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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 17:39:28 UTC

Update Date

2022-03-07 02:52:43 UTC

HMDB ID

HMDB0030863

Secondary Accession Numbers

HMDB30863

Metabolite Identification

Common Name

Kuwanon F

Description

Kuwanon F 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, kuwanon F is considered to be a flavonoid. Based on a literature review a significant number of articles have been published on Kuwanon F.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

  Mrv0541 05061305332D          

 31 34  0  0  0  0            999 V2000
   10.6427   -3.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5481   -4.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4269   -3.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4875   -2.9637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2999   -2.8205    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
    7.9572   -2.3317    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
    5.0013   -1.2375    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
    2.1434   -0.4125    0.0000 C   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
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8302   -3.4525    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
    1.4289    0.0000    0.0000 C   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
    2.1434    1.2375    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
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   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
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  4  1  0  0  0  0
  8  6  2  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14  5  2  0  0  0  0
 15  6  1  0  0  0  0
 15  9  1  0  0  0  0
 16 10  2  0  0  0  0
 16 11  1  0  0  0  0
 17  9  2  0  0  0  0
 18 12  2  0  0  0  0
 18 17  1  0  0  0  0
 19 10  1  0  0  0  0
 20 13  1  0  0  0  0
 21 12  1  0  0  0  0
 21 15  2  0  0  0  0
 22 13  1  0  0  0  0
 22 17  1  0  0  0  0
 23 11  2  0  0  0  0
 24 19  2  0  0  0  0
 24 20  1  0  0  0  0
 24 23  1  0  0  0  0
 25  3  1  0  0  0  0
 25  7  1  0  0  0  0
 25  8  1  0  0  0  0
 26 16  1  0  0  0  0
 27 18  1  0  0  0  0
 28 19  1  0  0  0  0
 29 20  2  0  0  0  0
 30 22  1  0  0  0  0
 30 23  1  0  0  0  0
 31 21  1  0  0  0  0
 31 25  1  0  0  0  0
M  END

HMDB0030863
     RDKit          3D
Kuwanon F
 57 60  0  0  0  0  0  0  0  0999 V2000
   -7.3691    0.4658   -1.2783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2155   -0.5259   -0.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4155   -1.0973    0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0115   -0.9001    0.1908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8046   -0.3499   -0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9904    0.3432    0.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7119    0.9467   -0.0197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1303    1.9711   -1.1046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9812    1.7149    0.9955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7171    1.4991    1.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0537    0.4775    0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3903    0.2466    0.8524 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0252   -0.7349    0.1459 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4539   -1.0073    0.4216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9766   -0.1513    1.5664 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4599   -0.4210    1.6423 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0291   -0.8231    2.6828 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2126   -0.1853    0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5475    0.1647    0.4830 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2629    0.3236    1.6436 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1734    0.3637   -0.7657 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4801    0.2137   -1.9420 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1397    0.4213   -3.1696 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1494   -0.1360   -1.9605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5125   -0.3369   -0.7689 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1705   -0.6914   -0.7830 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3867   -1.4798   -0.8151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0628   -2.4899   -1.5315 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0646   -1.2454   -1.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6241   -0.2486   -0.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9400    0.0011   -0.6479 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8424    1.4087   -1.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9227    0.0819   -2.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4356    0.7147   -1.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1444   -1.4628    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8185   -1.9798   -0.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2483   -0.3616    0.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8848   -1.6285    1.0017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2658   -1.2350   -0.9093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1268    0.3397   -1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6710   -0.3936    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6198    1.1501    1.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9269    1.5792   -2.1207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2011    2.2039   -0.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5566    2.9143   -1.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4725    2.5118    1.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1851    2.0900    2.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8381    0.8636    1.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6394   -2.0677    0.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4513   -0.4366    2.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8310    0.9145    1.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8895    0.2206    2.5401 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2322    0.6421   -0.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6505    0.3162   -4.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5858   -0.2585   -2.8777 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0293   -2.6350   -1.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4648   -1.8217   -1.8479 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
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 13 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31  7  1  0
 30 11  1  0
 26 14  1  0
 25 18  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  8 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
 10 47  1  0
 12 48  1  0
 14 49  1  0
 15 50  1  0
 15 51  1  0
 20 52  1  0
 21 53  1  0
 23 54  1  0
 24 55  1  0
 28 56  1  0
 29 57  1  0
M  END

