NP-MRD: Showing NP-Card for (1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane (NP0238227)

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Record Information

Version

2.0

Created at

2022-09-06 21:34:55 UTC

Updated at

2022-09-06 21:34:56 UTC

NP-MRD ID

NP0238227

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane

Description

Chlorofucin belongs to the class of organic compounds known as oxolanes. These are organic compounds containing an oxolane (tetrahydrofuran) ring, which is a saturated aliphatic five-member ring containing one oxygen and five carbon atoms. (1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane was first documented in 2011 (PMID: 21802699). Based on a literature review very few articles have been published on chlorofucin (PMID: 29222867).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    6.7218   -0.4678   -0.4145 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5613   -0.2792   -0.1816 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1666   -0.0759    0.1074 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5447    1.0699   -0.0846 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1272    1.2601    0.2142 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4620    0.0401    0.7526 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2605   -0.9501   -0.2389 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2962   -1.8002    0.2447 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4038   -1.0698    1.4008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0291    0.3542    1.0324 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4940    0.8036   -0.1515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7979    1.0138   -0.3709 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6679    1.4558    0.7417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1010    1.6161    0.2047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3792   -0.2541   -1.0110 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6039    0.2350   -2.4560 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -1.2663   -1.0947   -1.6089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7756   -2.1818   -0.7164 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1946   -2.8122    0.1850 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    7.7382   -0.6375   -0.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6061   -0.9167    0.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1142    1.8992   -0.4801 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5684    1.5687   -0.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0314    2.0615    0.9688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9399   -0.4412    1.5988 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7967   -2.7169    0.6226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4503   -1.2838    1.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1637   -1.3078    2.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0690    1.0459    1.8783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8652    1.7784   -1.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4084    2.4330    1.1724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7718    0.6983    1.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4560    0.5805    0.0209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0685    2.1956   -0.7233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7519    2.0620    0.9923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9809   -0.7971   -0.2863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4582   -0.4407   -1.9947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7011   -1.5890   -2.5154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4041   -3.0552   -1.3157 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  3  0
  8 18  1  0
 18 19  1  0
 18 17  1  0
 17 15  1  0
 15 16  1  0
 15 12  1  0
  6 10  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
 13 31  1  0
 13 32  1  0
 12 30  1  6
 10 29  1  1
  9 27  1  0
  9 28  1  0
  8 26  1  1
  6 25  1  1
  5 23  1  0
  5 24  1  0
  4 22  1  0
  3 21  1  0
  1 20  1  0
 18 39  1  6
 17 37  1  0
 17 38  1  0
 15 36  1  1
M  END


  Mrv1652309062223342D          

 19 20  0  0  1  0            999 V2000
   -3.2680   -0.6920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6360   -0.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0040    0.3686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2287    0.0865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5968    0.6168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1785    0.3346    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1785   -0.4904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7088   -1.1224    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9699   -0.0779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7088    0.9666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5213    1.1098    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2357    0.6973    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8677    1.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7245    2.0401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5179   -0.0779    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3429   -0.0779    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.2357   -0.8531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5213   -1.2656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6645   -2.0781    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
 10  9  1  6  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0238227

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1O[C@H]2C[C@H](O[C@H]2C\C=C\C#C)[C@@H](Cl)C[C@@H]1Br

> <INCHI_IDENTIFIER>
InChI=1S/C15H20BrClO2/c1-3-5-6-7-13-15-9-14(19-13)11(17)8-10(16)12(4-2)18-15/h1,5-6,10-15H,4,7-9H2,2H3/b6-5+/t10-,11-,12+,13-,14-,15-/m0/s1

> <INCHI_KEY>
VRGYZGMXCGNRKB-KZZJSKRPSA-N

> <FORMULA>
C15H20BrClO2

> <MOLECULAR_WEIGHT>
347.68

> <EXACT_MASS>
346.033521

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
33.01369788693734

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,4S,6S,7S,9S)-4-bromo-6-chloro-3-ethyl-9-[(2E)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane

