NP-MRD: Showing NP-Card for Gancaonin F (NP0057056)

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Record Information

Version

2.0

Created at

2022-04-28 02:36:54 UTC

Updated at

2022-04-28 02:36:54 UTC

NP-MRD ID

NP0057056

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Gancaonin F

Description

Gancaonin f belongs to the class of organic compounds known as coumestans. These are polycyclic aromatic compounds containing a coumestan moiety, which consists of a benzoxole fused to a chromen-2-one to form 1-Benzoxolo[3,2-c]chromen-6-one. They are oxidation products of pterocarpan. Thus, gancaonin F is considered to be a flavonoid. Gancaonin F is found in Glycyrrhiza glabra and Glycyrrhiza spp.. Based on a literature review very few articles have been published on Gancaonin f.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282204362D          

 27 31  0  0  0  0            999 V2000
    5.1234   -0.2126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8512    0.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0407    0.7200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5023    0.0949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7744   -0.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5850   -0.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2360   -1.3091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4254   -1.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8870   -1.7804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1533   -0.3765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6917    0.2486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2636    0.9538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4606    0.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3924   -0.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -0.4097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0316    0.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0365    0.8826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7826    1.2347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6414    1.3527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7685    1.4988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9580    1.6525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3896    1.1913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2002    1.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4723    0.2588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9339   -0.3663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2602    0.5036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1158   -0.2575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  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  2  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 17 19  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  1 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
M  END

     RDKit          3D

 43 47  0  0  0  0  0  0  0  0999 V2000
    0.3737    2.7492   -0.3723 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0204    1.7519    0.5113 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5164    0.5253    0.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8764    0.3551    0.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4230   -0.8745   -0.0412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5638   -1.9425   -0.2533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1946   -1.7814   -0.2111 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6238   -2.7923   -0.4119 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9443   -2.6735   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7038   -3.6699   -0.5770 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5569   -1.4701   -0.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8692   -1.0579   -0.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0761   -1.7008   -0.1592 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2461   -1.0063   -0.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1710    0.3553    0.2676 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3522    1.0727    0.4219 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9519    0.9886    0.3887 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7694    0.3115    0.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4838    0.6514    0.3033 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7335   -0.3834    0.0872 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3706   -0.5266    0.0487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7879   -0.9957   -0.0752 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6866    0.0496    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5405    0.2271   -1.1313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6018   -0.3899    1.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0810    1.3610    0.4053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7595    1.4849    0.4389 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5154    3.3583   -0.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6730    2.2530   -1.3430 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2486    3.3533   -0.0729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0022   -2.9113   -0.4540 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1090   -2.7529   -0.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1841   -1.5207   -0.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7396    1.4863   -0.4199 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9442    2.0455    0.6043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0168    1.2297   -1.0970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2765   -0.5742   -1.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8305    0.2479   -1.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2927   -1.1300    0.8552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9502   -0.8012    2.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1538    0.4601    1.7107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7487    2.1879    0.5701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3269    2.4496    0.6393 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 21  2  0
 21 20  1  0
 20 11  2  0
 11 12  1  0
 12 18  2  0
 18 19  1  0
 18 17  1  0
 17 15  2  0
 15 16  1  0
 15 14  1  0
 14 13  2  0
 11  9  1  0
  9 10  2  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4 27  1  0
 27 26  2  0
 26 23  1  0
 23 24  1  0
 23 25  1  0
 23 22  1  0
  4  3  1  0
  7 21  1  0
 22  5  1  0
 19 20  1  0
 13 12  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 17 35  1  0
 16 34  1  0
 14 33  1  0
 13 32  1  0
  6 31  1  0
 27 43  1  0
 26 42  1  0
 24 36  1  0
 24 37  1  0
 24 38  1  0
 25 39  1  0
 25 40  1  0
 25 41  1  0
M  END


  Mrv1652304282204362D          

 27 31  0  0  0  0            999 V2000
    5.1234   -0.2126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8512    0.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0407    0.7200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5023    0.0949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7744   -0.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5850   -0.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2360   -1.3091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4254   -1.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8870   -1.7804    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1533   -0.3765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6917    0.2486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2636    0.9538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4606    0.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3924   -0.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -0.4097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0316    0.0604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0365    0.8826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7826    1.2347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6414    1.3527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7685    1.4988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9580    1.6525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3896    1.1913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2002    1.0376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4723    0.2588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9339   -0.3663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2602    0.5036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1158   -0.2575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  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  2  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 17 19  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  1 25  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057056

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C3=C(C4=C(O3)C=C(O)C=C4)C(=O)OC2=CC2=C1C=CC(C)(C)O2

> <INCHI_IDENTIFIER>
InChI=1S/C21H16O6/c1-21(2)7-6-12-14(27-21)9-15-17(18(12)24-3)19-16(20(23)26-15)11-5-4-10(22)8-13(11)25-19/h4-9,22H,1-3H3

