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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 18:31:04 UTC

Update Date

2022-03-07 02:53:50 UTC

HMDB ID

HMDB0033756

Secondary Accession Numbers

HMDB33756

Metabolite Identification

Common Name

Albanin C

Description

Albanin C belongs to the class of organic compounds known as 8-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 8-position. Albanin C has been detected, but not quantified in, fruits. This could make albanin C a potential biomarker for the consumption of these foods. Based on a literature review a significant number of articles have been published on Albanin C.

Structure

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


  Mrv0541 05061307202D          

 32 35  0  0  0  0            999 V2000
   -2.5839    0.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6285    1.7377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0626    1.6514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267    1.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4140    2.4905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9793    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1994    3.2432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1939    1.0365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0240    3.2175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1547    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2352    2.5420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3613    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586    3.9187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0598    2.5677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   -1.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0655   -1.0415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7959    0.5156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 12  5  2  0  0  0  0
 13  6  1  0  0  0  0
 13  9  2  0  0  0  0
 14  8  1  0  0  0  0
 15  7  1  0  0  0  0
 16 10  1  0  0  0  0
 17  9  1  0  0  0  0
 17 14  2  0  0  0  0
 18 11  2  0  0  0  0
 19 11  1  0  0  0  0
 19 16  2  0  0  0  0
 20 10  1  0  0  0  0
 21 18  1  0  0  0  0
 22 15  1  0  0  0  0
 22 21  1  0  0  0  0
 23 14  1  0  0  0  0
 23 15  2  0  0  0  0
 24 16  1  0  0  0  0
 24 21  2  0  0  0  0
 25  3  1  0  0  0  0
 25  4  1  0  0  0  0
 25 20  1  0  0  0  0
 26 13  1  0  0  0  0
 27 17  1  0  0  0  0
 28 18  1  0  0  0  0
 29 22  2  0  0  0  0
 30 25  1  0  0  0  0
 31 19  1  0  0  0  0
 31 20  1  0  0  0  0
 32 23  1  0  0  0  0
 32 24  1  0  0  0  0
M  END

HMDB0033756
     RDKit          3D
Albanin C
 58 61  0  0  0  0  0  0  0  0999 V2000
   -5.5275   -1.8842    1.9613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9465   -1.6873    0.6129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2820   -2.6564   -0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1278   -0.6435    0.3694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5207   -0.3952   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0391   -0.3530   -0.9326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2951    0.6447   -0.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7897    1.8387    0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0051    2.3794    0.0757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3895    3.5019    0.8418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5398    4.0453    1.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9864    5.1554    2.4908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2986    3.5060    1.9674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9402    2.4184    1.2182 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3297    1.8555    1.4127 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0313    0.5214   -0.4281 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6823   -0.4632   -0.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0596   -0.4710   -0.9290 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7537   -1.5188   -1.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0402   -2.5556   -2.0524 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6644   -2.5878   -2.0924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0901   -3.6048   -2.6527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0016   -1.5220   -1.5292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3618   -1.4417   -1.5081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0018   -2.3933   -2.0313 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1380   -1.2813   -1.3315 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2524   -0.4460   -0.1961 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5442    0.3145   -0.1614 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6614   -0.7334   -0.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5973    1.1001    1.1311 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6503    1.1160   -1.2735 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0557    0.4864   -0.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6207   -2.0872    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3535   -0.9718    2.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9771   -2.7440    2.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9901   -3.4087   -0.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6698   -2.1077   -1.3529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3191   -3.1366   -0.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9267    0.0103    1.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9980    0.3794   -1.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7997   -1.3462   -1.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7281    2.0411   -0.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3869    3.9241    0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3739    5.5693    3.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6275    3.9243    2.6910 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9373    2.2679    2.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5850   -3.3980   -2.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4130   -4.3927   -3.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0921   -1.0800    0.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5503   -0.3507   -0.6798 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3166   -1.6845   -0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9230   -0.9666    0.9236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9891    0.5878    1.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2574    2.1431    0.9701 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6745    1.1300    1.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6123    1.2318   -1.5404 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3333    1.2420   -1.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7697    0.9782    0.5334 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  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 25  2  0
 19 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 28 31  1  0
 27 32  1  0
 24  6  1  0
 14  8  1  0
 23 17  1  0
 32 18  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
  9 42  1  0
 10 43  1  0
 12 44  1  0
 13 45  1  0
 15 46  1  0
 20 47  1  0
 22 48  1  0
 27 49  1  0
 29 50  1  0
 29 51  1  0
 29 52  1  0
 30 53  1  0
 30 54  1  0
 30 55  1  0
 31 56  1  0
 32 57  1  0
 32 58  1  0
M  END