  Mrv0541 05061305332D          

 31 34  0  0  0  0            999 V2000
   10.6427   -3.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5481   -4.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4269   -3.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4875   -2.9637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2999   -2.8205    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
    7.9572   -2.3317    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
    5.0013   -1.2375    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
    2.1434   -0.4125    0.0000 C   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
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8302   -3.4525    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
    1.4289    0.0000    0.0000 C   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
    2.1434    1.2375    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
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    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
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   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
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  4  1  0  0  0  0
  8  6  2  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 14  5  2  0  0  0  0
 15  6  1  0  0  0  0
 15  9  1  0  0  0  0
 16 10  2  0  0  0  0
 16 11  1  0  0  0  0
 17  9  2  0  0  0  0
 18 12  2  0  0  0  0
 18 17  1  0  0  0  0
 19 10  1  0  0  0  0
 20 13  1  0  0  0  0
 21 12  1  0  0  0  0
 21 15  2  0  0  0  0
 22 13  1  0  0  0  0
 22 17  1  0  0  0  0
 23 11  2  0  0  0  0
 24 19  2  0  0  0  0
 24 20  1  0  0  0  0
 24 23  1  0  0  0  0
 25  3  1  0  0  0  0
 25  7  1  0  0  0  0
 25  8  1  0  0  0  0
 26 16  1  0  0  0  0
 27 18  1  0  0  0  0
 28 19  1  0  0  0  0
 29 20  2  0  0  0  0
 30 22  1  0  0  0  0
 30 23  1  0  0  0  0
 31 21  1  0  0  0  0
 31 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0030863

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)=CCCC1(C)OC2=C(C=C1)C=C(C1CC(=O)C3=C(O)C=C(O)C=C3O1)C(O)=C2

> <INCHI_IDENTIFIER>
InChI=1S/C25H26O6/c1-14(2)5-4-7-25(3)8-6-15-9-17(18(27)12-21(15)31-25)22-13-20(29)24-19(28)10-16(26)11-23(24)30-22/h5-6,8-12,22,26-28H,4,7,13H2,1-3H3

> <INCHI_KEY>
FZAZNGMSARSUNC-UHFFFAOYSA-N

> <FORMULA>
C25H26O6

> <MOLECULAR_WEIGHT>
422.4703

> <EXACT_MASS>
422.172938564

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
46.32026316999137

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,7-dihydroxy-2-[7-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-2H-chromen-6-yl]-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
4.25

> <JCHEM_LOGP>
5.4733994573333336

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.135715043415296

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.895145302585832

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8613247142892915

> <JCHEM_POLAR_SURFACE_AREA>
96.22

> <JCHEM_REFRACTIVITY>
119.40879999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.76e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
kuwanon F

