NP-MRD: Showing NP-Card for lophirone i (NP0202711)

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Record Information

Version

2.0

Created at

2022-09-04 21:58:56 UTC

Updated at

2022-09-04 21:58:56 UTC

NP-MRD ID

NP0202711

Secondary Accession Numbers

None

Natural Product Identification

Common Name

lophirone i

Description

Lophirone i belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. Thus, lophirone I is considered to be a flavonoid. lophirone i is found in Lophira lanceolata. Based on a literature review very few articles have been published on Lophirone i.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042223582D          

 28 32  0  0  1  0            999 V2000
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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  1  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
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0420    1.3770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7065    2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1190    2.8452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9440    2.8452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3565    3.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9440    4.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3565    4.9886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1190    4.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7065    3.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8860    2.0445    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
    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
    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
    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
    2.1434   -1.2375    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  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 10 18  2  0  0  0  0
 18 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  2  0  0  0  0
  5 20  1  0  0  0  0
  4 21  1  0  0  0  0
 21 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
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
  2 28  1  0  0  0  0
M  END

     RDKit          3D

 44 48  0  0  0  0  0  0  0  0999 V2000
   -4.3730   -1.9038   -2.0893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9780   -1.0936   -1.1938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5375   -1.0432   -0.8248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3904   -0.3876    0.5267 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9799   -0.0351    0.8203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6115    0.7792    1.8505 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7218    1.0613    2.0595 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7178    0.5395    1.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0339    0.6512    1.2343 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5534   -0.0383    0.2600 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9655   -0.1860   -0.1082 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9494    0.4546    0.6170 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2832    0.3255    0.2829 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6907   -0.4461   -0.7860 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0268   -0.5607   -1.1013 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6968   -1.0865   -1.5098 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3610   -0.9586   -1.1771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5237   -0.6472   -0.4177 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3524   -0.2771    0.2147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.5616    0.0048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1844    0.8015    0.6060 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5514    0.7013    0.3335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4982    1.4980    0.9188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8466    1.4050    0.6552 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8047    2.2118    1.2481 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2802    0.4597   -0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3363   -0.3636   -0.8571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9810   -0.2476   -0.5720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9485   -0.4787   -1.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1940   -2.0945   -0.7631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7175   -1.1238    1.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3963    1.1956    2.4967 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0130    1.7072    2.8767 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6348    1.0717    1.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0478    0.8395    0.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4481    0.0915   -1.7413 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0017   -1.6890   -2.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5900   -1.4607   -1.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6070   -1.2950   -1.2835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2017   -1.2146   -0.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1615    2.2434    1.6301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2659    1.9448    2.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3332    0.3333   -0.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6473   -1.1222   -1.5767 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11 17  1  0
 17 16  2  0
 11 10  1  0
 10 18  2  0
 18 19  1  0
 19 20  2  0
 20  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 28  1  0
 28 27  2  0
 27 26  1  0
 26 24  2  0
 24 25  1  0
 24 23  1  0
 23 22  2  0
 22 21  1  0
 16 14  1  0
  9 10  1  0
 21  4  1  0
  8 19  1  0
 22 28  1  0
 15 36  1  0
 13 35  1  0
 12 34  1  0
 17 38  1  0
 16 37  1  0
 18 39  1  0
 20 40  1  0
  6 32  1  0
  7 33  1  0
  4 31  1  1
  3 29  1  0
  3 30  1  0
 27 44  1  0
 26 43  1  0
 25 42  1  0
 23 41  1  0
M  END


  Mrv1652309042223582D          

 28 32  0  0  1  0            999 V2000
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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  1  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
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0420    1.3770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7065    2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1190    2.8452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9440    2.8452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3565    3.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9440    4.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3565    4.9886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1190    4.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7065    3.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8860    2.0445    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
    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
    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
    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
    2.1434   -1.2375    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  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 11 17  1  0  0  0  0
 10 18  2  0  0  0  0
 18 19  1  0  0  0  0
  8 19  1  0  0  0  0
 19 20  2  0  0  0  0
  5 20  1  0  0  0  0
  4 21  1  0  0  0  0
 21 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
 24 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 22 28  1  0  0  0  0
  2 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0202711