  Mrv0541 05061307202D          

 32 35  0  0  0  0            999 V2000
   -2.5839    0.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6285    1.7377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0626    1.6514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267    1.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3693    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4140    2.4905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9793    1.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1994    3.2432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1939    1.0365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0240    3.2175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1547    1.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2352    2.5420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3613    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586    3.9187    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0598    2.5677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   -1.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0655   -1.0415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7959    0.5156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 12  5  2  0  0  0  0
 13  6  1  0  0  0  0
 13  9  2  0  0  0  0
 14  8  1  0  0  0  0
 15  7  1  0  0  0  0
 16 10  1  0  0  0  0
 17  9  1  0  0  0  0
 17 14  2  0  0  0  0
 18 11  2  0  0  0  0
 19 11  1  0  0  0  0
 19 16  2  0  0  0  0
 20 10  1  0  0  0  0
 21 18  1  0  0  0  0
 22 15  1  0  0  0  0
 22 21  1  0  0  0  0
 23 14  1  0  0  0  0
 23 15  2  0  0  0  0
 24 16  1  0  0  0  0
 24 21  2  0  0  0  0
 25  3  1  0  0  0  0
 25  4  1  0  0  0  0
 25 20  1  0  0  0  0
 26 13  1  0  0  0  0
 27 17  1  0  0  0  0
 28 18  1  0  0  0  0
 29 22  2  0  0  0  0
 30 25  1  0  0  0  0
 31 19  1  0  0  0  0
 31 20  1  0  0  0  0
 32 23  1  0  0  0  0
 32 24  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0033756

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)=CCC1=C(OC2=C(C(O)=CC3=C2CC(O3)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H26O7/c1-12(2)5-7-15-22(29)21-18(28)11-19-16(10-20(31-19)25(3,4)30)24(21)32-23(15)14-8-6-13(26)9-17(14)27/h5-6,8-9,11,20,26-28,30H,7,10H2,1-4H3

> <INCHI_KEY>
ZDJLVJJUSHPYOI-UHFFFAOYSA-N

> <FORMULA>
C25H26O7

> <MOLECULAR_WEIGHT>
438.4697

> <EXACT_MASS>
438.167853186

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_AVERAGE_POLARIZABILITY>
46.845645981841706

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-3-(3-methylbut-2-en-1-yl)-4H,8H,9H-furo[2,3-h]chromen-4-one

> <ALOGPS_LOGP>
3.87

> <JCHEM_LOGP>
4.266419224666667

> <ALOGPS_LOGS>
-4.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.864322749907338

