NP-MRD: Showing NP-Card for 2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate (NP0315392)

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Record Information

Version

2.0

Created at

2022-09-11 14:00:04 UTC

Updated at

2022-09-11 14:00:05 UTC

NP-MRD ID

NP0315392

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate

Description

2-{7-Hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]Nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen. 2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate is found in Fusarium proliferatum. Based on a literature review very few articles have been published on 2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]Nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112216002D          

 32 34  0  0  0  0            999 V2000
    0.6776   -4.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921   -4.0553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3921   -3.2303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1065   -4.4678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8210   -4.0553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5355   -4.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5355   -5.2928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  8 32  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309112216002D          

 32 34  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
NP0315392

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(COC(C)=O)C1=C(O)C(=O)C2(C)CC=C(C)CC=CC3(C)CCC(O3)C(C)=CCC12

> <INCHI_IDENTIFIER>
InChI=1S/C27H38O5/c1-17-8-7-13-26(5)14-12-22(32-26)18(2)9-10-21-23(19(3)16-31-20(4)28)24(29)25(30)27(21,6)15-11-17/h7,9,11,13,19,21-22,29H,8,10,12,14-16H2,1-6H3

> <INCHI_KEY>
ZEIXQVUXYJFZIW-UHFFFAOYSA-N

> <FORMULA>
C27H38O5

> <MOLECULAR_WEIGHT>
442.596

> <EXACT_MASS>
442.271924324

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
49.36842985480326

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0^{5,9}]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate

> <JCHEM_LOGP>
4.774305733666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.030079677517003

> <JCHEM_PKA_STRONGEST_BASIC>
-3.778503149054292

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
129.6477

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0^{5,9}]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

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       1.265  -8.340   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.599  -7.570   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.599  -6.030   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.932  -8.340   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.266  -7.570   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.600  -8.340   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.600  -9.880   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.933  -7.570   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.094  -6.038   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.950  -5.008   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       9.601  -5.718   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.227  -4.311   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.371  -7.052   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.276  -5.806   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.877  -7.372   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.907  -6.228   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.414  -6.548   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.444  -5.403   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.890  -8.012   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.859  -9.157   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.335 -10.621   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.305 -11.766   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.742 -12.318   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.305 -13.306   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.840 -13.782   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.768 -12.590   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.798 -11.446   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.261 -12.270   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.231 -13.414   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.786 -10.805   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.816  -9.661   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.340  -8.196   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   32                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   32                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   27                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26   22                                                       
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    8   13                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0,]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetic acid	Generator

Chemical Formula

C₂₇H₃₈O₅

Average Mass

442.5960 Da

Monoisotopic Mass

442.27192 Da

IUPAC Name

2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0^{5,9}]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate

Traditional Name

2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0^{5,9}]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate

CAS Registry Number

Not Available

SMILES

CC(COC(C)=O)C1=C(O)C(=O)C2(C)CC=C(C)CC=CC3(C)CCC(O3)C(C)=CCC12

InChI Identifier

InChI=1S/C27H38O5/c1-17-8-7-13-26(5)14-12-22(32-26)18(2)9-10-21-23(19(3)16-31-20(4)28)24(29)25(30)27(21,6)15-11-17/h7,9,11,13,19,21-22,29H,8,10,12,14-16H2,1-6H3

InChI Key

ZEIXQVUXYJFZIW-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

Species Name	Source	Reference
Fusarium proliferatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydrofurans

Sub Class

Not Available

Direct Parent

Tetrahydrofurans

Alternative Parents

Substituents

Tetrahydrofuran
Ketone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Enol
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	4.77	ChemAxon
pKa (Strongest Acidic)	9.03	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	129.65 m³·mol⁻¹	ChemAxon
Polarizability	49.37 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

78115834

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate (NP0315392)

MOL for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

3D MOL for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

3D SDF for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

3D-SDF for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

PDB for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

3D PDB for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

SMILES for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

INCHI for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

Structure for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)

3D Structure for NP0315392 (2-{7-hydroxy-2,9,12,16-tetramethyl-8-oxo-19-oxatricyclo[14.2.1.0⁵,⁹]nonadeca-2,6,11,14-tetraen-6-yl}propyl acetate)