NP-MRD: Showing NP-Card for (2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate (NP0199236)

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Record Information

Version

2.0

Created at

2022-09-04 17:50:21 UTC

Updated at

2022-09-04 17:50:22 UTC

NP-MRD ID

NP0199236

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate

Description

4-[(2S,3S)-3,7-bis(acetyloxy)-5-methoxy-6-methyl-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl]phenyl acetate belongs to the class of organic compounds known as 5-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone. Based on a literature review very few articles have been published on 4-[(2S,3S)-3,7-bis(acetyloxy)-5-methoxy-6-methyl-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl]phenyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042219502D          

 32 34  0  0  1  0            999 V2000
    0.7145    1.2375    0.0000 C   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
    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 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   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   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
   -2.8579   -1.6500    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
    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 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
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  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
    2.8579    0.8250    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
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  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
    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
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   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
    1.4289   -1.6500    0.0000 O   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
  4  5  1  0  0  0  0
  4  6  1  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
  8 10  2  0  0  0  0
  6 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 25 30  1  0  0  0  0
 30 31  2  0  0  0  0
 22 31  1  0  0  0  0
 21 32  1  0  0  0  0
 12 32  1  0  0  0  0
M  END

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
   -3.9475   -3.2131    0.7823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7833   -2.3291   -0.3195 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3436   -1.0221   -0.0373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2413   -0.0085    0.2209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6966   -0.3565    0.1884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8183    1.2942    0.5027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7674    2.2719    0.7544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3384    3.0734   -0.2029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3547    4.1172    0.0823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9901    2.9269   -1.3990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4589    1.5304    0.5130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5188    0.5530    0.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9986   -0.7325   -0.0144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0667   -1.8206   -0.2906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4965   -2.9020   -0.7690 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3652   -1.5696    0.0207 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2349   -2.4190   -0.6813 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1098   -3.2751   -0.0530 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0212   -4.1652   -0.8373 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1257   -3.2921    1.2010 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6664   -0.1510   -0.4175 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1059    0.1852   -0.2663 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9026    0.1314   -1.3834 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2352    0.4365   -1.2740 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8101    0.7963   -0.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1485    1.0923   -0.0267 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7008    2.3400   -0.2073 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1797    2.5603   -0.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9167    3.2956   -0.4463 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0068    0.8492    1.0349 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6565    0.5435    0.9417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1513    0.7897    0.2718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4614   -2.8040    1.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4972   -4.1999    0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0312   -3.3885    1.0051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8990   -1.1619   -0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0052   -0.7923    1.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3237    0.5058   -0.0448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1850    3.9678   -0.6238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7617    4.0214    1.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9401    5.1380   -0.0637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1380    2.5396    0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4819   -1.6850    1.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4358   -3.6370   -1.7200 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8778   -4.5071   -0.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4607   -5.0446   -1.1961 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777   -0.0756   -1.4853 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4715   -0.1570   -2.3682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8656    0.3946   -2.1541 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4669    2.4769    0.9463 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6364    1.6701   -0.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4879    3.4915   -0.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4576    1.1329    1.9753 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0087    0.5836    1.8316 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
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
  6 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 16 21  1  0
 21 32  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 25 30  1  0
 30 31  2  0
 13  3  1  0
 31 22  1  0
 32 12  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  0
  5 37  1  0
  5 38  1  0
  9 39  1  0
  9 40  1  0
  9 41  1  0
 11 42  1  0
 16 43  1  1
 19 44  1  0
 19 45  1  0
 19 46  1  0
 21 47  1  6
 23 48  1  0
 24 49  1  0
 28 50  1  0
 28 51  1  0
 28 52  1  0
 30 53  1  0
 31 54  1  0
M  END


  Mrv1652309042219502D          

 32 34  0  0  1  0            999 V2000
    0.7145    1.2375    0.0000 C   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
    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 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   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   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
   -2.8579   -1.6500    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
    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 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
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  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
    2.8579    0.8250    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
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  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
    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
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   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
    1.4289   -1.6500    0.0000 O   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
  4  5  1  0  0  0  0
  4  6  1  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
  8 10  2  0  0  0  0
  6 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 25 30  1  0  0  0  0
 30 31  2  0  0  0  0
 22 31  1  0  0  0  0
 21 32  1  0  0  0  0
 12 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0199236

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C)C(OC(C)=O)=CC2=C1C(=O)[C@@H](OC(C)=O)[C@@H](O2)C1=CC=C(OC(C)=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O9/c1-11-17(30-13(3)25)10-18-19(21(11)28-5)20(27)23(31-14(4)26)22(32-18)15-6-8-16(9-7-15)29-12(2)24/h6-10,22-23H,1-5H3/t22-,23+/m0/s1

> <INCHI_KEY>
ASHPMUOPXZTLQY-XZOQPEGZSA-N

> <FORMULA>
C23H22O9

> <MOLECULAR_WEIGHT>
442.42

> <EXACT_MASS>
442.126382288

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
44.1970455894363

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl acetate

> <JCHEM_LOGP>
2.3920430373333335

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.095244453175898

> <JCHEM_PKA_STRONGEST_BASIC>
-4.620334228281429

> <JCHEM_POLAR_SURFACE_AREA>
114.43000000000002

> <JCHEM_REFRACTIVITY>
109.60600000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -2.310   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       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12                                                       
CONECT   12   11   13   32                                                  
CONECT   13   12    3   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22   32                                                  
CONECT   22   21   23   31                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   31                                                       
CONECT   31   30   22                                                       
CONECT   32   21   12                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
4-[(2S,3S)-3,7-Bis(acetyloxy)-5-methoxy-6-methyl-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl]phenyl acetic acid	Generator

Chemical Formula

C₂₃H₂₂O₉

Average Mass

442.4200 Da

Monoisotopic Mass

442.12638 Da

IUPAC Name

(2S,3S)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl acetate

Traditional Name

(2S,3S)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate

CAS Registry Number

Not Available

SMILES

COC1=C(C)C(OC(C)=O)=CC2=C1C(=O)[C@@H](OC(C)=O)[C@@H](O2)C1=CC=C(OC(C)=O)C=C1

InChI Identifier

InChI=1S/C23H22O9/c1-11-17(30-13(3)25)10-18-19(21(11)28-5)20(27)23(31-14(4)26)22(32-18)15-6-8-16(9-7-15)29-12(2)24/h6-10,22-23H,1-5H3/t22-,23+/m0/s1

InChI Key

ASHPMUOPXZTLQY-XZOQPEGZSA-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 5-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

5-O-methylated flavonoids

Alternative Parents

Substituents

5-methoxyflavonoid-skeleton
Flavanonol
Flavanone
Flavan
Chromone
1-benzopyran
Phenol ester
Benzopyran
Chromane
Tricarboxylic acid or derivatives
Phenoxy compound
Aryl alkyl ketone
Aryl ketone
Anisole
Alpha-acyloxy ketone
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	2.39	ChemAxon
pKa (Strongest Acidic)	11.1	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	114.43 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	109.61 m³·mol⁻¹	ChemAxon
Polarizability	44.2 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163066038

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate (NP0199236)

MOL for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

3D MOL for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

3D SDF for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

3D-SDF for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

PDB for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

3D PDB for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

SMILES for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

INCHI for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

Structure for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)

3D Structure for NP0199236 ((2s,3s)-3-(acetyloxy)-2-[4-(acetyloxy)phenyl]-5-methoxy-6-methyl-4-oxo-2,3-dihydro-1-benzopyran-7-yl acetate)