> <JCHEM_LOGP>
3.650811162666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.894239248101129

> <JCHEM_POLAR_SURFACE_AREA>
18.46

> <JCHEM_REFRACTIVITY>
81.4665

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,4S,6S,7S,9S)-4-bromo-6-chloro-3-ethyl-9-[(2E)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane

> <JCHEM_VEBER_RULE>
1

$$$$

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      -6.100  -1.292   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.920  -0.302   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.741   0.688   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.294   0.161   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.114   1.151   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.333   0.625   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.333  -0.915   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.323  -2.095   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.811  -0.145   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.323   1.804   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.840   2.072   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.173   1.302   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.353   2.292   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.086   3.808   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.700  -0.145   0.000  0.00  0.00           C+0
HETATM   16 Br   UNK     0       6.240  -0.145   0.000  0.00  0.00          Br+0
HETATM   17  C   UNK     0       4.173  -1.593   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.840  -2.363   0.000  0.00  0.00           C+0
HETATM   19 Cl   UNK     0       3.107  -3.879   0.000  0.00  0.00          Cl+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9    6   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    8   19                                                  
CONECT   19   18                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   40    0
END

View in JSmol

Synonyms

Value	Source
(3Z)-Chlorofucin	MeSH

Chemical Formula

C₁₅H₂₀BrClO₂

Average Mass

347.6800 Da

Monoisotopic Mass

346.03352 Da

IUPAC Name

(1S,3R,4S,6S,7S,9S)-4-bromo-6-chloro-3-ethyl-9-[(2E)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane

Traditional Name

(1S,3R,4S,6S,7S,9S)-4-bromo-6-chloro-3-ethyl-9-[(2E)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane

CAS Registry Number

Not Available

SMILES

CC[C@H]1O[C@H]2C[C@H](O[C@H]2C\C=C\C#C)[C@@H](Cl)C[C@@H]1Br

InChI Identifier

InChI=1S/C15H20BrClO2/c1-3-5-6-7-13-15-9-14(19-13)11(17)8-10(16)12(4-2)18-15/h1,5-6,10-15H,4,7-9H2,2H3/b6-5+/t10-,11-,12+,13-,14-,15-/m0/s1

InChI Key

VRGYZGMXCGNRKB-KZZJSKRPSA-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 oxolanes. These are organic compounds containing an oxolane (tetrahydrofuran) ring, which is a saturated aliphatic five-member ring containing one oxygen and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxolanes

Sub Class

Not Available

Direct Parent

Oxolanes

Alternative Parents

Substituents

Oxolane
Acetylide
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organobromide
Organohalogen compound
Alkyl halide
Alkyl chloride
Alkyl bromide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	3.65	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	18.46 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	81.47 m³·mol⁻¹	ChemAxon
Polarizability	33.01 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

C00033720

Chemspider ID

109121098

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90475817

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Dias DA, Urban S: Phytochemical studies of the southern Australian marine alga, Laurencia elata. Phytochemistry. 2011 Nov;72(16):2081-9. doi: 10.1016/j.phytochem.2011.06.012. Epub 2011 Jul 28. [PubMed:21802699 ]
Kim B, Sohn TI, Kim D, Paton RS: Asymmetric Total Syntheses and Structure Confirmation of Chlorofucins and Bromofucins. Chemistry. 2018 Feb 21;24(11):2634-2642. doi: 10.1002/chem.201704564. Epub 2018 Jan 25. [PubMed:29222867 ]
LOTUS database [Link]

Showing NP-Card for (1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane (NP0238227)

MOL for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

3D MOL for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

3D SDF for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

3D-SDF for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

PDB for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

3D PDB for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

SMILES for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

INCHI for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

Structure for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)

3D Structure for NP0238227 ((1s,3r,4s,6s,7s,9s)-4-bromo-6-chloro-3-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,8-dioxabicyclo[5.2.1]decane)