NP-MRD: Showing NP-Card for 3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione (NP0258764)

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Record Information

Version

2.0

Created at

2022-09-08 00:22:51 UTC

Updated at

2022-09-08 00:22:51 UTC

NP-MRD ID

NP0258764

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione

Description

3-Methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)-2,5-dihydrofuran-2,5-dione belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. 3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione is found in Graphis scripta. 3-Methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)-2,5-dihydrofuran-2,5-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
    6.1357   -0.2778    0.0982 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8451   -0.7777   -0.4584 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8370   -1.6965   -1.2875 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6151   -0.1531    0.0040 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6177    0.9514    1.0001 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4687   -0.5711   -0.4668 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1932    0.0073   -0.0498 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0363   -0.4157   -0.5261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1878    0.2046   -0.0672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3527   -0.2046   -0.5316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6362    0.3702   -0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8229   -0.0379   -0.5838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0160   -1.1141   -1.5701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8544    0.7798    0.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0731    0.6629   -0.1363 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2427    1.6601    0.9130 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8531    1.4529    0.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9767    2.0720    1.4701 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4028    0.7027   -0.3537 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0987   -0.2133    1.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9338   -0.9882   -0.1577 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6360    1.2098    1.3208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0083    0.5838    1.8747 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0624    1.8240    0.5811 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4177   -1.3773   -1.1980 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2498    0.8195    0.6872 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0236   -1.2106   -1.2440 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1499    0.9935    0.6474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3830   -1.0253   -1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9044   -2.1183   -1.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1670   -1.0591   -2.3119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9622   -1.0539   -2.1139 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  4  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 11  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  7 26  1  0
  8 27  1  0
  9 28  1  0
 10 29  1  0
 13 30  1  0
 13 31  1  0
 13 32  1  0
M  END


  Mrv1533004201502222D          

 18 18  0  0  0  0            999 V2000
   -2.2901    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    6.0643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0198    0.8843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8843    0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    4.4143    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
  4 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258764

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)C(C)=CC=CC=CC1=C(C)C(=O)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H14O4/c1-9(11(3)15)7-5-4-6-8-12-10(2)13(16)18-14(12)17/h4-8H,1-3H3

> <INCHI_KEY>
DPZNQXPHRMGJIG-UHFFFAOYSA-N

> <FORMULA>
C14H14O4

> <MOLECULAR_WEIGHT>
246.262

> <EXACT_MASS>
246.089208931

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
26.33697337356506

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)-2,5-dihydrofuran-2,5-dione

> <ALOGPS_LOGP>
2.72

> <JCHEM_LOGP>
2.6973517376666667

> <ALOGPS_LOGS>
-4.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.601244861055804

> <JCHEM_PKA_STRONGEST_BASIC>
-4.52038473094882

> <JCHEM_POLAR_SURFACE_AREA>
60.440000000000005

> <JCHEM_REFRACTIVITY>
70.62190000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.61e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      -4.275  11.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.941  10.550   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.608  11.320   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -2.941   9.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.608   8.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.608   6.700   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.274   5.930   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.274   4.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.770   1.651   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.735  -1.536   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       0.290  -0.290   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.651   1.651   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -4.275   8.240   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   18                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16                                                            
CONECT   18    4                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₄O₄

Average Mass

246.2620 Da

Monoisotopic Mass

246.08921 Da

IUPAC Name

3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)-2,5-dihydrofuran-2,5-dione

Traditional Name

3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione

CAS Registry Number

Not Available

SMILES

CC(=O)C(C)=CC=CC=CC1=C(C)C(=O)OC1=O

InChI Identifier

InChI=1S/C14H14O4/c1-9(11(3)15)7-5-4-6-8-12-10(2)13(16)18-14(12)17/h4-8H,1-3H3

InChI Key

DPZNQXPHRMGJIG-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
Graphis scripta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

2-furanone
Dicarboxylic acid or derivatives
Alpha-branched alpha,beta-unsaturated-ketone
Acryloyl-group
Carboxylic acid anhydride
Alpha,beta-unsaturated ketone
Enone
Ketone
Oxacycle
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic oxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	2.72	ALOGPS
logP	2.7	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	19.6	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	60.44 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	70.62 m³·mol⁻¹	ChemAxon
Polarizability	26.34 Å³	ChemAxon
Number of Rings	1	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

190912

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione (NP0258764)

MOL for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

3D MOL for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

3D SDF for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

3D-SDF for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

PDB for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

3D PDB for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

SMILES for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

INCHI for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

Structure for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)

3D Structure for NP0258764 (3-methyl-4-(6-methyl-7-oxoocta-1,3,5-trien-1-yl)furan-2,5-dione)