NP-MRD: Showing NP-Card for 6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid (NP0227768)

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Record Information

Version

2.0

Created at

2022-09-06 07:12:25 UTC

Updated at

2022-09-06 07:12:25 UTC

NP-MRD ID

NP0227768

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

Description

6-Hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid belongs to the class of organic compounds known as salicylic acid and derivatives. Salicylic acid and derivatives are compounds containing a 2-hydroxybenzoic acid moiety or a derivative thereof. 6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid is found in Lepra amara. 6-Hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241511122D          

 30 32  0  0  0  0            999 V2000
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1854   -2.6145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8499   -3.3682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2926   -3.9700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0294   -3.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2843   -4.0666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7323   -4.6797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9253   -4.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3733   -5.1213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6704   -3.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2224   -3.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9675   -2.3258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5195   -1.7127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0913   -4.2381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3463   -5.0227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942   -5.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    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  2  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
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 18 30  1  0  0  0  0
  6 30  1  0  0  0  0
 14 30  2  0  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
    4.6928    0.7756   -1.2189 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4084    1.4207   -1.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3729    0.5098   -2.1608 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8274   -0.5415   -1.2574 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1446    0.0396   -0.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5174   -0.9610    0.8435 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2656   -1.7043    1.7142 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966   -1.5629    1.9457 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2399   -2.3085    2.8149 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5542   -0.6947    1.3228 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5625   -2.6652    2.4759 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2964   -3.4351    3.3650 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7874   -2.8380    2.3500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4943   -2.0511    1.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8793   -1.1002    0.6775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8802   -0.4068   -0.1751 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1623   -1.1160    0.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2624   -0.8055   -0.3231 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8540   -2.0420    1.1553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1088    1.0068    0.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2468    1.3098    1.6243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4200    2.7398    1.9858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2248    3.5818    1.6052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1763    1.9694   -0.7021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0223    1.6839   -2.1360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0818    2.5844   -3.0106 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7941    0.3032   -2.5252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7334   -0.6344   -1.6091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5140   -1.9567   -2.0100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4949   -2.5919   -2.7918 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5735    1.0936   -1.8516 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9416    1.1233   -0.1837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6449   -0.3399   -1.2346 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9938    2.0673   -0.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6792    2.1224   -2.4809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7882    0.0086   -3.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5260    1.1387   -2.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0533   -1.0916   -1.8841 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5911   -1.2898   -1.0453 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9025    0.5972    0.5443 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3907    0.8036   -0.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5312   -0.9438    1.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8100   -4.1234    3.9148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3090   -3.5936    2.9560 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1430    0.7720    2.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3962    0.9175    2.2260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7052    2.8889    3.0455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3180    3.1302    1.4124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4831    4.5149    1.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5251    2.9962    0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7575    3.8988    2.5714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3580    3.0109   -0.4832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6683    0.0046   -3.5643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4311   -2.6107   -2.2215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5882   -1.9884   -3.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1852   -3.6163   -3.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8 10  1  0
  8  9  2  0
  7 11  1  0
 11 12  1  0
 11 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  1
 17 18  2  0
 17 19  1  0
 16 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 20 24  2  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  1  0
 15  6  1  0
 28 16  1  0
 19 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  2 34  1  0
  2 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
 10 42  1  0
 12 43  1  0
 13 44  1  0
 21 45  1  0
 21 46  1  0
 22 47  1  0
 22 48  1  0
 23 49  1  0
 23 50  1  0
 23 51  1  0
 24 52  1  0
 27 53  1  0
 30 54  1  0
 30 55  1  0
 30 56  1  0
M  END


  Mrv1533004241511122D          

 30 32  0  0  0  0            999 V2000
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1854   -2.6145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8499   -3.3682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2926   -3.9700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0294   -3.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2843   -4.0666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7323   -4.6797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9253   -4.5082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3733   -5.1213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6704   -3.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2224   -3.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9675   -2.3258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5195   -1.7127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0913   -4.2381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3463   -5.0227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7942   -5.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    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  2  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
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 18 30  1  0  0  0  0
  6 30  1  0  0  0  0
 14 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0227768

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC1=C(C(O)=O)C(O)=CC2=C1C1(C(=O)O2)C(CCC)=CC(=O)C=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C23H26O7/c1-4-6-7-9-15-19(21(26)27)16(25)12-17-20(15)23(22(28)30-17)13(8-5-2)10-14(24)11-18(23)29-3/h10-12,25H,4-9H2,1-3H3,(H,26,27)

> <INCHI_KEY>
YKIVLKOVDRIXKW-UHFFFAOYSA-N

> <FORMULA>
C23H26O7

> <MOLECULAR_WEIGHT>
414.454

> <EXACT_MASS>
414.167853177

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.97332393417686

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

> <ALOGPS_LOGP>
4.14

> <JCHEM_LOGP>
5.097203448333334

> <ALOGPS_LOGS>
-4.62

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.158193621485678

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.750532115117683

> <JCHEM_PKA_STRONGEST_BASIC>
-4.817704197901372

> <JCHEM_POLAR_SURFACE_AREA>
110.13000000000001

> <JCHEM_REFRACTIVITY>
112.56839999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.94e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

> <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      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.813  -4.880   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.186  -6.287   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.013  -7.411   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.655  -6.126   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.131  -7.591   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.100  -8.735   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.594  -8.415   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.564  -9.560   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.118  -6.951   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.149  -5.806   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       3.673  -4.342   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.703  -3.197   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.637  -7.911   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.113  -9.376   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.083 -10.520   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   30                                                  
CONECT    7    6    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   30                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   24   30                                             
CONECT   19   18   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   18   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   19   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   18    6   14                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
6-Hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylate	Generator

Chemical Formula

C₂₃H₂₆O₇

Average Mass

414.4540 Da

Monoisotopic Mass

414.16785 Da

IUPAC Name

6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

Traditional Name

6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

CAS Registry Number

Not Available

SMILES

CCCCCC1=C(C(O)=O)C(O)=CC2=C1C1(C(=O)O2)C(CCC)=CC(=O)C=C1OC

InChI Identifier

InChI=1S/C23H26O7/c1-4-6-7-9-15-19(21(26)27)16(25)12-17-20(15)23(22(28)30-17)13(8-5-2)10-14(24)11-18(23)29-3/h10-12,25H,4-9H2,1-3H3,(H,26,27)

InChI Key

YKIVLKOVDRIXKW-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
Lepra amara	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as salicylic acid and derivatives. Salicylic acid and derivatives are compounds containing a 2-hydroxybenzoic acid moiety or a derivative thereof.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Salicylic acid and derivatives

Alternative Parents

Substituents

Salicylic acid or derivatives
Benzofuran
Coumaran
1-hydroxy-2-unsubstituted benzenoid
Dicarboxylic acid or derivatives
Vinylogous ester
Vinylogous acid
Carboxylic acid ester
Ketone
Lactone
Cyclic ketone
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
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	4.14	ALOGPS
logP	5.1	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	2.75	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.13 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	112.57 m³·mol⁻¹	ChemAxon
Polarizability	42.97 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

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 6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid (NP0227768)

MOL for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D MOL for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D SDF for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D-SDF for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

PDB for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D PDB for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

SMILES for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

INCHI for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

Structure for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D Structure for NP0227768 (6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-6'-propylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)