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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 22:44:24 UTC

Update Date

2022-03-07 02:55:21 UTC

HMDB ID

HMDB0037488

Secondary Accession Numbers

HMDB37488

Metabolite Identification

Common Name

Albanin A

Description

Albanin A belongs to the class of organic compounds known as 3-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 3-position. Thus, albanin a is considered to be a flavonoid. Albanin A has been detected, but not quantified in, fruits. This could make albanin a a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Albanin A.

Structure

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


  Mrv0541 05061309482D          

 26 28  0  0  0  0            999 V2000
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    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
    5.0013    1.2375    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   -1.6500    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
    5.7158    2.4750    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
    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
    4.2868    0.8250    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
    2.1434    1.2375    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
    3.5724    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
    7.1447   -1.6500    0.0000 O   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
    4.2868   -1.6500    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
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
 10  1  1  0  0  0  0
 10  2  1  0  0  0  0
 10  3  2  0  0  0  0
 11  4  1  0  0  0  0
 11  7  2  0  0  0  0
 12  8  2  0  0  0  0
 12  9  1  0  0  0  0
 13  6  1  0  0  0  0
 14  5  1  0  0  0  0
 15  7  1  0  0  0  0
 15 13  2  0  0  0  0
 16  8  1  0  0  0  0
 17  9  2  0  0  0  0
 18 16  2  0  0  0  0
 18 17  1  0  0  0  0
 19 14  1  0  0  0  0
 19 18  1  0  0  0  0
 20 13  1  0  0  0  0
 20 14  2  0  0  0  0
 21 11  1  0  0  0  0
 22 12  1  0  0  0  0
 23 15  1  0  0  0  0
 24 16  1  0  0  0  0
 25 19  2  0  0  0  0
 26 17  1  0  0  0  0
 26 20  1  0  0  0  0
M  END

HMDB0037488
     RDKit          3D
Albanin A
 44 46  0  0  0  0  0  0  0  0999 V2000
   -4.2201   -0.9577    1.3877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3620   -1.0543    0.1687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6170   -2.1370   -0.8275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968   -0.1683    0.0117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5204   -0.2200   -1.1753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0872   -0.3385   -0.8249 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6637    0.6727   -0.2867 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2059    2.0086    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    2.6395   -0.5229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3039    3.9212   -0.1465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047    4.5740    0.8262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0344    5.8557    1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4715    4.0061    1.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8898    2.7236    1.0065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9878    2.2683    1.6719 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480    0.3987    0.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5540   -0.7078   -0.1704 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9057   -0.8454    0.1813 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5352   -2.0506   -0.0158 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8885   -2.2537    0.3157 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8163   -3.0886   -0.5541 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926   -2.9621   -0.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7463   -4.0101   -1.4507 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8332   -1.7508   -0.7109 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5201   -1.5812   -1.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0891   -2.5660   -1.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6982   -1.5728    2.1705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2372   -1.3620    1.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2506    0.1107    1.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5611   -2.6680   -0.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7670   -2.8448   -0.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7261   -1.7821   -1.8501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2463    0.5893    0.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7633    0.4094   -2.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7767   -1.2760   -1.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4391    2.2124   -1.3007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1611    4.3878   -0.5971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7126    5.8812    1.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040    4.5467    2.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5533    1.5118    1.7204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4519   -0.0013    0.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4664   -1.5521    0.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2874   -4.0683   -0.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2146   -4.8981   -1.5946 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  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
  7 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
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  2  0
 25  6  1  0
 14  8  1  0
 24 17  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  9 36  1  0
 10 37  1  0
 12 38  1  0
 13 39  1  0
 15 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 23 44  1  0
M  END


  Mrv0541 05061309482D          

 26 28  0  0  0  0            999 V2000
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    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
    5.0013    1.2375    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   -1.6500    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
    5.7158    2.4750    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
    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
    4.2868    0.8250    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
    2.1434    1.2375    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
    3.5724    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
    7.1447   -1.6500    0.0000 O   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
    4.2868   -1.6500    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
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
 10  1  1  0  0  0  0
 10  2  1  0  0  0  0
 10  3  2  0  0  0  0
 11  4  1  0  0  0  0
 11  7  2  0  0  0  0
 12  8  2  0  0  0  0
 12  9  1  0  0  0  0
 13  6  1  0  0  0  0
 14  5  1  0  0  0  0
 15  7  1  0  0  0  0
 15 13  2  0  0  0  0
 16  8  1  0  0  0  0
 17  9  2  0  0  0  0
 18 16  2  0  0  0  0
 18 17  1  0  0  0  0
 19 14  1  0  0  0  0
 19 18  1  0  0  0  0
 20 13  1  0  0  0  0
 20 14  2  0  0  0  0
 21 11  1  0  0  0  0
 22 12  1  0  0  0  0
 23 15  1  0  0  0  0
 24 16  1  0  0  0  0
 25 19  2  0  0  0  0
 26 17  1  0  0  0  0
 26 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0037488

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C(O)C=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O6/c1-10(2)3-5-14-19(25)18-16(24)8-12(22)9-17(18)26-20(14)13-6-4-11(21)7-15(13)23/h3-4,6-9,21-24H,5H2,1-2H3

> <INCHI_KEY>
KEIIIPKLVSSAEI-UHFFFAOYSA-N

> <FORMULA>
C20H18O6

> <MOLECULAR_WEIGHT>
354.3533

> <EXACT_MASS>
354.110338308

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
36.64963456346732

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-3-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

> <ALOGPS_LOGP>
3.36

> <JCHEM_LOGP>
4.013819911333333

> <ALOGPS_LOGS>
-4.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.122461982746882

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.5981578477717155

> <JCHEM_PKA_STRONGEST_BASIC>
-5.177059826926301

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
98.45349999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.24e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
albanin A

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0037488
     RDKit          3D
Albanin A
 44 46  0  0  0  0  0  0  0  0999 V2000
   -4.2201   -0.9577    1.3877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3620   -1.0543    0.1687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6170   -2.1370   -0.8275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968   -0.1683    0.0117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5204   -0.2200   -1.1753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0872   -0.3385   -0.8249 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6637    0.6727   -0.2867 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2059    2.0086    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    2.6395   -0.5229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3039    3.9212   -0.1465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047    4.5740    0.8262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0344    5.8557    1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4715    4.0061    1.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8898    2.7236    1.0065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9878    2.2683    1.6719 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480    0.3987    0.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5540   -0.7078   -0.1704 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9057   -0.8454    0.1813 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5352   -2.0506   -0.0158 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8885   -2.2537    0.3157 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8163   -3.0886   -0.5541 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926   -2.9621   -0.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7463   -4.0101   -1.4507 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8332   -1.7508   -0.7109 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5201   -1.5812   -1.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0891   -2.5660   -1.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6982   -1.5728    2.1705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2372   -1.3620    1.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2506    0.1107    1.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5611   -2.6680   -0.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7670   -2.8448   -0.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7261   -1.7821   -1.8501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2463    0.5893    0.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7633    0.4094   -2.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7767   -1.2760   -1.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4391    2.2124   -1.3007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1611    4.3878   -0.5971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7126    5.8812    1.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040    4.5467    2.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5533    1.5118    1.7204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4519   -0.0013    0.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4664   -1.5521    0.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2874   -4.0683   -0.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2146   -4.8981   -1.5946 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  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
  7 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
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  2  0
 25  6  1  0
 14  8  1  0
 24 17  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  9 36  1  0
 10 37  1  0
 12 38  1  0
 13 39  1  0
 15 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 23 44  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      10.669   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.003   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
CONECT    1   10                                                            
CONECT    2   10                                                            
CONECT    3    5   10                                                       
CONECT    4    6   11                                                       
CONECT    5    3   14                                                       
CONECT    6    4   13                                                       
CONECT    7   11   15                                                       
CONECT    8   12   16                                                       
CONECT    9   12   17                                                       
CONECT   10    1    2    3                                                  
CONECT   11    4    7   21                                                  
CONECT   12    8    9   22                                                  
CONECT   13    6   15   20                                                  
CONECT   14    5   19   20                                                  
CONECT   15    7   13   23                                                  
CONECT   16    8   18   24                                                  
CONECT   17    9   18   26                                                  
CONECT   18   16   17   19                                                  
CONECT   19   14   18   25                                                  
CONECT   20   13   14   26                                                  
CONECT   21   11                                                            
CONECT   22   12                                                            
CONECT   23   15                                                            
CONECT   24   16                                                            
CONECT   25   19                                                            
CONECT   26   17   20                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

