NP-MRD: Showing NP-Card for 5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate (NP0171102)

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Record Information

Version

2.0

Created at

2022-09-03 07:28:56 UTC

Updated at

2022-09-03 07:28:56 UTC

NP-MRD ID

NP0171102

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate

Description

5-(Furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]Pentadec-2(6)-en-11-yl 4-hydroxybenzoate belongs to the class of organic compounds known as p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group. 5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate is found in Fallopia multiflora. 5-(Furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]Pentadec-2(6)-en-11-yl 4-hydroxybenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241518032D          

 34 39  0  0  0  0            999 V2000
    1.5999    2.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5672    1.1972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4206    0.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3424    0.3935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8178   -0.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0698   -0.0482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9972    0.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4636    1.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2837    1.7932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651    1.2078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699    0.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5198    0.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6825   -0.7643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0785    0.6516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8980    0.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6739    1.3705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0177    2.1205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6130    2.8394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1717    3.4464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9217    3.1026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8265    2.2831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0223    1.0066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2920    0.2270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2933   -0.3543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0959    1.3732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8439    1.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3857    0.4031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5193    1.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4467    2.3208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1221    2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8701    2.4466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5455    2.9204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9427    1.6249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2673    1.1510    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
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 14 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 17 21  1  0  0  0  0
  8 22  1  0  0  0  0
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  6 23  1  0  0  0  0
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  3 25  1  0  0  0  0
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 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 28 34  1  0  0  0  0
M  END

     RDKit          3D

 60 65  0  0  0  0  0  0  0  0999 V2000
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   -0.1903    1.7123    1.1798 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.4014    0.3532    0.3176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9287    1.2366   -0.5443 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6059    0.0338   -1.6458 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8149    0.8504   -1.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0087   -0.7348   -0.4888 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9687   -1.5372    0.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0359   -1.1360    1.0371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6323   -2.2720    1.5439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9713   -3.3133    1.1101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9632   -2.9113    0.3377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9550    2.2273   -0.0448 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0271    2.7158   -1.0316 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3503    2.0072   -0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2176    0.5720   -0.4898 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5331    0.0723   -0.3226 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0437   -1.0027   -1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3247   -1.5714   -1.8588 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4264   -1.4072   -0.7480 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1974   -0.7496    0.1854 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4958   -1.1267    0.4517 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0872   -2.1824   -0.2043 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3826   -2.5140    0.1006 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3126   -2.8407   -1.1400 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0130   -2.4702   -1.4128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7478    3.2941    0.6220 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9787    0.2668    2.9039 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0171    1.4972    3.1925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2859    0.7898    2.1801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9353   -0.4263    2.2459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8021   -0.5702   -2.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7166    0.2202   -1.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0902    1.5694   -2.0602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6010    1.4674   -0.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2060   -1.3744   -0.9548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3769   -0.1335    1.2368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4930   -2.3217    2.1870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2986   -3.6376   -0.1164 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2317    3.8064   -0.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3956    2.6983   -2.0711 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0717    2.5410   -0.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4416   -3.0015   -2.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
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 12  6  1  0
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  3 39  1  1
  4 40  1  1
  5 41  1  0
  5 42  1  0
M  END


  Mrv1533004241518032D          

 34 39  0  0  0  0            999 V2000
    1.5999    2.0692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5672    1.1972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4206    0.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3424    0.3935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8178   -0.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0698   -0.0482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9972    0.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4636    1.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2837    1.7932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8651    1.2078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699    0.3883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5198    0.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6825   -0.7643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0785    0.6516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8980    0.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6739    1.3705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0177    2.1205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6130    2.8394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1717    3.4464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9217    3.1026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8265    2.2831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0223    1.0066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2920    0.2270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2933   -0.3543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0959    1.3732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8439    1.0252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3857    0.4031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5193    1.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4467    2.3208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1221    2.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8701    2.4466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5455    2.9204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9427    1.6249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2673    1.1510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  2  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
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 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
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 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 28 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171102

