NP-MRD: Showing NP-Card for Calopogoniumisoflavone A (NP0056532)

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Record Information

Version

2.0

Created at

2022-04-28 02:16:58 UTC

Updated at

2022-04-28 02:16:58 UTC

NP-MRD ID

NP0056532

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Calopogoniumisoflavone A

Description

Calopogoniumisoflavone a belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton. Thus, calopogoniumisoflavone a is considered to be a flavonoid lipid molecule. Calopogoniumisoflavone A is found in Calopogonium mucunoides and Millettia dura. Calopogoniumisoflavone a is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161521432D          

 25 28  0  0  0  0            999 V2000
   -3.8230   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -1.5322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -2.5928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -3.4914    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
  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
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 12 23  1  0  0  0  0
 23 24  1  0  0  0  0
  9 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
    7.9949   -0.5913   -0.7666 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3020   -0.0765    0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8996   -0.0546    0.3254 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1799    0.4442    1.3896 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7977    0.4672    1.3848 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0974   -0.0149    0.3005 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6406   -0.0073    0.2587 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8413   -0.4039    1.3101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4719   -0.3775    1.2199 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1136    0.0206    0.1427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5004    0.0065    0.1601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2149    0.4161   -0.9491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4958    0.8416   -2.0796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1167    0.8433   -2.0635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4015    0.4358   -0.9600 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9709    0.4152   -0.8845 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6306    0.7893   -1.8778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5678    0.3942   -0.9105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3366   -0.0134    0.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1787    1.2168    0.5789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3353   -1.0999   -0.2102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5266   -0.4378    1.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2247   -0.4342    1.3311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8436   -0.5090   -0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2113   -0.5311   -0.7460 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7607   -1.6556   -0.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0938   -0.5363   -0.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8715    0.0067   -1.6950 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7586    0.8229    2.2425 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2922    0.8698    2.2465 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3510   -0.7377    2.2130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0839    1.1529   -2.9232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5736    1.1723   -2.9376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1270    0.9004    1.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5298    1.8245    1.2071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4515    1.8124   -0.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7855   -2.0665   -0.1733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1267   -1.0767    0.5567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6929   -0.8708   -1.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0903   -0.7750    2.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6759   -0.7646    2.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3230   -0.8948   -1.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7608   -0.9234   -1.5835 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 24  1  0
 24 25  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 23  1  0
 23 22  2  0
 22 19  1  0
 19 20  1  0
 19 21  1  0
 19 18  1  0
 18 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 25  3  1  0
 16  7  1  0
 15 10  1  0
 12 11  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  0
 24 42  1  0
 25 43  1  0
  8 31  1  0
 23 41  1  0
 22 40  1  0
 20 34  1  0
 20 35  1  0
 20 36  1  0
 21 37  1  0
 21 38  1  0
 21 39  1  0
 13 32  1  0
 14 33  1  0
M  END


  Mrv1533004161521432D          

 25 28  0  0  0  0            999 V2000
   -3.8230   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -1.5322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -2.5928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -3.4914    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
  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
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 12 23  1  0  0  0  0
 23 24  1  0  0  0  0
  9 24  1  0  0  0  0
 24 25  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0056532

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C1=COC2=C3C=CC(C)(C)OC3=CC=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H18O4/c1-21(2)11-10-15-18(25-21)9-8-16-19(22)17(12-24-20(15)16)13-4-6-14(23-3)7-5-13/h4-12H,1-3H3

> <INCHI_KEY>
QLPJSBWLIFSIMS-UHFFFAOYSA-N

> <FORMULA>
C21H18O4

> <MOLECULAR_WEIGHT>
334.371

> <EXACT_MASS>
334.12050906

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
36.75985186439681

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(4-methoxyphenyl)-8,8-dimethyl-4H,8H-pyrano[2,3-h]chromen-4-one

> <ALOGPS_LOGP>
4.39

> <JCHEM_LOGP>
4.080520491

> <ALOGPS_LOGS>
-5.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.508186290786872

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
96.5968

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.23e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
calopogoniumisoflavone A

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -7.136  -5.184   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.366  -3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -4.826  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.056  -2.516   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.516  -2.516   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.746  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.516  -5.184   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.056  -5.184   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.206  -3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.564  -2.516   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.104  -2.516   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.874  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.414  -3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.184  -2.516   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.724  -2.516   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.494  -3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.673  -2.860   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.673  -4.840   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.724  -5.184   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.184  -5.184   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.414  -6.517   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.874  -6.517   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.104  -5.184   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.564  -5.184   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.206  -6.517   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    6   10   24                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14   20                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16   20                                                       
CONECT   20   19   13   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   12   24                                                  
CONECT   24   23    9   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₈O₄

Average Mass

334.3710 Da

Monoisotopic Mass

334.12051 Da

IUPAC Name

3-(4-methoxyphenyl)-8,8-dimethyl-4H,8H-pyrano[2,3-h]chromen-4-one

Traditional Name

calopogoniumisoflavone A

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C1=COC2=C3C=CC(C)(C)OC3=CC=C2C1=O

InChI Identifier

InChI=1S/C21H18O4/c1-21(2)11-10-15-18(25-21)9-8-16-19(22)17(12-24-20(15)16)13-4-6-14(23-3)7-5-13/h4-12H,1-3H3

InChI Key

QLPJSBWLIFSIMS-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
Calopogonium mucunoides	Plant	KNApSAcK
Millettia dura	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Pyranoisoflavonoids

Direct Parent

Pyranoisoflavonoids

Alternative Parents

Substituents

Pyranoisoflavonoid
4p-o-methylisoflavone
Isoflavone
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Benzopyran
1-benzopyran
Methoxybenzene
Anisole
Phenoxy compound
Phenol ether
Alkyl aryl ether
Pyranone
Benzenoid
Monocyclic benzene moiety
Pyran
Heteroaromatic compound
Ether
Organoheterocyclic compound
Oxacycle
Organic oxide
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Isoflavonoids (LMPK12050035 )

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	4.39	ALOGPS
logP	4.08	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	96.6 m³·mol⁻¹	ChemAxon
Polarizability	36.76 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

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

354119

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Calopogoniumisoflavone A (NP0056532)

MOL for NP0056532 (Calopogoniumisoflavone A)

3D MOL for NP0056532 (Calopogoniumisoflavone A)

3D SDF for NP0056532 (Calopogoniumisoflavone A)

3D-SDF for NP0056532 (Calopogoniumisoflavone A)

PDB for NP0056532 (Calopogoniumisoflavone A)

3D PDB for NP0056532 (Calopogoniumisoflavone A)

SMILES for NP0056532 (Calopogoniumisoflavone A)

INCHI for NP0056532 (Calopogoniumisoflavone A)

Structure for NP0056532 (Calopogoniumisoflavone A)

3D Structure for NP0056532 (Calopogoniumisoflavone A)