NP-MRD: Showing NP-Card for [11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate (NP0288186)

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Record Information

Version

2.0

Created at

2022-09-09 17:47:34 UTC

Updated at

2022-09-09 17:47:34 UTC

NP-MRD ID

NP0288186

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate

Description

[11-(Acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]Hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond. Based on a literature review very few articles have been published on [11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]Hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092219472D          

 34 37  0  0  0  0            999 V2000
    6.1362    1.8981    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


  Mrv1652309092219472D          

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M  END
> <DATABASE_ID>
NP0288186

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)OCC1(C)C(CC2COC34CCC(C)(C=C)C=C3C(=O)C(O)=C1C24O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H34O8/c1-7-23(5)8-9-25-17(11-23)19(28)20(29)21-24(6,13-32-22(30)14(2)3)18(34-15(4)27)10-16(12-33-25)26(21,25)31/h7,11,14,16,18,29,31H,1,8-10,12-13H2,2-6H3

> <INCHI_KEY>
NPLMEFDXIMEPNJ-UHFFFAOYSA-N

> <FORMULA>
C26H34O8

> <MOLECULAR_WEIGHT>
474.55

> <EXACT_MASS>
474.225368055

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
49.87774064585773

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0^{1,6}.0^{13,16}]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate

> <JCHEM_LOGP>
2.0826301036666637

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.189504525123997

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.805736777294637

> <JCHEM_PKA_STRONGEST_BASIC>
-3.825697531909225

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000001

> <JCHEM_REFRACTIVITY>
123.96399999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0^{1,6}.0^{13,16}]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      11.454   3.543   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.007   4.070   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.827   3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.007   2.090   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.057   1.746   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.517   1.746   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.747   0.413   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.517  -0.921   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.207   0.413   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.437  -0.921   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.437   1.746   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.897   1.746   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.450   1.220   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.165   0.230   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.985  -0.760   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.252  -2.277   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.700  -2.803   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.073  -3.267   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.340  -4.783   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.374  -2.740   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.127   3.080   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.413   3.080   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.183   1.746   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.413   0.413   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.723   1.746   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.897   4.414   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.437   4.414   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.977   5.450   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.069   4.699   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.747   3.080   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.517   4.414   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.057   4.414   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.207   3.080   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.977   1.746   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   32                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   30                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   33                                                  
CONECT   12   11   13   14   21                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   12   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   27                                                       
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    6   31   33                                             
CONECT   31   30   32                                                       
CONECT   32   31    3                                                       
CONECT   33   30   11   27   34                                             
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Value	Source
[11-(Acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0,.0,]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoic acid	Generator

Chemical Formula

C₂₆H₃₄O₈

Average Mass

474.5500 Da

Monoisotopic Mass

474.22537 Da

IUPAC Name

[11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0^{1,6}.0^{13,16}]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate

Traditional Name

[11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0^{1,6}.0^{13,16}]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)OCC1(C)C(CC2COC34CCC(C)(C=C)C=C3C(=O)C(O)=C1C24O)OC(C)=O

InChI Identifier

InChI=1S/C26H34O8/c1-7-23(5)8-9-25-17(11-23)19(28)20(29)21-24(6,13-32-22(30)14(2)3)18(34-15(4)27)10-16(12-33-25)26(21,25)31/h7,11,14,16,18,29,31H,1,8-10,12-13H2,2-6H3

InChI Key

NPLMEFDXIMEPNJ-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 cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Cyclohexenones

Alternative Parents

Substituents

Cyclohexenone
Dicarboxylic acid or derivatives
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Enol
Dialkyl ether
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.08	ChemAxon
pKa (Strongest Acidic)	8.81	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	123.96 m³·mol⁻¹	ChemAxon
Polarizability	49.88 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162815259

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate (NP0288186)

MOL for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

3D MOL for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

3D SDF for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

3D-SDF for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

PDB for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

3D PDB for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

SMILES for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

INCHI for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

Structure for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)

3D Structure for NP0288186 ([11-(acetyloxy)-4-ethenyl-8,16-dihydroxy-4,10-dimethyl-7-oxo-15-oxatetracyclo[7.6.1.0¹,⁶.0¹³,¹⁶]hexadeca-5,8-dien-10-yl]methyl 2-methylpropanoate)