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.062830686781226

> <JCHEM_PKA_STRONGEST_BASIC>
-3.106437461616533

> <JCHEM_POLAR_SURFACE_AREA>
116.45

> <JCHEM_REFRACTIVITY>
121.26489999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-3-(3-methylbut-2-en-1-yl)-8H,9H-furo[2,3-h]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0033756
     RDKit          3D
Albanin C
 58 61  0  0  0  0  0  0  0  0999 V2000
   -5.5275   -1.8842    1.9613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9465   -1.6873    0.6129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2820   -2.6564   -0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1278   -0.6435    0.3694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5207   -0.3952   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0391   -0.3530   -0.9326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2951    0.6447   -0.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7897    1.8387    0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0051    2.3794    0.0757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3895    3.5019    0.8418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5398    4.0453    1.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9864    5.1554    2.4908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2986    3.5060    1.9674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9402    2.4184    1.2182 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3297    1.8555    1.4127 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0313    0.5214   -0.4281 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6823   -0.4632   -0.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0596   -0.4710   -0.9290 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7537   -1.5188   -1.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0402   -2.5556   -2.0524 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6644   -2.5878   -2.0924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0901   -3.6048   -2.6527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0016   -1.5220   -1.5292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3618   -1.4417   -1.5081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0018   -2.3933   -2.0313 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1380   -1.2813   -1.3315 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2524   -0.4460   -0.1961 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5442    0.3145   -0.1614 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6614   -0.7334   -0.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5973    1.1001    1.1311 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6503    1.1160   -1.2735 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0557    0.4864   -0.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6207   -2.0872    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3535   -0.9718    2.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9771   -2.7440    2.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9901   -3.4087   -0.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6698   -2.1077   -1.3529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3191   -3.1366   -0.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9267    0.0103    1.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9980    0.3794   -1.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7997   -1.3462   -1.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7281    2.0411   -0.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3869    3.9241    0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3739    5.5693    3.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6275    3.9243    2.6910 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9373    2.2679    2.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5850   -3.3980   -2.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4130   -4.3927   -3.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0921   -1.0800    0.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5503   -0.3507   -0.6798 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3166   -1.6845   -0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9230   -0.9666    0.9236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9891    0.5878    1.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2574    2.1431    0.9701 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6745    1.1300    1.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6123    1.2318   -1.5404 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3333    1.2420   -1.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7697    0.9782    0.5334 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  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 25  2  0
 19 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 28 31  1  0
 27 32  1  0
 24  6  1  0
 14  8  1  0
 23 17  1  0
 32 18  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
  9 42  1  0
 10 43  1  0
 12 44  1  0
 13 45  1  0
 15 46  1  0
 20 47  1  0
 22 48  1  0
 27 49  1  0
 29 50  1  0
 29 51  1  0
 29 52  1  0
 30 53  1  0
 30 54  1  0
 30 55  1  0
 31 56  1  0
 32 57  1  0
 32 58  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      -4.823   0.578   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.907   3.244   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.450   3.083   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.330   3.580   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.556   1.983   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.639   4.649   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.745   0.674   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.828   3.340   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.372   6.054   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.406   2.042   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.495  -1.800   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.095   1.935   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.911   6.006   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.289   3.388   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.206   0.722   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.412   0.866   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.439   4.745   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.956  -1.848   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.223  -0.443   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.832   1.460   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.145  -0.539   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.606  -0.587   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.522   2.079   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.873   0.818   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.141   2.271   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.723   7.315   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       1.978   4.793   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.228  -3.205   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -0.122  -1.944   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       8.952   0.962   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       6.719  -0.076   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       2.062   2.127   0.000  0.00  0.00           O+0
CONECT    1   12                                                            
CONECT    2   12                                                            
CONECT    3   25                                                            
CONECT    4   25                                                            
CONECT    5    7   12                                                       
CONECT    6    8   13                                                       
CONECT    7    5   15                                                       
CONECT    8    6   14                                                       
CONECT    9   13   17                                                       
CONECT   10   16   20                                                       
CONECT   11   18   19                                                       
CONECT   12    1    2    5                                                  
CONECT   13    6    9   26                                                  
CONECT   14    8   17   23                                                  
CONECT   15    7   22   23                                                  
CONECT   16   10   19   24                                                  
CONECT   17    9   14   27                                                  
CONECT   18   11   21   28                                                  
CONECT   19   11   16   31                                                  
CONECT   20   10   25   31                                                  
CONECT   21   18   22   24                                                  
CONECT   22   15   21   29                                                  
CONECT   23   14   15   32                                                  
CONECT   24   16   21   32                                                  
CONECT   25    3    4   20   30                                             
CONECT   26   13                                                            
CONECT   27   17                                                            
CONECT   28   18                                                            
CONECT   29   22                                                            
CONECT   30   25                                                            
CONECT   31   19   20                                                       
CONECT   32   23   24                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

