NP-MRD: Showing NP-Card for methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate (NP0212962)

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Record Information

Version

2.0

Created at

2022-09-05 11:47:08 UTC

Updated at

2022-09-05 11:47:08 UTC

NP-MRD ID

NP0212962

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate

Description

Methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1E)-prop-1-en-1-yl]-4H-pyran-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 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1E)-prop-1-en-1-yl]-4H-pyran-3-carbonyl}benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052213472D          

 27 28  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 O   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
    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
  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  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
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  4 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    6.8560   -0.1605    0.2603 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4228   -0.2858   -0.0534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4701   -0.6218    0.8125 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0758   -0.7127    0.3850 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5348   -1.6076   -0.3750 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2384   -1.5550   -0.7090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3885   -0.5532   -0.2746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9353   -0.4449   -0.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7954   -0.1688   -2.1651 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2682   -0.5341   -0.4429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8727   -1.7963   -0.3080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0343   -2.8593   -0.4003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4016   -4.1973   -0.2875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1985   -1.9504   -0.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9997   -0.8187   -0.0086 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3782   -0.9477    0.1932 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4498    0.4333   -0.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0960    0.5748   -0.3388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5695    1.9304   -0.4204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4361    2.1541   -0.8906 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3303    2.9733    0.0647 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8506    4.3271    0.1164 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763    0.3944    0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2959    1.3280    1.0095 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2942    0.3256    0.8712 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9182    1.3044    1.6860 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4113    2.3796    0.8178 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0319   -0.2024    1.3533 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1390    0.9180    0.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5000   -0.8601   -0.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0714   -0.0657   -1.0755 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7370   -0.8410    1.8170 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8672   -2.3529   -1.3579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2586   -4.3945    0.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7074   -4.5293   -1.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5152   -4.8017    0.0743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6766   -2.9394    0.0195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7785   -1.8967    0.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1260    1.2971   -0.0664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6465    5.0571    0.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2073    4.3377    1.0849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1792    4.4932   -0.7231 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6046    3.1242    0.7220 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3529    2.7656    1.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5251    1.9800   -0.2361 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 19  1  0
 19 20  2  0
 19 18  1  0
 18 17  2  0
 17 15  1  0
 15 16  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 25  2  0
 25 26  1  0
 26 27  1  0
 25 23  1  0
 23 24  2  0
 10 18  1  0
 23  7  1  0
 22 40  1  0
 22 41  1  0
 22 42  1  0
 17 39  1  0
 16 38  1  0
 14 37  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
  6 33  1  0
  3 32  1  0
  2 31  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 27 43  1  0
 27 44  1  0
 27 45  1  0
M  END


  Mrv1652309052213472D          

 27 28  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 O   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
    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
  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  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
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  4 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0212962

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O8/c1-5-6-13-18(25-3)17(22)12(9-27-13)16(21)15-11(19(23)26-4)7-10(20)8-14(15)24-2/h5-9,20H,1-4H3/b6-5+

> <INCHI_KEY>
RKPUWEPREOHXHS-AATRIKPKSA-N

> <FORMULA>
C19H18O8

> <MOLECULAR_WEIGHT>
374.345

> <EXACT_MASS>
374.10016754

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.314620639015246

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1E)-prop-1-en-1-yl]-4H-pyran-3-carbonyl}benzoate

> <JCHEM_LOGP>
2.304054685999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.164755849500134

> <JCHEM_PKA_STRONGEST_BASIC>
-4.567194695268311

> <JCHEM_POLAR_SURFACE_AREA>
108.36000000000001

> <JCHEM_REFRACTIVITY>
98.92159999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1E)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-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  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+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       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   27  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   25                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   23                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   18                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   10   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21                                                            
CONECT   23    7   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    4   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

View in JSmol

Synonyms

Value	Source
Methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1E)-prop-1-en-1-yl]-4H-pyran-3-carbonyl}benzoic acid	Generator

Chemical Formula

C₁₉H₁₈O₈

Average Mass

374.3450 Da

Monoisotopic Mass

374.10017 Da

IUPAC Name

methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1E)-prop-1-en-1-yl]-4H-pyran-3-carbonyl}benzoate

Traditional Name

methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1E)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C19H18O8/c1-5-6-13-18(25-3)17(22)12(9-27-13)16(21)15-11(19(23)26-4)7-10(20)8-14(15)24-2/h5-9,20H,1-4H3/b6-5+

InChI Key

RKPUWEPREOHXHS-AATRIKPKSA-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-hydroxybenzoic acid ester
M-methoxybenzoic acid or derivatives
Benzoate ester
Methoxyphenol
Benzoic acid or derivatives
Benzoyl
Phenoxy compound
Phenol ether
Anisole
Methoxybenzene
Pyranone
Phenol
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyran
Benzenoid
Monocyclic benzene moiety
Methyl ester
Heteroaromatic compound
Cyclic ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
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	2.3	ChemAxon
pKa (Strongest Acidic)	7.16	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	108.36 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	98.92 m³·mol⁻¹	ChemAxon
Polarizability	37.31 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

8746809

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10571422

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate (NP0212962)

MOL for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

3D MOL for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

3D SDF for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

3D-SDF for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

PDB for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

3D PDB for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

SMILES for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

INCHI for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

Structure for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)

3D Structure for NP0212962 (methyl 5-hydroxy-3-methoxy-2-{5-methoxy-4-oxo-6-[(1e)-prop-1-en-1-yl]pyran-3-carbonyl}benzoate)