NP-MRD: Showing NP-Card for 4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one (NP0320730)

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Record Information

Version

2.0

Created at

2022-09-11 22:33:14 UTC

Updated at

2022-09-11 22:33:14 UTC

NP-MRD ID

NP0320730

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one

Description

4,8-Dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-1H-2-benzopyran-1-one belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position. 4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one is found in Aigialus parvus. 4,8-Dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-1H-2-benzopyran-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161506332D          

 28 29  0  0  0  0            999 V2000
   -2.1434   -1.2375    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
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    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
   -2.1434    2.8875    0.0000 O   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
    0.7145    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    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
    2.8579    1.6500    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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    1.6500    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 O   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  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
  5  6  1  0  0  0  0
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  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 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
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 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
  3 28  1  0  0  0  0
M  END

     RDKit          3D

 54 55  0  0  0  0  0  0  0  0999 V2000
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   -6.0127   -1.9167   -0.7083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2088   -0.8780   -0.2389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2736   -0.4629    1.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4825    0.5646    1.5512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5375    0.9950    2.8786 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5898    1.2249    0.7323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5254    0.8097   -0.5822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3179   -0.2206   -1.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5700    1.5117   -1.4658 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2955    2.5617   -2.0737 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4405    2.1352   -0.7223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4444    1.1524   -0.1800 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1284    0.2460   -1.2370 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.2080    0.5986   -0.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4743   -0.2275   -0.5015 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9721   -0.6068    0.8778 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2284   -1.4219    0.7077 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.2365   -0.5743   -0.0145 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6947   -1.9398    1.9020 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8971    2.9224    0.3617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7654    2.3098    1.2525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8458    2.6709    2.4692 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.9604   -0.9557    1.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1522    0.5862    3.5705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2723   -0.5528   -2.0927 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7039   -0.3487   -1.6453 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3827   -1.1415   -1.0868 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2668    0.4241   -0.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1934   -1.2917    1.3040 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9714   -2.2811    0.0176 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0456   -0.5761   -1.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2566   -0.9615    0.2515 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2020    0.4945    0.3352 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3169   -2.6880    1.7221 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
  5  6  1  0
  5  7  2  0
  7 27  1  0
 27 28  2  0
 27 26  1  0
 26 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 12 10  1  0
 10 11  1  0
 10  8  1  0
  8  9  2  0
  9  3  1  0
  8  7  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  4 32  1  0
  6 33  1  0
 12 37  1  6
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 13 39  1  0
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 23 50  1  6
 24 51  1  0
 24 52  1  0
 24 53  1  0
 25 54  1  0
 10 35  1  6
 11 36  1  0
  9 34  1  0
M  END


  Mrv1533004161506332D          

 28 29  0  0  0  0            999 V2000
   -2.1434   -1.2375    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
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    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
   -2.1434    2.8875    0.0000 O   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
    0.7145    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    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
    2.8579    1.6500    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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    1.6500    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 O   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  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
  5  6  1  0  0  0  0
  5  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  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
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
  3 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320730

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(=O)OC(CC(O)C(O)C(=O)CCCC(C)O)C(O)C2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H26O9/c1-9(20)4-3-5-12(21)18(25)14(23)8-15-17(24)11-6-10(27-2)7-13(22)16(11)19(26)28-15/h6-7,9,14-15,17-18,20,22-25H,3-5,8H2,1-2H3

> <INCHI_KEY>
SQYAYCYQGHSUJQ-UHFFFAOYSA-N

> <FORMULA>
C19H26O9

> <MOLECULAR_WEIGHT>
398.408

> <EXACT_MASS>
398.157682417

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
39.99658738870172

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-1H-2-benzopyran-1-one

> <ALOGPS_LOGP>
0.07

> <JCHEM_LOGP>
0.4748031106666659

> <ALOGPS_LOGS>
-2.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.35721467847386

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.472791254702011

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5917509056209602

> <JCHEM_POLAR_SURFACE_AREA>
153.75

> <JCHEM_REFRACTIVITY>
97.39230000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.81e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.667  -1.540   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -5.335   3.080   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.001   5.390   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -1.334   5.390   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.667   3.080   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.001   6.930   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.335   3.080   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.668   5.390   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336   5.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.003   5.390   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.669   3.080   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   28                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   27                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   11   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    7   28                                                  
CONECT   28   27    3                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₆O₉

Average Mass

398.4080 Da

Monoisotopic Mass

398.15768 Da

IUPAC Name

4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-1H-2-benzopyran-1-one

Traditional Name

4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=O)OC(CC(O)C(O)C(=O)CCCC(C)O)C(O)C2=C1

InChI Identifier

InChI=1S/C19H26O9/c1-9(20)4-3-5-12(21)18(25)14(23)8-15-17(24)11-6-10(27-2)7-13(22)16(11)19(26)28-15/h6-7,9,14-15,17-18,20,22-25H,3-5,8H2,1-2H3

InChI Key

SQYAYCYQGHSUJQ-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
Aigialus parvus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

2-benzopyrans

Direct Parent

2-benzopyrans

Alternative Parents

Substituents

2-benzopyran
Fatty alcohol
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Acyloin
Fatty acyl
Monosaccharide
Benzenoid
Beta-hydroxy ketone
Alpha-hydroxy ketone
Vinylogous acid
Lactone
Ketone
Carboxylic acid ester
Secondary alcohol
Oxacycle
Polyol
Carboxylic acid derivative
Ether
Monocarboxylic acid or derivatives
Alcohol
Carbonyl group
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
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	0.07	ALOGPS
logP	0.47	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	9.47	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	153.75 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	97.39 m³·mol⁻¹	ChemAxon
Polarizability	40 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

74928175

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one (NP0320730)

MOL for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

3D MOL for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

3D SDF for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

3D-SDF for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

PDB for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

3D PDB for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

SMILES for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

INCHI for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

Structure for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)

3D Structure for NP0320730 (4,8-dihydroxy-6-methoxy-3-(2,3,8-trihydroxy-4-oxononyl)-3,4-dihydro-2-benzopyran-1-one)