NP-MRD: Showing NP-Card for petalopurpurenol (NP0252173)

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Record Information

Version

2.0

Created at

2022-09-07 15:36:09 UTC

Updated at

2022-09-07 15:36:10 UTC

NP-MRD ID

NP0252173

Secondary Accession Numbers

None

Natural Product Identification

Common Name

petalopurpurenol

Description

Petalopurpurenol belongs to the class of organic compounds known as pyranoflavonoids. Pyranoflavonoids are compounds containing a pyran ring fused to a 2-phenyl-1,4-benzopyran skeleton. Thus, petalopurpurenol is considered to be a flavonoid lipid molecule. Petalopurpurenol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261501152D          

 32 35  0  0  0  0            999 V2000
    3.7865    3.1772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0686    2.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5383    1.7700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8205    0.9947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902    0.3627    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
    2.7599   -0.5558    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
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   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
    4.8811    2.2587    0.0000 C   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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 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
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 15 28  1  0  0  0  0
 14 29  2  0  0  0  0
  9 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
  6 31  1  0  0  0  0
  2 32  1  0  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
    6.6178    1.3513   -1.6796 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3640    0.1495   -0.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3478   -0.9369   -0.7895 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2101    0.0698   -0.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2374    1.1685   -0.2457 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9361    0.9518   -0.8860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -0.1017   -0.2531 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7180   -1.4759   -0.3157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7843   -0.2252   -0.9817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3771   -0.0741   -0.3863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5372    0.2235    1.0177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7426    0.3712    1.6311 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9983    0.2319    0.9126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9404   -0.5905    1.3500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1026   -0.7707    0.7703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0194   -1.6605    1.3156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2313   -1.8572    0.7225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1467   -2.7603    1.2865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6116   -1.2040   -0.4224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7095   -0.2882   -1.0128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1106    0.3490   -2.1510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4813   -0.1016   -0.3945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5403    0.7670   -0.8910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7801    1.4115   -1.9244 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3133    0.9210   -0.2272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4148    1.8401   -0.7895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7443    0.6324    3.0081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5913    0.7484    3.7453 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5978    0.5995    3.0951 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7923    0.7090    3.7850 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6723    0.3336    1.7245 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8558    0.1757    1.0925 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7619    2.2226   -0.9959 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5125    1.1713   -2.3087 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7850    1.5974   -2.3714 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1680   -1.7079   -1.5631 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3277   -1.4126    0.2301 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3933   -0.5798   -0.9426 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1137   -0.8202    0.4344 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7530    2.0877   -0.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0732    1.5168    0.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1301    0.5798   -1.9404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3878    1.9174   -0.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5058   -1.4662   -1.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0912   -1.8371    0.6414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9210   -2.2276   -0.6140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7745   -0.4505   -2.0588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2816   -0.2454   -0.9744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7648   -2.1912    2.2073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1134   -3.7228    0.9905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5486   -1.3257   -0.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6430    0.9917   -2.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6166    2.3556   -1.6175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7247    0.7376    3.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6298    0.9548    4.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8200    0.8965    4.7602 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  7  6  1  6
  7  8  1  0
  7 32  1  0
 32 31  1  0
 31 29  2  0
 29 30  1  0
 29 28  1  0
 28 27  2  0
 27 12  1  0
 12 13  1  0
 13 25  2  0
 25 26  1  0
 25 23  1  0
 23 24  2  0
 23 22  1  0
 22 20  2  0
 20 21  1  0
 20 19  1  0
 19 17  2  0
 17 18  1  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
 12 11  2  0
 11 10  1  0
 10  9  2  0
  9  7  1  0
 11 31  1  0
 14 13  1  0
 15 22  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  5 40  1  0
  5 41  1  0
  6 42  1  0
  6 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
 30 56  1  0
 28 55  1  0
 27 54  1  0
 26 53  1  0
 21 52  1  0
 19 51  1  0
 18 50  1  0
 16 49  1  0
 10 48  1  0
  9 47  1  0
M  END


