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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:50:59 UTC

Update Date

2022-03-07 02:54:39 UTC

HMDB ID

HMDB0035826

Secondary Accession Numbers

HMDB35826

Metabolite Identification

Common Name

Faradiol

Description

Faradiol belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review a significant number of articles have been published on Faradiol.

Structure

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


  Mrv0541 02241217372D          

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M  END

HMDB0035826
     RDKit          3D
Faradiol
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M  END


  Mrv0541 02241217372D          

 32 36  0  0  0  0            999 V2000
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 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 30  1  0  0  0  0
 25 26  1  0  0  0  0
 25 32  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035826

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1C2C3CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CC(O)C2(C)CC=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O2/c1-18-11-14-28(6)24(32)17-30(8)20(25(28)19(18)2)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h11,19-25,31-32H,9-10,12-17H2,1-8H3

> <INCHI_KEY>
BNHIQKVOPNHQKO-UHFFFAOYSA-N

> <FORMULA>
C30H50O2

> <MOLECULAR_WEIGHT>
442.7168

> <EXACT_MASS>
442.381080844

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
54.94906768552386

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,12,12a,12b,13,14,14a,14b-icosahydropicene-3,8-diol

> <ALOGPS_LOGP>
5.70

> <JCHEM_LOGP>
6.159301743666667

> <ALOGPS_LOGS>
-5.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.489433390177712

> <JCHEM_PKA_STRONGEST_BASIC>
-0.22091100973876043

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
133.49629999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.49e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,12,12a,12b,13,14,14a-tetradecahydro-1H-picene-3,8-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035826
     RDKit          3D
Faradiol
 82 86  0  0  0  0  0  0  0  0999 V2000
    5.1738    1.3500   -1.7484 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8954    0.6151   -0.5131 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3379   -0.6554   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9759   -1.2684    0.9359 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4814   -1.0928    1.2549 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4418   -1.4068    2.7704 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7869   -2.2491    0.6163 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8303   -3.4082    1.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3145   -1.9989    0.3925 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0583   -0.7168   -0.4148 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6883   -1.0949   -1.7790 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7873    0.4557    0.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9711    1.5909    0.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4962    1.4587    0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9665    0.7479   -0.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4408    0.8757   -0.7120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7755    0.8597   -2.1654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9007    2.2608   -0.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4059    2.4303   -0.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1846    1.3874    0.2813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4829    1.3671   -0.2687 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6322    0.0050    0.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0351   -0.6812    1.5349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3147   -0.7486   -0.8724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1303   -0.0573    0.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6442   -1.4548    0.2822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1537   -1.4409    0.5214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4238   -0.6318   -0.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7829   -1.4319   -1.8216 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9465    0.2414    1.0144 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1591    1.1134    0.6560 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8757    2.5582    0.5611 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1466    1.0663   -2.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2167    2.4403   -1.5846 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3831    1.1479   -2.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8966   -1.1523   -1.1518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6081   -0.9092    1.7680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2066   -2.3581    0.8320 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9209   -0.5399    3.2630 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0286   -2.3278    2.9622 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4012   -1.4926    3.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2684   -2.5752   -0.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7318   -3.8217    1.4066 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9826   -2.8356   -0.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8559   -1.9571    1.3854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7858   -1.0989   -1.6213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5335   -0.2591   -2.5012 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3969   -2.0738   -2.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2926    0.9471   -0.8223 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2358    2.5943    0.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2483    1.7646    1.7359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9132    2.5073    0.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8488    0.9638    1.5946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5029    1.2811   -1.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8534    0.7406   -2.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5205    0.1464   -2.4959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1423    1.8613   -2.5564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3202    3.0732   -0.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8896    2.2207    0.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6352    3.4132    0.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6853    2.5856   -1.4767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3434    1.7062    1.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1171    1.0429    0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9641   -0.2247    1.9322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1073   -1.7759    1.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2508   -0.5103    2.3078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7401   -0.0126   -1.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7426   -1.5522   -1.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2498   -1.2470   -0.4705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8710    0.3497    1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0713   -1.8847    1.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9918   -2.1491   -0.4774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8733   -2.5151    0.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9756   -1.0701    1.5252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8577   -1.4944   -2.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5115   -2.5015   -1.5679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3006   -1.0806   -2.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    0.6876    2.0160 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8520    0.9711    1.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2848    2.9687    1.3770 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5203    2.8809   -0.4618 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8799    3.0797    0.6437 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 12 30  1  0
 30 31  1  0
 31 32  1  0
 31  2  1  0
 30  5  1  0
 28 10  1  0
 28 15  1  0
 25 16  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  6 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 11 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 17 55  1  0
 17 56  1  0
 17 57  1  0
 18 58  1  0
 18 59  1  0
 19 60  1  0
 19 61  1  0
 20 62  1  0
 21 63  1  0
 23 64  1  0
 23 65  1  0
 23 66  1  0
 24 67  1  0
 24 68  1  0
 24 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 27 73  1  0
 27 74  1  0
 29 75  1  0
 29 76  1  0
 29 77  1  0
 30 78  1  0
 31 79  1  0
 32 80  1  0
 32 81  1  0
 32 82  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0       0.666  -3.260   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.668  -4.030   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.001  -3.260   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.001   3.670   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.333   2.900   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.333   1.360   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.001   0.590   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.666   1.360   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.668   0.590   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.668  -0.950   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.666  -1.720   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.001  -2.490   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.668   5.210   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.668   3.670   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.002   2.900   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.002   1.360   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.668   0.590   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.002  -0.180   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.001  -0.180   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.001  -1.720   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.335  -0.950   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.667  -1.720   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.667  -3.260   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -6.002  -4.030   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.001  -0.950   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.333  -1.720   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.668  -0.950   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.002  -1.720   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.324  -5.210   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.335  -4.030   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.345  -5.210   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.771  -2.284   0.000  0.00  0.00           C+0
CONECT    1    2   11                                                       
CONECT    2    1    3                                                       
CONECT    3    2   20   30                                                  
CONECT    4    5                                                            
CONECT    5    4    6   14                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8   25                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   20                                                  
CONECT   11    1   10   12   25                                             
CONECT   12   11                                                            
CONECT   13   14                                                            
CONECT   14    5   13   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17    6   16   18   27                                             
CONECT   18   17                                                            
CONECT   19   20                                                            
CONECT   20    3   10   19   21                                             
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   30                                                  
CONECT   24   23                                                            
CONECT   25    7   11   26   32                                             
CONECT   26   25   27                                                       
CONECT   27   17   26   28                                                  
CONECT   28   27                                                            
CONECT   29   30                                                            
CONECT   30    3   23   29   31                                             
CONECT   31   30                                                            
CONECT   32   25                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