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0030863
     RDKit          3D
Kuwanon F
 57 60  0  0  0  0  0  0  0  0999 V2000
   -7.3691    0.4658   -1.2783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2155   -0.5259   -0.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4155   -1.0973    0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0115   -0.9001    0.1908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8046   -0.3499   -0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9904    0.3432    0.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7119    0.9467   -0.0197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1303    1.9711   -1.1046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9812    1.7149    0.9955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7171    1.4991    1.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0537    0.4775    0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3903    0.2466    0.8524 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0252   -0.7349    0.1459 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4539   -1.0073    0.4216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9766   -0.1513    1.5664 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4599   -0.4210    1.6423 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0291   -0.8231    2.6828 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2126   -0.1853    0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5475    0.1647    0.4830 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2629    0.3236    1.6436 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1734    0.3637   -0.7657 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4801    0.2137   -1.9420 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1397    0.4213   -3.1696 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1494   -0.1360   -1.9605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5125   -0.3369   -0.7689 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1705   -0.6914   -0.7830 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3867   -1.4798   -0.8151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0628   -2.4899   -1.5315 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0646   -1.2454   -1.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6241   -0.2486   -0.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9400    0.0011   -0.6479 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8424    1.4087   -1.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9227    0.0819   -2.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4356    0.7147   -1.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1444   -1.4628    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8185   -1.9798   -0.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2483   -0.3616    0.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8848   -1.6285    1.0017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2658   -1.2350   -0.9093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1268    0.3397   -1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6710   -0.3936    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6198    1.1501    1.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9269    1.5792   -2.1207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2011    2.2039   -0.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5566    2.9143   -1.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4725    2.5118    1.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1851    2.0900    2.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8381    0.8636    1.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6394   -2.0677    0.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4513   -0.4366    2.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8310    0.9145    1.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8895    0.2206    2.5401 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2322    0.6421   -0.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6505    0.3162   -4.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5858   -0.2585   -2.8777 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0293   -2.6350   -1.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4648   -1.8217   -1.8479 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
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 13 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31  7  1  0
 30 11  1  0
 26 14  1  0
 25 18  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  8 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
 10 47  1  0
 12 48  1  0
 14 49  1  0
 15 50  1  0
 15 51  1  0
 20 52  1  0
 21 53  1  0
 23 54  1  0
 24 55  1  0
 28 56  1  0
 29 57  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      19.866  -6.177   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.823  -7.892   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.864  -6.067   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.843  -5.532   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      17.360  -5.265   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.853  -4.353   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      18.350  -6.445   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.002   0.000   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       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
CONECT    1   14                                                            
CONECT    2   14                                                            
CONECT    3   25                                                            
CONECT    4    5    7                                                       
CONECT    5    4   14                                                       
CONECT    6    8   15                                                       
CONECT    7    4   25                                                       
CONECT    8    6   25                                                       
CONECT    9   15   17                                                       
CONECT   10   16   19                                                       
CONECT   11   16   23                                                       
CONECT   12   18   21                                                       
CONECT   13   20   22                                                       
CONECT   14    1    2    5                                                  