COMPND    HMDB0037488
HETATM    1  C1  UNL     1      -4.220  -0.958   1.388  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.362  -1.054   0.169  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.617  -2.137  -0.828  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.397  -0.168   0.012  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.520  -0.220  -1.175  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.087  -0.339  -0.825  1.00  0.00           C  
HETATM    7  C7  UNL     1       0.664   0.673  -0.287  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.206   2.009   0.010  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.861   2.639  -0.523  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.304   3.921  -0.146  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.605   4.574   0.826  1.00  0.00           C  
HETATM   12  O1  UNL     1      -1.034   5.856   1.213  1.00  0.00           O  
HETATM   13  C12 UNL     1       0.472   4.006   1.403  1.00  0.00           C  
HETATM   14  C13 UNL     1       0.890   2.724   1.007  1.00  0.00           C  
HETATM   15  O2  UNL     1       1.988   2.268   1.672  1.00  0.00           O  
HETATM   16  O3  UNL     1       1.948   0.399   0.002  1.00  0.00           O  
HETATM   17  C14 UNL     1       2.554  -0.708  -0.170  1.00  0.00           C  
HETATM   18  C15 UNL     1       3.906  -0.845   0.181  1.00  0.00           C  
HETATM   19  C16 UNL     1       4.535  -2.051  -0.016  1.00  0.00           C  
HETATM   20  O4  UNL     1       5.889  -2.254   0.316  1.00  0.00           O  
HETATM   21  C17 UNL     1       3.816  -3.089  -0.554  1.00  0.00           C  
HETATM   22  C18 UNL     1       2.493  -2.962  -0.901  1.00  0.00           C  
HETATM   23  O5  UNL     1       1.746  -4.010  -1.451  1.00  0.00           O  
HETATM   24  C19 UNL     1       1.833  -1.751  -0.711  1.00  0.00           C  
HETATM   25  C20 UNL     1       0.520  -1.581  -1.041  1.00  0.00           C  
HETATM   26  O6  UNL     1      -0.089  -2.566  -1.530  1.00  0.00           O  
HETATM   27  H1  UNL     1      -3.698  -1.573   2.171  1.00  0.00           H  
HETATM   28  H2  UNL     1      -5.237  -1.362   1.198  1.00  0.00           H  
HETATM   29  H3  UNL     1      -4.251   0.111   1.683  1.00  0.00           H  
HETATM   30  H4  UNL     1      -4.561  -2.668  -0.561  1.00  0.00           H  
HETATM   31  H5  UNL     1      -2.767  -2.845  -0.779  1.00  0.00           H  
HETATM   32  H6  UNL     1      -3.726  -1.782  -1.850  1.00  0.00           H  
HETATM   33  H7  UNL     1      -2.246   0.589   0.759  1.00  0.00           H  
HETATM   34  H8  UNL     1      -1.763   0.409  -2.020  1.00  0.00           H  
HETATM   35  H9  UNL     1      -1.777  -1.276  -1.605  1.00  0.00           H  
HETATM   36  H10 UNL     1      -1.439   2.212  -1.301  1.00  0.00           H  
HETATM   37  H11 UNL     1      -2.161   4.388  -0.597  1.00  0.00           H  
HETATM   38  H12 UNL     1      -1.713   5.881   1.978  1.00  0.00           H  
HETATM   39  H13 UNL     1       1.004   4.547   2.170  1.00  0.00           H  
HETATM   40  H14 UNL     1       2.553   1.512   1.720  1.00  0.00           H  
HETATM   41  H15 UNL     1       4.452  -0.001   0.608  1.00  0.00           H  
HETATM   42  H16 UNL     1       6.466  -1.552   0.707  1.00  0.00           H  
HETATM   43  H17 UNL     1       4.287  -4.068  -0.726  1.00  0.00           H  
HETATM   44  H18 UNL     1       2.215  -4.898  -1.595  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3    4    4
CONECT    3   30   31   32
CONECT    4    5   33
CONECT    5    6   34   35
CONECT    6    7    7   25
CONECT    7    8   16
CONECT    8    9    9   14
CONECT    9   10   36
CONECT   10   11   11   37
CONECT   11   12   13
CONECT   12   38
CONECT   13   14   14   39
CONECT   14   15
CONECT   15   40
CONECT   16   17
CONECT   17   18   18   24
CONECT   18   19   41
CONECT   19   20   21   21
CONECT   20   42
CONECT   21   22   43
CONECT   22   23   24   24
CONECT   23   44
CONECT   24   25
CONECT   25   26   26
END

