NP-MRD: Showing NP-Card for Moracin Q (NP0074736)

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Record Information

Version

2.0

Created at

2022-04-28 20:03:33 UTC

Updated at

2022-04-28 20:03:33 UTC

NP-MRD ID

NP0074736

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Moracin Q

Description

Moracin Q belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. Moracin Q is found in Morus alba, Morus mesozygia and Morus sp.. Based on a literature review very few articles have been published on moracin Q.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222032D          

 26 28  0  0  0  0            999 V2000
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 O   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  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  5  9  1  0  0  0  0
  8 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
 14 16  1  0  0  0  0
 12 17  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 26  1  0  0  0  0
M  END

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
   -4.0610    2.3484    0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0662    2.2117    1.0555 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7006    2.1275    0.8147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9831    3.3222    0.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6729    4.5331    0.9775 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3718    3.3008    0.5423 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0132    2.0973    0.3489 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2760    1.7807    0.1111 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4387    0.5052   -0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -0.2350   -0.2677 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8736    0.4156   -0.4275 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0630   -0.2516   -0.6773 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2584    0.4434   -0.8328 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0236   -1.6107   -0.7657 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8498   -2.3038   -0.6137 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8794   -3.6930   -0.7159 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6770   -1.6090   -0.3648 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1995   -0.0791    0.1655 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2830    0.9293    0.3923 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0784    0.9119    0.6236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7913   -0.3608    0.6507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5614   -0.6986   -0.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6560   -0.0414   -1.5578 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3072   -2.0098   -0.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0559   -2.2434   -1.7900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3104   -1.9607    0.6220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5369    2.5021   -0.8972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6313    1.3935    0.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7737    3.1737    0.2868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1335    5.3868    0.9448 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9287    4.2257    0.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8973    1.4792   -0.3570 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5287    0.7507   -1.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9554   -2.1543   -0.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0441   -4.2146    0.1579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7391   -2.1541   -0.2427 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9179   -1.1234    0.1408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4608   -0.3495    1.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0754   -1.1974    0.8353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5287   -2.8009   -0.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5196   -1.8283   -2.6666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0693   -1.7872   -1.6745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2336   -3.3337   -1.9155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8006   -0.9566    0.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0426   -2.7757    0.5187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8392   -2.0663    1.6195 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
  4  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 20  3  1  0
 17 10  1  0
 19  7  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  6 31  1  0
 18 37  1  0
 21 38  1  0
 21 39  1  0
 24 40  1  0
 25 41  1  0
 25 42  1  0
 25 43  1  0
 26 44  1  0
 26 45  1  0
 26 46  1  0
 11 32  1  0
 13 33  1  0
 14 34  1  0
 16 35  1  0
 17 36  1  0
M  END


  Mrv1652304282222032D          

 26 28  0  0  0  0            999 V2000
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 O   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  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  5  9  1  0  0  0  0
  8 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
 14 16  1  0  0  0  0
 12 17  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
  2 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0074736

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C2OC(=CC2=C1CC(=O)C(C)C)C1=CC(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O6/c1-10(2)16(23)7-15-14-8-18(11-4-12(21)6-13(22)5-11)26-19(14)9-17(24)20(15)25-3/h4-6,8-10,21-22,24H,7H2,1-3H3

> <INCHI_KEY>
WMDVTEYZKOEFEB-UHFFFAOYSA-N

> <FORMULA>
C20H20O6

> <MOLECULAR_WEIGHT>
356.374

> <EXACT_MASS>
356.125988364

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
37.50365885987479

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[2-(3,5-dihydroxyphenyl)-6-hydroxy-5-methoxy-1-benzofuran-4-yl]-3-methylbutan-2-one

> <ALOGPS_LOGP>
3.84

> <JCHEM_LOGP>
3.8421244089999997

> <ALOGPS_LOGS>
-3.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.090349355538477

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.501442543609135

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8496316404008746

> <JCHEM_POLAR_SURFACE_AREA>
100.13000000000002

> <JCHEM_REFRACTIVITY>
96.37879999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.80e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[2-(3,5-dihydroxyphenyl)-6-hydroxy-5-methoxy-1-benzofuran-4-yl]-3-methylbutan-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       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.322   2.016   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.877   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.107  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.433  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.203   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.433   2.104   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.107   2.104   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.203   3.437   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -2.203  -1.897   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.121  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.454  -3.080   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.788  -2.310   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.454  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.788  -5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.121  -5.390   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.788  -0.770   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.122  -0.000   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.788   2.310   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   26                                                  
CONECT    3    2    4   24                                                  
CONECT    4    3    5   18                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8    5                                                       
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14   10                                                       
CONECT   16   14                                                            
CONECT   17   12                                                            
CONECT   18    4   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24    3   25                                                       
CONECT   25   24                                                            
CONECT   26    2                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₀O₆

Average Mass

356.3740 Da

Monoisotopic Mass

356.12599 Da

IUPAC Name

1-[2-(3,5-dihydroxyphenyl)-6-hydroxy-5-methoxy-1-benzofuran-4-yl]-3-methylbutan-2-one

Traditional Name

1-[2-(3,5-dihydroxyphenyl)-6-hydroxy-5-methoxy-1-benzofuran-4-yl]-3-methylbutan-2-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C2OC(=CC2=C1CC(=O)C(C)C)C1=CC(O)=CC(O)=C1

InChI Identifier

InChI=1S/C20H20O6/c1-10(2)16(23)7-15-14-8-18(11-4-12(21)6-13(22)5-11)26-19(14)9-17(24)20(15)25-3/h4-6,8-10,21-22,24H,7H2,1-3H3

InChI Key

WMDVTEYZKOEFEB-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
Morus alba	LOTUS Database	35616633
Morus mesozygia	Plant	KNApSAcK
Morus sp.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
4-prenylated 2-arybenzofuran
Phenylbenzofuran
2-phenylbenzofuran
Benzofuran
Phenol ether
Resorcinol
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Furan
Heteroaromatic compound
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Organic oxide
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
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	3.84	ALOGPS
logP	3.84	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	8.5	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	100.13 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	96.38 m³·mol⁻¹	ChemAxon
Polarizability	37.5 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	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00036159

Chemspider ID

24626238

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25208125

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Moracin Q (NP0074736)

MOL for NP0074736 (Moracin Q)

3D MOL for NP0074736 (Moracin Q)

3D SDF for NP0074736 (Moracin Q)

3D-SDF for NP0074736 (Moracin Q)

PDB for NP0074736 (Moracin Q)

3D PDB for NP0074736 (Moracin Q)

SMILES for NP0074736 (Moracin Q)

INCHI for NP0074736 (Moracin Q)

Structure for NP0074736 (Moracin Q)

3D Structure for NP0074736 (Moracin Q)