NP-MRD: Showing NP-Card for methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate (NP0321482)

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Record Information

Version

2.0

Created at

2022-09-11 23:42:42 UTC

Updated at

2022-09-11 23:42:42 UTC

NP-MRD ID

NP0321482

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate

Description

Methyl 2-{6-[2-(acetyloxy)propyl]-4-oxo-4H-pyran-3-carbonyl}-3,5-dimethoxybenzoate 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. methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate is found in Talaromyces flavus. Methyl 2-{6-[2-(acetyloxy)propyl]-4-oxo-4H-pyran-3-carbonyl}-3,5-dimethoxybenzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171516282D          

 30 31  0  0  0  0            999 V2000
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    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
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    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
   -1.4289    1.6500    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    2.8875    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
    0.0000    1.6500    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
   -0.7145    0.4125    0.0000 O   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
    1.4289    2.4750    0.0000 C   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    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  2  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
   -0.7119   -3.5379   -0.8965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2804   -2.2373   -0.8277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4491   -1.9309   -0.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0552   -2.9180    0.3367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0688   -0.6274   -0.1146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3349   -0.5581    0.5043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0080    0.6388    0.5994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2529    0.6644    1.2176 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9206   -0.4156    1.7755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4271    1.7687    0.0778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1976    1.7724   -0.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5919    2.8982   -1.0724 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2690    4.1156   -0.9801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5388    0.5167   -0.6118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2309    0.5491   -1.2405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2110    0.6923   -2.4906 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0299    0.4390   -0.5146 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0942   -0.3112   -0.9918 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2512   -0.3934   -0.3542 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5066    0.2104    0.7721 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7519    0.1615    1.5274 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8753   -0.5937    0.9029 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0372   -0.5001    1.9163 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3173   -0.0337   -0.3218 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3545   -0.8101   -1.4529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8178   -0.2567   -2.7466 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9865   -2.0212   -1.3900 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4699    0.9781    1.2939 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2588    1.0942    0.6698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6475    1.7987    1.1740 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3067   -3.6083   -0.5145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7459   -3.8443   -1.9523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3286   -4.2764   -0.3269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7830   -1.4513    0.9102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2329   -0.9209    2.4908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7501    0.0296    2.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2991   -1.1261    1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9419    2.7103    0.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1881    4.4788    0.0633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8696    4.8720   -1.7010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3605    4.0615   -1.2456 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0311   -0.8678   -1.9146 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1032    1.2017    1.7490 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5760   -0.3317    2.5315 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5881   -1.6461    0.7502 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8351   -1.2091    1.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3614    0.5559    1.9482 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5984   -0.7773    2.9047 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9774    0.2497   -3.2458 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6966    0.4385   -2.6018 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2222   -1.0802   -3.4002 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6484    1.5109    2.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  2  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  2  0
 20 28  2  0
 28 29  1  0
 29 30  2  0
 14  5  1  0
 29 17  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  6 34  1  0
  9 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 13 39  1  0
 13 40  1  0
 13 41  1  0
 18 42  1  0
 21 43  1  0
 21 44  1  0
 22 45  1  6
 23 46  1  0
 23 47  1  0
 23 48  1  0
 26 49  1  0
 26 50  1  0
 26 51  1  0
 28 52  1  0
M  END


  Mrv1533004171516282D          

 30 31  0  0  0  0            999 V2000
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    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
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    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
   -1.4289    1.6500    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    2.8875    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
    0.0000    1.6500    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
   -0.7145    0.4125    0.0000 O   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
    1.4289    2.4750    0.0000 C   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    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  2  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321482

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CC(OC)=CC(OC)=C1C(=O)C1=COC(CC(C)OC(C)=O)=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H22O9/c1-11(30-12(2)22)6-14-8-17(23)16(10-29-14)20(24)19-15(21(25)28-5)7-13(26-3)9-18(19)27-4/h7-11H,6H2,1-5H3

> <INCHI_KEY>
VSHBHDIKPQHDHQ-UHFFFAOYSA-N

> <FORMULA>
C21H22O9

> <MOLECULAR_WEIGHT>
418.398

> <EXACT_MASS>
418.126382288

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
41.76609605679892

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-{6-[2-(acetyloxy)propyl]-4-oxo-4H-pyran-3-carbonyl}-3,5-dimethoxybenzoate

> <ALOGPS_LOGP>
2.22

> <JCHEM_LOGP>
1.6936190446666657

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.494260257435807

> <JCHEM_POLAR_SURFACE_AREA>
114.43

> <JCHEM_REFRACTIVITY>
106.57709999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.20e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -5.335  -0.000   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -6.668   0.770   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -8.002  -0.000   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002   3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -9.336   5.390   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -9.336   6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668   5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.001   5.390   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.335   3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.001   0.770   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.334   5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.334   0.770   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+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   5.390   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.668   5.390   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   14                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11    5   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   17   23                                                  
CONECT   23   22                                                            
CONECT   24   20   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-{6-[2-(acetyloxy)propyl]-4-oxo-4H-pyran-3-carbonyl}-3,5-dimethoxybenzoic acid	Generator

Chemical Formula

C₂₁H₂₂O₉

Average Mass

418.3980 Da

Monoisotopic Mass

418.12638 Da

IUPAC Name

methyl 2-{6-[2-(acetyloxy)propyl]-4-oxo-4H-pyran-3-carbonyl}-3,5-dimethoxybenzoate

Traditional Name

methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC(OC)=CC(OC)=C1C(=O)C1=COC(CC(C)OC(C)=O)=CC1=O

InChI Identifier

InChI=1S/C21H22O9/c1-11(30-12(2)22)6-14-8-17(23)16(10-29-14)20(24)19-15(21(25)28-5)7-13(26-3)9-18(19)27-4/h7-11H,6H2,1-5H3

InChI Key

VSHBHDIKPQHDHQ-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
Talaromyces flavus	LOTUS Database	35616633

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
Benzoate ester
M-dimethoxybenzene
Dimethoxybenzene
Benzoic acid or derivatives
Phenoxy compound
Anisole
Methoxybenzene
Benzoyl
Phenol ether
Alkyl aryl ether
Pyranone
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Benzenoid
Pyran
Heteroaromatic compound
Methyl ester
Carboxylic acid ester
Cyclic ketone
Ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
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	2.22	ALOGPS
logP	1.69	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	114.43 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	106.58 m³·mol⁻¹	ChemAxon
Polarizability	41.77 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

9953797

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate (NP0321482)

MOL for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

3D MOL for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

3D SDF for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

3D-SDF for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

PDB for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

3D PDB for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

SMILES for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

INCHI for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

Structure for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)

3D Structure for NP0321482 (methyl 2-{6-[2-(acetyloxy)propyl]-4-oxopyran-3-carbonyl}-3,5-dimethoxybenzoate)