  Mrv1533004261501152D          

 32 35  0  0  0  0            999 V2000
    3.7865    3.1772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0686    2.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5383    1.7700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8205    0.9947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2902    0.3627    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
    2.7599   -0.5558    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
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   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
    4.8811    2.2587    0.0000 C   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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 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
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 20 27  1  0  0  0  0
 27 28  1  0  0  0  0
 15 28  1  0  0  0  0
 14 29  2  0  0  0  0
  9 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
  6 31  1  0  0  0  0
  2 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0252173

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC1(C)OC2=C(O)C=CC(C3=C(O)C(=O)C4=C(O)C=C(O)C=C4O3)=C2C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H24O7/c1-13(2)5-4-9-25(3)10-8-16-15(6-7-17(27)23(16)32-25)24-22(30)21(29)20-18(28)11-14(26)12-19(20)31-24/h5-8,10-12,26-28,30H,4,9H2,1-3H3

> <INCHI_KEY>
LBBKHSYDJWHLOM-UHFFFAOYSA-N

> <FORMULA>
C25H24O7

> <MOLECULAR_WEIGHT>
436.46

> <EXACT_MASS>
436.152203113

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
45.78439515792107

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,5,7-trihydroxy-2-[8-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-2H-chromen-5-yl]-4H-chromen-4-one

> <ALOGPS_LOGP>
4.33

> <JCHEM_LOGP>
5.098156192666668

> <ALOGPS_LOGS>
-4.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.916617668142969

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.381912036890941

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8763264375849777

> <JCHEM_POLAR_SURFACE_AREA>
116.45

> <JCHEM_REFRACTIVITY>
123.00029999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.69e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
petalopurpurenol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0       7.068   5.931   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.595   4.484   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.605   3.304   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.132   1.857   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.142   0.677   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.152  -1.037   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.002   0.000   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.337  -4.620   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      13.337  -7.700   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      12.003 -10.010   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.111   4.216   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   31                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   29                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   29                                                  
CONECT   15   14   16   28                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   27                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   20   28                                                  
CONECT   28   27   15                                                       
CONECT   29   14    9   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30    6                                                       
CONECT   32    2                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₄O₇

Average Mass

436.4600 Da

Monoisotopic Mass

436.15220 Da

IUPAC Name

3,5,7-trihydroxy-2-[8-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-2H-chromen-5-yl]-4H-chromen-4-one

Traditional Name

petalopurpurenol

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC1(C)OC2=C(O)C=CC(C3=C(O)C(=O)C4=C(O)C=C(O)C=C4O3)=C2C=C1

InChI Identifier

InChI=1S/C25H24O7/c1-13(2)5-4-9-25(3)10-8-16-15(6-7-17(27)23(16)32-25)24-22(30)21(29)20-18(28)11-14(26)12-19(20)31-24/h5-8,10-12,26-28,30H,4,9H2,1-3H3

InChI Key

LBBKHSYDJWHLOM-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoflavonoids. Pyranoflavonoids are compounds containing a pyran ring fused to a 2-phenyl-1,4-benzopyran skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Pyranoflavonoids

Direct Parent

Pyranoflavonoids

Alternative Parents

Substituents

Pyranoflavonoid
3-hydroxyflavone
Flavone
3-hydroxyflavonoid
4'-hydroxyflavonoid
5-hydroxyflavonoid
Hydroxyflavonoid
7-hydroxyflavonoid
Chromone
Benzopyran
1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Pyranone
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Oxacycle
Organoheterocyclic compound
Polyol
Ether
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12112298 )

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	4.33	ALOGPS
logP	5.1	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	6.38	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	123 m³·mol⁻¹	ChemAxon
Polarizability	45.78 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

10478165

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for petalopurpurenol (NP0252173)

MOL for NP0252173 (petalopurpurenol)

3D MOL for NP0252173 (petalopurpurenol)

3D SDF for NP0252173 (petalopurpurenol)

3D-SDF for NP0252173 (petalopurpurenol)

PDB for NP0252173 (petalopurpurenol)

3D PDB for NP0252173 (petalopurpurenol)

SMILES for NP0252173 (petalopurpurenol)

INCHI for NP0252173 (petalopurpurenol)

Structure for NP0252173 (petalopurpurenol)

3D Structure for NP0252173 (petalopurpurenol)