> <INCHI_KEY>
YURHIASRSSMERJ-UHFFFAOYSA-N

> <FORMULA>
C21H16O6

> <MOLECULAR_WEIGHT>
364.353

> <EXACT_MASS>
364.094688235

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
38.165853679320136

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6-hydroxy-21-methoxy-17,17-dimethyl-3,12,16-trioxapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{15,20}]henicosa-1(21),2(10),4(9),5,7,13,15(20),18-octaen-11-one

> <ALOGPS_LOGP>
3.99

> <JCHEM_LOGP>
3.4438387803333326

> <ALOGPS_LOGS>
-4.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.103919814099825

> <JCHEM_PKA_STRONGEST_BASIC>
-3.064852453103734

> <JCHEM_POLAR_SURFACE_AREA>
78.13000000000001

> <JCHEM_REFRACTIVITY>
98.49520000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.01e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxy-21-methoxy-17,17-dimethyl-3,12,16-trioxapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{15,20}]henicosa-1(21),2(10),4(9),5,7,13,15(20),18-octaen-11-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       9.564  -0.397   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.056   1.057   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.543   1.344   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.538   0.177   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.046  -1.277   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.559  -1.564   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.041  -2.444   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.527  -2.157   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.522  -3.323   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.019  -0.703   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.025   0.464   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.225   1.780   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.726   1.427   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.599  -0.108   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.206  -0.765   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.059   0.113   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.068   1.648   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.461   2.305   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.197   2.525   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       7.035   2.798   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.522   3.085   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.061   2.224   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.574   1.937   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.082   0.483   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.077  -0.684   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      13.552   0.940   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.283  -0.481   0.000  0.00  0.00           C+0
CONECT    1    2    6   25                                                  
CONECT    2    1    3   22                                                  
CONECT    3    2    4   20                                                  
CONECT    4    3    5   11                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   14                                                  
CONECT   11   10    4   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   10   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17   13                                                       
CONECT   19   17                                                            
CONECT   20    3   21                                                       
CONECT   21   20                                                            
CONECT   22    2   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   27                                             
CONECT   25   24    1                                                       
CONECT   26   24                                                            
CONECT   27   24                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₆O₆

Average Mass

364.3530 Da

Monoisotopic Mass

364.09469 Da

IUPAC Name

6-hydroxy-21-methoxy-17,17-dimethyl-3,12,16-trioxapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{15,20}]henicosa-1(21),2(10),4(9),5,7,13,15(20),18-octaen-11-one

Traditional Name

6-hydroxy-21-methoxy-17,17-dimethyl-3,12,16-trioxapentacyclo[11.8.0.0^{2,10}.0^{4,9}.0^{15,20}]henicosa-1(21),2(10),4(9),5,7,13,15(20),18-octaen-11-one

CAS Registry Number

Not Available

SMILES

COC1=C2C3=C(C4=C(O3)C=C(O)C=C4)C(=O)OC2=CC2=C1C=CC(C)(C)O2

InChI Identifier

InChI=1S/C21H16O6/c1-21(2)7-6-12-14(27-21)9-15-17(18(12)24-3)19-16(20(23)26-15)11-5-4-10(22)8-13(11)25-19/h4-9,22H,1-3H3

InChI Key

YURHIASRSSMERJ-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, 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
Glycyrrhiza glabra	Plant	KNApSAcK
Glycyrrhiza spp.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumestans. These are polycyclic aromatic compounds containing a coumestan moiety, which consists of a benzoxole fused to a chromen-2-one to form 1-Benzoxolo[3,2-c]chromen-6-one. They are oxidation products of pterocarpan.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Coumestans

Direct Parent

Coumestans

Alternative Parents

Substituents

Coumestan
Linear pyranocoumarin
Pyranocoumarin
Angular furanocoumarin
Furanocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Coumarin
Benzopyran
1-benzopyran
Benzofuran
Furopyran
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Benzenoid
Pyran
Furan
Heteroaromatic compound
Lactone
Organoheterocyclic compound
Ether
Oxacycle
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Coumestan flavonoids (LMPK12090043 )

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	3.99	ALOGPS
logP	3.44	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	9.1	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	78.13 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	98.5 m³·mol⁻¹	ChemAxon
Polarizability	38.17 Å³	ChemAxon
Number of Rings	5	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

C00010062

Chemspider ID

4476337

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5317482

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Gancaonin F (NP0057056)

MOL for NP0057056 (Gancaonin F)

3D MOL for NP0057056 (Gancaonin F)

3D SDF for NP0057056 (Gancaonin F)

3D-SDF for NP0057056 (Gancaonin F)

PDB for NP0057056 (Gancaonin F)

3D PDB for NP0057056 (Gancaonin F)

SMILES for NP0057056 (Gancaonin F)

INCHI for NP0057056 (Gancaonin F)

Structure for NP0057056 (Gancaonin F)

3D Structure for NP0057056 (Gancaonin F)