NP-MRD: Showing NP-Card for 2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione (NP0186461)

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Record Information

Version

2.0

Created at

2022-09-04 02:19:05 UTC

Updated at

2022-09-04 02:19:06 UTC

NP-MRD ID

NP0186461

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione

Description

2-(3,7-Dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione belongs to the class of organic compounds known as prenylquinones. These are quinones with a structure characterized by the quinone ring substituted by an prenyl side-chain. 2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione is found in Lettowianthus stellatus. 2-(3,7-Dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 04121517342D          

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M  END

     RDKit          3D

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M  END


  Mrv0541 04121517342D          

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    1.9233    4.6646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2089    5.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    5.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668   -1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    0.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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  4  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  4  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 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
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 20 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 19 35  1  0  0  0  0
 35 36  1  0  0  0  0
 17 36  2  0  0  0  0
  6 37  1  0  0  0  0
  2 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0186461

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC(C)=CCC1=C2OC(=CC2=CC(O)=C1)C1=CC(=O)C=C(CC=C(C)CCC=C(C)C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H40O4/c1-22(2)9-7-11-24(5)13-15-26-17-30(36)21-31(33(26)37)32-20-28-19-29(35)18-27(34(28)38-32)16-14-25(6)12-8-10-23(3)4/h9-10,13-14,17-21,35H,7-8,11-12,15-16H2,1-6H3

> <INCHI_KEY>
OLVOHJVDFSHOFA-UHFFFAOYSA-N

> <FORMULA>
C34H40O4

> <MOLECULAR_WEIGHT>
512.69

> <EXACT_MASS>
512.292659768

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
61.36783338753264

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione

> <ALOGPS_LOGP>
6.86

> <JCHEM_LOGP>
9.126452458000003

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.49335958984721

> <JCHEM_PKA_STRONGEST_BASIC>
-2.979965470900258

> <JCHEM_POLAR_SURFACE_AREA>
67.51

> <JCHEM_REFRACTIVITY>
161.5871

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.77e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-APR-15         0                                  
HETATM    1  C   UNK     0     -11.870   0.031   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -10.330   0.031   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.560  -1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.020  -1.303   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.250  -2.637   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.710  -2.637   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.940  -3.970   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.400  -3.970   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.630  -2.637   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.400  -1.303   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.630   0.031   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.400   1.365   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.090   0.031   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.320  -1.303   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.090  -2.637   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.320  -3.970   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.126  -0.057   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.924   1.777   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.590   2.547   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.590   4.087   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.924   4.857   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.257   4.857   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.257   6.397   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.590   7.167   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.590   8.707   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.257   9.477   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.924   9.477   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.591  -2.843   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -4.940  -1.303   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -9.560   1.365   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   38                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   37                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14    9   16                                                  
CONECT   16   15                                                            
CONECT   17   14   18   36                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   35                                                  
CONECT   20   19   21   31                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   20   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   19   36                                                  
CONECT   36   35   17                                                       
CONECT   37    6                                                            
CONECT   38    2                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₀O₄

Average Mass

512.6900 Da

Monoisotopic Mass

512.29266 Da

IUPAC Name

2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione

Traditional Name

2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)=CCC1=C2OC(=CC2=CC(O)=C1)C1=CC(=O)C=C(CC=C(C)CCC=C(C)C)C1=O

InChI Identifier

InChI=1S/C34H40O4/c1-22(2)9-7-11-24(5)13-15-26-17-30(36)21-31(33(26)37)32-20-28-19-29(35)18-27(34(28)38-32)16-14-25(6)12-8-10-23(3)4/h9-10,13-14,17-21,35H,7-8,11-12,15-16H2,1-6H3

InChI Key

OLVOHJVDFSHOFA-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
Lettowianthus stellatus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylquinones. These are quinones with a structure characterized by the quinone ring substituted by an prenyl side-chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Quinone and hydroquinone lipids

Direct Parent

Prenylquinones

Alternative Parents

Substituents

Prenylbenzoquinone
Aromatic monoterpenoid
Bicyclic monoterpenoid
Monoterpenoid
Benzofuran
P-benzoquinone
Quinone
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Furan
Heteroaromatic compound
Ketone
Cyclic ketone
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
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	6.86	ALOGPS
logP	9.13	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	8.49	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	67.51 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	161.59 m³·mol⁻¹	ChemAxon
Polarizability	61.37 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

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 2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione (NP0186461)

MOL for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

3D MOL for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

3D SDF for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

3D-SDF for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

PDB for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

3D PDB for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

SMILES for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

INCHI for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

Structure for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)

3D Structure for NP0186461 (2-(3,7-dimethylocta-2,6-dien-1-yl)-6-[7-(3,7-dimethylocta-2,6-dien-1-yl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione)