NP-MRD: Showing NP-Card for 6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate (NP0299739)

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Record Information

Version

2.0

Created at

2022-09-10 11:44:26 UTC

Updated at

2022-09-10 11:44:27 UTC

NP-MRD ID

NP0299739

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate

Description

6-(Acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate belongs to the class of organic compounds known as guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative. 6-(Acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191518472D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004191518472D          

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 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  4  0  0  0
 31 34  1  0  0  0  0
 26 35  1  0  0  0  0
  8 35  1  0  0  0  0
 22 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0299739

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1CC(C)(OC(C)=O)C2CC=C(C)C2C2OC(=O)C(C)(OC(=O)C(C)=CC)C12

> <INCHI_IDENTIFIER>
InChI=1S/C27H36O8/c1-9-14(3)23(29)32-19-13-26(7,34-17(6)28)18-12-11-16(5)20(18)22-21(19)27(8,25(31)33-22)35-24(30)15(4)10-2/h9-11,18-22H,12-13H2,1-8H3

> <INCHI_KEY>
MQLRFXKOLJMLHW-UHFFFAOYSA-N

> <FORMULA>
C27H36O8

> <MOLECULAR_WEIGHT>
488.577

> <EXACT_MASS>
488.241018119

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
52.50490969432808

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate

> <ALOGPS_LOGP>
4.53

> <JCHEM_LOGP>
4.6369423403333325

> <ALOGPS_LOGS>
-4.82

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.39253702903411

> <JCHEM_POLAR_SURFACE_AREA>
105.20000000000002

> <JCHEM_REFRACTIVITY>
128.7535

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.42e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3aH,4H,5H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       1.533   8.307   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.737   7.347   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.507   5.824   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.073   5.261   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.711   4.864   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.145   5.426   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.482   3.341   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.686   2.381   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.073   3.049   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.461   2.381   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.001   2.381   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.803   3.882   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.674   4.929   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.203   4.476   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.017   6.431   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.803   0.879   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.245   0.338   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.176  -1.200   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.691  -1.610   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.150  -3.052   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.843  -0.325   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.303  -0.325   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.455  -1.610   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.970  -1.200   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.766  -2.161   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.901   0.338   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.378   0.109   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.514   1.829   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.029   2.238   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.642   3.729   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.068   1.157   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.552   1.567   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.650   0.486   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.320  -0.333   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.343   0.879   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   35                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   16                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   10   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   16   22                                                  
CONECT   22   21   23   35                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28   35                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31                                                            
CONECT   35   26    8   22                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   74    0
END

View in JSmol

Synonyms

Value	Source
6-(Acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-2H,3H,3ah,4H,5H,6H,6ah,7H,9ah,9BH-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₇H₃₆O₈

Average Mass

488.5770 Da

Monoisotopic Mass

488.24102 Da

IUPAC Name

6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-2H,3H,3aH,4H,5H,6H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate

Traditional Name

6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3aH,4H,5H,6aH,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1CC(C)(OC(C)=O)C2CC=C(C)C2C2OC(=O)C(C)(OC(=O)C(C)=CC)C12

InChI Identifier

InChI=1S/C27H36O8/c1-9-14(3)23(29)32-19-13-26(7,34-17(6)28)18-12-11-16(5)20(18)22-21(19)27(8,25(31)33-22)35-24(30)15(4)10-2/h9-11,18-22H,12-13H2,1-8H3

InChI Key

MQLRFXKOLJMLHW-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 guaianolides and derivatives. These are diterpene lactones with a structure characterized by the presence of a gamma-lactone fused to a guaiane, forming 3,6,9-trimethyl-azuleno[4,5-b]furan-2-one or a derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Guaianolides and derivatives

Alternative Parents

Substituents

Guaianolide-skeleton
Guaiane sesquiterpenoid
Sesquiterpenoid
Tetracarboxylic acid or derivatives
Fatty acid ester
Gamma butyrolactone
Fatty acyl
Enoate ester
Tetrahydrofuran
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
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	4.53	ALOGPS
logP	4.64	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-6.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	105.2 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	128.75 m³·mol⁻¹	ChemAxon
Polarizability	52.5 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

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 6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate (NP0299739)

MOL for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

3D MOL for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

3D SDF for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

3D-SDF for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

PDB for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

3D PDB for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

SMILES for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

INCHI for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

Structure for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)

3D Structure for NP0299739 (6-(acetyloxy)-3,6,9-trimethyl-3-[(2-methylbut-2-enoyl)oxy]-2-oxo-3ah,4h,5h,6ah,7h,9ah,9bh-azuleno[4,5-b]furan-4-yl 2-methylbut-2-enoate)