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)C1=CC2=CC(=CC=C2O1)[C@@H]1CC(=O)C2=CC=C(O)C=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C23H16O5/c24-16-4-1-13(2-5-16)21-10-15-9-14(3-8-20(15)27-21)22-12-19(26)18-7-6-17(25)11-23(18)28-22/h1-11,22,24-25H,12H2/t22-/m0/s1

> <INCHI_KEY>
FKAOXSDPCYTXNP-QFIPXVFZSA-N

> <FORMULA>
C23H16O5

> <MOLECULAR_WEIGHT>
372.376

> <EXACT_MASS>
372.099773615

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
39.32058464302811

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-7-hydroxy-2-[2-(4-hydroxyphenyl)-1-benzofuran-5-yl]-3,4-dihydro-2H-1-benzopyran-4-one

> <JCHEM_LOGP>
4.215023258333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.414112016828154

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.787334713602059

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9090413044266334

> <JCHEM_POLAR_SURFACE_AREA>
79.9

> <JCHEM_REFRACTIVITY>
103.1637

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
lophirone I

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.667  -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       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.812   2.570   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -3.185   3.977   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.955   5.311   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.495   5.311   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.265   6.645   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.495   7.978   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -6.265   9.312   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -3.955   7.978   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.185   6.645   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.654   3.816   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   21                                                  
CONECT    5    4    6   20                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   18                                                  
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   11                                                       
CONECT   18   10   19                                                       
CONECT   19   18    8   20                                                  
CONECT   20   19    5                                                       
CONECT   21    4   22                                                       
CONECT   22   21   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   22    2                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₁₆O₅

Average Mass

372.3760 Da

Monoisotopic Mass

372.09977 Da

IUPAC Name

(2S)-7-hydroxy-2-[2-(4-hydroxyphenyl)-1-benzofuran-5-yl]-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

lophirone I

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)C1=CC2=CC(=CC=C2O1)[C@@H]1CC(=O)C2=CC=C(O)C=C2O1

InChI Identifier

InChI=1S/C23H16O5/c24-16-4-1-13(2-5-16)21-10-15-9-14(3-8-20(15)27-21)22-12-19(26)18-7-6-17(25)11-23(18)28-22/h1-11,22,24-25H,12H2/t22-/m0/s1

InChI Key

FKAOXSDPCYTXNP-QFIPXVFZSA-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
Lophira lanceolata	LOTUS Database	35616633

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
Flavonolignan
Furanoflavonoid or dihydroflavonoid
7-hydroxyflavonoid
Flavanone
Hydroxyflavonoid
Flavan
2-phenylbenzofuran
Phenylbenzofuran
Chromone
Chromane
Benzopyran
1-benzopyran
Benzofuran
Aryl alkyl ketone
Aryl ketone
Phenol
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Furan
Heteroaromatic compound
Ketone
Organoheterocyclic compound
Ether
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavanones (LMPK12140048 )

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	4.22	ChemAxon
pKa (Strongest Acidic)	7.79	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.9 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	103.16 m³·mol⁻¹	ChemAxon
Polarizability	39.32 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

C00014712

Chemspider ID

24846234

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

42607815

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for lophirone i (NP0202711)

MOL for NP0202711 (lophirone i)

3D MOL for NP0202711 (lophirone i)

3D SDF for NP0202711 (lophirone i)

3D-SDF for NP0202711 (lophirone i)

PDB for NP0202711 (lophirone i)

3D PDB for NP0202711 (lophirone i)

SMILES for NP0202711 (lophirone i)

INCHI for NP0202711 (lophirone i)

Structure for NP0202711 (lophirone i)

3D Structure for NP0202711 (lophirone i)