NP-MRD: Showing NP-Card for (6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione (NP0193769)

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Record Information

Version

2.0

Created at

2022-09-04 11:18:39 UTC

Updated at

2022-09-04 11:18:39 UTC

NP-MRD ID

NP0193769

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione

Description

(6AR)-3-[(4R)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2R)-2-methyloctanoyl]-6H,6aH,8H-furo[2,3-h]isochromene-6,8-dione belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain. (6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione is found in Jackrogersella cohaerens. Based on a literature review very few articles have been published on (6aR)-3-[(4R)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2R)-2-methyloctanoyl]-6H,6aH,8H-furo[2,3-h]isochromene-6,8-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042213182D          

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M  END

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  Mrv1652309042213182D          

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 26 27  1  0  0  0  0
 13 27  1  0  0  0  0
 27 28  2  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
 12 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 11 34  1  0  0  0  0
 34 35  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0193769

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC[C@@H](C)C(=O)C1=C2C3=COC(=CC3=CC(=O)[C@]2(C)OC1=O)C1=C(C)C[C@@H](O)CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H32O7/c1-5-6-7-8-9-15(2)26(32)24-25-19-14-34-21(23-16(3)10-18(29)13-20(23)30)11-17(19)12-22(31)28(25,4)35-27(24)33/h11-12,14-15,18,29H,5-10,13H2,1-4H3/t15-,18-,28+/m1/s1

> <INCHI_KEY>
LFNOEQKIIMCRRH-YGOAZIPFSA-N

> <FORMULA>
C28H32O7

> <MOLECULAR_WEIGHT>
480.557

> <EXACT_MASS>
480.21480337

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
51.808835059868024

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6aR)-3-[(4R)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2R)-2-methyloctanoyl]-6H,6aH,8H-furo[2,3-h]isochromene-6,8-dione

> <JCHEM_LOGP>
3.941226779999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.591221195089183

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.994152574129231

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7963155586551736

> <JCHEM_POLAR_SURFACE_AREA>
106.97

> <JCHEM_REFRACTIVITY>
133.15119999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(6aR)-3-[(4R)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2R)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.261  -6.263   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.928  -5.493   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.594  -6.263   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.260  -5.493   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.926  -6.263   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.593  -5.493   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.259  -6.263   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.259  -7.803   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.925  -5.493   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.925  -3.953   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.408  -6.263   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.815  -5.637   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.291  -4.172   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.261  -3.028   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.736  -1.563   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.243  -1.243   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.719   0.222   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.688   1.366   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.182   1.046   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.164   2.831   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.670   3.151   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.146   4.616   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.701   2.007   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.225   0.542   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.255  -0.602   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.273  -2.387   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.797  -3.852   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.828  -4.996   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.352  -6.461   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.382  -7.605   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.846  -6.781   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.751  -8.027   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       2.076  -8.115   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       0.569  -7.795   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -0.575  -8.825   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   34                                                  
CONECT   12   11   13   31                                                  
CONECT   13   12   14   27                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16   18   24                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   17   25                                                  
CONECT   25   24                                                            
CONECT   26   16   27                                                       
CONECT   27   26   13   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   12   32   33                                             
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   11   35                                                  
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₂O₇

Average Mass

480.5570 Da

Monoisotopic Mass

480.21480 Da

IUPAC Name

(6aR)-3-[(4R)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2R)-2-methyloctanoyl]-6H,6aH,8H-furo[2,3-h]isochromene-6,8-dione

Traditional Name

(6aR)-3-[(4R)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2R)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione

CAS Registry Number

Not Available

SMILES

CCCCCC[C@@H](C)C(=O)C1=C2C3=COC(=CC3=CC(=O)[C@]2(C)OC1=O)C1=C(C)C[C@@H](O)CC1=O

InChI Identifier

InChI=1S/C28H32O7/c1-5-6-7-8-9-15(2)26(32)24-25-19-14-34-21(23-16(3)10-18(29)13-20(23)30)11-17(19)12-22(31)28(25,4)35-27(24)33/h11-12,14-15,18,29H,5-10,13H2,1-4H3/t15-,18-,28+/m1/s1

InChI Key

LFNOEQKIIMCRRH-YGOAZIPFSA-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
Jackrogersella cohaerens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Annonaceous acetogenins

Alternative Parents

Substituents

Annonaceae acetogenin skeleton
Cyclohexenone
Alpha-acyloxy ketone
2-furanone
Pyran
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Ketone
Lactone
Secondary alcohol
Cyclic ketone
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Organooxygen compound
Organic oxide
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	3.94	ChemAxon
pKa (Strongest Acidic)	14.99	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	106.97 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	133.15 m³·mol⁻¹	ChemAxon
Polarizability	51.81 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	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

162951413

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione (NP0193769)

MOL for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

3D MOL for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

3D SDF for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

3D-SDF for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

PDB for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

3D PDB for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

SMILES for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

INCHI for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

Structure for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)

3D Structure for NP0193769 ((6ar)-3-[(4r)-4-hydroxy-2-methyl-6-oxocyclohex-1-en-1-yl]-6a-methyl-9-[(2r)-2-methyloctanoyl]furo[2,3-h]isochromene-6,8-dione)