NP-MRD: Showing NP-Card for methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate (NP0265861)

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Record Information

Version

2.0

Created at

2022-09-08 09:59:57 UTC

Updated at

2022-09-08 09:59:57 UTC

NP-MRD ID

NP0265861

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate

Description

Methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)-2,5-dihydrofuran-3-yl]-2,3-diphenylpropanoate belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate is found in Pulveroboletus ravenelii. Methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)-2,5-dihydrofuran-3-yl]-2,3-diphenylpropanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171503522D          

 32 35  0  0  0  0            999 V2000
   -2.7512    3.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    2.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    2.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9897   -0.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8147   -0.6697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7347   -1.4544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2197   -2.1218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8841   -2.8755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0636   -2.9617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7281   -3.7154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2130   -4.3828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0335   -4.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3690   -3.5429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9097   -1.4544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6548   -0.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1298   -0.4148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    1.0527    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  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  4  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
  6 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
  5 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -1.4477    3.6685   -1.4301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834    2.3403   -0.9959 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4171    1.8982    0.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7877    2.7074    0.9933 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7692    0.5303    0.7011 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2298    0.3009    0.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9456    0.2395   -0.4799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3163    0.0274   -0.4903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9858   -0.1266    0.7030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2975   -0.0700    1.8911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9184    0.1444    1.8749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0141   -0.4361   -0.1554 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4397   -0.1783    0.0254 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2720    0.3412   -0.8871 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8883    0.7241   -2.1687 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6263    0.4543   -0.3682 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6543    0.9389   -1.0644 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9446    0.9965   -0.4313 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4135    0.0179    0.4298 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6450    0.0807    1.0366 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4734    1.1376    0.8070 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0456    2.1442   -0.0505 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8041    2.0714   -0.6563 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6061   -0.0202    0.9176 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839   -0.4142    1.1879 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9153   -0.8993    2.2903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4020   -1.8422   -0.0022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5207   -2.6741   -1.1151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8935   -3.9973   -1.0412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1674   -4.5436    0.1933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0680   -3.7722    1.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6851   -2.4267    1.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6966    4.3662   -0.5901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1609    3.8922   -2.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4004    3.7384   -1.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4242    0.4563    1.7745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4707    0.3538   -1.4479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8405   -0.0138   -1.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0567   -0.2917    0.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8518   -0.1943    2.8086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4354    0.1781    2.8428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2261   -0.1677   -1.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9466    0.0107   -2.8881 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5325    1.2806   -2.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7781   -0.8208    0.6225 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9433   -0.7131    1.6923 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4347    1.1768    1.2874 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7027    2.9812   -0.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5091    2.8679   -1.3122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3132   -2.2757   -2.1006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9745   -4.6153   -1.9394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4642   -5.5732    0.3167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2811   -4.1872    2.3218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6136   -1.8119    2.1045 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 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 24  1  0
 24 25  1  0
 25 26  2  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 12 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 25 13  1  0
 23 18  1  0
 32 27  1  0
 11  6  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  1
 12 42  1  6
 15 43  1  0
 17 44  1  0
 19 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
 28 50  1  0
 29 51  1  0
 30 52  1  0
 31 53  1  0
 32 54  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 11 41  1  0
M  END


  Mrv1533004171503522D          

 32 35  0  0  0  0            999 V2000
   -2.7512    3.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    2.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    2.2902    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0367    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3222   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9897   -0.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8147   -0.6697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7347   -1.4544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2197   -2.1218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8841   -2.8755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0636   -2.9617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7281   -3.7154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2130   -4.3828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0335   -4.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3690   -3.5429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9097   -1.4544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6548   -0.6697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1298   -0.4148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    1.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8212    1.0527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7512   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656   -0.5973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801   -0.1848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    0.6402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    1.0527    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  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  4  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
  6 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
  5 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0265861

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(C(C1=C(O)C(OC1=O)=CC1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H22O5/c1-31-26(29)23(20-15-9-4-10-16-20)22(19-13-7-3-8-14-19)24-25(28)21(32-27(24)30)17-18-11-5-2-6-12-18/h2-17,22-23,28H,1H3

> <INCHI_KEY>
DFRUUMWSIQRNGP-UHFFFAOYSA-N

> <FORMULA>
C27H22O5

> <MOLECULAR_WEIGHT>
426.468

> <EXACT_MASS>
426.146723808

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
45.58909876598631

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
4.95

> <JCHEM_LOGP>
4.897066909333334

> <ALOGPS_LOGS>
-5.42

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.527842324516618

> <JCHEM_PKA_STRONGEST_BASIC>
-6.504521767371565

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
122.97760000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.61e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -5.136   5.815   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.136   4.275   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.802   3.505   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.468   4.275   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -3.802   1.965   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.468   1.195   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.468  -0.345   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.714  -1.250   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -5.254  -1.250   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -3.238  -2.715   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.143  -3.961   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.517  -5.368   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.985  -5.529   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.359  -6.935   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.264  -8.181   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.796  -8.020   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.422  -6.613   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.698  -2.715   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -1.222  -1.250   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.242  -0.774   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.134   1.965   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.134   3.505   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.199   4.275   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.533   3.505   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.533   1.965   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.199   1.195   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.136   1.195   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.136  -0.345   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -6.469  -1.115   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -7.803  -0.345   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -7.803   1.195   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -6.469   1.965   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   27                                                  
CONECT    6    5    7   21                                                  
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    6   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21                                                       
CONECT   27    5   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

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

Chemical Formula

C₂₇H₂₂O₅

Average Mass

426.4680 Da

Monoisotopic Mass

426.14672 Da

IUPAC Name

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

Traditional Name

methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate

CAS Registry Number

Not Available

SMILES

COC(=O)C(C(C1=C(O)C(OC1=O)=CC1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1

InChI Identifier

InChI=1S/C27H22O5/c1-31-26(29)23(20-15-9-4-10-16-20)22(19-13-7-3-8-14-19)24-25(28)21(32-27(24)30)17-18-11-5-2-6-12-18/h2-17,22-23,28H,1H3

InChI Key

DFRUUMWSIQRNGP-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, 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 stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Fatty acid ester
Monocyclic benzene moiety
2-furanone
Dicarboxylic acid or derivatives
Fatty acyl
Benzenoid
Dihydrofuran
Enol ester
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Vinylogous acid
Lactone
Carboxylic acid ester
Oxacycle
Enol
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
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	4.95	ALOGPS
logP	4.9	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	6.53	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	7	ChemAxon
Refractivity	122.98 m³·mol⁻¹	ChemAxon
Polarizability	45.59 Å³	ChemAxon
Number of Rings	4	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

76170733

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate (NP0265861)

MOL for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

3D MOL for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

3D SDF for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

3D-SDF for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

PDB for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

3D PDB for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

SMILES for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

INCHI for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

Structure for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)

3D Structure for NP0265861 (methyl 3-[4-hydroxy-2-oxo-5-(phenylmethylidene)furan-3-yl]-2,3-diphenylpropanoate)