2-yl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 30 31  0  0  0  0  0  0  0  0999 V2000
    3.2617    0.1455   -2.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4341    0.9295   -1.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9999    2.1801   -1.3859 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0793    0.6053    0.3451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6278    0.3435    0.5344 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0885   -0.8260   -0.2651 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7359   -2.0074    0.0813 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065   -2.9053    0.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0119   -4.0992    0.9863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4998   -2.2682    0.5172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6987   -2.8756    0.9274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3507   -1.0511    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4561   -0.1205   -0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4531   -0.0358    0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5199    0.8264    0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5826    1.6125   -0.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6158    1.5613   -1.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610    0.6843   -1.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0085    2.8785   -0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3499    1.4702    0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7143   -0.2395    0.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0567    1.2482    0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4551    0.1194    1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1804   -0.6117   -1.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4928   -2.9421    0.2819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3924   -0.6626    1.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3094    0.9024    1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4075    2.3129   -0.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6762    2.1913   -2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7945    0.6337   -2.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 12  6  1  0
 18 13  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  6
 11 25  1  0
 14 26  1  0
 15 27  1  0
 16 28  1  0
 17 29  1  0
 18 30  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  O   UNK     0       3.262   0.146  -2.024  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.434   0.930  -1.061  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.000   2.180  -1.386  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.079   0.605   0.345  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.628   0.344   0.534  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.089  -0.826  -0.265  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.736  -2.007   0.081  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.807  -2.905   0.563  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.012  -4.099   0.986  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.500  -2.268   0.517  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.699  -2.876   0.927  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.351  -1.051   0.034  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.456  -0.121  -0.152  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.453  -0.036   0.817  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.520   0.826   0.663  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.583   1.613  -0.482  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.616   1.561  -1.469  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.561   0.684  -1.278  0.00  0.00           C+0
HETATM   19  H   UNK     0       4.008   2.878  -0.671  0.00  0.00           H+0
HETATM   20  H   UNK     0       3.350   1.470   0.977  0.00  0.00           H+0
HETATM   21  H   UNK     0       3.714  -0.240   0.728  0.00  0.00           H+0
HETATM   22  H   UNK     0       1.057   1.248   0.295  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.455   0.119   1.613  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.180  -0.612  -1.344  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.493  -2.942   0.282  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.392  -0.663   1.712  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.309   0.902   1.417  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.407   2.313  -0.649  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.676   2.191  -2.378  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.795   0.634  -2.046  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2   19                                                       
CONECT    4    2    5   20   21                                             
CONECT    5    4    6   22   23                                             
CONECT    6    5    7   12   24                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10   25                                                       
CONECT   12   10   13    6                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15   26                                                  
CONECT   15   14   16   27                                                  
CONECT   16   15   17   28                                                  
CONECT   17   16   18   29                                                  
CONECT   18   17   13   30                                                  
CONECT   19    3                                                            
CONECT   20    4                                                            
CONECT   21    4                                                            
CONECT   22    5                                                            
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25   11                                                            
CONECT   26   14                                                            
CONECT   27   15                                                            
CONECT   28   16                                                            
CONECT   29   17                                                            
CONECT   30   18                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

RDKit          3D

30 31  0  0  0  0  0  0  0  0999 V2000
    3.2617    0.1455   -2.0242 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4341    0.9295   -1.0610 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9999    2.1801   -1.3859 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0793    0.6053    0.3451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6278    0.3435    0.5344 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0885   -0.8260   -0.2651 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7359   -2.0074    0.0813 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065   -2.9053    0.5629 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0119   -4.0992    0.9863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4998   -2.2682    0.5172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6987   -2.8756    0.9274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3507   -1.0511    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4561   -0.1205   -0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4531   -0.0358    0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5199    0.8264    0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5826    1.6125   -0.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6158    1.5613   -1.4692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5610    0.6843   -1.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0085    2.8785   -0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3499    1.4702    0.9772 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7143   -0.2395    0.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0567    1.2482    0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4551    0.1194    1.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1804   -0.6117   -1.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4928   -2.9421    0.2819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3924   -0.6626    1.7124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3094    0.9024    1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4075    2.3129   -0.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6762    2.1913   -2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7945    0.6337   -2.0465 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0
  8 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 12  6  1  0
 18 13  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  5 23  1  0
  6 24  1  6
 11 25  1  0
 14 26  1  0
 15 27  1  0
 16 28  1  0
 17 29  1  0
 18 30  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
3-(4-Hydroxy-5-oxo-3-phenyl-2,5-dihydrofuran-2-yl)propanoate	Generator
3-(4-Hydroxy-5-oxo-3-phenyl-2,5-dihydro-2-furan)propionic acid	MeSH

Chemical Formula

C₁₃H₁₂O₅

Average Mass

248.2340 Da

Monoisotopic Mass

248.06847 Da

IUPAC Name

3-[(2R)-4-hydroxy-5-oxo-3-phenyl-2,5-dihydrofuran-2-yl]propanoic acid

Traditional Name

3-[(2R)-4-hydroxy-5-oxo-3-phenyl-2H-furan-2-yl]propanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CCC1OC(=O)C(O)=C1C1=CC=CC=C1

InChI Identifier

InChI=1S/C13H12O5/c14-10(15)7-6-9-11(12(16)13(17)18-9)8-4-2-1-3-5-8/h1-5,9,16H,6-7H2,(H,14,15)

InChI Key

PPZVSYXNLXFYAD-UHFFFAOYSA-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
Chaetomella raphigera	NPAtlas	3119547

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

Monocyclic benzene moiety
2-furanone
Dicarboxylic acid or derivatives
Benzenoid
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Enol
Carboxylic acid
Carboxylic acid derivative
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organooxygen compound
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	1.31	ALOGPS
logP	1.6	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	4.06	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	62.8 m³·mol⁻¹	ChemAxon
Polarizability	24.26 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

NPAtlas ID

NPA015467

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

113787

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

128356

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for WF 3681 (NP0019921)

MOL for NP0019921 (WF 3681)

3D MOL for NP0019921 (WF 3681)

3D SDF for NP0019921 (WF 3681)

3D-SDF for NP0019921 (WF 3681)

PDB for NP0019921 (WF 3681)

3D PDB for NP0019921 (WF 3681)

SMILES for NP0019921 (WF 3681)

INCHI for NP0019921 (WF 3681)

Structure for NP0019921 (WF 3681)

3D Structure for NP0019921 (WF 3681)