NP-MRD: Showing NP-Card for (2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane (NP0226542)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 05:37:07 UTC

Updated at

2022-09-06 05:37:08 UTC

NP-MRD ID

NP0226542

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane

Description

Bisezakyne A belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen. Based on a literature review very few articles have been published on Bisezakyne A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 38  0  0  0  0  0  0  0  0999 V2000
    3.9155    3.1325    1.9920 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7281    2.1488    1.3129 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4880    0.9904    0.4914 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7563   -0.1893    1.0142 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5291   -1.4266    0.2144 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0099   -1.1218   -1.1131 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8436   -1.5639   -1.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9203   -2.4153   -0.7790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4040   -1.8140   -0.5149 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3563   -0.5575    0.1417 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7116   -0.2665    0.2946 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0289    1.1698    0.4957 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5987    2.3012   -0.9984 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.5461    1.2672    0.7008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9300    2.7237    0.9912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4411   -0.7996   -0.9172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2536   -1.4425   -1.6933 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6021   -0.1379   -2.6894 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    4.0743    4.0084    2.5759 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0981    1.0831   -0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1399   -0.3017    2.0132 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9374   -2.0986    0.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5536   -1.9108    0.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5610   -0.4989   -1.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5317   -1.2981   -2.5983 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3281   -2.8094    0.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7418   -3.3571   -1.3971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0436   -2.5115    0.1008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0666   -0.8139    1.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5287    1.6021    1.3870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0821    1.0072   -0.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8400    0.6256    1.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0304    3.2717    0.0333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8689    2.7445    1.5768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1262    3.1930    1.6078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1287   -1.6188   -0.6519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9078   -0.0350   -1.5343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6612   -2.2807   -2.2535 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 12  1  0
 12 13  1  0
 12 11  1  0
 11 16  1  0
 16 17  1  0
 17 18  1  0
 17  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  3  0
  9 10  1  0
 10 11  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 14 31  1  0
 14 32  1  0
 12 30  1  1
 11 29  1  1
 16 36  1  0
 16 37  1  0
 17 38  1  6
  9 28  1  1
  8 26  1  0
  8 27  1  0
  7 25  1  0
  6 24  1  0
  5 22  1  0
  5 23  1  0
  4 21  1  0
  3 20  1  0
  1 19  1  0
M  END


  Mrv1652309062207372D          

 18 18  0  0  1  0            999 V2000
    1.2822    6.4768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2857   -0.7365    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.1296   -1.5764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6145   -2.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8843    0.8843    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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0226542

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C15H20BrClO/c1-3-5-6-7-8-9-10-14-13(17)11-15(18-14)12(16)4-2/h1,5-6,8-9,12-15H,4,7,10-11H2,2H3/b6-5+,9-8-/t12-,13+,14+,15+/m0/s1

> <INCHI_KEY>
CUPRGZVKNKNTTN-LDISCDDKSA-N

> <FORMULA>
C15H20BrClO

> <MOLECULAR_WEIGHT>
331.68

> <EXACT_MASS>
330.038606

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
31.929947592841337

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R,5R)-5-[(1S)-1-bromopropyl]-3-chloro-2-[(2Z,5E)-octa-2,5-dien-7-yn-1-yl]oxolane

> <JCHEM_LOGP>
4.661602073666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.186955236807781

> <JCHEM_POLAR_SURFACE_AREA>
9.23

> <JCHEM_REFRACTIVITY>
83.10580000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,5R)-5-[(1S)-1-bromopropyl]-3-chloro-2-[(2Z,5E)-octa-2,5-dien-7-yn-1-yl]oxolane

> <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       2.393  12.090   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.393  10.550   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.393   9.010   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.060   8.240   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.060   6.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.274   5.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.274   4.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.306   1.175   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.735  -1.536   0.000  0.00  0.00           C+0
HETATM   13 Br   UNK     0       4.267  -1.375   0.000  0.00  0.00          Br+0
HETATM   14  C   UNK     0       2.109  -2.943   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.014  -4.188   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   18 Cl   UNK     0      -1.651   1.651   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                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16   11   17                                                       
CONECT   17   16    9   18                                                  
CONECT   18   17                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀BrClO

Average Mass

331.6800 Da

Monoisotopic Mass

330.03861 Da

IUPAC Name

(2R,3R,5R)-5-[(1S)-1-bromopropyl]-3-chloro-2-[(2Z,5E)-octa-2,5-dien-7-yn-1-yl]oxolane

Traditional Name

(2R,3R,5R)-5-[(1S)-1-bromopropyl]-3-chloro-2-[(2Z,5E)-octa-2,5-dien-7-yn-1-yl]oxolane

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C15H20BrClO/c1-3-5-6-7-8-9-10-14-13(17)11-15(18-14)12(16)4-2/h1,5-6,8-9,12-15H,4,7,10-11H2,2H3/b6-5+,9-8-/t12-,13+,14+,15+/m0/s1

InChI Key

CUPRGZVKNKNTTN-LDISCDDKSA-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 tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydrofurans

Sub Class

Not Available

Direct Parent

Tetrahydrofurans

Alternative Parents

Substituents

Tetrahydrofuran
Acetylide
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organobromide
Organohalogen compound
Alkyl halide
Alkyl chloride
Alkyl bromide
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	4.66	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	9.23 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	83.11 m³·mol⁻¹	ChemAxon
Polarizability	31.93 Å³	ChemAxon
Number of Rings	1	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

C00038606

Chemspider ID

29212860

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

132516924

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane (NP0226542)

MOL for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

3D MOL for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

3D SDF for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

3D-SDF for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

PDB for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

3D PDB for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

SMILES for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

INCHI for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

Structure for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)

3D Structure for NP0226542 ((2r,3r,5r)-5-[(1s)-1-bromopropyl]-3-chloro-2-[(2z,5e)-octa-2,5-dien-7-yn-1-yl]oxolane)