NP-MRD: Showing NP-Card for 2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one (NP0225538)

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Record Information

Version

2.0

Created at

2022-09-06 04:17:22 UTC

Updated at

2022-09-06 04:17:22 UTC

NP-MRD ID

NP0225538

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one

Description

Amomol A belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. Based on a literature review a small amount of articles have been published on amomol A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062206172D          

 31 32  0  0  1  0            999 V2000
    0.0657  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7801  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4946  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2091  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9236  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6380  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3525  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0670  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7814  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4959  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2104  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9249  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6393  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3538  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0683  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7827  -11.3689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7827  -12.1939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4972  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2117  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7268  -12.0364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0623  -12.7900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5472  -10.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3677  -10.7015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5392  -11.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2067  -11.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9604  -11.3591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0466  -12.1796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8003  -12.5151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3792  -12.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6255  -12.3289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8248  -11.9209    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  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 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  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 24 30  1  0  0  0  0
 24 31  1  0  0  0  0
 19 31  1  0  0  0  0
M  END


  Mrv1652309062206172D          

 31 32  0  0  1  0            999 V2000
    0.0657  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7801  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4946  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2091  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9236  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6380  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3525  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0670  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7814  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4959  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2104  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9249  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6393  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3538  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0683  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7827  -11.3689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7827  -12.1939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4972  -10.9564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2117  -11.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7268  -12.0364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0623  -12.7900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5472  -10.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3677  -10.7015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5392  -11.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2067  -11.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9604  -11.3591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0466  -12.1796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8003  -12.5151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3792  -12.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6255  -12.3289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8248  -11.9209    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  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 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  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 24 30  1  0  0  0  0
 24 31  1  0  0  0  0
 19 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0225538

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCC[C@@H](O)CC1(CCC2(O1)C=CC(=O)C=C2)OC

> <INCHI_IDENTIFIER>
InChI=1S/C27H46O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-25(29)23-27(30-2)22-21-26(31-27)19-17-24(28)18-20-26/h17-20,25,29H,3-16,21-23H2,1-2H3/t25-,27?/m1/s1

> <INCHI_KEY>
LOBKLUVDTHVJSR-CSMDKSQMSA-N

> <FORMULA>
C27H46O4

> <MOLECULAR_WEIGHT>
434.661

> <EXACT_MASS>
434.339609961

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
54.640263165197446

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(2R)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one

> <JCHEM_LOGP>
7.964829560666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.087171251555556

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7606712945695984

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
129.47629999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2R)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       0.123 -20.452   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.456 -21.222   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.790 -20.452   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.124 -21.222   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.457 -20.452   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.791 -21.222   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.125 -20.452   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.458 -21.222   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.792 -20.452   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.126 -21.222   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.459 -20.452   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.793 -21.222   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.127 -20.452   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.460 -21.222   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.794 -20.452   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      20.128 -21.222   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      20.128 -22.762   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      21.461 -20.452   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      22.795 -21.222   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      21.890 -22.468   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      22.516 -23.875   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      23.422 -19.815   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      24.953 -19.976   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.273 -21.482   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.519 -20.577   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      27.926 -21.204   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      28.087 -22.735   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      29.494 -23.362   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      26.841 -23.640   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      25.434 -23.014   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      23.940 -22.252   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   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   22   31                                             
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   30   31                                             
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   24                                                       
CONECT   31   24   19                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Value	Source
(-)-Amomol a	ChEBI
2XI,12R-2-(2-hydroxyheptadecyl)-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one	ChEBI

Chemical Formula

C₂₇H₄₆O₄

Average Mass

434.6610 Da

Monoisotopic Mass

434.33961 Da

IUPAC Name

2-[(2R)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one

Traditional Name

2-[(2R)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCC[C@@H](O)CC1(CCC2(O1)C=CC(=O)C=C2)OC

InChI Identifier

InChI=1S/C27H46O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-25(29)23-27(30-2)22-21-26(31-27)19-17-24(28)18-20-26/h17-20,25,29H,3-16,21-23H2,1-2H3/t25-,27?/m1/s1

InChI Key

LOBKLUVDTHVJSR-CSMDKSQMSA-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 long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Long-chain fatty alcohols

Alternative Parents

Substituents

Long chain fatty alcohol
Ketal
Tetrahydrofuran
Ketone
Secondary alcohol
Cyclic ketone
Acetal
Organoheterocyclic compound
Oxacycle
Organic oxide
Alcohol
Organooxygen compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

long-chain fatty alcohol (CHEBI:65405 )

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	7.96	ChemAxon
pKa (Strongest Acidic)	15.09	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	129.48 m³·mol⁻¹	ChemAxon
Polarizability	54.64 Å³	ChemAxon
Number of Rings	2	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

Not Available

Chemspider ID

23314587

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44448222

PDB ID

Not Available

ChEBI ID

65404

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one (NP0225538)

MOL for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

3D MOL for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

3D SDF for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

3D-SDF for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

PDB for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

3D PDB for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

SMILES for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

INCHI for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

Structure for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)

3D Structure for NP0225538 (2-[(2r)-2-hydroxyheptadecyl]-2-methoxy-1-oxaspiro[4.5]deca-6,9-dien-8-one)