NP-MRD: Showing NP-Card for Kumepaloxane (NP0058180)

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Record Information

Version

2.0

Created at

2022-04-28 03:33:06 UTC

Updated at

2022-04-28 03:33:06 UTC

NP-MRD ID

NP0058180

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Kumepaloxane

Description

(2S,5R,6R)-2-[(1S)-1-bromoethyl]-6-[(2E)-3-chloroprop-2-en-1-yl]-2,5-dimethyloxane belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms. Kumepaloxane is found in Haminoea cymbalum. Based on a literature review very few articles have been published on (2S,5R,6R)-2-[(1S)-1-bromoethyl]-6-[(2E)-3-chloroprop-2-en-1-yl]-2,5-dimethyloxane.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 35  0  0  0  0  0  0  0  0999 V2000
    3.1611    1.3341    0.3633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3888    0.7770   -0.7945 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4773    2.1120   -1.8193 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.4382   -0.3416   -0.3555 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3187   -1.4190    0.2560 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7304   -0.8141   -1.5928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4481   -1.6730   -1.2259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3873   -0.9548   -0.2677 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7602   -1.9033    0.8110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7189    0.2926    0.1776 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4866    1.0604    1.2218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8293    1.4737    0.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1874    2.7459    0.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7951    3.1154    0.0679 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.5782    0.0958    0.6402 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4755    1.3065    1.2529 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4197    2.3885    0.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0755    0.7465    0.5343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1282    0.2729   -1.4701 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3505   -1.4052   -0.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4757   -1.1689    1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8642   -2.4194    0.1951 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4254    0.0578   -2.2019 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4452   -1.4675   -2.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0449   -2.6027   -0.7613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9754   -2.0062   -2.1500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2803   -0.6686   -0.8882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7500   -2.3724    0.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8014   -1.4998    1.8180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0545   -2.7845    0.8519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6303    0.9686   -0.7095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6411    0.5051    2.1572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9268    1.9827    1.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5321    0.7105    0.4240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5030    3.5549    0.9643 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  1
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 10 15  1  0
 15  4  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  6
  5 20  1  0
  5 21  1  0
  5 22  1  0
  6 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  6
  9 28  1  0
  9 29  1  0
  9 30  1  0
 10 31  1  6
 11 32  1  0
 11 33  1  0
 12 34  1  0
 13 35  1  0
M  END


  Mrv1652304282205332D          

 15 15  0  0  1  0            999 V2000
    1.4289    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
   -0.0000    0.0000    0.0000 C   0  0  2  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
    0.7145    1.2375    0.0000 C   0  0  1  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
    0.3272    1.9659    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4973    1.9947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7643    2.6656    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.1018    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  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
   -1.4289   -2.4750    0.0000 Cl  0  0  0  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  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  6  0  0  0
  7  8  1  0  0  0  0
  7  9  1  6  0  0  0
  5 10  1  1  0  0  0
  3 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
  2 15  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0058180

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C12H20BrClO/c1-9-6-7-12(3,10(2)13)15-11(9)5-4-8-14/h4,8-11H,5-7H2,1-3H3/b8-4+/t9-,10+,11-,12+/m1/s1

> <INCHI_KEY>
RPUPJNLDKRSQRY-QJBXBYQYSA-N

> <FORMULA>
C12H20BrClO

> <MOLECULAR_WEIGHT>
295.65

> <EXACT_MASS>
294.038606

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
27.79152545477955

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,5R,6R)-2-[(1S)-1-bromoethyl]-6-[(2E)-3-chloroprop-2-en-1-yl]-2,5-dimethyloxane

> <ALOGPS_LOGP>
4.69

> <JCHEM_LOGP>
4.343667887999999

> <ALOGPS_LOGS>
-5.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.197867253821023

> <JCHEM_POLAR_SURFACE_AREA>
9.23

> <JCHEM_REFRACTIVITY>
69.06960000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.48e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5R,6R)-2-[(1S)-1-bromoethyl]-6-[(2E)-3-chloroprop-2-en-1-yl]-2,5-dimethyloxane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.611   3.670   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.928   3.723   0.000  0.00  0.00           C+0
HETATM    9 Br   UNK     0       1.427   4.976   0.000  0.00  0.00          Br+0
HETATM   10  C   UNK     0       2.057   3.670   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   14 Cl   UNK     0      -2.667  -4.620   0.000  0.00  0.00          Cl+0
HETATM   15  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   15                                                  
CONECT    3    2    4   11                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   10                                             
CONECT    6    5    1                                                       
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5                                                            
CONECT   11    3   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15    2                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₂₀BrClO

Average Mass

295.6500 Da

Monoisotopic Mass

294.03861 Da

IUPAC Name

(2S,5R,6R)-2-[(1S)-1-bromoethyl]-6-[(2E)-3-chloroprop-2-en-1-yl]-2,5-dimethyloxane

Traditional Name

(2S,5R,6R)-2-[(1S)-1-bromoethyl]-6-[(2E)-3-chloroprop-2-en-1-yl]-2,5-dimethyloxane

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C12H20BrClO/c1-9-6-7-12(3,10(2)13)15-11(9)5-4-8-14/h4,8-11H,5-7H2,1-3H3/b8-4+/t9-,10+,11-,12+/m1/s1

InChI Key

RPUPJNLDKRSQRY-QJBXBYQYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Haminoea cymbalum	Animalia	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxanes

Sub Class

Not Available

Direct Parent

Oxanes

Alternative Parents

Substituents

Oxane
Dialkyl ether
Ether
Vinyl chloride
Vinyl halide
Haloalkene
Chloroalkene
Oxacycle
Organooxygen compound
Organochloride
Organic oxygen compound
Alkyl halide
Alkyl bromide
Organohalogen compound
Organobromide
Hydrocarbon derivative
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	4.69	ALOGPS
logP	4.34	ChemAxon
logS	-5.8	ALOGPS
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	3	ChemAxon
Refractivity	69.07 m³·mol⁻¹	ChemAxon
Polarizability	27.79 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

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

163093842

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Kumepaloxane (NP0058180)

MOL for NP0058180 (Kumepaloxane)

3D MOL for NP0058180 (Kumepaloxane)

3D SDF for NP0058180 (Kumepaloxane)

3D-SDF for NP0058180 (Kumepaloxane)

PDB for NP0058180 (Kumepaloxane)

3D PDB for NP0058180 (Kumepaloxane)

SMILES for NP0058180 (Kumepaloxane)

INCHI for NP0058180 (Kumepaloxane)

Structure for NP0058180 (Kumepaloxane)

3D Structure for NP0058180 (Kumepaloxane)