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(C2=COC=C2)C2=C(C1=O)C13CCC(OC(=O)C4=CC=C(O)C=C4)C(C)C1C(C2)OC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H26O7/c1-13-19(33-25(30)15-3-5-17(28)6-4-15)7-9-27-22(13)20(34-26(27)31)11-18-21(16-8-10-32-12-16)14(2)24(29)23(18)27/h3-6,8,10,12-14,19-22,28H,7,9,11H2,1-2H3

> <INCHI_KEY>
PEOXODGBZUAOSU-UHFFFAOYSA-N

> <FORMULA>
C27H26O7

> <MOLECULAR_WEIGHT>
462.498

> <EXACT_MASS>
462.167853177

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
47.99210240745186

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate

> <ALOGPS_LOGP>
3.83

> <JCHEM_LOGP>
4.226711638333333

> <ALOGPS_LOGS>
-3.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.858550504539718

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.496687749273383

> <JCHEM_PKA_STRONGEST_BASIC>
-2.87897318472151

> <JCHEM_POLAR_SURFACE_AREA>
103.04

> <JCHEM_REFRACTIVITY>
121.24369999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.81e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       2.986   3.863   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.926   2.235   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.518   1.679   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.373   0.735   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.393  -0.740   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.997  -0.090   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.861   1.444   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.865   3.180   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.396   3.347   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.481   2.255   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.304   0.725   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.704   0.083   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.007  -1.427   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.747   1.216   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.276   1.039   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.991   2.558   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.633   3.958   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.878   5.300   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.921   6.433   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.320   5.792   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.143   4.262   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.042   1.879   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.545   0.424   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.548  -0.661   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       5.779   2.563   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.175   1.914   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.187   0.752   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.436   2.798   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.300   4.332   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.561   5.217   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.957   4.567   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      12.218   5.452   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      11.093   3.033   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.832   2.149   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11   23                                             
CONECT    7    6    2    8                                                  
CONECT    8    7    9   22                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10    6   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10   17                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   17                                                       
CONECT   22    8   23                                                       
CONECT   23   22    6   24                                                  
CONECT   24   23                                                            
CONECT   25    3   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   28                                                       
MASTER        0    0    0    0    0    0    0    0   34    0   78    0
END

View in JSmol

Synonyms

Value	Source
5-(Furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0,.0,]pentadec-2(6)-en-11-yl 4-hydroxybenzoic acid	Generator
5-(Furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoic acid	Generator

Chemical Formula

C₂₇H₂₆O₇

Average Mass

462.4980 Da

Monoisotopic Mass

462.16785 Da

IUPAC Name

5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate

Traditional Name

5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate

CAS Registry Number

Not Available

SMILES

CC1C(C2=COC=C2)C2=C(C1=O)C13CCC(OC(=O)C4=CC=C(O)C=C4)C(C)C1C(C2)OC3=O

InChI Identifier

InChI=1S/C27H26O7/c1-13-19(33-25(30)15-3-5-17(28)6-4-15)7-9-27-22(13)20(34-26(27)31)11-18-21(16-8-10-32-12-16)14(2)24(29)23(18)27/h3-6,8,10,12-14,19-22,28H,7,9,11H2,1-2H3

InChI Key

PEOXODGBZUAOSU-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
Fallopia multiflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as p-hydroxybenzoic acid alkyl esters. These are aromatic compounds containing a benzoic acid, which is esterified with an alkyl group and para-substituted with a hydroxyl group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

p-Hydroxybenzoic acid alkyl esters

Alternative Parents

Substituents

P-hydroxybenzoic acid alkyl ester
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Dicarboxylic acid or derivatives
Gamma butyrolactone
Furan
Heteroaromatic compound
Tetrahydrofuran
Lactone
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	3.83	ALOGPS
logP	4.23	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	8.5	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	103.04 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	121.24 m³·mol⁻¹	ChemAxon
Polarizability	47.99 Å³	ChemAxon
Number of Rings	6	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate (NP0171102)

MOL for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

3D MOL for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

3D SDF for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

3D-SDF for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

PDB for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

3D PDB for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

SMILES for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

INCHI for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

Structure for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)

3D Structure for NP0171102 (5-(furan-3-yl)-4,10-dimethyl-3,14-dioxo-15-oxatetracyclo[6.5.2.0¹,⁹.0²,⁶]pentadec-2(6)-en-11-yl 4-hydroxybenzoate)