CONECT   15    6    9   21                                                  
CONECT   16   10   11   26                                                  
CONECT   17    9   18   22                                                  
CONECT   18   12   17   27                                                  
CONECT   19   10   24   28                                                  
CONECT   20   13   24   29                                                  
CONECT   21   12   15   31                                                  
CONECT   22   13   17   30                                                  
CONECT   23   11   24   30                                                  
CONECT   24   19   20   23                                                  
CONECT   25    3    7    8   31                                             
CONECT   26   16                                                            
CONECT   27   18                                                            
CONECT   28   19                                                            
CONECT   29   20                                                            
CONECT   30   22   23                                                       
CONECT   31   21   25                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0030863
HETATM    1  C1  UNL     1      -7.369   0.466  -1.278  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.215  -0.526  -0.173  1.00  0.00           C  
HETATM    3  C3  UNL     1      -8.416  -1.097   0.524  1.00  0.00           C  
HETATM    4  C4  UNL     1      -6.012  -0.900   0.191  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.805  -0.350  -0.482  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.990   0.343   0.577  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.712   0.947  -0.020  1.00  0.00           C  
HETATM    8  C8  UNL     1      -3.130   1.971  -1.105  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.981   1.715   0.995  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.717   1.499   1.263  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.054   0.478   0.568  1.00  0.00           C  
HETATM   12  C12 UNL     1       1.390   0.247   0.852  1.00  0.00           C  
HETATM   13  C13 UNL     1       2.025  -0.735   0.146  1.00  0.00           C  
HETATM   14  C14 UNL     1       3.454  -1.007   0.422  1.00  0.00           C  
HETATM   15  C15 UNL     1       3.977  -0.151   1.566  1.00  0.00           C  
HETATM   16  C16 UNL     1       5.460  -0.421   1.642  1.00  0.00           C  
HETATM   17  O1  UNL     1       6.029  -0.823   2.683  1.00  0.00           O  
HETATM   18  C17 UNL     1       6.213  -0.185   0.414  1.00  0.00           C  
HETATM   19  C18 UNL     1       7.547   0.165   0.483  1.00  0.00           C  
HETATM   20  O2  UNL     1       8.263   0.324   1.644  1.00  0.00           O  
HETATM   21  C19 UNL     1       8.173   0.364  -0.766  1.00  0.00           C  
HETATM   22  C20 UNL     1       7.480   0.214  -1.942  1.00  0.00           C  
HETATM   23  O3  UNL     1       8.140   0.421  -3.170  1.00  0.00           O  
HETATM   24  C21 UNL     1       6.149  -0.136  -1.961  1.00  0.00           C  
HETATM   25  C22 UNL     1       5.512  -0.337  -0.769  1.00  0.00           C  
HETATM   26  O4  UNL     1       4.170  -0.691  -0.783  1.00  0.00           O  
HETATM   27  C23 UNL     1       1.387  -1.480  -0.815  1.00  0.00           C  
HETATM   28  O5  UNL     1       2.063  -2.490  -1.531  1.00  0.00           O  
HETATM   29  C24 UNL     1       0.065  -1.245  -1.091  1.00  0.00           C  
HETATM   30  C25 UNL     1      -0.624  -0.249  -0.390  1.00  0.00           C  
HETATM   31  O6  UNL     1      -1.940   0.001  -0.648  1.00  0.00           O  
HETATM   32  H1  UNL     1      -6.842   1.409  -1.026  1.00  0.00           H  
HETATM   33  H2  UNL     1      -6.923   0.082  -2.222  1.00  0.00           H  
HETATM   34  H3  UNL     1      -8.436   0.715  -1.455  1.00  0.00           H  
HETATM   35  H4  UNL     1      -8.144  -1.463   1.536  1.00  0.00           H  
HETATM   36  H5  UNL     1      -8.819  -1.980  -0.043  1.00  0.00           H  
HETATM   37  H6  UNL     1      -9.248  -0.362   0.559  1.00  0.00           H  
HETATM   38  H7  UNL     1      -5.885  -1.628   1.002  1.00  0.00           H  
HETATM   39  H8  UNL     1      -4.266  -1.235  -0.909  1.00  0.00           H  
HETATM   40  H9  UNL     1      -5.127   0.340  -1.290  1.00  0.00           H  
HETATM   41  H10 UNL     1      -3.671  -0.394   1.319  1.00  0.00           H  
HETATM   42  H11 UNL     1      -4.620   1.150   1.005  1.00  0.00           H  
HETATM   43  H12 UNL     1      -2.927   1.579  -2.121  1.00  0.00           H  
HETATM   44  H13 UNL     1      -4.201   2.204  -1.000  1.00  0.00           H  
HETATM   45  H14 UNL     1      -2.557   2.914  -1.002  1.00  0.00           H  
HETATM   46  H15 UNL     1      -2.472   2.512   1.577  1.00  0.00           H  
HETATM   47  H16 UNL     1      -0.185   2.090   2.034  1.00  0.00           H  
HETATM   48  H17 UNL     1       1.838   0.864   1.620  1.00  0.00           H  
HETATM   49  H18 UNL     1       3.639  -2.068   0.725  1.00  0.00           H  
HETATM   50  H19 UNL     1       3.451  -0.437   2.475  1.00  0.00           H  
HETATM   51  H20 UNL     1       3.831   0.915   1.300  1.00  0.00           H  
HETATM   52  H21 UNL     1       7.889   0.221   2.540  1.00  0.00           H  
HETATM   53  H22 UNL     1       9.232   0.642  -0.771  1.00  0.00           H  
HETATM   54  H23 UNL     1       7.651   0.316  -4.026  1.00  0.00           H  
HETATM   55  H24 UNL     1       5.586  -0.258  -2.878  1.00  0.00           H  
HETATM   56  H25 UNL     1       3.029  -2.635  -1.294  1.00  0.00           H  
HETATM   57  H26 UNL     1      -0.465  -1.822  -1.848  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3    4    4
CONECT    3   35   36   37
CONECT    4    5   38
CONECT    5    6   39   40
CONECT    6    7   41   42
CONECT    7    8    9   31
CONECT    8   43   44   45
CONECT    9   10   10   46
CONECT   10   11   47
CONECT   11   12   12   30
CONECT   12   13   48
CONECT   13   14   27   27
CONECT   14   15   26   49
CONECT   15   16   50   51
CONECT   16   17   17   18
CONECT   18   19   19   25
CONECT   19   20   21
CONECT   20   52
CONECT   21   22   22   53
CONECT   22   23   24
CONECT   23   54
CONECT   24   25   25   55
CONECT   25   26
CONECT   27   28   29
CONECT   28   56
CONECT   29   30   30   57
CONECT   30   31
END

