NP-MRD: Showing NP-Card for 3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one (NP0328625)

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Record Information

Version

2.0

Created at

2022-09-12 12:15:50 UTC

Updated at

2022-09-12 12:15:50 UTC

NP-MRD ID

NP0328625

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one

Description

3-[5-(1,2,4A,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-hexahydrofuro[3,2-b]furan-2-one belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 3-[5-(1,2,4A,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-hexahydrofuro[3,2-b]furan-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171509042D          

 32 35  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004171509042D          

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M  END
> <DATABASE_ID>
NP0328625

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC2(C)C(CCC=C2C)C1(C)CCC(C)=CCC1(O)C(=O)OC2C(O)COC12O

> <INCHI_IDENTIFIER>
InChI=1S/C26H40O6/c1-16(10-14-25(29)22(28)32-21-19(27)15-31-26(21,25)30)9-12-23(4)18(3)11-13-24(5)17(2)7-6-8-20(23)24/h7,10,18-21,27,29-30H,6,8-9,11-15H2,1-5H3

> <INCHI_KEY>
GUGKETBJPXLNIM-UHFFFAOYSA-N

> <FORMULA>
C26H40O6

> <MOLECULAR_WEIGHT>
448.6

> <EXACT_MASS>
448.282489008

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
49.860127115779434

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[5-(1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-hexahydrofuro[3,2-b]furan-2-one

> <ALOGPS_LOGP>
4.26

> <JCHEM_LOGP>
4.211319325666667

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.324339764036694

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.654850589496059

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5798326828219684

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
122.32069999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.09e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5H-furo[3,2-b]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -6.188   7.367   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.004   8.673   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.281  10.033   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.097  11.339   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.636  11.285   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.913  12.645   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.359   9.926   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.898   9.872   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -11.715  11.178   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -10.992  12.538   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.452  12.591   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.729  13.951   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -8.543   8.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.820   7.758   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.543   7.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -9.877   6.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -9.877   4.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -11.211   4.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -11.211   2.460   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.877   1.690   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -9.251   3.096   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0     -10.782   0.444   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0     -12.322   0.444   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -9.877  -0.802   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -8.412  -0.326   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.948  -0.802   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -6.472  -2.267   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -6.043   0.444   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.948   1.690   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -8.412   1.214   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -8.412   2.754   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -8.543   4.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   11                                             
CONECT    6    5                                                            
CONECT    7    5    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    5   12                                                  
CONECT   12   11                                                            
CONECT   13    7    2   14   15                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   32                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   30                                             
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   20   25   31                                             
CONECT   31   30                                                            
CONECT   32   17                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₄₀O₆

Average Mass

448.6000 Da

Monoisotopic Mass

448.28249 Da

IUPAC Name

3-[5-(1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-hexahydrofuro[3,2-b]furan-2-one

Traditional Name

3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5H-furo[3,2-b]furan-2-one

CAS Registry Number

Not Available

SMILES

CC1CCC2(C)C(CCC=C2C)C1(C)CCC(C)=CCC1(O)C(=O)OC2C(O)COC12O

InChI Identifier

InChI=1S/C26H40O6/c1-16(10-14-25(29)22(28)32-21-19(27)15-31-26(21,25)30)9-12-23(4)18(3)11-13-24(5)17(2)7-6-8-20(23)24/h7,10,18-21,27,29-30H,6,8-9,11-15H2,1-5H3

InChI Key

GUGKETBJPXLNIM-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 diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Isosorbide
Furofuran
Gamma butyrolactone
Monosaccharide
Tetrahydrofuran
Tertiary alcohol
Lactone
Hemiacetal
Carboxylic acid ester
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	4.26	ALOGPS
logP	4.21	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	9.65	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	122.32 m³·mol⁻¹	ChemAxon
Polarizability	49.86 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

85147955

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one (NP0328625)

MOL for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

3D MOL for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

3D SDF for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

3D-SDF for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

PDB for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

3D PDB for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

SMILES for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

INCHI for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

Structure for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)

3D Structure for NP0328625 (3-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl]-3,3a,6-trihydroxy-dihydro-5h-furo[3,2-b]furan-2-one)