NP-MRD: Showing NP-Card for (2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine (NP0311013)

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Record Information

Version

2.0

Created at

2022-09-11 06:43:17 UTC

Updated at

2022-09-11 06:43:18 UTC

NP-MRD ID

NP0311013

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine

Description

(2R,3S,10S)-3-bromo-10-[(1Z)-but-1-en-3-yn-1-yl]-2-ethyl-3,4,7,10-tetrahydro-2H-oxecine belongs to the class of organic compounds known as oxocins. Oxocins are compounds containing an oxocin ring, which is a eight-member unsaturated aromatic ring containing one oxygen atom and seven carbon atoms. (2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine is found in Laurencia tenera. Based on a literature review very few articles have been published on (2R,3S,10S)-3-bromo-10-[(1Z)-but-1-en-3-yn-1-yl]-2-ethyl-3,4,7,10-tetrahydro-2H-oxecine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 36  0  0  0  0  0  0  0  0999 V2000
    2.2042   -1.3943    2.4402 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4527   -1.6600    1.2960 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7751   -1.9708   -0.0755 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2418   -1.3432   -1.0882 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2397   -0.2383   -0.8548 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0293    1.0051   -0.8163 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4415    2.1589   -0.9738 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0068    2.2542   -1.1908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7391    3.1119   -0.2397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0893    2.6430    0.9387 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7941    1.3000    1.4078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6015    0.1864    0.7840 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8462   -0.4940    2.1333 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.6314   -0.9216    0.4195 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1294   -1.8025   -0.6753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5759   -2.2221   -0.4871 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6629   -0.4979    0.3438 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9848   -1.1738    3.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4985   -2.7690   -0.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5083   -1.6011   -2.0954 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5704   -0.3142   -1.7272 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0889    0.9646   -0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0197    3.0832   -0.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0901    2.7954   -2.1976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5196    1.3184   -1.3859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0062    4.1639   -0.5207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6444    3.3662    1.5708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0248    1.2905    2.5284 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2962    1.0529    1.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2490    0.5074   -0.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6344   -1.5943    1.3456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5510   -2.7467   -0.7553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0982   -1.3436   -1.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7205   -2.7772    0.4640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2794   -1.3870   -0.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7961   -2.9506   -1.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 14  1  0
 14 17  1  0
 17  5  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  3  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 16 34  1  0
 16 35  1  0
 16 36  1  0
 15 32  1  0
 15 33  1  0
 14 31  1  1
  5 21  1  6
  4 20  1  0
  3 19  1  0
  1 18  1  0
  6 22  1  0
  7 23  1  0
  8 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  6
M  END


  Mrv1652309112208432D          

 17 17  0  0  1  0            999 V2000
   -0.7508    1.7854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1563    2.3574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4381    2.9295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2308    2.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.8998    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2216    1.6710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4197    0.8701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8253    0.2981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0234   -0.5028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.0748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6363   -0.8460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4381   -0.0451    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3545    0.1837    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.0326    0.5269    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2400    0.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0418    1.5566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8345    1.3278    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
  5 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0311013

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C15H19BrO/c1-3-5-10-13-11-8-6-7-9-12-14(16)15(4-2)17-13/h1,5,7-11,13-15H,4,6,12H2,2H3/b9-7-,10-5-,11-8-/t13-,14+,15-/m1/s1

> <INCHI_KEY>
KQEYHIDELOKBAL-QMRJKOCLSA-N

> <FORMULA>
C15H19BrO

> <MOLECULAR_WEIGHT>
295.22

> <EXACT_MASS>
294.061928

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
28.373333681192854

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3S,10S)-3-bromo-10-[(1Z)-but-1-en-3-yn-1-yl]-2-ethyl-3,4,7,10-tetrahydro-2H-oxecine

> <JCHEM_LOGP>
4.404601093999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.229431484898411

> <JCHEM_POLAR_SURFACE_AREA>
9.23

> <JCHEM_REFRACTIVITY>
79.54549999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,10S)-3-bromo-10-[(1Z)-but-1-en-3-yn-1-yl]-2-ethyl-3,4,7,10-tetrahydro-2H-oxecine

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.401   3.333   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.292   4.401   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.818   5.468   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.297   5.041   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   3.546   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.147   3.119   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.517   1.624   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.407   0.556   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.777  -0.938   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -2.006   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.188  -1.579   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.818  -0.084   0.000  0.00  0.00           C+0
HETATM   13 Br   UNK     0      -0.662   0.343   0.000  0.00  0.00          Br+0
HETATM   14  C   UNK     0       1.928   0.984   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.448   1.411   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.078   2.906   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.558   2.478   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   17                                                  
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   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14    5                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₉BrO

Average Mass

295.2200 Da

Monoisotopic Mass

294.06193 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C15H19BrO/c1-3-5-10-13-11-8-6-7-9-12-14(16)15(4-2)17-13/h1,5,7-11,13-15H,4,6,12H2,2H3/b9-7-,10-5-,11-8-/t13-,14+,15-/m1/s1

InChI Key

KQEYHIDELOKBAL-QMRJKOCLSA-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 tenera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxocins. Oxocins are compounds containing an oxocin ring, which is a eight-member unsaturated aromatic ring containing one oxygen atom and seven carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxocins

Sub Class

Not Available

Direct Parent

Oxocins

Alternative Parents

Substituents

Oxocin
Acetylide
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organobromide
Organohalogen compound
Alkyl halide
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

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

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

162872642

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine (NP0311013)

MOL for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

3D MOL for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

3D SDF for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

3D-SDF for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

PDB for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

3D PDB for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

SMILES for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

INCHI for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

Structure for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)

3D Structure for NP0311013 ((2s,3z,6z,9s,10r)-9-bromo-2-[(1z)-but-1-en-3-yn-1-yl]-10-ethyl-5,8,9,10-tetrahydro-2h-oxecine)