HMDB0030863
     RDKit          3D
Kuwanon F
 57 60  0  0  0  0  0  0  0  0999 V2000
   -7.3691    0.4658   -1.2783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2155   -0.5259   -0.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4155   -1.0973    0.5235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0115   -0.9001    0.1908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8046   -0.3499   -0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9904    0.3432    0.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7119    0.9467   -0.0197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1303    1.9711   -1.1046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9812    1.7149    0.9955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7171    1.4991    1.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0537    0.4775    0.5681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3903    0.2466    0.8524 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0252   -0.7349    0.1459 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4539   -1.0073    0.4216 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9766   -0.1513    1.5664 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4599   -0.4210    1.6423 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0291   -0.8231    2.6828 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2126   -0.1853    0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5475    0.1647    0.4830 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2629    0.3236    1.6436 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1734    0.3637   -0.7657 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4801    0.2137   -1.9420 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1397    0.4213   -3.1696 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1494   -0.1360   -1.9605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5125   -0.3369   -0.7689 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1705   -0.6914   -0.7830 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3867   -1.4798   -0.8151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0628   -2.4899   -1.5315 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0646   -1.2454   -1.0906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6241   -0.2486   -0.3899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9400    0.0011   -0.6479 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8424    1.4087   -1.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9227    0.0819   -2.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4356    0.7147   -1.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1444   -1.4628    1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8185   -1.9798   -0.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2483   -0.3616    0.5585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8848   -1.6285    1.0017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2658   -1.2350   -0.9093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1268    0.3397   -1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6710   -0.3936    1.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6198    1.1501    1.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9269    1.5792   -2.1207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2011    2.2039   -0.9995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5566    2.9143   -1.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4725    2.5118    1.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1851    2.0900    2.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8381    0.8636    1.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6394   -2.0677    0.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4513   -0.4366    2.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8310    0.9145    1.3001 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8895    0.2206    2.5401 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2322    0.6421   -0.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6505    0.3162   -4.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5858   -0.2585   -2.8777 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0293   -2.6350   -1.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4648   -1.8217   -1.8479 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
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 13 27  2  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31  7  1  0
 30 11  1  0
 26 14  1  0
 25 18  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  4 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  8 43  1  0
  8 44  1  0
  8 45  1  0
  9 46  1  0
 10 47  1  0
 12 48  1  0
 14 49  1  0
 15 50  1  0
 15 51  1  0
 20 52  1  0
 21 53  1  0
 23 54  1  0
 24 55  1  0
 28 56  1  0
 29 57  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
4-Methyl-2-(1-methyl-1-butenyl)-1,3-dioxolane	HMDB
5,7,7'-Trihydroxy-2'-methyl-2'-(4-methyl-3-pentenyl)-(2,6'-bi-2H-1-benzopyran)-4(3H)-one, 9ci	HMDB