COMPND    HMDB0033756
HETATM    1  C1  UNL     1      -5.527  -1.884   1.961  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.946  -1.687   0.613  1.00  0.00           C  
HETATM    3  C3  UNL     1      -5.282  -2.656  -0.461  1.00  0.00           C  
HETATM    4  C4  UNL     1      -4.128  -0.643   0.369  1.00  0.00           C  
HETATM    5  C5  UNL     1      -3.521  -0.395  -0.947  1.00  0.00           C  
HETATM    6  C6  UNL     1      -2.039  -0.353  -0.933  1.00  0.00           C  
HETATM    7  C7  UNL     1      -1.295   0.645  -0.384  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.790   1.839   0.261  1.00  0.00           C  
HETATM    9  C9  UNL     1      -3.005   2.379   0.076  1.00  0.00           C  
HETATM   10  C10 UNL     1      -3.389   3.502   0.842  1.00  0.00           C  
HETATM   11  C11 UNL     1      -2.540   4.045   1.769  1.00  0.00           C  
HETATM   12  O1  UNL     1      -2.986   5.155   2.491  1.00  0.00           O  
HETATM   13  C12 UNL     1      -1.299   3.506   1.967  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.940   2.418   1.218  1.00  0.00           C  
HETATM   15  O2  UNL     1       0.330   1.856   1.413  1.00  0.00           O  
HETATM   16  O3  UNL     1       0.031   0.521  -0.428  1.00  0.00           O  
HETATM   17  C14 UNL     1       0.682  -0.463  -0.948  1.00  0.00           C  
HETATM   18  C15 UNL     1       2.060  -0.471  -0.929  1.00  0.00           C  
HETATM   19  C16 UNL     1       2.754  -1.519  -1.482  1.00  0.00           C  
HETATM   20  C17 UNL     1       2.040  -2.556  -2.052  1.00  0.00           C  
HETATM   21  C18 UNL     1       0.664  -2.588  -2.092  1.00  0.00           C  
HETATM   22  O4  UNL     1      -0.090  -3.605  -2.653  1.00  0.00           O  
HETATM   23  C19 UNL     1      -0.002  -1.522  -1.529  1.00  0.00           C  
HETATM   24  C20 UNL     1      -1.362  -1.442  -1.508  1.00  0.00           C  
HETATM   25  O5  UNL     1      -2.002  -2.393  -2.031  1.00  0.00           O  
HETATM   26  O6  UNL     1       4.138  -1.281  -1.331  1.00  0.00           O  
HETATM   27  C21 UNL     1       4.252  -0.446  -0.196  1.00  0.00           C  
HETATM   28  C22 UNL     1       5.544   0.315  -0.161  1.00  0.00           C  
HETATM   29  C23 UNL     1       6.661  -0.733  -0.125  1.00  0.00           C  
HETATM   30  C24 UNL     1       5.597   1.100   1.131  1.00  0.00           C  
HETATM   31  O7  UNL     1       5.650   1.116  -1.273  1.00  0.00           O  
HETATM   32  C25 UNL     1       3.056   0.486  -0.396  1.00  0.00           C  
HETATM   33  H1  UNL     1      -6.621  -2.087   1.934  1.00  0.00           H  
HETATM   34  H2  UNL     1      -5.354  -0.972   2.595  1.00  0.00           H  
HETATM   35  H3  UNL     1      -4.977  -2.744   2.423  1.00  0.00           H  
HETATM   36  H4  UNL     1      -5.990  -3.409  -0.094  1.00  0.00           H  
HETATM   37  H5  UNL     1      -5.670  -2.108  -1.353  1.00  0.00           H  
HETATM   38  H6  UNL     1      -4.319  -3.137  -0.760  1.00  0.00           H  
HETATM   39  H7  UNL     1      -3.927   0.010   1.200  1.00  0.00           H  
HETATM   40  H8  UNL     1      -3.998   0.379  -1.532  1.00  0.00           H  
HETATM   41  H9  UNL     1      -3.800  -1.346  -1.580  1.00  0.00           H  
HETATM   42  H10 UNL     1      -3.728   2.041  -0.644  1.00  0.00           H  
HETATM   43  H11 UNL     1      -4.387   3.924   0.672  1.00  0.00           H  
HETATM   44  H12 UNL     1      -2.374   5.569   3.178  1.00  0.00           H  
HETATM   45  H13 UNL     1      -0.628   3.924   2.691  1.00  0.00           H  
HETATM   46  H14 UNL     1       0.937   2.268   2.095  1.00  0.00           H  
HETATM   47  H15 UNL     1       2.585  -3.398  -2.497  1.00  0.00           H  
HETATM   48  H16 UNL     1       0.413  -4.393  -3.069  1.00  0.00           H  
HETATM   49  H17 UNL     1       4.092  -1.080   0.687  1.00  0.00           H  
HETATM   50  H18 UNL     1       7.550  -0.351  -0.680  1.00  0.00           H  
HETATM   51  H19 UNL     1       6.317  -1.685  -0.593  1.00  0.00           H  
HETATM   52  H20 UNL     1       6.923  -0.967   0.924  1.00  0.00           H  
HETATM   53  H21 UNL     1       4.989   0.588   1.928  1.00  0.00           H  
HETATM   54  H22 UNL     1       5.257   2.143   0.970  1.00  0.00           H  
HETATM   55  H23 UNL     1       6.674   1.130   1.430  1.00  0.00           H  
HETATM   56  H24 UNL     1       6.612   1.232  -1.540  1.00  0.00           H  
HETATM   57  H25 UNL     1       3.333   1.242  -1.167  1.00  0.00           H  
HETATM   58  H26 UNL     1       2.770   0.978   0.533  1.00  0.00           H  
CONECT    1    2   33   34   35
CONECT    2    3    4    4
CONECT    3   36   37   38
CONECT    4    5   39
CONECT    5    6   40   41
CONECT    6    7    7   24
CONECT    7    8   16
CONECT    8    9    9   14
CONECT    9   10   42
CONECT   10   11   11   43
CONECT   11   12   13
CONECT   12   44
CONECT   13   14   14   45
CONECT   14   15
CONECT   15   46
CONECT   16   17
CONECT   17   18   18   23
CONECT   18   19   32
CONECT   19   20   20   26
CONECT   20   21   47
CONECT   21   22   23   23
CONECT   22   48
CONECT   23   24
CONECT   24   25   25
CONECT   26   27
CONECT   27   28   32   49
CONECT   28   29   30   31
CONECT   29   50   51   52
CONECT   30   53   54   55
CONECT   31   56
CONECT   32   57   58
END

