NP-MRD: Showing NP-Card for 5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate (NP0319091)

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Record Information

Version

2.0

Created at

2022-09-11 19:56:48 UTC

Updated at

2022-09-11 19:56:48 UTC

NP-MRD ID

NP0319091

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate

Description

5-Hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate belongs to the class of organic compounds known as acyloins. These are organic compounds containing an alpha hydroxy ketone. Acyloins are formally derived from reductive coupling of carboxylic acyl groups. 5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate is found in Hygrophorus persoonii and Hygrophorus pustulatus. 5-Hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 57 57  0  0  0  0  0  0  0  0999 V2000
    6.7513   -2.4437   -0.5471 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3999   -1.2955   -1.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1538   -0.0863   -0.5960 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0097   -0.4700    0.3145 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7000    0.6863    1.2534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3072    1.9392    0.5817 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1628    1.9833   -0.3278 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7936    1.6680    0.0996 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4530    0.3228    0.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0101    0.2429    0.9645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9069    0.5289   -0.2000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3844    0.4099    0.2154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2418    0.6953   -0.9455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7499    0.9690   -2.0101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7085    0.6467   -0.8079 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3739    0.9365   -1.9787 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0922    1.6020    0.2795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4458    2.7761    0.1092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9595    0.8667    1.5177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0015   -0.4307    1.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1725   -0.6734   -0.1953 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.5492   -0.8629   -0.4103 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1057   -1.9964   -0.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5686   -2.0872   -1.1455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3601   -2.9331   -1.3109 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8258   -2.9159   -0.2220 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2418   -2.0246    0.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3930   -3.1542   -1.0853 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4705   -1.5968   -2.0148 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1893   -1.1120   -2.2358 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9044    0.8062   -1.1976 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0635    0.1451   -0.0081 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1317   -0.8230   -0.2382 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3584   -1.3039    0.9713 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1083    0.3221    2.0807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7602    0.9165    1.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2420    2.2949    0.0181 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2522    2.7259    1.4000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1139    3.0622   -0.7267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4532    1.4348   -1.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4257    2.4818    0.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1374    1.8469   -0.8226 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5490   -0.3821   -0.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0520   -0.0148    1.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2412    0.8685    1.8501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2129   -0.8057    1.2747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6745   -0.1811   -1.0163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7722    1.5713   -0.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5264    1.0996    1.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5096   -0.6295    0.5849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6024    0.1223   -2.4840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8408    1.3142    2.5143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9278   -1.2238    2.0068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5460   -1.5171   -0.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9894   -3.0339   -0.7612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8454   -2.0377   -2.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0847   -1.2508   -0.6181 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  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  6
 15 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 21 20  1  0
 20 19  2  0
 19 17  1  0
 17 18  2  0
 17 15  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 16 51  1  0
 21 54  1  6
 24 55  1  0
 24 56  1  0
 24 57  1  0
 20 53  1  0
 19 52  1  0
M  END


  Mrv1533004161508402D          

 25 25  0  0  0  0            999 V2000
   -0.2331   -8.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4814   -8.5267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1959   -8.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9104   -8.5267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6248   -8.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3393   -8.5267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0538   -8.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7682   -8.5267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4827   -8.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1972   -8.5267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9117   -8.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6261   -8.5267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3406   -8.1142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3406   -7.2892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0551   -8.5267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5701   -9.1941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3906   -7.7730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9781   -7.0585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3906   -6.3441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2156   -6.3441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9781   -5.6296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2111   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3826   -8.6662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6682   -9.0787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5819   -9.8992    0.0000 O   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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0319091

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCC(=O)C1(O)C(OC(C)=O)C=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O5/c1-3-4-5-6-7-8-9-10-11-12-13-17(22)20(24)18(23)14-15-19(20)25-16(2)21/h14-15,19,24H,3-13H2,1-2H3

> <INCHI_KEY>
NTQWRCCBLDPDFL-UHFFFAOYSA-N

> <FORMULA>
C20H32O5

> <MOLECULAR_WEIGHT>
352.471

> <EXACT_MASS>
352.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
41.149473616154815

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate

> <ALOGPS_LOGP>
4.36

> <JCHEM_LOGP>
5.026680126666667

> <ALOGPS_LOGS>
-5.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.092703896187032

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.917147022014555

> <JCHEM_PKA_STRONGEST_BASIC>
-4.814131651641357

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
96.97839999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.19e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -0.435 -15.146   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.899 -15.916   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.232 -15.146   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.566 -15.916   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.900 -15.146   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.233 -15.916   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.567 -15.146   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.901 -15.916   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.234 -15.146   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.568 -15.916   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.902 -15.146   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.235 -15.916   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.569 -15.146   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      15.569 -13.606   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      16.903 -15.916   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      15.998 -17.162   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      17.529 -14.510   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      16.759 -13.176   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      17.529 -11.842   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      19.069 -11.842   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      16.759 -10.509   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      19.061 -14.671   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.381 -16.177   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      18.047 -16.947   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      17.886 -18.479   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   24                                             
CONECT   16   15                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   15   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Value	Source
5-Hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetic acid	Generator

Chemical Formula

C₂₀H₃₂O₅

Average Mass

352.4710 Da

Monoisotopic Mass

352.22497 Da

IUPAC Name

5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate

Traditional Name

5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCC(=O)C1(O)C(OC(C)=O)C=CC1=O

InChI Identifier

InChI=1S/C20H32O5/c1-3-4-5-6-7-8-9-10-11-12-13-17(22)20(24)18(23)14-15-19(20)25-16(2)21/h14-15,19,24H,3-13H2,1-2H3

InChI Key

NTQWRCCBLDPDFL-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
Hygrophorus persoonii	LOTUS Database	35616633
Hygrophorus pustulatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyloins. These are organic compounds containing an alpha hydroxy ketone. Acyloins are formally derived from reductive coupling of carboxylic acyl groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Acyloins

Alternative Parents

Substituents

Acyloin
Tertiary alcohol
Alpha-hydroxy ketone
Cyclic ketone
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	4.36	ALOGPS
logP	5.03	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	8.92	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	80.67 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	96.98 m³·mol⁻¹	ChemAxon
Polarizability	41.15 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

11360147

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-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate (NP0319091)

MOL for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

3D MOL for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

3D SDF for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

3D-SDF for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

PDB for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

3D PDB for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

SMILES for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

INCHI for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

Structure for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)

3D Structure for NP0319091 (5-hydroxy-4-oxo-5-tridecanoylcyclopent-2-en-1-yl acetate)