Chemical Formula

C₂₅H₂₆O₆

Average Molecular Weight

422.4703

Monoisotopic Molecular Weight

422.172938564

IUPAC Name

5,7-dihydroxy-2-[7-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-2H-chromen-6-yl]-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

kuwanon F

CAS Registry Number

71344-07-5

SMILES

CC(C)=CCCC1(C)OC2=C(C=C1)C=C(C1CC(=O)C3=C(O)C=C(O)C=C3O1)C(O)=C2

InChI Identifier

InChI=1S/C25H26O6/c1-14(2)5-4-7-25(3)8-6-15-9-17(18(27)12-21(15)31-25)22-13-20(29)24-19(28)10-16(26)11-23(24)30-22/h5-6,8-12,22,26-28H,4,7,13H2,1-3H3

InChI Key

FZAZNGMSARSUNC-UHFFFAOYSA-N

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
5-hydroxyflavonoid
7-hydroxyflavonoid
Flavanone
Hydroxyflavonoid
Flavan
Chromone
Chromane
Benzopyran
1-benzopyran
Aryl ketone
Aryl alkyl ketone
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Vinylogous acid
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavanones (LMPK12140513 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0030863)
Cell membrane (HMDB: HMDB0030863)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0030863)

Source

Endogenous

Endogenous (HMDB: HMDB0030863)

Plant

Plant (HMDB: HMDB0030863)

Exogenous

Food

Food (HMDB: HMDB0030863)

Fruit

Fruits (FooDB: FOOD00871)

Exogenous (HMDB: HMDB0030863)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	0.021 mg/L @ 25 °C (est)	The Good Scents Company Information System
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0048 g/L	ALOGPS
logP	4.25	ALOGPS
logP	5.47	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	7.9	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	119.41 m³·mol⁻¹	ChemAxon
Polarizability	46.32 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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	204.965	31661259
DarkChem	[M-H]-	204.695	31661259
DeepCCS	[M+H]+	203.428	30932474
DeepCCS	[M-H]-	201.038	30932474
DeepCCS	[M-2H]-	234.291	30932474
DeepCCS	[M+Na]+	209.519	30932474
AllCCS	[M+H]+	208.8	32859911
AllCCS	[M+H-H2O]+	206.1	32859911
AllCCS	[M+NH4]+	211.3	32859911
AllCCS	[M+Na]+	212.0	32859911
AllCCS	[M-H]-	202.2	32859911
AllCCS	[M+Na-2H]-	202.7	32859911
AllCCS	[M+HCOO]-	203.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Kuwanon F	CC(C)=CCCC1(C)OC2=C(C=C1)C=C(C1CC(=O)C3=C(O)C=C(O)C=C3O1)C(O)=C2	5102.7	Standard polar	33892256
Kuwanon F	CC(C)=CCCC1(C)OC2=C(C=C1)C=C(C1CC(=O)C3=C(O)C=C(O)C=C3O1)C(O)=C2	3571.3	Standard non polar	33892256
Kuwanon F	CC(C)=CCCC1(C)OC2=C(C=C1)C=C(C1CC(=O)C3=C(O)C=C(O)C=C3O1)C(O)=C2	3839.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Kuwanon F,1TMS,isomer #1	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(C=C(O)C=C4O[Si](C)(C)C)O3)=C(O)C=C2O1	3644.2	Semi standard non polar	33892256
Kuwanon F,1TMS,isomer #2	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)=C(O)C=C2O1	3657.1	Semi standard non polar	33892256
Kuwanon F,1TMS,isomer #3	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(O)C=C(O)C=C4O3)=C(O[Si](C)(C)C)C=C2O1	3596.6	Semi standard non polar	33892256
Kuwanon F,2TMS,isomer #1	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(C=C(O[Si](C)(C)C)C=C4O[Si](C)(C)C)O3)=C(O)C=C2O1	3565.8	Semi standard non polar	33892256
Kuwanon F,2TMS,isomer #2	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(C=C(O)C=C4O[Si](C)(C)C)O3)=C(O[Si](C)(C)C)C=C2O1	3515.7	Semi standard non polar	33892256
Kuwanon F,2TMS,isomer #3	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)=C(O[Si](C)(C)C)C=C2O1	3535.3	Semi standard non polar	33892256
Kuwanon F,3TMS,isomer #1	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(C=C(O[Si](C)(C)C)C=C4O[Si](C)(C)C)O3)=C(O[Si](C)(C)C)C=C2O1	3505.9	Semi standard non polar	33892256
Kuwanon F,1TBDMS,isomer #1	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(C=C(O)C=C4O[Si](C)(C)C(C)(C)C)O3)=C(O)C=C2O1	3882.7	Semi standard non polar	33892256
Kuwanon F,1TBDMS,isomer #2	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4O3)=C(O)C=C2O1	3897.2	Semi standard non polar	33892256
Kuwanon F,1TBDMS,isomer #3	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(O)C=C(O)C=C4O3)=C(O[Si](C)(C)C(C)(C)C)C=C2O1	3835.1	Semi standard non polar	33892256
Kuwanon F,2TBDMS,isomer #1	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(C=C(O[Si](C)(C)C(C)(C)C)C=C4O[Si](C)(C)C(C)(C)C)O3)=C(O)C=C2O1	4031.0	Semi standard non polar	33892256
Kuwanon F,2TBDMS,isomer #2	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(C=C(O)C=C4O[Si](C)(C)C(C)(C)C)O3)=C(O[Si](C)(C)C(C)(C)C)C=C2O1	3980.8	Semi standard non polar	33892256
Kuwanon F,2TBDMS,isomer #3	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4O3)=C(O[Si](C)(C)C(C)(C)C)C=C2O1	4003.4	Semi standard non polar	33892256
Kuwanon F,3TBDMS,isomer #1	CC(C)=CCCC1(C)C=CC2=CC(C3CC(=O)C4=C(C=C(O[Si](C)(C)C(C)(C)C)C=C4O[Si](C)(C)C(C)(C)C)O3)=C(O[Si](C)(C)C(C)(C)C)C=C2O1	4146.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Kuwanon F GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-9003400000-ed36eebcb34535309678	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kuwanon F GC-MS (3 TMS) - 70eV, Positive	splash10-00di-6200039000-bdba174d0786800463f0	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Kuwanon F GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 10V, Positive-QTOF	splash10-00di-0343900000-7373149a9cb255a4405e	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 20V, Positive-QTOF	splash10-0udi-3955200000-3609bc09add6a5613ce0	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 40V, Positive-QTOF	splash10-0uxs-4910000000-6e9d9847682d3fa74f48	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 10V, Negative-QTOF	splash10-00di-0110900000-bd00da9db975d62be9d4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 20V, Negative-QTOF	splash10-00di-0544900000-7b380558af9c9a25c041	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 40V, Negative-QTOF	splash10-0py0-2895300000-d2151e4aff25c1915956	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 10V, Negative-QTOF	splash10-00di-0000900000-992577a540f8cfc09aec	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 20V, Negative-QTOF	splash10-0fk9-0900800000-6894b5264cbeee2f0128	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 40V, Negative-QTOF	splash10-066r-0591000000-9834b86f96001c28b6a3	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 10V, Positive-QTOF	splash10-00di-0000900000-9a76091e85d6c52ac33b	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 20V, Positive-QTOF	splash10-0uka-0900400000-872be7ec0fc3ceeab907	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Kuwanon F 40V, Positive-QTOF	splash10-0udi-0920000000-eb8701d07ca342bb06cf	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB002823

