NP-MRD: Showing NP-Card for repenone (NP0196593)

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Record Information

Version

2.0

Created at

2022-09-04 14:42:45 UTC

Updated at

2022-09-04 14:42:45 UTC

NP-MRD ID

NP0196593

Secondary Accession Numbers

None

Natural Product Identification

Common Name

repenone

Description

Repenone belongs to the class of organic compounds known as rotenones. These are rotenoids with a structure based on a 6a,12a-dihydrochromeno[3,4-b]chromen-12(6H)-one skeleton. Thus, repenone is considered to be a flavonoid. repenone is found in Boerhavia repens. Based on a literature review very few articles have been published on Repenone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042216422D          

 27 30  0  0  0  0            999 V2000
    3.6850   -4.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -3.4853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149   -2.7057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -2.5498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748   -2.0821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -1.3025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9058    0.1007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  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
  9 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
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END

     RDKit          3D

 39 42  0  0  0  0  0  0  0  0999 V2000
    4.7504    3.8288    0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9938    2.7256    0.4714 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3396    1.8674   -0.4089 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149    2.0691   -1.6585 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6057    0.7967    0.0221 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9223   -0.1028   -0.8586 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4577   -1.3547   -0.6943 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8444   -2.4779   -0.2419 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5387   -3.6925   -0.1315 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9226   -4.8348    0.3265 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5907   -4.7583    0.6790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1249   -3.5750    0.5822 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5067   -2.4486    0.1239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1997   -1.1595   -0.0018 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4967   -0.0399   -0.4765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1590    1.0920   -0.5769 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4223    1.2200   -0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0909    2.4248   -0.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4400    2.5466   -0.0256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0533    3.7732   -0.1617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1273    1.4650    0.4370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4453    1.5154    0.7921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4785    0.2413    0.5623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1481   -0.8666    1.0266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1561    0.1657    0.2123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5074   -1.0852    0.3445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1703   -2.0377    0.7680 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8807    3.7738   -1.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7144    3.9324    0.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1489    4.7614    0.2143 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0825    0.2049   -1.9233 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5860   -3.6751   -0.4281 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4969   -5.7489    0.3952 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1102   -5.6462    1.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1364   -3.6267    0.8774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5898    3.3081   -0.7327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0050    3.9146    0.0685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0310    2.3311    0.7513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1187   -0.8274    1.2877 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 25 26  1  0
 26 27  2  0
 15  6  1  0
 25 17  1  0
 13  8  1  0
 26 14  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  6 31  1  6
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 18 36  1  0
 20 37  1  0
 22 38  1  0
 24 39  1  0
M  END


  Mrv1652309042216422D          

 27 30  0  0  0  0            999 V2000
    3.6850   -4.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -3.4853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4149   -2.7057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -2.5498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748   -2.0821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1449   -1.3025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550   -1.1466    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2251   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0352   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3052    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7651    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9550    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6850    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946   -0.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4444   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9058    0.1007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3657    1.6598    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9845    1.1921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2546    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5246    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3347    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6048    1.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  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
  9 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
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  0  0  0  0
 14 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0196593

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)OC1OC2=CC=CC=C2C2=C1OC1=CC(O)=C(O)C(O)=C1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H12O9/c1-24-18(23)27-17-16-11(7-4-2-3-5-9(7)26-17)14(21)12-10(25-16)6-8(19)13(20)15(12)22/h2-6,17,19-20,22H,1H3

> <INCHI_KEY>
JHFAKPWBUSBCCY-UHFFFAOYSA-N

> <FORMULA>
C18H12O9

> <MOLECULAR_WEIGHT>
372.285

> <EXACT_MASS>
372.048131966

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
34.354786979710184

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 9,10,11-trihydroxy-12-oxo-6,12-dihydro-5,7-dioxatetraphen-6-yl carbonate

> <JCHEM_LOGP>
3.289133540666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.279147837538014

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.692295908844931

> <JCHEM_PKA_STRONGEST_BASIC>
-4.812803142422193

> <JCHEM_POLAR_SURFACE_AREA>
131.75000000000003

> <JCHEM_REFRACTIVITY>
89.05259999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
repenone

> <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  C   UNK     0       6.879  -7.670   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.870  -6.506   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.375  -5.051   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.887  -4.760   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       5.366  -3.887   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.870  -2.431   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.383  -2.140   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.887  -0.685   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.399  -0.394   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.903   1.061   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.895   2.225   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.383   1.934   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.879   0.479   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.366   0.188   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.862  -1.267   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.350  -1.558   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.342  -0.394   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.830  -0.685   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.179   0.479   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.691   0.188   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.326   1.934   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.683   3.098   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.838   2.225   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.342   3.680   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.846   1.061   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.358   1.352   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.862   2.807   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13   15   26                                                  
CONECT   15   14    6   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   17   26                                                  
CONECT   26   25   14   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₂O₉

Average Mass

372.2850 Da

Monoisotopic Mass

372.04813 Da

IUPAC Name

methyl 9,10,11-trihydroxy-12-oxo-6,12-dihydro-5,7-dioxatetraphen-6-yl carbonate

Traditional Name

repenone

CAS Registry Number

Not Available

SMILES

COC(=O)OC1OC2=CC=CC=C2C2=C1OC1=CC(O)=C(O)C(O)=C1C2=O

InChI Identifier

InChI=1S/C18H12O9/c1-24-18(23)27-17-16-11(7-4-2-3-5-9(7)26-17)14(21)12-10(25-16)6-8(19)13(20)15(12)22/h2-6,17,19-20,22H,1H3

InChI Key

JHFAKPWBUSBCCY-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Boerhavia repens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as rotenones. These are rotenoids with a structure based on a 6a,12a-dihydrochromeno[3,4-b]chromen-12(6H)-one skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Rotenoids

Direct Parent

Rotenones

Alternative Parents

Substituents

Rotenone or derivatives
Isoflavone
Chromone
Benzopyran
1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Pyranone
1-hydroxy-4-unsubstituted benzenoid
Carbonic acid diester
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Carbonic acid derivative
Oxacycle
Polyol
Acetal
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Rotenoid flavonoids (LMPK12060079 )

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	3.29	ChemAxon
pKa (Strongest Acidic)	6.69	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	131.75 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	89.05 m³·mol⁻¹	ChemAxon
Polarizability	34.35 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	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00009987

Chemspider ID

24842975

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44257427

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for repenone (NP0196593)

MOL for NP0196593 (repenone)

3D MOL for NP0196593 (repenone)

3D SDF for NP0196593 (repenone)

3D-SDF for NP0196593 (repenone)

PDB for NP0196593 (repenone)

3D PDB for NP0196593 (repenone)

SMILES for NP0196593 (repenone)

INCHI for NP0196593 (repenone)

Structure for NP0196593 (repenone)

3D Structure for NP0196593 (repenone)