NP-MRD: Showing NP-Card for 4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate (NP0237609)

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Record Information

Version

2.0

Created at

2022-09-06 20:48:18 UTC

Updated at

2022-09-06 20:48:18 UTC

NP-MRD ID

NP0237609

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate

Description

4-Hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxo-4H-chromen-2-yl)phenyl acetate belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone. 4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate is found in Notholaena aliena. 4-Hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxo-4H-chromen-2-yl)phenyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171516272D          

 29 31  0  0  0  0            999 V2000
    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 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
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    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
    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
    5.0013   -0.4125    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
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    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
    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 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
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    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
  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
  6  7  2  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
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  2  0  0  0  0
  4 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -5.0514    2.9337   -0.7773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8030    2.6252   -0.1768 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0031    1.5853   -0.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4301    0.8468   -1.7434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6510   -0.1643   -2.2158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0192   -0.9601   -3.3104 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4291   -0.4710   -1.6330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6742   -1.4956   -2.1289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0117   -2.1910   -3.0952 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5603   -1.7815   -1.5089 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3170   -2.7987   -2.0116 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695   -4.1610   -1.8103 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9148   -1.0077   -0.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1573   -1.1473    0.3030 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7287   -2.3304    0.6192 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9676   -2.3823    1.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4939   -3.6219    1.5271 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6223   -1.2308    1.5280 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0695   -0.0170    1.2218 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8156    0.0380    0.5975 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2932    1.3016    0.2947 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8413    2.2223    1.1789 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3446    3.5284    0.6317 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8558    1.9636    2.3891 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1123   -0.0148   -0.0235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0281    0.2908   -0.5496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7968    1.3204   -0.0485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4009    2.0833    1.0408 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7909    1.6278    2.3284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5944    1.9475   -0.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6690    3.5835   -0.1572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9032    3.3167   -1.8121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3633    1.0623   -2.2088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9082   -0.7396   -3.7373 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9537   -4.7447   -2.7094 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6155   -4.4316   -0.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3033   -4.5345   -1.5936 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1873   -3.2572    0.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0401   -4.4841    1.3251 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6012   -1.2660    2.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5634    0.8985    1.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5824    3.9780    1.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8456    3.3440   -0.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1756    4.2429    0.4732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9329    1.1467    2.8340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1406    2.4485    2.9730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6305    0.8974    2.2680 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  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 10 13  2  0
 13 25  1  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 27  3  1  0
 20 14  1  0
 26  7  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  4 33  1  0
  6 34  1  0
 12 35  1  0
 12 36  1  0
 12 37  1  0
 29 45  1  0
 29 46  1  0
 29 47  1  0
 15 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 23 42  1  0
 23 43  1  0
 23 44  1  0
M  END


  Mrv1533004171516272D          

 29 31  0  0  0  0            999 V2000
    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 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
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    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
    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
    5.0013   -0.4125    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
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    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
    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 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
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    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
  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
  6  7  2  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
 10 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  2  0  0  0  0
  4 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 19 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237609

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=C2C(=O)C(OC)=C(OC2=C1OC)C1=CC(O)=CC=C1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O9/c1-9(21)28-13-6-5-10(22)7-11(13)17-20(27-4)16(24)15-12(23)8-14(25-2)18(26-3)19(15)29-17/h5-8,22-23H,1-4H3

> <INCHI_KEY>
OAEULSJISUDEJO-UHFFFAOYSA-N

> <FORMULA>
C20H18O9

> <MOLECULAR_WEIGHT>
402.355

> <EXACT_MASS>
402.09508216

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
39.046267358400186

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxo-4H-chromen-2-yl)phenyl acetate

> <ALOGPS_LOGP>
2.98

> <JCHEM_LOGP>
2.168175939666666

> <ALOGPS_LOGS>
-4.04

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.109263004452352

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.647521761109037

> <JCHEM_PKA_STRONGEST_BASIC>
-4.449529450738313

> <JCHEM_POLAR_SURFACE_AREA>
120.75

> <JCHEM_REFRACTIVITY>
101.7104

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.65e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate

> <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       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  -2.310   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  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -2.310   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  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000   1.540   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   3.850   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5   19                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   16                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    6   17                                                  
CONECT   17   16    3   18                                                  
CONECT   18   17                                                            
CONECT   19    4   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   19   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Value	Source
4-Hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxo-4H-chromen-2-yl)phenyl acetic acid	Generator

Chemical Formula

C₂₀H₁₈O₉

Average Mass

402.3550 Da

Monoisotopic Mass

402.09508 Da

IUPAC Name

4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxo-4H-chromen-2-yl)phenyl acetate

Traditional Name

4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(=O)C(OC)=C(OC2=C1OC)C1=CC(O)=CC=C1OC(C)=O

InChI Identifier

InChI=1S/C20H18O9/c1-9(21)28-13-6-5-10(22)7-11(13)17-20(27-4)16(24)15-12(23)8-14(25-2)18(26-3)19(15)29-17/h5-8,22-23H,1-4H3

InChI Key

OAEULSJISUDEJO-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
Notholaena aliena	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

8-O-methylated flavonoids

Alternative Parents

Substituents

3-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
8-methoxyflavonoid-skeleton
Flavone
3'-hydroxyflavonoid
5-hydroxyflavonoid
Hydroxyflavonoid
3-methoxychromone
Chromone
Benzopyran
Phenol ester
1-benzopyran
Phenoxy compound
Anisole
Pyranone
Phenol
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyran
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Vinylogous acid
Carboxylic acid ester
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Ether
Carbonyl group
Organooxygen compound
Organic oxide
Organic oxygen compound
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	2.98	ALOGPS
logP	2.17	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	7.65	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	120.75 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	101.71 m³·mol⁻¹	ChemAxon
Polarizability	39.05 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

14134166

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate (NP0237609)

MOL for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

3D MOL for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

3D SDF for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

3D-SDF for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

PDB for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

3D PDB for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

SMILES for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

INCHI for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

Structure for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)

3D Structure for NP0237609 (4-hydroxy-2-(5-hydroxy-3,7,8-trimethoxy-4-oxochromen-2-yl)phenyl acetate)