NP-MRD: Showing NP-Card for 6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one (NP0322060)

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Record Information

Version

2.0

Created at

2022-09-12 00:37:08 UTC

Updated at

2022-09-12 00:37:08 UTC

NP-MRD ID

NP0322060

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one

Description

6-{5A,9-dimethyl-3-methylidene-2-oxo-dodecahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-dodecahydronaphtho[1,2-b]furan-2-one belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. 6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one is found in Frullania muscicola. 6-{5A,9-dimethyl-3-methylidene-2-oxo-dodecahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-dodecahydronaphtho[1,2-b]furan-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161520442D          

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M  END

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M  END


  Mrv1533004161520442D          

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    5.0758   -1.6293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3140   -0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9440    0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2535   -0.8508    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 18  1  0  0  0  0
  2 18  1  0  0  0  0
  7 18  1  0  0  0  0
  6 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 28 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 35  1  0  0  0  0
 19 35  1  0  0  0  0
 24 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322060

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(O)CCC(C2(C)CCC3C(OC(=O)C3=C)C12)C1(C)CCCC2(C)CCC3C(OC(=O)C3=C)C12

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O5/c1-16-18-8-13-27(3)11-7-12-28(4,23(27)21(18)34-25(16)31)20-10-15-30(6,33)24-22-19(9-14-29(20,24)5)17(2)26(32)35-22/h18-24,33H,1-2,7-15H2,3-6H3

> <INCHI_KEY>
ZSWWFQJBWLZPLZ-UHFFFAOYSA-N

> <FORMULA>
C30H42O5

> <MOLECULAR_WEIGHT>
482.661

> <EXACT_MASS>
482.303224452

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
55.072045233825875

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-{5a,9-dimethyl-3-methylidene-2-oxo-dodecahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-dodecahydronaphtho[1,2-b]furan-2-one

> <ALOGPS_LOGP>
4.77

> <JCHEM_LOGP>
5.449748481666665

> <ALOGPS_LOGS>
-6.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.68872041702923

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9349536895914143

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
132.36560000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.01e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one

> <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       3.179  -8.777   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.451  -7.420   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.241  -8.372   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.914  -6.938   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.229  -5.431   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.081  -4.405   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.618  -4.886   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.932  -3.378   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.470  -3.860   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.993  -4.341   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.308  -5.848   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.160  -6.875   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.781  -8.284   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.313  -8.128   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -3.339  -9.277   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.639  -6.623   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.048  -6.002   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.303  -6.393   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.395  -2.897   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.825  -3.469   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.856  -2.849   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.128  -1.492   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.939  -0.183   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.479  -0.231   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.751   1.126   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.290   1.078   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.829   1.030   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.557  -0.327   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.746  -1.636   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.740  -2.812   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.166  -2.230   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.475  -3.041   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       8.053  -0.694   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.229   0.300   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.207  -1.588   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   18                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   19                                                  
CONECT    7    6    8    9   18                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   11   17                                                  
CONECT   17   16                                                            
CONECT   18   12    2    7                                                  
CONECT   19    6   20   21   35                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   35                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   28   34                                                  
CONECT   34   33                                                            
CONECT   35   29   19   24                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂O₅

Average Mass

482.6610 Da

Monoisotopic Mass

482.30322 Da

IUPAC Name

6-{5a,9-dimethyl-3-methylidene-2-oxo-dodecahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-dodecahydronaphtho[1,2-b]furan-2-one

Traditional Name

6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one

CAS Registry Number

Not Available

SMILES

CC1(O)CCC(C2(C)CCC3C(OC(=O)C3=C)C12)C1(C)CCCC2(C)CCC3C(OC(=O)C3=C)C12

InChI Identifier

InChI=1S/C30H42O5/c1-16-18-8-13-27(3)11-7-12-28(4,23(27)21(18)34-25(16)31)20-10-15-30(6,33)24-22-19(9-14-29(20,24)5)17(2)26(32)35-22/h18-24,33H,1-2,7-15H2,3-6H3

InChI Key

ZSWWFQJBWLZPLZ-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
Frullania muscicola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Eudesmanolide
Naphthofuran
Dicarboxylic acid or derivatives
Gamma butyrolactone
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
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	ALOGPS
logP	5.45	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	14.69	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	132.37 m³·mol⁻¹	ChemAxon
Polarizability	55.07 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

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-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one (NP0322060)

MOL for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

3D MOL for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

3D SDF for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

3D-SDF for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

PDB for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

3D PDB for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

SMILES for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

INCHI for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

Structure for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)

3D Structure for NP0322060 (6-{5a,9-dimethyl-3-methylidene-2-oxo-octahydronaphtho[1,2-b]furan-9-yl}-9-hydroxy-5a,9-dimethyl-3-methylidene-octahydronaphtho[1,2-b]furan-2-one)