NP-MRD: Showing NP-Card for 5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate (NP0270783)

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Record Information

Version

2.0

Created at

2022-09-08 16:50:59 UTC

Updated at

2022-09-08 16:50:59 UTC

NP-MRD ID

NP0270783

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate

Description

5-Hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5,6,7-tetrahydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate belongs to the class of organic compounds known as furanoid fatty acids. These are fatty acids containing a 5-alkylfuran-2-alkanoic acid. Based on a literature review very few articles have been published on 5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5,6,7-tetrahydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082218512D          

 27 29  0  0  0  0            999 V2000
   -2.6909   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8659   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3522    0.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8825   -0.4287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4128    0.2033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1307    0.9785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2253    0.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7556    0.6920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4734    1.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5681    0.5488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8502   -0.2265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6627   -0.3698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3199   -0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5075   -0.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9772   -1.3472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  4  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  6 27  1  0  0  0  0
M  END

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    7.8105   -1.4455   -0.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4589   -0.8741   -0.4057 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4269   -1.4861    0.1424 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0841   -0.8998    0.0700 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7650    0.2862   -0.5420 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3967    0.4704   -0.3811 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9532   -0.6232    0.3267 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9853   -1.4082    0.5723 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5320   -0.6941    0.6434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0568   -1.7972    0.6323 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1659    0.5727    0.9721 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1120    0.7991    2.4665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5588    0.3609    0.8159 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1097   -0.0212   -0.4022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2853   -0.1601   -1.3328 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5286   -0.2445   -0.5926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3871   -0.0694    0.4923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8065    0.3385    1.7965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7691   -0.2704    0.3693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3341   -0.6470   -0.8208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7157   -0.8499   -0.9518 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4986   -0.8193   -1.8843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0994   -0.6224   -1.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3399   -0.8200   -2.9101 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3494    1.7630    0.2400 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8818    2.7251    1.1296 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4059    1.4959   -0.7769 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5153   -0.6184   -0.0457 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1687   -1.8607   -1.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8884   -2.2387    0.4118 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2942    0.0742   -0.9125 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6127   -2.4259    0.6403 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3830    0.9932   -1.0637 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2307    0.8270    2.5865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2431   -0.0651    3.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3010    1.7640    2.8044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3562    1.3515    1.7853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1439   -0.4265    2.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6840    0.3673    2.5249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4027   -0.1238    1.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2941   -0.0566   -1.2195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8978   -1.1182   -2.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3868   -0.7422   -3.0604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4971    2.2721   -0.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5973    3.2488    0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0034    1.2780   -1.7996 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0069    2.4408   -0.9374 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 11 13  1  1
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 23 24  1  0
 11 25  1  0
 25 26  1  0
 25 27  1  0
  8  4  1  0
 23 16  1  0
 27  6  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  3 32  1  0
  5 33  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
 18 37  1  0
 18 38  1  0
 18 39  1  0
 19 40  1  0
 21 41  1  0
 22 42  1  0
 24 43  1  0
 25 44  1  6
 26 45  1  0
 27 46  1  0
 27 47  1  0
M  END


  Mrv1652309082218512D          

 27 29  0  0  0  0            999 V2000
   -2.6909   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8659   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4534   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3522    0.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8825   -0.4287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4128    0.2033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1307    0.9785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2253    0.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7556    0.6920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4734    1.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5681    0.5488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8502   -0.2265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6627   -0.3698    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3199   -0.8585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5075   -0.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9772   -1.3472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  4  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  6 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270783

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=CC1=CC2=C(O1)C(=O)C(C)(OC(=O)C1=C(C)C=C(O)C=C1O)C(O)C2

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O7/c1-4-5-13-7-11-8-15(23)20(3,18(24)17(11)26-13)27-19(25)16-10(2)6-12(21)9-14(16)22/h4-7,9,15,21-23H,8H2,1-3H3

> <INCHI_KEY>
JOYCBRUDRSSQCN-UHFFFAOYSA-N

> <FORMULA>
C20H20O7

> <MOLECULAR_WEIGHT>
372.373

> <EXACT_MASS>
372.120902984

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
37.27209659781689

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5,6,7-tetrahydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate

> <JCHEM_LOGP>
3.923096451666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.546129485119348

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.68765806536759

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0470872436160485

> <JCHEM_POLAR_SURFACE_AREA>
117.2

> <JCHEM_REFRACTIVITY>
98.34689999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.023  -2.637   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.483  -2.637   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.713  -1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.268  -2.549   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.268  -0.057   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.530   1.777   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.864  -0.533   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.391   0.914   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.381  -0.800   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.371   0.379   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.844   1.827   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.887   0.112   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.877   1.292   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.350   2.739   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.394   1.024   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.920  -0.423   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.437  -0.690   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.931  -1.602   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.414  -1.335   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       7.424  -2.515   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.864  -2.073   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.198  -2.843   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   27                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    4                                                       
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13   25                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   23                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   16   24                                                  
CONECT   24   23                                                            
CONECT   25   11   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    6                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
5-Hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5,6,7-tetrahydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoic acid	Generator

Chemical Formula

C₂₀H₂₀O₇

Average Mass

372.3730 Da

Monoisotopic Mass

372.12090 Da

IUPAC Name

5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5,6,7-tetrahydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate

Traditional Name

5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate

CAS Registry Number

Not Available

SMILES

CC=CC1=CC2=C(O1)C(=O)C(C)(OC(=O)C1=C(C)C=C(O)C=C1O)C(O)C2

InChI Identifier

InChI=1S/C20H20O7/c1-4-5-13-7-11-8-15(23)20(3,18(24)17(11)26-13)27-19(25)16-10(2)6-12(21)9-14(16)22/h4-7,9,15,21-23H,8H2,1-3H3

InChI Key

JOYCBRUDRSSQCN-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furanoid fatty acids. These are fatty acids containing a 5-alkylfuran-2-alkanoic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Furanoid fatty acids

Alternative Parents

Substituents

P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Furanoid fatty acid
Salicylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Benzofuran
Aryl alkyl ketone
Aryl ketone
Resorcinol
M-cresol
Benzoyl
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Toluene
Phenol
Hydroxy fatty acid
Benzenoid
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Furan
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	3.92	ChemAxon
pKa (Strongest Acidic)	8.69	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	117.2 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	98.35 m³·mol⁻¹	ChemAxon
Polarizability	37.27 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

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

163064033

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate (NP0270783)

MOL for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

3D MOL for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

3D SDF for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

3D-SDF for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

PDB for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

3D PDB for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

SMILES for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

INCHI for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

Structure for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)

3D Structure for NP0270783 (5-hydroxy-6-methyl-7-oxo-2-(prop-1-en-1-yl)-4,5-dihydro-1-benzofuran-6-yl 2,4-dihydroxy-6-methylbenzoate)