NP-MRD: Showing NP-Card for 5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside (NP0057200)

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Record Information

Version

2.0

Created at

2022-04-28 02:42:19 UTC

Updated at

2022-04-28 02:42:19 UTC

NP-MRD ID

NP0057200

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside

Description

CHEMBL469863 belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety. Thus, CHEMBL469863 is considered to be a flavonoid. 5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside is found in Exostema caribaeum. Based on a literature review very few articles have been published on CHEMBL469863.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282204422D          

 33 36  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   -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
    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 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
    0.7145    2.0625    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    2.0625    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
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  1  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
   -2.1434    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    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 O   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
   -1.4289   -0.0000    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  3  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
  4 18  2  0  0  0  0
 18 19  1  0  0  0  0
  1 19  2  0  0  0  0
 18 20  1  0  0  0  0
 21 20  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 25 27  1  1  0  0  0
 27 28  1  0  0  0  0
 24 29  1  1  0  0  0
 23 30  1  1  0  0  0
 22 31  1  6  0  0  0
  1 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
    0.9234   -2.9246    4.7636 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4231   -2.9387    3.4595 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6249   -1.7670    2.7218 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3238   -0.5518    3.2869 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5451    0.5790    2.5074 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0401    0.5143    1.2299 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3055    1.7569    0.5232 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3623    2.5759    0.9841 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7002    3.7243    0.3316 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6474    4.4368    0.7630 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0278    4.0542   -0.7288 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0342    3.3162   -1.1882 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3590    3.7407   -2.3288 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3175    3.0197   -2.8468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3241    3.4852   -3.9864 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0889    4.6885   -4.6066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0658    1.8539   -2.2249 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5633    1.3778   -1.0911 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2015    0.2315   -0.4527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8214   -0.6547   -0.7263 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7916   -0.6848    0.3110 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9383   -1.2198   -0.2811 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2001   -0.9358    0.4910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4209    0.4362    0.6010 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7288   -2.6995   -0.4620 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4653   -3.3760    0.5339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2536   -3.0420   -0.3025 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8953   -2.9299    1.0293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4283   -2.0456   -1.0975 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7392   -2.3317   -2.4519 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6238    2.1404   -0.5932 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3309   -0.7115    0.6924 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1208   -1.8465    1.4442 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5338   -3.9366    5.0399 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0787   -2.2327    4.9320 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7785   -2.7374    5.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9285   -0.4732    4.3008 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2954    1.5394    2.9858 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8847    2.2324    1.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7082    4.6760   -2.7796 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1390    4.4990   -4.9577 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1777    5.5294   -3.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5074    4.9254   -5.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8939    1.2959   -2.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4127   -0.2597   -1.5996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9883   -0.7198   -1.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1236   -1.4205    1.4738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0350   -1.3619   -0.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5382    0.7850   -0.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0673   -3.0294   -1.4767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9282   -4.1258    0.0918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1296   -4.0733   -0.6954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6239   -3.1648    1.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6421   -2.2787   -1.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4901   -3.2784   -2.5912 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7294   -0.8214   -0.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3512   -2.8407    1.0218 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  2  0
  6 32  1  0
 32 33  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
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 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
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 29 30  1  0
 18 31  2  0
 33  3  1  0
 31  7  1  0
 31 12  1  0
 29 20  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  4 37  1  0
  5 38  1  0
 32 56  1  0
 33 57  1  0
  8 39  1  0
 13 40  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 20 45  1  6
 22 46  1  6
 23 47  1  0
 23 48  1  0
 24 49  1  0
 25 50  1  6
 26 51  1  0
 27 52  1  6
 28 53  1  0
 29 54  1  6
 30 55  1  0
M  END


  Mrv1652304282204422D          

 33 36  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   -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
    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 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
    0.7145    2.0625    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    2.0625    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
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  1  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
   -2.1434    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    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 O   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
   -1.4289   -0.0000    0.0000 O   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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  3  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
  4 18  2  0  0  0  0
 18 19  1  0  0  0  0
  1 19  2  0  0  0  0
 18 20  1  0  0  0  0
 21 20  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
 25 27  1  1  0  0  0
 27 28  1  0  0  0  0
 24 29  1  1  0  0  0
 23 30  1  1  0  0  0
 22 31  1  6  0  0  0
  1 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057200

