NP-MRD: Showing NP-Card for 6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione (NP0301498)

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Record Information

Version

2.0

Created at

2022-09-10 14:29:57 UTC

Updated at

2022-09-10 14:29:57 UTC

NP-MRD ID

NP0301498

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione

Description

6,9-Dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl}oxy)-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. 6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione is found in Lactuca indica. 6,9-Dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl}oxy)-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161508212D          

 37 42  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004161508212D          

 37 42  0  0  0  0            999 V2000
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    3.8305   -1.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6417    1.7897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 15 16  2  0  0  0  0
 13 17  1  0  0  0  0
  6 18  1  0  0  0  0
  4 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 20 31  1  0  0  0  0
 25 31  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 23 34  1  0  0  0  0
 34 35  2  0  0  0  0
 32 36  1  0  0  0  0
 22 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0301498

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(OC1=O)C1C(C)=CC(=O)C1=C(C)CC2OC1CC(C)=C2C(C3OC(=O)C(=C)C13)C(C)=CC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H32O7/c1-11-7-17(31)21-13(3)9-19(25-15(5)29(33)36-27(25)23(11)21)35-20-10-14(4)22-18(32)8-12(2)24(22)28-26(20)16(6)30(34)37-28/h7-8,16,19-20,23-28H,5,9-10H2,1-4,6H3

> <INCHI_KEY>
AULGBYCWKJOWIY-UHFFFAOYSA-N

> <FORMULA>
C30H32O7

> <MOLECULAR_WEIGHT>
504.579

> <EXACT_MASS>
504.21480337

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
53.02500303501286

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-({6,9-dimethyl-3-methylidene-2,7-dioxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl}oxy)-3,6,9-trimethyl-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

> <ALOGPS_LOGP>
3.32

> <JCHEM_LOGP>
3.5461089419999987

> <ALOGPS_LOGS>
-4.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.210109657502855

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.56400907742243

> <JCHEM_PKA_STRONGEST_BASIC>
-4.12462296432306

> <JCHEM_POLAR_SURFACE_AREA>
95.97

> <JCHEM_REFRACTIVITY>
136.8673

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.59e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-({6,9-dimethyl-3-methylidene-2,7-dioxo-3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-4-yl}oxy)-3,6,9-trimethyl-3H,3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       0.649   3.651   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.014   5.147   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.439   5.731   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.711   4.864   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.183   5.317   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.745   6.751   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.975   8.085   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.452   8.314   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.324   7.267   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.827   7.632   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.018   6.322   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.518   6.207   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.200   9.833   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.567  10.543   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.664   9.462   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.183   9.714   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.823  10.522   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.281   6.866   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.482   3.341   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.686   2.381   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.073   3.049   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.461   2.381   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.803   0.879   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.843  -0.325   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.303  -0.325   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.455  -1.610   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.970  -1.200   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.766  -2.161   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.901   0.338   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.616   1.186   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.343   0.879   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.691  -1.610   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.176  -1.200   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.245   0.338   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      10.530   1.186   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       7.150  -3.052   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.665   3.341   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5   19                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10    2   12                                                  
CONECT   12   11                                                            
CONECT   13    8   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14    7   16                                                  
CONECT   16   15                                                            
CONECT   17   13                                                            
CONECT   18    6                                                            
CONECT   19    4   20                                                       
CONECT   20   19   21   31                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   37                                                  
CONECT   23   22   24   34                                                  
CONECT   24   23   25   32                                                  
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   20   25                                                  
CONECT   32   24   33   36                                                  
CONECT   33   32   34                                                       
CONECT   34   33   23   35                                                  
CONECT   35   34                                                            
CONECT   36   32                                                            
CONECT   37   22                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₂O₇

Average Mass

504.5790 Da

Monoisotopic Mass

504.21480 Da

IUPAC Name

4-({6,9-dimethyl-3-methylidene-2,7-dioxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-4-yl}oxy)-3,6,9-trimethyl-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

Traditional Name

4-({6,9-dimethyl-3-methylidene-2,7-dioxo-3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-4-yl}oxy)-3,6,9-trimethyl-3H,3aH,4H,5H,9aH,9bH-azuleno[4,5-b]furan-2,7-dione

CAS Registry Number

Not Available

SMILES

CC1C2C(OC1=O)C1C(C)=CC(=O)C1=C(C)CC2OC1CC(C)=C2C(C3OC(=O)C(=C)C13)C(C)=CC2=O

InChI Identifier

InChI=1S/C30H32O7/c1-11-7-17(31)21-13(3)9-19(25-15(5)29(33)36-27(25)23(11)21)35-20-10-14(4)22-18(32)8-12(2)24(22)28-26(20)16(6)30(34)37-28/h7-8,16,19-20,23-28H,5,9-10H2,1-4,6H3

InChI Key

AULGBYCWKJOWIY-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
Lactuca indica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Gamma butyrolactones

Direct Parent

Gamma butyrolactones

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Gamma butyrolactone
Oxolane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Ketone
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Carbonyl group
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
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	3.32	ALOGPS
logP	3.55	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	14.56	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	95.97 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	136.87 m³·mol⁻¹	ChemAxon
Polarizability	53.03 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	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

85306611

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione (NP0301498)

MOL for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D MOL for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D SDF for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D-SDF for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

PDB for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D PDB for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

SMILES for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

INCHI for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

Structure for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)

3D Structure for NP0301498 (6,9-dimethyl-3-methylidene-4-({3,6,9-trimethyl-2,7-dioxo-3h,3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-4-yl}oxy)-3ah,4h,5h,9ah,9bh-azuleno[4,5-b]furan-2,7-dione)