NP-MRD: Showing NP-Card for methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate (NP0259489)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 01:22:47 UTC

Updated at

2022-09-08 01:22:47 UTC

NP-MRD ID

NP0259489

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate

Description

Methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxo-4H-chromen-8-yl)-2,4-dimethoxybutanoate belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety. Based on a literature review very few articles have been published on methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxo-4H-chromen-8-yl)-2,4-dimethoxybutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082203222D          

 26 27  0  0  0  0            999 V2000
    2.3349    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599    2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724    0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1099    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -1.5099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -1.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -2.2243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099   -1.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974   -0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099   -0.0809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099    2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349    2.7770    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  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
  7 10  1  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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 10 24  2  0  0  0  0
 17 24  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 48 49  0  0  0  0  0  0  0  0999 V2000
    5.8908    0.6420   -0.9127 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7112   -0.1557   -0.7374 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8510    0.0165    0.3116 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0722    0.8947    1.1664 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6092   -0.8977    0.4090 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4613    0.0443    0.4989 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0802   -0.5060    0.4703 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1664   -1.2585   -0.6691 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4350   -2.5919   -0.3240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9792    0.5544    0.5160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7833    1.7766    1.1076 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4098    2.1852    1.6598 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6486    3.4105    2.2699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8106    2.7329    1.1976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0454    2.4369    0.6783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1214    3.3404    0.7313 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2857    1.2261    0.0756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5298    0.9243   -0.4582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4458    1.7729   -0.3799 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7291   -0.2970   -1.0614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6638   -1.1890   -1.1123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9039   -2.5095   -1.7744 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5495   -0.8228   -0.5911 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2578    0.3079    0.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7229   -1.6890   -0.6881 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2237   -2.9569   -0.4989 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7400    0.0935   -0.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0072    0.7452   -2.0211 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6691    1.6085   -0.4230 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8211   -1.4238    1.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5517    0.5316    1.5433 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6300    0.8666   -0.2189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0966   -1.1759    1.3573 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4840   -2.9935    0.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7382   -3.1315   -1.2250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2721   -2.6836    0.4256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1424    3.6399    3.0379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6343    3.4696    2.7712 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6183    4.2473    1.5477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6602    3.6957    1.6627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9593    4.2195    1.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6625   -0.5816   -1.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8232   -2.3535   -2.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9044   -2.9052   -1.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1369   -3.2542   -1.5173 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2507   -3.4656   -1.4908 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7154   -3.6007    0.2034 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2998   -2.9397   -0.1681 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 25  1  0
 25  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  7 10  1  0
 10 24  2  0
 24 23  1  0
 23 21  1  0
 21 22  1  0
 21 20  2  0
 20 18  1  0
 18 19  2  0
 18 17  1  0
 17 15  2  0
 15 16  1  0
 15 14  1  0
 14 11  2  0
 11 12  1  0
 12 13  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  1  0
 11 10  1  0
 17 24  1  0
 26 46  1  0
 26 47  1  0
 26 48  1  0
  5 30  1  1
  6 31  1  0
  6 32  1  0
  7 33  1  1
  9 34  1  0
  9 35  1  0
  9 36  1  0
 22 43  1  0
 22 44  1  0
 22 45  1  0
 20 42  1  0
 16 41  1  0
 14 40  1  0
 13 37  1  0
 13 38  1  0
 13 39  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END


  Mrv1652309082203222D          

 26 27  0  0  0  0            999 V2000
    2.3349    2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599    2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724    0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1099    1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849   -1.5099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -1.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474   -2.2243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099   -1.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974   -0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099   -0.0809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349   -0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8099    2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6349    2.7770    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  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
  7 10  1  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
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 10 24  2  0  0  0  0
 17 24  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0259489

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(CC(OC)C1=C2OC(C)=CC(=O)C2=C(O)C=C1OC)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C18H22O8/c1-9-6-10(19)15-11(20)7-12(22-2)16(17(15)26-9)13(23-3)8-14(24-4)18(21)25-5/h6-7,13-14,20H,8H2,1-5H3

> <INCHI_KEY>
BKVHVYLMRZGKDR-UHFFFAOYSA-N

> <FORMULA>
C18H22O8

> <MOLECULAR_WEIGHT>
366.366

> <EXACT_MASS>
366.131467668

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
36.2709773745469

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxo-4H-chromen-8-yl)-2,4-dimethoxybutanoate

> <JCHEM_LOGP>
1.8446783709999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.047781420321932

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.325912661511209

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8200835823487806

> <JCHEM_POLAR_SURFACE_AREA>
100.52000000000001

> <JCHEM_REFRACTIVITY>
93.29649999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       4.358   5.184   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.898   5.184   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.898   2.516   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.208   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.978   2.516   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.518   2.516   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.288   3.850   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.828   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.288   1.183   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.828   1.183   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      13.598   2.516   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      15.138   2.516   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.598  -0.151   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.828  -1.485   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.598  -2.818   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      11.288  -1.485   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.518  -2.818   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.288  -4.152   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.978  -2.818   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.208  -1.485   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668  -1.485   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.978  -0.151   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.518  -0.151   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.978   5.184   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.518   5.184   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   25                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   24                                                  
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   24                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   10   17                                                  
CONECT   25    5   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxo-4H-chromen-8-yl)-2,4-dimethoxybutanoic acid	Generator

Chemical Formula

C₁₈H₂₂O₈

Average Mass

366.3660 Da

Monoisotopic Mass

366.13147 Da

IUPAC Name

methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxo-4H-chromen-8-yl)-2,4-dimethoxybutanoate

Traditional Name

methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate

CAS Registry Number

Not Available

SMILES

COC(CC(OC)C1=C2OC(C)=CC(=O)C2=C(O)C=C1OC)C(=O)OC

InChI Identifier

InChI=1S/C18H22O8/c1-9-6-10(19)15-11(20)7-12(22-2)16(17(15)26-9)13(23-3)8-14(24-4)18(21)25-5/h6-7,13-14,20H,8H2,1-5H3

InChI Key

BKVHVYLMRZGKDR-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 chromones. Chromones are compounds containing a benzopyran-4-one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Chromones

Alternative Parents

Substituents

Chromone
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Pyranone
Fatty acyl
Benzenoid
Pyran
Vinylogous acid
Methyl ester
Heteroaromatic compound
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Organooxygen compound
Organic oxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	1.84	ChemAxon
pKa (Strongest Acidic)	7.33	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	100.52 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	93.3 m³·mol⁻¹	ChemAxon
Polarizability	36.27 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

162977063

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate (NP0259489)

MOL for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

3D MOL for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

3D SDF for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

3D-SDF for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

PDB for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

3D PDB for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

SMILES for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

INCHI for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

Structure for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)

3D Structure for NP0259489 (methyl 4-(5-hydroxy-7-methoxy-2-methyl-4-oxochromen-8-yl)-2,4-dimethoxybutanoate)