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C1=CC(=O)OC2=CC(OC)=CC(O[C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C23H24O10/c1-29-12-5-3-11(4-6-12)14-9-18(25)31-15-7-13(30-2)8-16(19(14)15)32-23-22(28)21(27)20(26)17(10-24)33-23/h3-9,17,20-24,26-28H,10H2,1-2H3/t17-,20+,21+,22-,23-/m1/s1

> <INCHI_KEY>
LQWQTQBLAULEDT-SUHOFRIBSA-N

> <FORMULA>
C23H24O10

> <MOLECULAR_WEIGHT>
460.435

> <EXACT_MASS>
460.136946973

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
45.30081747701594

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-methoxy-4-(4-methoxyphenyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H-chromen-2-one

> <ALOGPS_LOGP>
0.92

> <JCHEM_LOGP>
0.3295822466666664

> <ALOGPS_LOGS>
-3.01

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.19607924791153

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.200109330673673

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092346264787

> <JCHEM_POLAR_SURFACE_AREA>
144.14000000000001

> <JCHEM_REFRACTIVITY>
122.15299999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.53e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-methoxy-4-(4-methoxyphenyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+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  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   3.850   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  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -4.001   6.930   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -5.335   4.620   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -5.335   1.540   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2   19   32                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   18                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    3                                                       
CONECT   10    5   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16   13   17                                                       
CONECT   17   16                                                            
CONECT   18    4   19   20                                                  
CONECT   19   18    1                                                       
CONECT   20   18   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23   31                                                  
CONECT   23   22   24   30                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25   21                                                       
CONECT   27   25   28                                                       
CONECT   28   27                                                            
CONECT   29   24                                                            
CONECT   30   23                                                            
CONECT   31   22                                                            
CONECT   32    1   33                                                       
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₄O₁₀

Average Mass

460.4350 Da

Monoisotopic Mass

460.13695 Da

IUPAC Name

7-methoxy-4-(4-methoxyphenyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H-chromen-2-one

Traditional Name

7-methoxy-4-(4-methoxyphenyl)-5-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C1=CC(=O)OC2=CC(OC)=CC(O[C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)=C12

InChI Identifier

InChI=1S/C23H24O10/c1-29-12-5-3-11(4-6-12)14-9-18(25)31-15-7-13(30-2)8-16(19(14)15)32-23-22(28)21(27)20(26)17(10-24)33-23/h3-9,17,20-24,26-28H,10H2,1-2H3/t17-,20+,21+,22-,23-/m1/s1

InChI Key

LQWQTQBLAULEDT-SUHOFRIBSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Exostema caribaeum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Coumarin glycosides

Direct Parent

Coumarin glycosides

Alternative Parents

Substituents

Coumarin-5-o-glycoside
Coumarin o-glycoside
4-phenylcoumarin
Neoflavonoid skeleton
Phenolic glycoside
Hexose monosaccharide
O-glycosyl compound
Glycosyl compound
Benzopyran
1-benzopyran
Phenoxy compound
Phenol ether
Anisole
Methoxybenzene
Alkyl aryl ether
Pyranone
Pyran
Monosaccharide
Monocyclic benzene moiety
Oxane
Benzenoid
Heteroaromatic compound
Lactone
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Ether
Polyol
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Primary alcohol
Organic oxide
Organooxygen 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	0.92	ALOGPS
logP	0.33	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	144.14 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	122.15 m³·mol⁻¹	ChemAxon
Polarizability	45.3 Å³	ChemAxon
Number of Rings	4	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

23327389

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44559791

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside (NP0057200)

MOL for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

3D MOL for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

3D SDF for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

3D-SDF for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

PDB for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

3D PDB for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

SMILES for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

INCHI for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

Structure for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)

3D Structure for NP0057200 (5-Hydroxy-7,4'-dimethoxy-4-phenylcoumarin 5-O-galactoside)