NP-MRD: Showing NP-Card for 4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione (NP0232337)

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Record Information

Version

2.0

Created at

2022-09-06 13:32:41 UTC

Updated at

2022-09-06 13:32:41 UTC

NP-MRD ID

NP0232337

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione

Description

4,7,8-Trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1H,2H,3aH,4H,5H,6H,7H,8H,8bH-indeno[5,4-b]furan-2,6-dione belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. 4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione is found in Acremonium rutilum. Based on a literature review very few articles have been published on 4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1H,2H,3aH,4H,5H,6H,7H,8H,8bH-indeno[5,4-b]furan-2,6-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062215322D          

 33 36  0  0  0  0            999 V2000
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   -1.1224   -2.7856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2753   -2.4885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0599   -2.7434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2315   -3.5504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6730   -2.1914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4576   -2.4463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5015   -1.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0535    0.6576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309062215322D          

 33 36  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
NP0232337

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC=C(C)C(O)C1C2C3=C(CC(O)C2(C)OC1=O)C(=O)C(O)(C3O)C1=CC=CC=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C26H32O7/c1-5-6-9-14(3)21(28)19-20-18-15(12-17(27)25(20,4)33-24(19)31)22(29)26(32,23(18)30)16-11-8-7-10-13(16)2/h7-11,17,19-21,23,27-28,30,32H,5-6,12H2,1-4H3

> <INCHI_KEY>
WFSQOASGVQNLMJ-UHFFFAOYSA-N

> <FORMULA>
C26H32O7

> <MOLECULAR_WEIGHT>
456.535

> <EXACT_MASS>
456.21480337

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
48.70170123543187

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1H,2H,3aH,4H,5H,6H,7H,8H,8bH-indeno[5,4-b]furan-2,6-dione

> <JCHEM_LOGP>
2.174653644666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.46248415545901

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.397015062687057

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1992086685097956

> <JCHEM_POLAR_SURFACE_AREA>
124.29000000000002

> <JCHEM_REFRACTIVITY>
122.35139999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1H,4H,5H,8H,8bH-indeno[5,4-b]furan-2,6-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.240  -6.230   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.095  -5.200   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.631  -5.676   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.514  -4.645   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.979  -5.121   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.299  -6.627   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.123  -4.091   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.588  -4.566   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.803  -2.584   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.396  -1.958   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.062  -2.728   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       1.557  -0.426   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.063  -0.106   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.158   1.140   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.833   1.228   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.063   2.561   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.373   1.228   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.143  -0.106   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.373  -1.440   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.404  -2.584   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.084  -4.091   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.811  -1.958   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.286  -3.422   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       9.317  -1.638   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.793  -0.173   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.299   0.147   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.330  -0.997   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.854  -2.462   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.347  -2.782   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.871  -4.247   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.650  -0.426   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.794   0.604   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       3.833  -1.440   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   33                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15   33                                             
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   31                                                  
CONECT   19   18   20   33                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24   31                                             
CONECT   23   22                                                            
CONECT   24   22   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   24   30                                                  
CONECT   30   29                                                            
CONECT   31   22   18   32                                                  
CONECT   32   31                                                            
CONECT   33   19    9   13                                                  
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₂O₇

Average Mass

456.5350 Da

Monoisotopic Mass

456.21480 Da

IUPAC Name

4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1H,2H,3aH,4H,5H,6H,7H,8H,8bH-indeno[5,4-b]furan-2,6-dione

Traditional Name

4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1H,4H,5H,8H,8bH-indeno[5,4-b]furan-2,6-dione

CAS Registry Number

Not Available

SMILES

CCCC=C(C)C(O)C1C2C3=C(CC(O)C2(C)OC1=O)C(=O)C(O)(C3O)C1=CC=CC=C1C

InChI Identifier

InChI=1S/C26H32O7/c1-5-6-9-14(3)21(28)19-20-18-15(12-17(27)25(20,4)33-24(19)31)22(29)26(32,23(18)30)16-11-8-7-10-13(16)2/h7-11,17,19-21,23,27-28,30,32H,5-6,12H2,1-4H3

InChI Key

WFSQOASGVQNLMJ-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
Acremonium rutilum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Toluene
Acyloin
Monocyclic benzene moiety
Gamma butyrolactone
Benzenoid
Cyclic alcohol
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Ketone
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Polyol
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.17	ChemAxon
pKa (Strongest Acidic)	11.4	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	124.29 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	122.35 m³·mol⁻¹	ChemAxon
Polarizability	48.7 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

163056985

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione (NP0232337)

MOL for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

3D MOL for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

3D SDF for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

3D-SDF for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

PDB for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

3D PDB for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

SMILES for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

INCHI for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

Structure for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)

3D Structure for NP0232337 (4,7,8-trihydroxy-1-(1-hydroxy-2-methylhex-2-en-1-yl)-3a-methyl-7-(2-methylphenyl)-1h,4h,5h,8h,8bh-indeno[5,4-b]furan-2,6-dione)