NP-MRD: Showing NP-Card for (1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane (NP0145639)

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Record Information

Version

2.0

Created at

2022-09-02 00:53:00 UTC

Updated at

2022-09-02 00:53:00 UTC

NP-MRD ID

NP0145639

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane

Description

Laureatin belongs to the class of organic compounds known as oxetanes. Oxetanes are compounds containing an oxetane ring, which is a four-member saturated aliphatic ring with an oxygen, and three carbon atoms. (1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane is found in Laurencia nipponica. (1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane was first documented in 2007 (PMID: 17279755). Based on a literature review a small amount of articles have been published on Laureatin (PMID: 19733868) (PMID: 22913294).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    3.0638    3.5398   -0.7079 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5953    2.4556   -0.5127 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2351    1.1888   -0.2979 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4820    0.1160   -0.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9994    0.2562   -0.5927 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2749   -0.3015    0.5811 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0807    0.3047    0.9098 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0869    0.1009    0.3320 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8927    1.3353    0.8253 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8352    2.8579    0.2031 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.2277    1.4434    0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2300    1.4235   -1.2948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9547   -1.0651    0.7401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4913   -2.4110    0.1154 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2962   -2.4770   -1.6383 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.0875   -2.1783    0.0474 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1299   -2.8511    0.0112 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4852   -1.7047    0.9314 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1996   -2.0276    1.4368 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5965    4.4748   -0.8797 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3155    1.1194   -0.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9085   -0.8618   -0.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8543   -0.1475   -1.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7333    1.3450   -0.6454 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8830    0.2172    1.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1439    0.2785   -0.7863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9517    1.3711    1.9091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0319    0.8157    0.6557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5796    2.4961    0.4684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4821    0.4056   -1.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0162    2.0969   -1.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2743    1.7796   -1.6769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7681   -1.2136    1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0114   -0.9278    0.6072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8313   -3.2286    0.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0454   -1.3315   -0.6390 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2148   -3.7902    0.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7816   -2.8939   -0.8984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3138   -2.0107    1.5911 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11  9  1  0
  9 10  1  0
  9  8  1  0
  8 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  3  0
  6  7  1  0
  7  8  1  0
 19 16  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 11 28  1  0
 11 29  1  0
  9 27  1  1
  8 26  1  6
 13 33  1  0
 13 34  1  0
 14 35  1  1
 16 36  1  6
 17 37  1  0
 17 38  1  0
 18 39  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
M  END


  Mrv1652309022202532D          

 19 20  0  0  1  0            999 V2000
    2.8075    3.6448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0930    3.2323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3785    2.8198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3785    1.9948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0930    1.5823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0930    0.7573    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8552    0.4416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1709   -0.3206    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9959   -0.3206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4084    0.3939    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.4084   -1.0351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2334   -1.0351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8552   -1.0828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0930   -1.3985    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0930   -2.2235    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.3308   -1.0828    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0151   -0.3206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3308    0.4416    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5214   -0.3206    0.0000 O   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
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  1  6  0  0  0
 16 19  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0145639

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](Br)[C@@H]1C[C@@H](Br)[C@@H]2C[C@H](O2)[C@@H](C\C=C/C#C)O1

> <INCHI_IDENTIFIER>
InChI=1S/C15H20Br2O2/c1-3-5-6-7-12-15-9-14(19-15)11(17)8-13(18-12)10(16)4-2/h1,5-6,10-15H,4,7-9H2,2H3/b6-5-/t10-,11+,12+,13-,14-,15-/m0/s1

> <INCHI_KEY>
QVSXXUNREJZJAN-LIEINVJGSA-N

> <FORMULA>
C15H20Br2O2

> <MOLECULAR_WEIGHT>
392.131

> <EXACT_MASS>
389.983006

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
33.419053797071385

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,4S,6R,7S)-6-bromo-4-[(1S)-1-bromopropyl]-2-[(2Z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane

> <ALOGPS_LOGP>
4.45

> <JCHEM_LOGP>
3.8363064253333334

> <ALOGPS_LOGS>
-4.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.893176144313253

