NP-MRD: Showing NP-Card for 4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one (NP0241282)

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Record Information

Version

2.0

Created at

2022-09-07 01:19:07 UTC

Updated at

2022-09-07 01:19:07 UTC

NP-MRD ID

NP0241282

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one

Description

Phomenin B belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone. 4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one is found in Leptosphaeria maculans and Plenodomus tracheiphilus. 4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one was first documented in 2005 (PMID: 15649514). Based on a literature review very few articles have been published on Phomenin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 35  0  0  0  0  0  0  0  0999 V2000
    2.6031    2.6317    0.8850 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5604    1.6119    0.4705 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1195    0.4058    0.0344 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1990   -0.5082   -0.3516 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6934    0.2248    0.0160 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9887   -0.8202   -0.3441 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7054   -2.0385   -0.8009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4845   -0.8680   -0.3135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2897    0.1456    0.0849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6744   -0.0403    0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5388    0.9648    0.4592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9889    2.2009    0.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2234   -1.2281   -0.3562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6892   -1.4714   -0.3976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3395   -2.2084   -0.7450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8296   -3.3113   -1.1339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0525   -1.9896   -0.7067 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0085    2.3449    1.7965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9040    2.8923    0.0624 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1156    3.5738    1.1591 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6225    1.8312    0.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4633   -1.2337    0.4465 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0032   -0.9781   -1.3281 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1592    0.0905   -0.5768 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0313    1.0716    0.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0451   -1.9787   -1.8323 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0093   -2.9339   -0.7096 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5008   -2.2562   -0.0801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8910    1.0767    0.4137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8330    2.8601    1.1494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3296    2.6236    0.1214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4254    1.9609    1.8346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8957   -2.2206    0.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0387   -1.9004   -1.3367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2081   -0.5253   -0.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 10  1  0
 10 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 17  8  1  0
  8  9  2  0
  8  6  1  0
  6  7  1  0
  6  5  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
  9 10  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 14 35  1  0
  9 29  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
  5 25  1  0
  4 22  1  0
  4 23  1  0
  4 24  1  0
  2 21  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
M  END


  Mrv1652309072203192D          

 17 17  0  0  0  0            999 V2000
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  8 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0241282

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C)C(=O)OC(=C1)C(\C)=C\C(\C)=C/C

> <INCHI_IDENTIFIER>
InChI=1S/C14H18O3/c1-6-9(2)7-10(3)12-8-13(16-5)11(4)14(15)17-12/h6-8H,1-5H3/b9-6-,10-7+

> <INCHI_KEY>
SHJHZIUPBJKXFY-PCCLLEMOSA-N

> <FORMULA>
C14H18O3

> <MOLECULAR_WEIGHT>
234.295

> <EXACT_MASS>
234.12559444

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
26.27017783501364

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-methoxy-3-methyl-6-[(2E,4Z)-4-methylhexa-2,4-dien-2-yl]-2H-pyran-2-one

> <JCHEM_LOGP>
2.8324746083333343

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.835071791667888

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
71.8854

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-methoxy-3-methyl-6-[(2E,4Z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   17                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    8                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₁₈O₃

Average Mass

234.2950 Da

Monoisotopic Mass

234.12559 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=C(C)C(=O)OC(=C1)C(\C)=C\C(\C)=C/C

InChI Identifier

InChI=1S/C14H18O3/c1-6-9(2)7-10(3)12-8-13(16-5)11(4)14(15)17-12/h6-8H,1-5H3/b9-6-,10-7+

InChI Key

SHJHZIUPBJKXFY-PCCLLEMOSA-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
Leptosphaeria maculans	LOTUS Database	35616633
Plenodomus tracheiphilus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Pyranones and derivatives

Direct Parent

Pyranones and derivatives

Alternative Parents

Substituents

Pyranone
Alkyl aryl ether
Heteroaromatic compound
Vinylogous ester
Lactone
Oxacycle
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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

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

78435928

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102217555

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pedras MS, Chumala PB: Phomapyrones from blackleg causing phytopathogenic fungi: isolation, structure determination, biosyntheses and biological activity. Phytochemistry. 2005 Jan;66(1):81-7. doi: 10.1016/j.phytochem.2004.10.011. [PubMed:15649514 ]
LOTUS database [Link]

Showing NP-Card for 4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one (NP0241282)

MOL for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

3D MOL for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

3D SDF for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

3D-SDF for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

PDB for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

3D PDB for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

SMILES for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

INCHI for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

Structure for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)

3D Structure for NP0241282 (4-methoxy-3-methyl-6-[(2e,4z)-4-methylhexa-2,4-dien-2-yl]pyran-2-one)