NP-MRD: Showing NP-Card for (2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate (NP0299146)

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Record Information

Version

2.0

Created at

2022-09-10 10:48:28 UTC

Updated at

2022-09-10 10:48:28 UTC

NP-MRD ID

NP0299146

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate

Description

(2S)-2,3-dihydroxypropyl 9-[(1R)-cyclopent-2-en-1-yl]nonanoate belongs to the class of organic compounds known as 1-monoacylglycerols. These are monoacylglycerols containing a glycerol acylated at the 1-position. Based on a literature review very few articles have been published on (2S)-2,3-dihydroxypropyl 9-[(1R)-cyclopent-2-en-1-yl]nonanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 51  0  0  0  0  0  0  0  0999 V2000
   -3.8320   -1.9169   -1.4338 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0208   -1.1818   -0.7659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5836   -1.4694   -0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8086   -0.2989   -0.1704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9668    0.9137   -0.9925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2712    2.1324   -0.5620 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1845    2.2793   -0.5662 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9778    1.3265    0.2288 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4863    1.7162    0.1864 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2079    0.7019    1.0291 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0972   -0.7111    0.5833 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8012   -1.0151   -0.6890 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0397   -1.4007   -0.4704 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2960   -1.3937    0.9869 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9181   -1.5617    1.5786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5978   -0.1378   -0.0843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9690    0.1118   -0.1065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7815   -1.0082    0.4598 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3803   -1.1807    1.7946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2500   -0.6272    0.4553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4339    0.5660    1.1629 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3591   -2.3863   -0.1692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2293   -1.6456   -1.8084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3292   -0.1147    0.8301 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1949   -0.6343    0.0653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6966    0.6165   -2.0539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0799    1.1252   -1.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6607    2.4545    0.4757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7027    3.0059   -1.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3981    3.3245   -0.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5842    2.2976   -1.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6782    1.2925    1.2611 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0343    0.3158   -0.2578 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6000    2.7355    0.5975 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8043    1.6598   -0.8752 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8294    0.7279    2.0937 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2704    1.0227    1.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0911   -1.1344    0.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3528   -0.9303   -1.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7597   -1.6807   -1.2439 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7101   -0.3889    1.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9880   -2.2078    1.2976 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8290   -1.1671    2.6003 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6074   -2.6234    1.4921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1782    1.0257    0.5110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3296    0.3132   -1.1428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6826   -1.9539   -0.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5923   -0.3433    2.2904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8374   -1.4153    0.9662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6000   -0.4720   -0.5830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5675    1.3361    0.5323 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 18  1  0
 18 19  1  0
 18 17  1  0
 17 16  1  0
 16  2  1  0
  2  1  2  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 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 21 51  1  0
 20 49  1  0
 20 50  1  0
 18 47  1  6
 19 48  1  0
 17 45  1  0
 17 46  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  6
 15 43  1  0
 15 44  1  0
 14 41  1  0
 14 42  1  0
 13 40  1  0
 12 39  1  0
M  END


  Mrv1652309102212482D          

 21 21  0  0  1  0            999 V2000
    6.7553   -1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7553   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0409   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1830   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4685   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7540   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0396   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3251   -0.6271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4286   -0.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9806   -0.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5681    0.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2389    0.1934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4698   -0.6271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1843   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8987   -0.6271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.8987    0.1979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6132   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3277   -0.6271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 15  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0299146

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H](O)COC(=O)CCCCCCCC[C@@H]1CCC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H30O4/c18-13-16(19)14-21-17(20)12-6-4-2-1-3-5-9-15-10-7-8-11-15/h7,10,15-16,18-19H,1-6,8-9,11-14H2/t15-,16-/m0/s1

> <INCHI_KEY>
UZRAFOVPRMUAFS-HOTGVXAUSA-N

> <FORMULA>
C17H30O4

> <MOLECULAR_WEIGHT>
298.423

> <EXACT_MASS>
298.214409446

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
35.89614174161869

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2,3-dihydroxypropyl 9-[(1R)-cyclopent-2-en-1-yl]nonanoate

> <JCHEM_LOGP>
3.2097054216666674

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.561713304317518

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.619245765321082

> <JCHEM_PKA_STRONGEST_BASIC>
-2.968684336972288

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
84.16749999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,3-dihydroxypropyl 9-[(1R)-cyclopent-2-en-1-yl]nonanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  O   UNK     0      12.610  -3.481   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      12.610  -1.941   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.276  -1.171   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.943  -1.941   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.609  -1.171   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.275  -1.941   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.942  -1.171   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.608  -1.941   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.274  -1.171   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.941  -1.941   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.607  -1.171   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.800  -1.797   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.830  -0.652   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.060   0.681   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.446   0.361   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.944  -1.171   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      15.277  -1.941   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.611  -1.171   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      16.611   0.369   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      17.945  -1.941   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      19.278  -1.171   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   16                                                  
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   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   11                                                       
CONECT   16    2   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
(2S)-2,3-Dihydroxypropyl 9-[(1R)-cyclopent-2-en-1-yl]nonanoic acid	Generator

Chemical Formula

C₁₇H₃₀O₄

Average Mass

298.4230 Da

Monoisotopic Mass

298.21441 Da

IUPAC Name

(2S)-2,3-dihydroxypropyl 9-[(1R)-cyclopent-2-en-1-yl]nonanoate

Traditional Name

(2S)-2,3-dihydroxypropyl 9-[(1R)-cyclopent-2-en-1-yl]nonanoate

CAS Registry Number

Not Available

SMILES

OC[C@H](O)COC(=O)CCCCCCCC[C@@H]1CCC=C1

InChI Identifier

InChI=1S/C17H30O4/c18-13-16(19)14-21-17(20)12-6-4-2-1-3-5-9-15-10-7-8-11-15/h7,10,15-16,18-19H,1-6,8-9,11-14H2/t15-,16-/m0/s1

InChI Key

UZRAFOVPRMUAFS-HOTGVXAUSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-monoacylglycerols. These are monoacylglycerols containing a glycerol acylated at the 1-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Monoradylglycerols

Direct Parent

1-monoacylglycerols

Alternative Parents

Substituents

1-acyl-sn-glycerol
Fatty acid ester
Fatty acyl
1,2-diol
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Organic oxide
Organooxygen compound
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	3.21	ChemAxon
pKa (Strongest Acidic)	13.62	ChemAxon
pKa (Strongest Basic)	-3	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	13	ChemAxon
Refractivity	84.17 m³·mol⁻¹	ChemAxon
Polarizability	35.9 Å³	ChemAxon
Number of Rings	1	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

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METLIN ID

Not Available

PubChem Compound

163015407

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate (NP0299146)

MOL for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

3D MOL for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

3D SDF for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

3D-SDF for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

PDB for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

3D PDB for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

SMILES for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

INCHI for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

Structure for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)

3D Structure for NP0299146 ((2s)-2,3-dihydroxypropyl 9-[(1r)-cyclopent-2-en-1-yl]nonanoate)