> <JCHEM_POLAR_SURFACE_AREA>
18.46

> <JCHEM_REFRACTIVITY>
84.44999999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.77e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4S,6R,7S)-6-bromo-4-[(1S)-1-bromopropyl]-2-[(2Z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       5.241   6.804   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.907   6.034   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.573   5.264   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.573   3.724   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.907   2.954   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.907   1.414   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.330   0.824   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.919  -0.598   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.459  -0.598   0.000  0.00  0.00           C+0
HETATM   10 Br   UNK     0       8.229   0.735   0.000  0.00  0.00          Br+0
HETATM   11  C   UNK     0       8.229  -1.932   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.769  -1.932   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.330  -2.021   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.907  -2.611   0.000  0.00  0.00           C+0
HETATM   15 Br   UNK     0       3.907  -4.151   0.000  0.00  0.00          Br+0
HETATM   16  C   UNK     0       2.484  -2.021   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.895  -0.598   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.484   0.824   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.840  -0.598   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   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17    6   19                                                  
CONECT   19   18   16                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   40    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀Br₂O₂

Average Mass

392.1310 Da

Monoisotopic Mass

389.98301 Da

IUPAC Name

(1S,2R,4S,6R,7S)-6-bromo-4-[(1S)-1-bromopropyl]-2-[(2Z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane

Traditional Name

(1S,2R,4S,6R,7S)-6-bromo-4-[(1S)-1-bromopropyl]-2-[(2Z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane

CAS Registry Number

Not Available

SMILES

CC[C@H](Br)[C@@H]1C[C@@H](Br)[C@@H]2C[C@H](O2)[C@@H](C\C=C/C#C)O1

InChI Identifier

InChI=1S/C15H20Br2O2/c1-3-5-6-7-12-15-9-14(19-15)11(17)8-13(18-12)10(16)4-2/h1,5-6,10-15H,4,7-9H2,2H3/b6-5-/t10-,11+,12+,13-,14-,15-/m0/s1

InChI Key

QVSXXUNREJZJAN-LIEINVJGSA-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
Laurencia nipponica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxetanes. Oxetanes are compounds containing an oxetane ring, which is a four-member saturated aliphatic ring with an oxygen, and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxetanes

Sub Class

Not Available

Direct Parent

Oxetanes

Alternative Parents

Substituents

Oxetane
Acetylide
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organobromide
Organohalogen compound
Alkyl halide
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	4.45	ALOGPS
logP	3.84	ChemAxon
logS	-4.8	ALOGPS
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	4	ChemAxon
Refractivity	84.45 m³·mol⁻¹	ChemAxon
Polarizability	33.42 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

C00000460

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101266075

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Suzuki M, Takahashi Y, Nakano S, Abe T, Masuda M, Ohnishi T, Noya Y, Seki K: An experimental approach to study the biosynthesis of brominated metabolites by the red algal genus Laurencia. Phytochemistry. 2009 Jul-Aug;70(11-12):1410-5. doi: 10.1016/j.phytochem.2009.07.038. Epub 2009 Sep 4. [PubMed:19733868 ]
Keshipeddy S, Martinez I, Castillo BF 2nd, Morton MD, Howell AR: Toward a formal synthesis of laureatin: unexpected rearrangements involving cyclic ether nucleophiles. J Org Chem. 2012 Sep 21;77(18):7883-90. doi: 10.1021/jo301048z. Epub 2012 Sep 5. [PubMed:22913294 ]
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LOTUS database [Link]

Showing NP-Card for (1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane (NP0145639)

MOL for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

3D MOL for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

3D SDF for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

3D-SDF for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

PDB for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

3D PDB for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

SMILES for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

INCHI for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

Structure for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)

3D Structure for NP0145639 ((1s,2r,4s,6r,7s)-6-bromo-4-[(1s)-1-bromopropyl]-2-[(2z)-pent-2-en-4-yn-1-yl]-3,8-dioxabicyclo[5.1.1]nonane)