HMDB0033756
     RDKit          3D
Albanin C
 58 61  0  0  0  0  0  0  0  0999 V2000
   -5.5275   -1.8842    1.9613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9465   -1.6873    0.6129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2820   -2.6564   -0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1278   -0.6435    0.3694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5207   -0.3952   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0391   -0.3530   -0.9326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2951    0.6447   -0.3840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7897    1.8387    0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0051    2.3794    0.0757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3895    3.5019    0.8418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5398    4.0453    1.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9864    5.1554    2.4908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2986    3.5060    1.9674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9402    2.4184    1.2182 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3297    1.8555    1.4127 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0313    0.5214   -0.4281 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6823   -0.4632   -0.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0596   -0.4710   -0.9290 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7537   -1.5188   -1.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0402   -2.5556   -2.0524 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6644   -2.5878   -2.0924 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0901   -3.6048   -2.6527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0016   -1.5220   -1.5292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3618   -1.4417   -1.5081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0018   -2.3933   -2.0313 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1380   -1.2813   -1.3315 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2524   -0.4460   -0.1961 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5442    0.3145   -0.1614 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6614   -0.7334   -0.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5973    1.1001    1.1311 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6503    1.1160   -1.2735 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0557    0.4864   -0.3963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6207   -2.0872    1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3535   -0.9718    2.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9771   -2.7440    2.4233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9901   -3.4087   -0.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6698   -2.1077   -1.3529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3191   -3.1366   -0.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9267    0.0103    1.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9980    0.3794   -1.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7997   -1.3462   -1.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7281    2.0411   -0.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3869    3.9241    0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3739    5.5693    3.1781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6275    3.9243    2.6910 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9373    2.2679    2.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5850   -3.3980   -2.4972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4130   -4.3927   -3.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0921   -1.0800    0.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5503   -0.3507   -0.6798 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3166   -1.6845   -0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9230   -0.9666    0.9236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9891    0.5878    1.9279 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2574    2.1431    0.9701 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6745    1.1300    1.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6123    1.2318   -1.5404 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3333    1.2420   -1.1669 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7697    0.9782    0.5334 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  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
 24 25  2  0
 19 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 28 31  1  0
 27 32  1  0
 24  6  1  0
 14  8  1  0
 23 17  1  0
 32 18  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
  9 42  1  0
 10 43  1  0
 12 44  1  0
 13 45  1  0
 15 46  1  0
 20 47  1  0
 22 48  1  0
 27 49  1  0
 29 50  1  0
 29 51  1  0
 29 52  1  0
 30 53  1  0
 30 54  1  0
 30 55  1  0
 31 56  1  0
 32 57  1  0
 32 58  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₅H₂₆O₇