KNApSAcK ID

C00008379

Chemspider ID

137512

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

156149

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1823241

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Enzymes

Enzyme Details

1. UDP-glucuronosyltransferase 1-1

General function:: Involved in transferase activity, transferring hexosyl groups
Specific function:: UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:: UGT1A1
Uniprot ID:: P22309
Molecular weight:: 59590.91

Reactions

Kuwanon F → 6-{[6-(5,7-dihydroxy-4-oxo-3,4-dihydro-2H-1-benzopyran-2-yl)-2-methyl-2-(4-methylpent-3-en-1-yl)-2H-chromen-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic acid	details
Kuwanon F → 3,4,5-trihydroxy-6-({5-hydroxy-2-[7-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-2H-chromen-6-yl]-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl}oxy)oxane-2-carboxylic acid	details
Kuwanon F → 3,4,5-trihydroxy-6-({7-hydroxy-2-[7-hydroxy-2-methyl-2-(4-methylpent-3-en-1-yl)-2H-chromen-6-yl]-4-oxo-3,4-dihydro-2H-1-benzopyran-5-yl}oxy)oxane-2-carboxylic acid	details

Showing metabocard for Kuwanon F (HMDB0030863)

MOL for HMDB0030863 (Kuwanon F)

3D MOL for HMDB0030863 (Kuwanon F)

3D SDF for HMDB0030863 (Kuwanon F)

3D-SDF for HMDB0030863 (Kuwanon F)

PDB for HMDB0030863 (Kuwanon F)

3D PDB for HMDB0030863 (Kuwanon F)

SMILES for HMDB0030863 (Kuwanon F)

INCHI for HMDB0030863 (Kuwanon F)

Structure for HMDB0030863 (Kuwanon F)

3D Structure for HMDB0030863 (Kuwanon F)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

Reactions