HMDB0037488
     RDKit          3D
Albanin A
 44 46  0  0  0  0  0  0  0  0999 V2000
   -4.2201   -0.9577    1.3877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3620   -1.0543    0.1687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6170   -2.1370   -0.8275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968   -0.1683    0.0117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5204   -0.2200   -1.1753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0872   -0.3385   -0.8249 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6637    0.6727   -0.2867 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2059    2.0086    0.0104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8610    2.6395   -0.5229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3039    3.9212   -0.1465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047    4.5740    0.8262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0344    5.8557    1.2133 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4715    4.0061    1.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8898    2.7236    1.0065 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9878    2.2683    1.6719 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480    0.3987    0.0023 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5540   -0.7078   -0.1704 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9057   -0.8454    0.1813 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5352   -2.0506   -0.0158 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8885   -2.2537    0.3157 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8163   -3.0886   -0.5541 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926   -2.9621   -0.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7463   -4.0101   -1.4507 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8332   -1.7508   -0.7109 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5201   -1.5812   -1.0407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0891   -2.5660   -1.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6982   -1.5728    2.1705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2372   -1.3620    1.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2506    0.1107    1.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5611   -2.6680   -0.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7670   -2.8448   -0.7790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7261   -1.7821   -1.8501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2463    0.5893    0.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7633    0.4094   -2.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7767   -1.2760   -1.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4391    2.2124   -1.3007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1611    4.3878   -0.5971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7126    5.8812    1.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0040    4.5467    2.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5533    1.5118    1.7204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4519   -0.0013    0.6079 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4664   -1.5521    0.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2874   -4.0683   -0.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2146   -4.8981   -1.5946 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  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
  7 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
 22 23  1  0
 22 24  2  0
 24 25  1  0
 25 26  2  0
 25  6  1  0
 14  8  1  0
 24 17  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  9 36  1  0
 10 37  1  0
 12 38  1  0
 13 39  1  0
 15 40  1  0
 18 41  1  0
 20 42  1  0
 21 43  1  0
 23 44  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one, 9ci	HMDB

Chemical Formula

C₂₀H₁₈O₆

Average Molecular Weight

354.3533

Monoisotopic Molecular Weight

354.110338308

IUPAC Name

2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-3-(3-methylbut-2-en-1-yl)-4H-chromen-4-one

Traditional Name

albanin A

CAS Registry Number

73343-42-7

SMILES

CC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C(O)C=C(O)C=C1

InChI Identifier

InChI=1S/C20H18O6/c1-10(2)3-5-14-19(25)18-16(24)8-12(22)9-17(18)26-20(14)13-6-4-11(21)7-15(13)23/h3-4,6-9,21-24H,5H2,1-2H3

InChI Key

KEIIIPKLVSSAEI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

3-prenylated flavones

Alternative Parents

Substituents

3-prenylated flavone
4'-hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
Hydroxyflavonoid
Chromone
Benzopyran
1-benzopyran
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Phenol
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12110891 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0037488)

Cellular substructure

Membrane (HMDB: HMDB0037488)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0037488)

Source

Exogenous

Food

Food (HMDB: HMDB0037488)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0037488)

