NP-MRD: Showing NP-Card for methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate (NP0314105)

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Record Information

Version

2.0

Created at

2022-09-11 12:01:49 UTC

Updated at

2022-09-11 12:01:49 UTC

NP-MRD ID

NP0314105

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate

Description

Methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1,4-dihydropyridine-3-carbonyl]benzoate belongs to the class of organic compounds known as aryl-phenylketones. These are aromatic compounds containing a ketone substituted by one aryl group, and a phenyl group. Based on a literature review very few articles have been published on methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1,4-dihydropyridine-3-carbonyl]benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112214012D          

 28 29  0  0  0  0            999 V2000
   -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
   -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   -1.6500    0.0000 N   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   -2.8875    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   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.1250    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
    0.7145   -2.8875    0.0000 O   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
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    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
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  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  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  4 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 49 50  0  0  0  0  0  0  0  0999 V2000
    5.9853    1.5440   -0.6394 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5414    1.1232   -0.6243 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1462    0.2431    0.2424 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7615   -0.2304    0.3427 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8412    0.2373   -0.5013 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5711   -0.1655   -0.4009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1449   -1.0609    0.5455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2960   -1.4158    0.6099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6040   -2.5150    1.0862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2110   -0.4019    0.0927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2158    0.7830    0.8634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4294    0.8473    1.9963 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4175    2.0086    2.7699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0136    1.8064    0.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7937    1.6969   -0.7299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5944    2.7363   -1.1728 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7261    3.9861   -0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7340    0.5197   -1.4156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9405   -0.5739   -1.0313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9012   -1.7656   -1.8472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5037   -2.0249   -2.8799 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0303   -2.8024   -1.4079 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9240   -3.9771   -2.1875 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0856   -1.5486    1.4134 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7458   -2.3826    2.3090 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4119   -1.1465    1.3346 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4013   -1.5904    2.1726 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2225   -2.6919    1.9910 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6120    0.6421   -0.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2231    2.1558   -1.5236 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2539    2.0845    0.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8624    1.5761   -1.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8664   -0.1824    0.9303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0620    0.9227   -1.2563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1852    0.2105   -1.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2744    2.0794    3.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4679    2.1026    3.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4100    2.8797    2.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0441    2.7149    0.9979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8910    4.2975    0.0750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8860    4.7187   -1.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6452    3.9940    0.0428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3142    0.3475   -2.3349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2425   -4.7308   -1.7761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5701   -3.6415   -3.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9230   -4.4318   -2.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0585   -2.6032    2.7341 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7136   -3.6434    2.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6783   -2.7315    0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
 23 22  1  0
 22 20  1  0
 20 21  2  0
 20 19  1  0
 19 18  2  0
 18 15  1  0
 15 16  1  0
 16 17  1  0
 15 14  2  0
 14 11  1  0
 11 12  1  0
 12 13  1  0
 11 10  2  0
 10  8  1  0
  8  9  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  4 26  2  0
 26 27  1  0
 27 28  1  0
 26 24  1  0
 24 25  2  0
 10 19  1  0
 24  7  1  0
 23 44  1  0
 23 45  1  0
 23 46  1  0
 18 43  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 14 39  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
  6 35  1  0
  5 34  1  0
  3 33  1  0
  2 32  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 28 47  1  0
 28 48  1  0
 28 49  1  0
M  END


  Mrv1652309112214012D          

 28 29  0  0  0  0            999 V2000
   -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
   -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   -1.6500    0.0000 N   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   -2.8875    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   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.1250    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
    0.7145   -2.8875    0.0000 O   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
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -6.6000    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
   -2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  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  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  4 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0314105

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CC(OC)=CC(OC)=C1C(=O)C1=CNC(C=CC)=C(OC)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H21NO7/c1-6-7-14-19(27-4)18(23)13(10-21-14)17(22)16-12(20(24)28-5)8-11(25-2)9-15(16)26-3/h6-10H,1-5H3,(H,21,23)

> <INCHI_KEY>
QBVKMDADEIDLEW-UHFFFAOYSA-N

> <FORMULA>
C20H21NO7

> <MOLECULAR_WEIGHT>
387.388

> <EXACT_MASS>
387.13180202

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
39.92184616434437

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1,4-dihydropyridine-3-carbonyl]benzoate

> <JCHEM_LOGP>
2.1325208353333336

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.016608027969696

> <JCHEM_PKA_STRONGEST_BASIC>
-4.427001980402053

> <JCHEM_POLAR_SURFACE_AREA>
100.16000000000001

> <JCHEM_REFRACTIVITY>
105.0848

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1H-pyridine-3-carbonyl]benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       0.000  -3.080   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   26                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   24                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   19                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19                                                       
CONECT   19   18   10   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22                                                            
CONECT   24    7   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    4   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Value	Source
Methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1,4-dihydropyridine-3-carbonyl]benzoic acid	Generator

Chemical Formula

C₂₀H₂₁NO₇

Average Mass

387.3880 Da

Monoisotopic Mass

387.13180 Da

IUPAC Name

methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1,4-dihydropyridine-3-carbonyl]benzoate

Traditional Name

methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1H-pyridine-3-carbonyl]benzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC(OC)=CC(OC)=C1C(=O)C1=CNC(C=CC)=C(OC)C1=O

InChI Identifier

InChI=1S/C20H21NO7/c1-6-7-14-19(27-4)18(23)13(10-21-14)17(22)16-12(20(24)28-5)8-11(25-2)9-15(16)26-3/h6-10H,1-5H3,(H,21,23)

InChI Key

QBVKMDADEIDLEW-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aryl-phenylketones. These are aromatic compounds containing a ketone substituted by one aryl group, and a phenyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Aryl-phenylketones

Alternative Parents

Substituents

Aryl-phenylketone
M-methoxybenzoic acid or derivatives
M-dimethoxybenzene
Dimethoxybenzene
Benzoate ester
Pyridine carboxylic acid or derivatives
Benzoic acid or derivatives
Phenoxy compound
Methoxybenzene
Phenol ether
Benzoyl
Anisole
Dihydropyridine
Alkyl aryl ether
Benzenoid
Pyridine
Hydropyridine
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous amide
Methyl ester
Cyclic ketone
Carboxylic acid ester
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen 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
logP	2.13	ChemAxon
pKa (Strongest Acidic)	10.02	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	100.16 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	105.08 m³·mol⁻¹	ChemAxon
Polarizability	39.92 Å³	ChemAxon
Number of Rings	2	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

162847321

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate (NP0314105)

MOL for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

3D MOL for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

3D SDF for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

3D-SDF for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

PDB for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

3D PDB for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

SMILES for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

INCHI for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

Structure for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)

3D Structure for NP0314105 (methyl 3,5-dimethoxy-2-[5-methoxy-4-oxo-6-(prop-1-en-1-yl)-1h-pyridine-3-carbonyl]benzoate)