NP-MRD: Showing NP-Card for 10-methyloxecan-2-one (NP0322951)

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Record Information

Version

2.0

Created at

2022-09-12 02:03:17 UTC

Updated at

2022-09-12 02:03:17 UTC

NP-MRD ID

NP0322951

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-methyloxecan-2-one

Description

10-Methyloxecan-2-one, also known as phoracantholide I, belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. Thus, 10-methyloxecan-2-one is considered to be a fatty ester lipid molecule. 10-Methyloxecan-2-one is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 30  0  0  0  0  0  0  0  0999 V2000
    2.5251   -1.0178    0.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9316   -0.7916   -0.5817 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4551    0.6130   -0.7115 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9093    1.2124    0.5408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2045    2.1703    0.2002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4095    1.5047   -0.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0274    0.5366    0.5746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2866   -0.8207   -0.0148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1365   -1.7727    0.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2840   -1.8572   -1.0724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8771   -1.9910   -2.1707 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0497   -1.7905   -0.9496 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7244   -1.2210    1.5425 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2246   -1.8789    0.7144 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1211   -0.1466    1.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8256   -0.9028   -1.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7688    0.6632   -1.5811 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3380    1.2469   -1.0202 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6216    0.4775    1.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6967    1.8469    1.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5024    2.6958    1.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2112    2.9096   -0.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1333    2.3417   -0.6242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2223    1.0300   -1.3798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9994    0.9494    0.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4082    0.3958    1.4807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1467   -1.2541    0.5398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6016   -0.7767   -1.0762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5732   -2.8040    0.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5900   -1.5682    1.0651 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12  2  1  0
  1 13  1  0
  1 14  1  0
  1 15  1  0
  2 16  1  6
  3 17  1  0
  3 18  1  0
  4 19  1  0
  4 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  0
  8 28  1  0
  9 29  1  0
  9 30  1  0
M  END

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0       1.659   3.971   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667   2.807   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.180   3.098   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.188   1.934   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.684   0.479   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.171   0.188   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -1.267   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.155  -1.558   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.147  -0.394   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.651   1.061   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.357   2.225   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       2.163   1.352   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
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                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    2                                                       
MASTER        0    0    0    0    0    0    0    0   12    0   24    0
END

View in JSmol

Synonyms

Value	Source
Phoracantholide I	MeSH

Chemical Formula

C₁₀H₁₈O₂

Average Mass

170.2520 Da

Monoisotopic Mass

170.13068 Da

IUPAC Name

10-methyloxecan-2-one

Traditional Name

10-methyloxecan-2-one

CAS Registry Number

Not Available

SMILES

CC1CCCCCCCC(=O)O1

InChI Identifier

InChI=1S/C10H18O2/c1-9-7-5-3-2-4-6-8-10(11)12-9/h9H,2-8H2,1H3

InChI Key

SAMJSVOFANTIOD-UHFFFAOYSA-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 lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Not Available

Direct Parent

Lactones

Alternative Parents

Substituents

Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Lactones (LMFA07040026 )

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	3.08	ALOGPS
logP	2.79	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Basic)	-7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	47.73 m³·mol⁻¹	ChemAxon
Polarizability	19.62 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

566646

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-methyloxecan-2-one (NP0322951)

MOL for NP0322951 (10-methyloxecan-2-one)

3D MOL for NP0322951 (10-methyloxecan-2-one)

3D SDF for NP0322951 (10-methyloxecan-2-one)

3D-SDF for NP0322951 (10-methyloxecan-2-one)

PDB for NP0322951 (10-methyloxecan-2-one)

3D PDB for NP0322951 (10-methyloxecan-2-one)

SMILES for NP0322951 (10-methyloxecan-2-one)

INCHI for NP0322951 (10-methyloxecan-2-one)

Structure for NP0322951 (10-methyloxecan-2-one)

3D Structure for NP0322951 (10-methyloxecan-2-one)