Not Available

Nutrient (HMDB: HMDB0037488)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	220 - 227 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	2.08 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	0.022 g/L	ALOGPS
logP	3.36	ALOGPS
logP	4.01	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	6.6	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	98.45 m³·mol⁻¹	ChemAxon
Polarizability	36.65 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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
DeepCCS	[M+H]+	185.313	30932474
DeepCCS	[M-H]-	182.956	30932474
DeepCCS	[M-2H]-	217.12	30932474
DeepCCS	[M+Na]+	192.348	30932474
AllCCS	[M+H]+	182.1	32859911
AllCCS	[M+H-H2O]+	178.9	32859911
AllCCS	[M+NH4]+	185.1	32859911
AllCCS	[M+Na]+	185.9	32859911
AllCCS	[M-H]-	182.3	32859911
AllCCS	[M+Na-2H]-	181.5	32859911
AllCCS	[M+HCOO]-	180.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Albanin A	CC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C(O)C=C(O)C=C1	5280.5	Standard polar	33892256
Albanin A	CC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C(O)C=C(O)C=C1	3282.5	Standard non polar	33892256
Albanin A	CC(C)=CCC1=C(OC2=CC(O)=CC(O)=C2C1=O)C1=C(O)C=C(O)C=C1	3455.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Albanin A,1TMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC(O[Si](C)(C)C)=CC(O)=C2C1=O	3391.1	Semi standard non polar	33892256
Albanin A,1TMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C1=O	3326.2	Semi standard non polar	33892256
Albanin A,1TMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=CC(O)=CC(O)=C2C1=O	3311.1	Semi standard non polar	33892256
Albanin A,1TMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=CC(O)=CC(O)=C2C1=O	3350.6	Semi standard non polar	33892256
Albanin A,2TMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=CC(O[Si](C)(C)C)=CC(O)=C2C1=O	3259.5	Semi standard non polar	33892256
Albanin A,2TMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=CC(O[Si](C)(C)C)=CC(O)=C2C1=O	3245.4	Semi standard non polar	33892256
Albanin A,2TMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2C1=O	3244.3	Semi standard non polar	33892256
Albanin A,2TMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C1=O	3235.8	Semi standard non polar	33892256
Albanin A,2TMS,isomer #5	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C1=O	3219.8	Semi standard non polar	33892256
Albanin A,2TMS,isomer #6	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=CC(O)=CC(O)=C2C1=O	3244.0	Semi standard non polar	33892256
Albanin A,3TMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=CC(O[Si](C)(C)C)=CC(O)=C2C1=O	3175.3	Semi standard non polar	33892256
Albanin A,3TMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2C1=O	3171.6	Semi standard non polar	33892256
Albanin A,3TMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2C1=O	3144.2	Semi standard non polar	33892256
Albanin A,3TMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=CC(O)=CC(O[Si](C)(C)C)=C2C1=O	3150.1	Semi standard non polar	33892256
Albanin A,4TMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2C1=O	3192.2	Semi standard non polar	33892256
Albanin A,1TBDMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C2C1=O	3663.5	Semi standard non polar	33892256
Albanin A,1TBDMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	3604.1	Semi standard non polar	33892256
Albanin A,1TBDMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC(O)=CC(O)=C2C1=O	3597.0	Semi standard non polar	33892256
Albanin A,1TBDMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=CC(O)=CC(O)=C2C1=O	3625.7	Semi standard non polar	33892256
Albanin A,2TBDMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C2C1=O	3801.3	Semi standard non polar	33892256
Albanin A,2TBDMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C2C1=O	3768.3	Semi standard non polar	33892256
Albanin A,2TBDMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	3777.8	Semi standard non polar	33892256
Albanin A,2TBDMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	3766.3	Semi standard non polar	33892256
Albanin A,2TBDMS,isomer #5	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	3732.0	Semi standard non polar	33892256
Albanin A,2TBDMS,isomer #6	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC(O)=CC(O)=C2C1=O	3767.0	Semi standard non polar	33892256
Albanin A,3TBDMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C2C1=O	3884.9	Semi standard non polar	33892256
Albanin A,3TBDMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	3882.4	Semi standard non polar	33892256
Albanin A,3TBDMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	3830.4	Semi standard non polar	33892256
Albanin A,3TBDMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	3843.2	Semi standard non polar	33892256
Albanin A,4TBDMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	4030.0	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 - Albanin A GC-MS (Non-derivatized) - 70eV, Positive	splash10-002u-3129000000-c9d52ea92a5a65fa6cc4	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Albanin A GC-MS (4 TMS) - 70eV, Positive	splash10-004i-1000049000-ec7b90ea96795905d9f1	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Albanin A 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 - Albanin A 10V, Positive-QTOF	splash10-0a4i-0019000000-df41a8c149f792eff7e7	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 20V, Positive-QTOF	splash10-05mk-3079000000-69b0b0db08ae1778080b	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 40V, Positive-QTOF	splash10-0fvi-5490000000-589d3f70d078ee8034f9	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 10V, Negative-QTOF	splash10-0udi-0009000000-5e69e3fee03c2d9b277d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 20V, Negative-QTOF	splash10-0udi-0029000000-13c8480c6e5e7d260334	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 40V, Negative-QTOF	splash10-0a4i-5984000000-2f2dbc8861a2889f750a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 10V, Positive-QTOF	splash10-0a4i-0009000000-b1e99b126fa654ba9739	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 20V, Positive-QTOF	splash10-0a4i-0009000000-b1e99b126fa654ba9739	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 40V, Positive-QTOF	splash10-0zfr-0945000000-54f0bbc5bdfe3864b650	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 10V, Negative-QTOF	splash10-0udi-0009000000-6f322a051fa53b6f9d02	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 20V, Negative-QTOF	splash10-0udi-0009000000-6f322a051fa53b6f9d02	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin A 40V, Negative-QTOF	splash10-0f6x-0692000000-8e0a6bd3a606e1ba10ad	2021-09-25	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

FDB016559

KNApSAcK ID

C00004024

Chemspider ID

4587689

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5481961

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1861491

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.. .

Showing metabocard for Albanin A (HMDB0037488)

MOL for HMDB0037488 (Albanin A)

3D MOL for HMDB0037488 (Albanin A)

3D SDF for HMDB0037488 (Albanin A)

3D-SDF for HMDB0037488 (Albanin A)

PDB for HMDB0037488 (Albanin A)

3D PDB for HMDB0037488 (Albanin A)

SMILES for HMDB0037488 (Albanin A)

INCHI for HMDB0037488 (Albanin A)

Structure for HMDB0037488 (Albanin A)

3D Structure for HMDB0037488 (Albanin A)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra