NP-MRD: Showing NP-Card for methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate (NP0308813)

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Record Information

Version

2.0

Created at

2022-09-11 02:53:33 UTC

Updated at

2022-09-11 02:53:33 UTC

NP-MRD ID

NP0308813

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate

Description

Methyl (2S)-3-[(5Z)-4-hydroxy-2-oxo-5-(phenylmethylidene)-2,5-dihydrofuran-3-yl]-2-phenylpropanoate belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate is found in Pulveroboletus ravenelii. Based on a literature review very few articles have been published on methyl (2S)-3-[(5Z)-4-hydroxy-2-oxo-5-(phenylmethylidene)-2,5-dihydrofuran-3-yl]-2-phenylpropanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112204532D          

 26 28  0  0  1  0            999 V2000
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5253   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3099   -0.5950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    0.4445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7553    1.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4197    1.8657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5993    1.9519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2637    2.7056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7486    3.3730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5691    3.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9047    2.5331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454    0.4445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1904   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3654   -0.3401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 C   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
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 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
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
  5 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
M  END

     RDKit          3D

 44 46  0  0  0  0  0  0  0  0999 V2000
   -2.9550    3.1739    1.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8885    2.0605    0.3683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1762    0.9156    0.6588 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5588    0.8671    1.7542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1849   -0.1876   -0.3444 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2281   -1.2784   -0.0603 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1999   -0.8915   -0.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8075    0.2244   -0.2697 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1961    1.4038   -0.6654 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2186    0.0590   -0.0737 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2009    0.9614   -0.2223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5809    0.6321    0.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4142    1.5376    0.6174 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7596    1.2192    0.8479 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2560   -0.0231    0.4656 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4124   -0.9277   -0.1382 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0801   -0.5881   -0.3569 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4393   -1.2477    0.3165 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2246   -1.8683    0.3623 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0533   -3.0801    0.6845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5451   -0.7485   -0.5413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2825   -0.5674   -1.7139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5461   -1.0993   -1.8658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1269   -1.8371   -0.8471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4353   -2.0337    0.3120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1739   -1.4962    0.4488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3590    2.9900    2.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0080    3.3881    1.5475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5895    4.1110    0.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9431    0.3289   -1.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5216   -1.7819    0.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3309   -2.0392   -0.8635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6424    2.3053   -0.6348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8571    1.9433   -0.5333 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0718    2.5195    0.9332 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3743    1.9563    1.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3054   -0.2358    0.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8090   -1.8824   -0.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4525   -1.3277   -0.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8481    0.0019   -2.5093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1237   -0.9556   -2.7897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1170   -2.2656   -0.9393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8373   -2.6084    1.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5760   -1.6276    1.3646 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 18  1  0
 18 19  1  0
 19 20  2  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  5 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 19  7  1  0
 17 12  1  0
 26 21  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  6
  6 31  1  0
  6 32  1  0
  9 33  1  0
 11 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
 17 39  1  0
 22 40  1  0
 23 41  1  0
 24 42  1  0
 25 43  1  0
 26 44  1  0
M  END


  Mrv1652309112204532D          

 26 28  0  0  1  0            999 V2000
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5253   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3099   -0.5950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704    0.4445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7553    1.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4197    1.8657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5993    1.9519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2637    2.7056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7486    3.3730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5691    3.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9047    2.5331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454    0.4445    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1904   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3654   -0.3401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 C   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
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 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
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  2  0  0  0  0
  5 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0308813

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](CC1=C(O)\C(OC1=O)=C\C1=CC=CC=C1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H18O5/c1-25-20(23)16(15-10-6-3-7-11-15)13-17-19(22)18(26-21(17)24)12-14-8-4-2-5-9-14/h2-12,16,22H,13H2,1H3/b18-12-/t16-/m0/s1

> <INCHI_KEY>
JBSVMXLHJAADOB-JIHKLPAASA-N

> <FORMULA>
C21H18O5

> <MOLECULAR_WEIGHT>
350.37

> <EXACT_MASS>
350.11542368

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
36.60115072073718

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2S)-3-[(5Z)-4-hydroxy-2-oxo-5-(phenylmethylidene)-2,5-dihydrofuran-3-yl]-2-phenylpropanoate

> <JCHEM_LOGP>
3.476243840333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.553996342761479

> <JCHEM_PKA_STRONGEST_BASIC>
-6.493081999789401

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
98.33400000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2S)-3-[(5Z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334  -3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.667  -1.540   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.581  -0.635   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.045  -1.111   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.105   0.830   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.010   2.076   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.384   3.483   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.852   3.644   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.226   5.050   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.131   6.296   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.662   6.135   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.289   4.728   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.565   0.830   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.089  -0.635   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.549  -0.635   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335  -6.160   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667  -6.160   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   19                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   10   19                                                       
CONECT   19   18    7   20                                                  
CONECT   20   19                                                            
CONECT   21    5   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S)-3-[(5Z)-4-hydroxy-2-oxo-5-(phenylmethylidene)-2,5-dihydrofuran-3-yl]-2-phenylpropanoic acid	Generator

Chemical Formula

C₂₁H₁₈O₅

Average Mass

350.3700 Da

Monoisotopic Mass

350.11542 Da

IUPAC Name

methyl (2S)-3-[(5Z)-4-hydroxy-2-oxo-5-(phenylmethylidene)-2,5-dihydrofuran-3-yl]-2-phenylpropanoate

Traditional Name

methyl (2S)-3-[(5Z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](CC1=C(O)\C(OC1=O)=C\C1=CC=CC=C1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C21H18O5/c1-25-20(23)16(15-10-6-3-7-11-15)13-17-19(22)18(26-21(17)24)12-14-8-4-2-5-9-14/h2-12,16,22H,13H2,1H3/b18-12-/t16-/m0/s1

InChI Key

JBSVMXLHJAADOB-JIHKLPAASA-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
Pulveroboletus ravenelii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid esters

Alternative Parents

Substituents

Fatty acid ester
Benzenoid
Dicarboxylic acid or derivatives
2-furanone
Monocyclic benzene moiety
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Enol ester
Dihydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Enol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	3.48	ChemAxon
pKa (Strongest Acidic)	6.55	ChemAxon
pKa (Strongest Basic)	-6.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	98.33 m³·mol⁻¹	ChemAxon
Polarizability	36.6 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163104525

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate (NP0308813)

MOL for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

3D MOL for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

3D SDF for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

3D-SDF for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

PDB for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

3D PDB for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

SMILES for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

INCHI for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

Structure for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)

3D Structure for NP0308813 (methyl (2s)-3-[(5z)-4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2-phenylpropanoate)