Average Molecular Weight

438.4697

Monoisotopic Molecular Weight

438.167853186

IUPAC Name

2-(2,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-3-(3-methylbut-2-en-1-yl)-4H,8H,9H-furo[2,3-h]chromen-4-one

Traditional Name

2-(2,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-3-(3-methylbut-2-en-1-yl)-8H,9H-furo[2,3-h]chromen-4-one

CAS Registry Number

73343-43-8

SMILES

CC(C)=CCC1=C(OC2=C(C(O)=CC3=C2CC(O3)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C1

InChI Identifier

InChI=1S/C25H26O7/c1-12(2)5-7-15-22(29)21-18(28)11-19-16(10-20(31-19)25(3,4)30)24(21)32-23(15)14-8-6-13(26)9-17(14)27/h5-6,8-9,11,20,26-28,30H,7,10H2,1-4H3

InChI Key

ZDJLVJJUSHPYOI-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 8-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

8-prenylated flavones

Alternative Parents

Substituents

3-prenylated flavone
8-prenylated flavone
4'-hydroxyflavonoid
5-hydroxyflavonoid
Hydroxyflavonoid
Chromone
1-benzopyran
Benzopyran
Coumaran
Resorcinol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Phenol
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Tertiary alcohol
Ether
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cell membrane (HMDB: HMDB0033756)

Cellular substructure

Membrane (HMDB: HMDB0033756)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0033756)

Source

Exogenous

Food

Food (HMDB: HMDB0033756)

Fruit

Fruits (FooDB: FOOD00871)

Endogenous

Plant

Plant (HMDB: HMDB0033756)

Not Available

Nutrient (HMDB: HMDB0033756)

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	0.4 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	0.0078 g/L	ALOGPS
logP	3.87	ALOGPS
logP	4.27	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.06	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	121.26 m³·mol⁻¹	ChemAxon
Polarizability	46.85 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	203.67	31661259
DarkChem	[M-H]-	199.403	31661259
DeepCCS	[M+H]+	205.93	30932474
DeepCCS	[M-H]-	203.534	30932474
DeepCCS	[M-2H]-	236.418	30932474
DeepCCS	[M+Na]+	211.842	30932474
AllCCS	[M+H]+	205.7	32859911
AllCCS	[M+H-H2O]+	203.2	32859911
AllCCS	[M+NH4]+	208.0	32859911
AllCCS	[M+Na]+	208.7	32859911
AllCCS	[M-H]-	208.0	32859911
AllCCS	[M+Na-2H]-	208.2	32859911
AllCCS	[M+HCOO]-	208.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Albanin C	CC(C)=CCC1=C(OC2=C(C(O)=CC3=C2CC(O3)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C1	5719.4	Standard polar	33892256
Albanin C	CC(C)=CCC1=C(OC2=C(C(O)=CC3=C2CC(O3)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C1	3678.4	Standard non polar	33892256
Albanin C	CC(C)=CCC1=C(OC2=C(C(O)=CC3=C2CC(O3)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C1	3922.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Albanin C,1TMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=C3CC(C(C)(C)O)OC3=CC(O[Si](C)(C)C)=C2C1=O	3673.6	Semi standard non polar	33892256
Albanin C,1TMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=C3CC(C(C)(C)O[Si](C)(C)C)OC3=CC(O)=C2C1=O	3786.1	Semi standard non polar	33892256
Albanin C,1TMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=C3CC(C(C)(C)O)OC3=CC(O)=C2C1=O	3658.3	Semi standard non polar	33892256
Albanin C,1TMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=C3CC(C(C)(C)O)OC3=CC(O)=C2C1=O	3692.4	Semi standard non polar	33892256
Albanin C,2TMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=C3CC(C(C)(C)O)OC3=CC(O[Si](C)(C)C)=C2C1=O	3614.7	Semi standard non polar	33892256
Albanin C,2TMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=C3CC(C(C)(C)O)OC3=CC(O[Si](C)(C)C)=C2C1=O	3574.3	Semi standard non polar	33892256
Albanin C,2TMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=C3CC(C(C)(C)O[Si](C)(C)C)OC3=CC(O[Si](C)(C)C)=C2C1=O	3688.3	Semi standard non polar	33892256
Albanin C,2TMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=C3CC(C(C)(C)O[Si](C)(C)C)OC3=CC(O)=C2C1=O	3704.0	Semi standard non polar	33892256
Albanin C,2TMS,isomer #5	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=C3CC(C(C)(C)O[Si](C)(C)C)OC3=CC(O)=C2C1=O	3675.4	Semi standard non polar	33892256
Albanin C,2TMS,isomer #6	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=C3CC(C(C)(C)O)OC3=CC(O)=C2C1=O	3605.2	Semi standard non polar	33892256
Albanin C,3TMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=C3CC(C(C)(C)O)OC3=CC(O[Si](C)(C)C)=C2C1=O	3568.9	Semi standard non polar	33892256
Albanin C,3TMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=C3CC(C(C)(C)O[Si](C)(C)C)OC3=CC(O[Si](C)(C)C)=C2C1=O	3621.3	Semi standard non polar	33892256
Albanin C,3TMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=C3CC(C(C)(C)O[Si](C)(C)C)OC3=CC(O[Si](C)(C)C)=C2C1=O	3595.7	Semi standard non polar	33892256
Albanin C,3TMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=C3CC(C(C)(C)O[Si](C)(C)C)OC3=CC(O)=C2C1=O	3623.7	Semi standard non polar	33892256
Albanin C,4TMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=C3CC(C(C)(C)O[Si](C)(C)C)OC3=CC(O[Si](C)(C)C)=C2C1=O	3607.9	Semi standard non polar	33892256
Albanin C,1TBDMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=C3CC(C(C)(C)O)OC3=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	3926.3	Semi standard non polar	33892256
Albanin C,1TBDMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=C3CC(C(C)(C)O[Si](C)(C)C(C)(C)C)OC3=CC(O)=C2C1=O	4033.1	Semi standard non polar	33892256
Albanin C,1TBDMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=C3CC(C(C)(C)O)OC3=CC(O)=C2C1=O	3905.4	Semi standard non polar	33892256
Albanin C,1TBDMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=C3CC(C(C)(C)O)OC3=CC(O)=C2C1=O	3942.4	Semi standard non polar	33892256
Albanin C,2TBDMS,isomer #1	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=C3CC(C(C)(C)O)OC3=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	4075.1	Semi standard non polar	33892256
