NP-MRD: Showing NP-Card for {8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate (NP0164543)

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Record Information

Version

2.0

Created at

2022-09-02 23:26:34 UTC

Updated at

2022-09-02 23:26:35 UTC

NP-MRD ID

NP0164543

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate

Description

{8-[3-(Butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]Hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. {8-[3-(Butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]Hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231523582D          

 33 34  0  0  0  0            999 V2000
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   -1.3184   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1533004231523582D          

 33 34  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
NP0164543

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)OCC(=C)C1CCC(COC(=O)CCC)=CCCC2=COC(CC(C)=CC1)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C28H40O5/c1-5-8-27(29)32-18-22(4)25-14-12-21(3)16-26-17-24(20-31-26)11-7-10-23(13-15-25)19-33-28(30)9-6-2/h10,12,17,20,25H,4-9,11,13-16,18-19H2,1-3H3

> <INCHI_KEY>
HRDQGQBHRFWIQU-UHFFFAOYSA-N

> <FORMULA>
C28H40O5

> <MOLECULAR_WEIGHT>
456.623

> <EXACT_MASS>
456.287574388

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
52.159625487142605

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate

> <ALOGPS_LOGP>
6.61

> <JCHEM_LOGP>
6.486577669

> <ALOGPS_LOGS>
-5.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.814606383810481

> <JCHEM_POLAR_SURFACE_AREA>
65.74000000000001

> <JCHEM_REFRACTIVITY>
132.8732

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.59e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      -6.311  -6.724   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.771  -6.724   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.461  -5.390   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.691  -6.724   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      -1.691  -4.056   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.151  -4.056   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.619  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.151  -6.724   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.159  -5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.929  -4.056   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.159  -2.723   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.929  -1.389   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.469  -1.389   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.239  -2.723   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.779  -2.723   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.549  -4.056   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.014  -4.532   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.014  -6.072   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.549  -6.724   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.779  -8.057   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.239  -8.057   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.469  -6.724   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.929  -6.724   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.469  -9.391   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.779  -5.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.159  -0.055   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.619  -0.055   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.151   1.278   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.619   2.612   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -1.691   1.278   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.461   2.612   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.001   2.612   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   24                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   26                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23   10                                                       
CONECT   25   22                                                            
CONECT   26   20   17                                                       
CONECT   27   13   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

View in JSmol

Synonyms

Value	Source
{8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoic acid	Generator

Chemical Formula

C₂₈H₄₀O₅

Average Mass

456.6230 Da

Monoisotopic Mass

456.28757 Da

IUPAC Name

{8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate

Traditional Name

{8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate

CAS Registry Number

Not Available

SMILES

CCCC(=O)OCC(=C)C1CCC(COC(=O)CCC)=CCCC2=COC(CC(C)=CC1)=C2

InChI Identifier

InChI=1S/C28H40O5/c1-5-8-27(29)32-18-22(4)25-14-12-21(3)16-26-17-24(20-31-26)11-7-10-23(13-15-25)19-33-28(30)9-6-2/h10,12,17,20,25H,4-9,11,13-16,18-19H2,1-3H3

InChI Key

HRDQGQBHRFWIQU-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 sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Furan
Heteroaromatic compound
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carbonyl group
Organic oxide
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	6.61	ALOGPS
logP	6.49	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	65.74 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	132.87 m³·mol⁻¹	ChemAxon
Polarizability	52.16 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate (NP0164543)

MOL for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

3D MOL for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

3D SDF for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

3D-SDF for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

PDB for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

3D PDB for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

SMILES for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

INCHI for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

Structure for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)

3D Structure for NP0164543 ({8-[3-(butanoyloxy)prop-1-en-2-yl]-11-methyl-14-oxabicyclo[11.2.1]hexadeca-1(15),4,10,13(16)-tetraen-5-yl}methyl butanoate)