NP-MRD: Showing NP-Card for methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate (NP0280927)

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Record Information

Version

2.0

Created at

2022-09-09 06:58:57 UTC

Updated at

2022-09-09 06:58:58 UTC

NP-MRD ID

NP0280927

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate

Description

Plakortide K belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2. methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate was first documented in 2016 (PMID: 26859086). Based on a literature review very few articles have been published on plakortide K.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 48  0  0  0  0  0  0  0  0999 V2000
    4.9820    0.6744   -0.5247 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2098    0.3585   -1.7808 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9384    1.1064   -1.9425 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9130    0.9039   -0.9262 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9569    0.1110    0.1269 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7819    0.0317    1.0878 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4580   -0.2739    2.4339 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2215   -1.5781    2.3622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0733   -1.0895    0.6355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5670   -0.8416    0.6938 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0877   -1.0203   -0.7015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7931   -2.4414   -1.1912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7768    0.4930    1.3003 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1459    0.9373    1.5935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1147    1.0453    0.5206 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1295    0.2881    0.5325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0193    1.9243   -0.5337 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9869    2.0109   -1.5808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9761    1.3978    0.6198 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2288    1.2883    1.0654 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3481    1.3421    0.1162 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1956   -0.2506    0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9385    1.2238   -0.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9079    0.4783   -2.6339 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9392   -0.7367   -1.7267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2089    2.2053   -1.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5897    0.9530   -2.9887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9647    1.4713   -1.0213 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8472   -0.4816    0.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1816    0.5802    2.5667 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7649   -0.3519    3.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2418   -1.3945    2.7618 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7776   -2.3392    3.0723 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2108   -2.0631    1.3864 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2283   -1.4478   -0.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1743   -1.9747    1.2942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0372   -1.6024    1.3453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1459   -0.8680   -0.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5524   -0.3182   -1.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2575   -2.9781   -0.3954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1570   -2.4178   -2.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7151   -2.9906   -1.4616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2845    0.4267    2.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5304    0.2663    2.4211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1270    1.9442    2.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1228    0.9792   -2.0094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6385    2.7419   -2.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9707    2.2767   -1.1377 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  2  0
  6  5  1  6
  6  7  1  0
  7  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 13 19  1  0
 19 20  1  0
 20  6  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  4 28  1  0
  5 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  8 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  1
 11 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  1
 14 44  1  0
 14 45  1  0
 18 46  1  0
 18 47  1  0
 18 48  1  0
M  END


  Mrv1652309092208582D          

 20 20  0  0  1  0            999 V2000
   -0.3121    4.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2182    4.0520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0640    3.2767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4663    2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9626    2.6447    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
    1.4289   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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  2  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
  6 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0280927

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC\C=C\[C@]1(CC)C[C@H](CC)[C@H](CC(=O)OC)OO1

> <INCHI_IDENTIFIER>
InChI=1S/C16H28O4/c1-5-8-9-10-16(7-3)12-13(6-2)14(19-20-16)11-15(17)18-4/h9-10,13-14H,5-8,11-12H2,1-4H3/b10-9+/t13-,14-,16+/m0/s1

> <INCHI_KEY>
RQEKRXRNGTYPJC-HNMZYKETSA-N

> <FORMULA>
C16H28O4

> <MOLECULAR_WEIGHT>
284.396

> <EXACT_MASS>
284.198759382

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
32.705608288837254

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-[(3S,4S,6S)-4,6-diethyl-6-[(1E)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate

> <JCHEM_LOGP>
4.3146034413333325

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.852303001439892

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
78.8013

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(3S,4S,6S)-4,6-diethyl-6-[(1E)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.583   8.743   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.407   7.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.119   6.117   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.870   4.937   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.344   3.490   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.324   3.490   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.797   4.937   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.000   1.540   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    9   20                                             
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   13   20                                                       
CONECT   20   19    6                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₈O₄

Average Mass

284.3960 Da

Monoisotopic Mass

284.19876 Da

IUPAC Name

methyl 2-[(3S,4S,6S)-4,6-diethyl-6-[(1E)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate

Traditional Name

methyl [(3S,4S,6S)-4,6-diethyl-6-[(1E)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate

CAS Registry Number

Not Available

SMILES

CCC\C=C\[C@]1(CC)C[C@H](CC)[C@H](CC(=O)OC)OO1

InChI Identifier

InChI=1S/C16H28O4/c1-5-8-9-10-16(7-3)12-13(6-2)14(19-20-16)11-15(17)18-4/h9-10,13-14H,5-8,11-12H2,1-4H3/b10-9+/t13-,14-,16+/m0/s1

InChI Key

RQEKRXRNGTYPJC-HNMZYKETSA-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 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxanes

Sub Class

1,2-dioxanes

Direct Parent

1,2-dioxanes

Alternative Parents

Substituents

Ortho-dioxane
Methyl ester
Dialkyl peroxide
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	4.31	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	78.8 m³·mol⁻¹	ChemAxon
Polarizability	32.71 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

10469791

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23424765

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Jamison MT, Dalisay DS, Molinski TF: Peroxide Natural Products from Plakortis zyggompha and the Sponge Association Plakortis halichondrioides-Xestospongia deweerdtae: Antifungal Activity against Cryptococcus gattii. J Nat Prod. 2016 Mar 25;79(3):555-63. doi: 10.1021/acs.jnatprod.5b00951. Epub 2016 Feb 9. [PubMed:26859086 ]
LOTUS database [Link]

Showing NP-Card for methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate (NP0280927)

MOL for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

3D MOL for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

3D SDF for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

3D-SDF for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

PDB for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

3D PDB for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

SMILES for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

INCHI for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

Structure for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)

3D Structure for NP0280927 (methyl 2-[(3s,4s,6s)-4,6-diethyl-6-[(1e)-pent-1-en-1-yl]-1,2-dioxan-3-yl]acetate)