NP-MRD: Showing NP-Card for methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate (NP0217524)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 17:53:58 UTC

Updated at

2022-09-05 17:53:58 UTC

NP-MRD ID

NP0217524

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate

Description

4'-Methoxyvulpinic acid, also known as pinastric acid, belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate is found in Flavoparmelia caperata. Based on a literature review very few articles have been published on 4'-Methoxyvulpinic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052219532D          

 26 28  0  0  0  0            999 V2000
    0.8212    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212   -0.4741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1953   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2897   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5052   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1696   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6546   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750   -4.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9600   -5.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804   -5.1522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8106   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3257   -3.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2752   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0598   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    0.7634    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
  3  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  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 11 18  1  0  0  0  0
 10 19  2  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  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

 42 44  0  0  0  0  0  0  0  0999 V2000
   -4.1569    3.7210    2.2703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1487    2.8930    1.7192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1137    1.5786    2.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9363    1.1376    2.9871 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1082    0.6180    1.6456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2094    1.0017    0.7602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1798    2.3302    0.2785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1341    2.3772   -0.6192 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2083    3.4038   -1.2607 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5319    1.0926   -0.7392 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6720    0.7122   -1.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7203    1.6097   -1.8012 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8092    1.2689   -2.5764 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8760    0.0259   -3.1312 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9448   -0.3666   -3.9155 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0060   -1.6548   -4.4850 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8531   -0.8705   -2.9082 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7523   -0.5204   -2.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376    0.2819    0.1027 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1721   -1.0466    0.2922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0441   -0.7361    2.1584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9373   -1.3018    2.7484 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9261   -2.6217    3.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0426   -3.4167    3.0660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1598   -2.8734    2.4809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1648   -1.5632    2.0358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7477    4.2536    1.5047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8663    3.1452    2.8967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6744    4.4506    2.9826 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6700    2.5812   -1.3689 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6065    1.9993   -2.7387 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9409   -2.4027   -3.6507 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9954   -1.8447   -4.9604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1646   -1.8869   -5.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9272   -1.8487   -3.3585 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0002   -1.2850   -2.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0857   -1.3369    0.6339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0391   -0.6946    2.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0553   -3.0644    3.6614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0670   -4.4501    3.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0344   -3.5168    2.3845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0526   -1.1794    1.5872 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 19  2  0
 19 20  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  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  6  1  0
 18 11  1  0
 26 21  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
 20 37  1  0
 12 30  1  0
 13 31  1  0
 16 32  1  0
 16 33  1  0
 16 34  1  0
 17 35  1  0
 18 36  1  0
 22 38  1  0
 23 39  1  0
 24 40  1  0
 25 41  1  0
 26 42  1  0
M  END


  Mrv1652309052219532D          

 26 28  0  0  0  0            999 V2000
    0.8212    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212   -0.4741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0597   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1953   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2897   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0203   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5052   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1696   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6546   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750   -4.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9600   -5.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7804   -5.1522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8106   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3257   -3.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2752   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0598   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    0.7634    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
  3  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  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  2  0  0  0  0
 11 18  1  0  0  0  0
 10 19  2  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  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>
NP0217524

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(=C1/OC(=O)C(=C1O)C1=CC=C(OC)C=C1)\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O6/c1-24-14-10-8-13(9-11-14)15-17(21)18(26-20(15)23)16(19(22)25-2)12-6-4-3-5-7-12/h3-11,21H,1-2H3/b18-16-

> <INCHI_KEY>
KXQKSBAGVQMQSN-VLGSPTGOSA-N

> <FORMULA>
C20H16O6

> <MOLECULAR_WEIGHT>
352.342

> <EXACT_MASS>
352.094688235

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
36.359869559609876

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[(2Z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-2-ylidene]-2-phenylacetate

> <JCHEM_LOGP>
3.0698446020000003

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.009473442005588

> <JCHEM_PKA_STRONGEST_BASIC>
-4.831197969842443

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
95.35450000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(2Z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene](phenyl)acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       1.533   2.195   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.199   1.425   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.199  -0.115   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.533  -0.885   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.134  -0.885   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.134  -2.425   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.111  -3.330   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.364  -4.795   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.541  -6.041   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.904  -4.795   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.810  -6.041   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.183  -7.448   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.088  -8.693   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.620  -8.532   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -5.525  -9.778   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -7.057  -9.617   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.246  -7.126   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.341  -5.880   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.380  -3.330   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.845  -2.854   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -2.468  -0.115   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.802  -0.885   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.136  -0.115   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.136   1.425   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.802   2.195   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.468   1.425   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   19                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   19                                                  
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   11                                                       
CONECT   19   10    6   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
4'-Methoxyvulpinate	Generator
Pinastric acid	MeSH
Pinastric acid, potassium salt	MeSH

Chemical Formula

C₂₀H₁₆O₆

Average Mass

352.3420 Da

Monoisotopic Mass

352.09469 Da

IUPAC Name

methyl 2-[(2Z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-2-ylidene]-2-phenylacetate

Traditional Name

methyl [(2Z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene](phenyl)acetate

CAS Registry Number

Not Available

SMILES

COC(=O)C(=C1/OC(=O)C(=C1O)C1=CC=C(OC)C=C1)\C1=CC=CC=C1

InChI Identifier

InChI=1S/C20H16O6/c1-24-14-10-8-13(9-11-14)15-17(21)18(26-20(15)23)16(19(22)25-2)12-6-4-3-5-7-12/h3-11,21H,1-2H3/b18-16-

InChI Key

KXQKSBAGVQMQSN-VLGSPTGOSA-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
Flavoparmelia caperata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Anisole
Methoxybenzene
Alkyl aryl ether
Monocyclic benzene moiety
2-furanone
Dicarboxylic acid or derivatives
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Dihydrofuran
Enol ester
Carboxylic acid ester
Lactone
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Ether
Enol
Carbonyl group
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen 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	3.07	ChemAxon
pKa (Strongest Acidic)	6.01	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	95.35 m³·mol⁻¹	ChemAxon
Polarizability	36.36 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	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

21249072

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54684142

PDB ID

Not Available

ChEBI ID

144195

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate (NP0217524)

MOL for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

3D MOL for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

3D SDF for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

3D-SDF for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

PDB for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

3D PDB for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

SMILES for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

INCHI for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

Structure for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)

3D Structure for NP0217524 (methyl 2-[(2z)-3-hydroxy-4-(4-methoxyphenyl)-5-oxofuran-2-ylidene]-2-phenylacetate)