COMPND    HMDB0035826
HETATM    1  C1  UNL     1       5.174   1.350  -1.748  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.895   0.615  -0.513  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.338  -0.655  -0.374  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.976  -1.268   0.936  1.00  0.00           C  
HETATM    5  C5  UNL     1       3.481  -1.093   1.255  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.442  -1.407   2.770  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.787  -2.249   0.616  1.00  0.00           C  
HETATM    8  O1  UNL     1       2.830  -3.408   1.436  1.00  0.00           O  
HETATM    9  C8  UNL     1       1.314  -1.999   0.393  1.00  0.00           C  
HETATM   10  C9  UNL     1       1.058  -0.717  -0.415  1.00  0.00           C  
HETATM   11  C10 UNL     1       1.688  -1.095  -1.779  1.00  0.00           C  
HETATM   12  C11 UNL     1       1.787   0.456   0.077  1.00  0.00           C  
HETATM   13  C12 UNL     1       0.971   1.591   0.647  1.00  0.00           C  
HETATM   14  C13 UNL     1      -0.496   1.459   0.641  1.00  0.00           C  
HETATM   15  C14 UNL     1      -0.966   0.748  -0.573  1.00  0.00           C  
HETATM   16  C15 UNL     1      -2.441   0.876  -0.712  1.00  0.00           C  
HETATM   17  C16 UNL     1      -2.776   0.860  -2.165  1.00  0.00           C  
HETATM   18  C17 UNL     1      -2.901   2.261  -0.199  1.00  0.00           C  
HETATM   19  C18 UNL     1      -4.406   2.430  -0.446  1.00  0.00           C  
HETATM   20  C19 UNL     1      -5.185   1.387   0.281  1.00  0.00           C  
HETATM   21  O2  UNL     1      -6.483   1.367  -0.269  1.00  0.00           O  
HETATM   22  C20 UNL     1      -4.632   0.005   0.213  1.00  0.00           C  
HETATM   23  C21 UNL     1      -5.035  -0.681   1.535  1.00  0.00           C  
HETATM   24  C22 UNL     1      -5.315  -0.749  -0.872  1.00  0.00           C  
HETATM   25  C23 UNL     1      -3.130  -0.057   0.201  1.00  0.00           C  
HETATM   26  C24 UNL     1      -2.644  -1.455   0.282  1.00  0.00           C  
HETATM   27  C25 UNL     1      -1.154  -1.441   0.521  1.00  0.00           C  
HETATM   28  C26 UNL     1      -0.424  -0.632  -0.563  1.00  0.00           C  
HETATM   29  C27 UNL     1      -0.783  -1.432  -1.822  1.00  0.00           C  
HETATM   30  C28 UNL     1       2.946   0.241   1.014  1.00  0.00           C  
HETATM   31  C29 UNL     1       4.159   1.113   0.656  1.00  0.00           C  
HETATM   32  C30 UNL     1       3.876   2.558   0.561  1.00  0.00           C  
HETATM   33  H1  UNL     1       6.147   1.066  -2.208  1.00  0.00           H  
HETATM   34  H2  UNL     1       5.217   2.440  -1.585  1.00  0.00           H  
HETATM   35  H3  UNL     1       4.383   1.148  -2.494  1.00  0.00           H  
HETATM   36  H4  UNL     1       5.897  -1.152  -1.152  1.00  0.00           H  
HETATM   37  H5  UNL     1       5.608  -0.909   1.768  1.00  0.00           H  
HETATM   38  H6  UNL     1       5.207  -2.358   0.832  1.00  0.00           H  
HETATM   39  H7  UNL     1       3.921  -0.540   3.263  1.00  0.00           H  
HETATM   40  H8  UNL     1       4.029  -2.328   2.962  1.00  0.00           H  
HETATM   41  H9  UNL     1       2.401  -1.493   3.112  1.00  0.00           H  
HETATM   42  H10 UNL     1       3.268  -2.575  -0.327  1.00  0.00           H  
HETATM   43  H11 UNL     1       3.732  -3.822   1.407  1.00  0.00           H  
HETATM   44  H12 UNL     1       0.983  -2.836  -0.255  1.00  0.00           H  
HETATM   45  H13 UNL     1       0.856  -1.957   1.385  1.00  0.00           H  
HETATM   46  H14 UNL     1       2.786  -1.099  -1.621  1.00  0.00           H  
HETATM   47  H15 UNL     1       1.533  -0.259  -2.501  1.00  0.00           H  
HETATM   48  H16 UNL     1       1.397  -2.074  -2.122  1.00  0.00           H  
HETATM   49  H17 UNL     1       2.293   0.947  -0.822  1.00  0.00           H  
HETATM   50  H18 UNL     1       1.236   2.594   0.192  1.00  0.00           H  
HETATM   51  H19 UNL     1       1.248   1.765   1.736  1.00  0.00           H  
HETATM   52  H20 UNL     1      -0.913   2.507   0.741  1.00  0.00           H  
HETATM   53  H21 UNL     1      -0.849   0.964   1.595  1.00  0.00           H  
HETATM   54  H22 UNL     1      -0.503   1.281  -1.455  1.00  0.00           H  
HETATM   55  H23 UNL     1      -1.853   0.741  -2.820  1.00  0.00           H  
HETATM   56  H24 UNL     1      -3.520   0.146  -2.496  1.00  0.00           H  
HETATM   57  H25 UNL     1      -3.142   1.861  -2.556  1.00  0.00           H  
HETATM   58  H26 UNL     1      -2.320   3.073  -0.620  1.00  0.00           H  
HETATM   59  H27 UNL     1      -2.890   2.221   0.934  1.00  0.00           H  
HETATM   60  H28 UNL     1      -4.635   3.413   0.070  1.00  0.00           H  
HETATM   61  H29 UNL     1      -4.685   2.586  -1.477  1.00  0.00           H  
HETATM   62  H30 UNL     1      -5.343   1.706   1.352  1.00  0.00           H  
HETATM   63  H31 UNL     1      -7.117   1.043   0.414  1.00  0.00           H  
HETATM   64  H32 UNL     1      -5.964  -0.225   1.932  1.00  0.00           H  
HETATM   65  H33 UNL     1      -5.107  -1.776   1.398  1.00  0.00           H  
HETATM   66  H34 UNL     1      -4.251  -0.510   2.308  1.00  0.00           H  
HETATM   67  H35 UNL     1      -5.740  -0.013  -1.619  1.00  0.00           H  
HETATM   68  H36 UNL     1      -4.743  -1.552  -1.334  1.00  0.00           H  
HETATM   69  H37 UNL     1      -6.250  -1.247  -0.470  1.00  0.00           H  
HETATM   70  H38 UNL     1      -2.871   0.350   1.241  1.00  0.00           H  
HETATM   71  H39 UNL     1      -3.071  -1.885   1.245  1.00  0.00           H  
HETATM   72  H40 UNL     1      -2.992  -2.149  -0.477  1.00  0.00           H  
HETATM   73  H41 UNL     1      -0.873  -2.515   0.493  1.00  0.00           H  
HETATM   74  H42 UNL     1      -0.976  -1.070   1.525  1.00  0.00           H  
HETATM   75  H43 UNL     1      -1.858  -1.494  -2.011  1.00  0.00           H  
HETATM   76  H44 UNL     1      -0.512  -2.501  -1.568  1.00  0.00           H  
HETATM   77  H45 UNL     1      -0.301  -1.081  -2.725  1.00  0.00           H  
HETATM   78  H46 UNL     1       2.648   0.688   2.016  1.00  0.00           H  
HETATM   79  H47 UNL     1       4.852   0.971   1.541  1.00  0.00           H  
HETATM   80  H48 UNL     1       3.285   2.969   1.377  1.00  0.00           H  
HETATM   81  H49 UNL     1       3.520   2.881  -0.462  1.00  0.00           H  
HETATM   82  H50 UNL     1       4.880   3.080   0.644  1.00  0.00           H  
CONECT    1    2   33   34   35
CONECT    2    3    3   31
CONECT    3    4   36
CONECT    4    5   37   38
CONECT    5    6    7   30
CONECT    6   39   40   41
CONECT    7    8    9   42
CONECT    8   43
CONECT    9   10   44   45
CONECT   10   11   12   28
CONECT   11   46   47   48
CONECT   12   13   30   49
CONECT   13   14   50   51
CONECT   14   15   52   53
CONECT   15   16   28   54
CONECT   16   17   18   25
CONECT   17   55   56   57
CONECT   18   19   58   59
CONECT   19   20   60   61
CONECT   20   21   22   62
CONECT   21   63
CONECT   22   23   24   25
CONECT   23   64   65   66
CONECT   24   67   68   69
CONECT   25   26   70
CONECT   26   27   71   72
CONECT   27   28   73   74
CONECT   28   29
CONECT   29   75   76   77
CONECT   30   31   78
CONECT   31   32   79
CONECT   32   80   81   82
END

HMDB0035826
     RDKit          3D
Faradiol
 82 86  0  0  0  0  0  0  0  0999 V2000
    5.1738    1.3500   -1.7484 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8954    0.6151   -0.5131 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3379   -0.6554   -0.3737 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9759   -1.2684    0.9359 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4814   -1.0928    1.2549 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4418   -1.4068    2.7704 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7869   -2.2491    0.6163 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8303   -3.4082    1.4357 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3145   -1.9989    0.3925 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0583   -0.7168   -0.4148 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6883   -1.0949   -1.7790 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7873    0.4557    0.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9711    1.5909    0.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4962    1.4587    0.6411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9665    0.7479   -0.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4408    0.8757   -0.7120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7755    0.8597   -2.1654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9007    2.2608   -0.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4059    2.4303   -0.4461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1846    1.3874    0.2813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4829    1.3671   -0.2687 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6322    0.0050    0.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0351   -0.6812    1.5349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3147   -0.7486   -0.8724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1303   -0.0573    0.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6442   -1.4548    0.2822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1537   -1.4409    0.5214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4238   -0.6318   -0.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7829   -1.4319   -1.8216 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9465    0.2414    1.0144 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1591    1.1134    0.6560 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8757    2.5582    0.5611 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1466    1.0663   -2.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2167    2.4403   -1.5846 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3831    1.1479   -2.4942 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8966   -1.1523   -1.1518 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6081   -0.9092    1.7680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2066   -2.3581    0.8320 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9209   -0.5399    3.2630 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0286   -2.3278    2.9622 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4012   -1.4926    3.1124 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2684   -2.5752   -0.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7318   -3.8217    1.4066 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9826   -2.8356   -0.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8559   -1.9571    1.3854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7858   -1.0989   -1.6213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5335   -0.2591   -2.5012 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3969   -2.0738   -2.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2926    0.9471   -0.8223 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2358    2.5943    0.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2483    1.7646    1.7359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9132    2.5073    0.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8488    0.9638    1.5946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5029    1.2811   -1.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8534    0.7406   -2.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5205    0.1464   -2.4959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1423    1.8613   -2.5564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3202    3.0732   -0.6199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8896    2.2207    0.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6352    3.4132    0.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6853    2.5856   -1.4767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3434    1.7062    1.3517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1171    1.0429    0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9641   -0.2247    1.9322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1073   -1.7759    1.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2508   -0.5103    2.3078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7401   -0.0126   -1.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7426   -1.5522   -1.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2498   -1.2470   -0.4705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8710    0.3497    1.2410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0713   -1.8847    1.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9918   -2.1491   -0.4774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8733   -2.5151    0.4933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9756   -1.0701    1.5252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8577   -1.4944   -2.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5115   -2.5015   -1.5679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3006   -1.0806   -2.7246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484    0.6876    2.0160 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8520    0.9711    1.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2848    2.9687    1.3770 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5203    2.8809   -0.4618 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8799    3.0797    0.6437 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 12 30  1  0
 30 31  1  0
 31 32  1  0
 31  2  1  0
 30  5  1  0
 28 10  1  0
 28 15  1  0
 25 16  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  3 36  1  0
  4 37  1  0
  4 38  1  0
  6 39  1  0
  6 40  1  0
  6 41  1  0
  7 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 11 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 17 55  1  0
 17 56  1  0
 17 57  1  0
 18 58  1  0
 18 59  1  0
 19 60  1  0
 19 61  1  0
 20 62  1  0
 21 63  1  0
 23 64  1  0
 23 65  1  0
 23 66  1  0
 24 67  1  0
 24 68  1  0
 24 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 27 73  1  0
 27 74  1  0
 29 75  1  0
 29 76  1  0
 29 77  1  0
 30 78  1  0
 31 79  1  0
 32 80  1  0
 32 81  1  0
 32 82  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(3beta,12beta,18alpha,19alpha)-Urs-20-ene-3,12-diol	HMDB
18alpha,19BetaH-urs-20-ene-3beta,16beta-diol	HMDB
Isoarnidendiol	HMDB
Faradiol	MeSH

Chemical Formula

C₃₀H₅₀O₂

Average Molecular Weight

442.7168

Monoisotopic Molecular Weight

442.381080844

IUPAC Name

4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,12,12a,12b,13,14,14a,14b-icosahydropicene-3,8-diol

Traditional Name

4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,12,12a,12b,13,14,14a-tetradecahydro-1H-picene-3,8-diol

CAS Registry Number

20554-95-4

SMILES

CC1C2C3CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CC(O)C2(C)CC=C1C

InChI Identifier

InChI=1S/C30H50O2/c1-18-11-14-28(6)24(32)17-30(8)20(25(28)19(18)2)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h11,19-25,31-32H,9-10,12-17H2,1-8H3

InChI Key

BNHIQKVOPNHQKO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Hydroxysteroid
12-hydroxysteroid
Steroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0035826)
Cell membrane (HMDB: HMDB0035826)

Cellular substructure

Extracellular (HMDB: HMDB0035826)
Membrane (HMDB: HMDB0035826)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035826)

Source

Endogenous

Endogenous (HMDB: HMDB0035826)

Plant

Plant (HMDB: HMDB0035826)

Animal

Animal (HMDB: HMDB0035826)

Exogenous

Food

Food (HMDB: HMDB0035826)

Herb and spice

Herb

Dandelion (FooDB: FOOD00181)

Oilseed crop

Sunflower (FooDB: FOOD00086)

Tea

Fat and oil

Fats and oils (FooDB: FOOD00864)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0035826)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0035826)

Cellular process

Cell signaling (HMDB: HMDB0035826)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0035826)

Role

Biological role

Nutrient

Nutrient (HMDB: HMDB0035826)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035826)

Emulsifier (HMDB: HMDB0035826)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	236 - 237 °C	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	0.00023 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	0.00045 g/L	ALOGPS
logP	5.7	ALOGPS
logP	6.16	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	19.49	ChemAxon
pKa (Strongest Basic)	-0.22	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	133.5 m³·mol⁻¹	ChemAxon
Polarizability	54.95 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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]+	201.326	31661259
DarkChem	[M-H]-	197.535	31661259
DeepCCS	[M+H]+	217.62	30932474
DeepCCS	[M-H]-	215.262	30932474
DeepCCS	[M-2H]-	248.979	30932474
DeepCCS	[M+Na]+	224.208	30932474
AllCCS	[M+H]+	214.7	32859911
AllCCS	[M+H-H2O]+	212.9	32859911
AllCCS	[M+NH4]+	216.3	32859911
AllCCS	[M+Na]+	216.8	32859911
AllCCS	[M-H]-	211.9	32859911
AllCCS	[M+Na-2H]-	213.9	32859911
AllCCS	[M+HCOO]-	216.2	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Faradiol	CC1C2C3CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CC(O)C2(C)CC=C1C	2721.5	Standard polar	33892256
Faradiol	CC1C2C3CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CC(O)C2(C)CC=C1C	3508.2	Standard non polar	33892256
Faradiol	CC1C2C3CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CC(O)C2(C)CC=C1C	3676.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Faradiol,1TMS,isomer #1	CC1=CCC2(C)C(O)CC3(C)C(CCC4C5(C)CCC(O[Si](C)(C)C)C(C)(C)C5CCC43C)C2C1C	3664.3	Semi standard non polar	33892256
Faradiol,1TMS,isomer #2	CC1=CCC2(C)C(O[Si](C)(C)C)CC3(C)C(CCC4C5(C)CCC(O)C(C)(C)C5CCC43C)C2C1C	3665.7	Semi standard non polar	33892256
Faradiol,2TMS,isomer #1	CC1=CCC2(C)C(O[Si](C)(C)C)CC3(C)C(CCC4C5(C)CCC(O[Si](C)(C)C)C(C)(C)C5CCC43C)C2C1C	3592.5	Semi standard non polar	33892256
Faradiol,1TBDMS,isomer #1	CC1=CCC2(C)C(O)CC3(C)C(CCC4C5(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C5CCC43C)C2C1C	3891.2	Semi standard non polar	33892256
Faradiol,1TBDMS,isomer #2	CC1=CCC2(C)C(O[Si](C)(C)C(C)(C)C)CC3(C)C(CCC4C5(C)CCC(O)C(C)(C)C5CCC43C)C2C1C	3897.2	Semi standard non polar	33892256
Faradiol,2TBDMS,isomer #1	CC1=CCC2(C)C(O[Si](C)(C)C(C)(C)C)CC3(C)C(CCC4C5(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C5CCC43C)C2C1C	4078.5	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 - Faradiol GC-MS (Non-derivatized) - 70eV, Positive	splash10-004i-0333900000-75ff6d236fb034e2a468	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Faradiol GC-MS (2 TMS) - 70eV, Positive	splash10-00di-1021190000-6b1363ba9e9f01bcda9e	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Faradiol 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 - Faradiol 10V, Positive-QTOF	splash10-004l-0000900000-65f57895eb17c3ef76bc	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 20V, Positive-QTOF	splash10-056r-1122900000-c9bb8ac0ee993031c8b7	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 40V, Positive-QTOF	splash10-0q4i-4496300000-ab6dca6fe00fd4015563	2015-04-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 10V, Negative-QTOF	splash10-0006-0000900000-26ca4118c5e45a7b1e1e	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 20V, Negative-QTOF	splash10-006x-0000900000-133a934ed942612a1462	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 40V, Negative-QTOF	splash10-0a6r-0001900000-ac60c38af99ad50d4643	2015-04-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 10V, Positive-QTOF	splash10-0006-0001900000-cc5ed05422006e619cb7	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 20V, Positive-QTOF	splash10-00di-1964200000-4615c466c7809829dfe1	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 40V, Positive-QTOF	splash10-00di-1912000000-f5e54ffc2f9ebfdf41aa	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 10V, Negative-QTOF	splash10-0006-0000900000-849799f7ece1fdb1b84b	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 20V, Negative-QTOF	splash10-0006-0000900000-75b268393786aaa36906	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Faradiol 40V, Negative-QTOF	splash10-0006-0000900000-13116301087bd0f054ca	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
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

FDB014590

KNApSAcK ID

Not Available

Chemspider ID

550855

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

634598

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1851871

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Faradiol (HMDB0035826)

MOL for HMDB0035826 (Faradiol)

3D MOL for HMDB0035826 (Faradiol)

3D SDF for HMDB0035826 (Faradiol)

3D-SDF for HMDB0035826 (Faradiol)

PDB for HMDB0035826 (Faradiol)

3D PDB for HMDB0035826 (Faradiol)

SMILES for HMDB0035826 (Faradiol)

INCHI for HMDB0035826 (Faradiol)

Structure for HMDB0035826 (Faradiol)

3D Structure for HMDB0035826 (Faradiol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra