NP-MRD: Showing NP-Card for 3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one (NP0212758)

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Record Information

Version

2.0

Created at

2022-09-05 11:31:22 UTC

Updated at

2022-09-05 11:31:22 UTC

NP-MRD ID

NP0212758

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one

Description

189508-31-4, Also known as cohibin C, belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain. 3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one is found in Annona muricata. Based on a literature review very few articles have been published on 189508-31-4.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052213312D          

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M  END

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M  END


  Mrv1652309052213312D          

 39 39  0  0  1  0            999 V2000
   11.3308    0.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3308   -0.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6163   -0.7201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6163   -1.5451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9019   -1.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9019   -2.7826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1874   -3.1951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1874   -4.0201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4729   -4.4326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4729   -5.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7585   -5.6701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7585   -6.4951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0440   -6.9076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0440   -7.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7585   -8.1451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4729   -7.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1874   -8.1451    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.1874   -8.9701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9019   -7.7326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.9019   -6.9076    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6163   -8.1451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3308   -7.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0453   -8.1451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7598   -7.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4742   -8.1451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1887   -7.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9032   -8.1451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6176   -7.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3321   -8.1451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0466   -7.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7611   -8.1451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4755   -7.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1900   -8.1451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9437   -7.8095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.4957   -8.4226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3162   -8.3364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0832   -9.1371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2762   -8.9656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6631   -9.5176    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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 33 38  1  0  0  0  0
 38 39  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0212758

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC\C=C/CC[C@@H](O)[C@H](O)CCCCCCCCCCCCC1=CC(C)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H64O4/c1-3-4-5-6-7-8-9-10-11-12-16-19-22-25-28-33(36)34(37)29-26-23-20-17-14-13-15-18-21-24-27-32-30-31(2)39-35(32)38/h19,22,30-31,33-34,36-37H,3-18,20-21,23-29H2,1-2H3/b22-19-/t31?,33-,34-/m1/s1

> <INCHI_KEY>
GFUJWCRMULHYHE-VYTNDSDZSA-N

> <FORMULA>
C35H64O4

> <MOLECULAR_WEIGHT>
548.893

> <EXACT_MASS>
548.480460541

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
72.53147359261135

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(13R,14R,17Z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
11.417688597000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.034716953438394

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.334538472118101

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1442581910954512

> <JCHEM_POLAR_SURFACE_AREA>
66.75999999999999

> <JCHEM_REFRACTIVITY>
167.59990000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
28

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-[(13R,14R,17Z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      21.151   0.966   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.151  -0.574   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.817  -1.344   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.817  -2.884   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.484  -3.654   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.484  -5.194   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.150  -5.964   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.150  -7.504   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.816  -8.274   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.816  -9.814   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.482 -10.584   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.482 -12.124   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.149 -12.894   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.149 -14.434   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.482 -15.204   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.816 -14.434   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.150 -15.204   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      17.150 -16.744   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      18.484 -14.434   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      18.484 -12.894   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      19.817 -15.204   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      21.151 -14.434   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.485 -15.204   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      23.818 -14.434   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      25.152 -15.204   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      26.486 -14.434   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      27.819 -15.204   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      29.153 -14.434   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      30.487 -15.204   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      31.820 -14.434   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      33.154 -15.204   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      34.488 -14.434   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      35.821 -15.204   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      37.228 -14.578   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      38.259 -15.722   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      39.790 -15.561   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      37.489 -17.056   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      35.982 -16.736   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      34.838 -17.766   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                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   33   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   78    0
END

View in JSmol

Synonyms

Value	Source
Cohibin C	MeSH

Chemical Formula

C₃₅H₆₄O₄

Average Mass

548.8930 Da

Monoisotopic Mass

548.48046 Da

IUPAC Name

3-[(13R,14R,17Z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-2,5-dihydrofuran-2-one

Traditional Name

3-[(13R,14R,17Z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC\C=C/CC[C@@H](O)[C@H](O)CCCCCCCCCCCCC1=CC(C)OC1=O

InChI Identifier

InChI=1S/C35H64O4/c1-3-4-5-6-7-8-9-10-11-12-16-19-22-25-28-33(36)34(37)29-26-23-20-17-14-13-15-18-21-24-27-32-30-31(2)39-35(32)38/h19,22,30-31,33-34,36-37H,3-18,20-21,23-29H2,1-2H3/b22-19-/t31?,33-,34-/m1/s1

InChI Key

GFUJWCRMULHYHE-VYTNDSDZSA-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
Annona muricata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Annonaceous acetogenins

Alternative Parents

Substituents

Annonaceae acetogenin skeleton
Long chain fatty alcohol
2-furanone
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
1,2-diol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Alcohol
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic oxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	11.42	ChemAxon
pKa (Strongest Acidic)	13.33	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	28	ChemAxon
Refractivity	167.6 m³·mol⁻¹	ChemAxon
Polarizability	72.53 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00044129

Chemspider ID

4948240

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6444316

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one (NP0212758)

MOL for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

3D MOL for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

3D SDF for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

3D-SDF for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

PDB for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

3D PDB for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

SMILES for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

INCHI for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

Structure for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)

3D Structure for NP0212758 (3-[(13r,14r,17z)-13,14-dihydroxytriacont-17-en-1-yl]-5-methyl-5h-furan-2-one)