Albanin C,2TBDMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=C3CC(C(C)(C)O)OC3=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	4034.7	Semi standard non polar	33892256
Albanin C,2TBDMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=C3CC(C(C)(C)O[Si](C)(C)C(C)(C)C)OC3=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	4141.1	Semi standard non polar	33892256
Albanin C,2TBDMS,isomer #4	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=C3CC(C(C)(C)O[Si](C)(C)C(C)(C)C)OC3=CC(O)=C2C1=O	4165.6	Semi standard non polar	33892256
Albanin C,2TBDMS,isomer #5	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=C3CC(C(C)(C)O[Si](C)(C)C(C)(C)C)OC3=CC(O)=C2C1=O	4129.0	Semi standard non polar	33892256
Albanin C,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=C3CC(C(C)(C)O)OC3=CC(O)=C2C1=O	4062.0	Semi standard non polar	33892256
Albanin C,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=C3CC(C(C)(C)O)OC3=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	4201.4	Semi standard non polar	33892256
Albanin C,3TBDMS,isomer #2	CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=C3CC(C(C)(C)O[Si](C)(C)C(C)(C)C)OC3=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	4261.0	Semi standard non polar	33892256
Albanin C,3TBDMS,isomer #3	CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=C3CC(C(C)(C)O[Si](C)(C)C(C)(C)C)OC3=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	4216.6	Semi standard non polar	33892256
Albanin C,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=C3CC(C(C)(C)O[Si](C)(C)C(C)(C)C)OC3=CC(O)=C2C1=O	4264.8	Semi standard non polar	33892256
Albanin C,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=C3CC(C(C)(C)O[Si](C)(C)C(C)(C)C)OC3=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O	4389.4	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 C GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-9004400000-432721926315737ad3b8	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Albanin C GC-MS (3 TMS) - 70eV, Positive	splash10-0a4u-9000048000-1f8e8d616d06b6af17b2	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Albanin C 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 C 10V, Positive-QTOF	splash10-0079-0005900000-12bd87ba925bd2b58d6d	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 20V, Positive-QTOF	splash10-01bi-4009700000-6bf5040b852b13436aed	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 40V, Positive-QTOF	splash10-052b-2269000000-1a0278b8d50237df8de9	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 10V, Negative-QTOF	splash10-000i-0000900000-f3b711da0d6ceb2a4715	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 20V, Negative-QTOF	splash10-00kr-0014900000-925375ef17dc2937b27d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 40V, Negative-QTOF	splash10-0a4i-1928100000-8a7a4194215b4f081d07	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 10V, Positive-QTOF	splash10-000i-0000900000-b5f2afccea7aeee35d79	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 20V, Positive-QTOF	splash10-000i-0000900000-b5f2afccea7aeee35d79	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 40V, Positive-QTOF	splash10-000i-0090400000-e95b8aeee33b028c9844	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 10V, Negative-QTOF	splash10-000i-0000900000-c34e42b820ea6128d411	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 20V, Negative-QTOF	splash10-000i-0000900000-c34e42b820ea6128d411	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Albanin C 40V, Negative-QTOF	splash10-000f-0190100000-9c94344a7f6b5010d825	2021-09-22	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

FDB011891

KNApSAcK ID

C00055330

Chemspider ID

35013663

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131676030

PDB ID

Not Available

ChEBI ID

175534

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1838211

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 C (HMDB0033756)

MOL for HMDB0033756 (Albanin C)

3D MOL for HMDB0033756 (Albanin C)

3D SDF for HMDB0033756 (Albanin C)

3D-SDF for HMDB0033756 (Albanin C)

PDB for HMDB0033756 (Albanin C)

3D PDB for HMDB0033756 (Albanin C)

SMILES for HMDB0033756 (Albanin C)

INCHI for HMDB0033756 (Albanin C)

Structure for HMDB0033756 (Albanin C)

3D Structure for HMDB0033756 (Albanin C)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra