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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2008-08-13 13:21:54 UTC

Update Date

2022-03-07 02:49:33 UTC

HMDB ID

HMDB0006845

Secondary Accession Numbers

HMDB0006925
HMDB06845
HMDB06925

Metabolite Identification

Common Name

4alpha-Methylfecosterol

Description

4alpha-Methylfecosterol belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Thus, 4alpha-methylfecosterol is considered to be a sterol lipid molecule. 4alpha-Methylfecosterol is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. 4alpha-Methylfecosterol is involved in the biosynthesis of steroids. 4alpha-Methylfecosterol is converted from delta8,14-sterol by delta14-sterol reductase (EC 1.3.1.70). 4alpha-Methylfecosterol is converted into 24-methylenelophenol by cholestenol delta-isomerase (EC 5.3.3.5).

Structure

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

  Mrv1652309042000332D          

 33 36  0  0  0  0            999 V2000
 9997.8391 9999.9734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.1267 9997.0766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.6978 9997.9037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.976210001.2192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.9762 9998.7390    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.8391 9997.4922    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 9997.1260 9999.5578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.4115 9999.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 9998.5519 9997.9078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.2664 9998.3202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.264410000.8031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.549910000.3906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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10001.2483 9999.9780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.763510000.6455    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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10001.479210001.8810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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10003.624210000.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.479210001.0560    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  8  1  0  0  0  0
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 11  1  1  1  0  0  0
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 14 18  1  0  0  0  0
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 29 32  1  0  0  0  0
 23 19  1  0  0  0  0
 23 22  1  0  0  0  0
 18 20  1  0  0  0  0
 20  5  1  6  0  0  0
 15 19  1  0  0  0  0
 19  4  1  1  0  0  0
M  END

HMDB0006845
     RDKit          3D
4alpha-Methylfecosterol
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.2082    0.2731   -1.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6268   -0.6100   -0.9916 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  3
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M  END

  Mrv1652309042000332D          

 33 36  0  0  0  0            999 V2000
 9997.8391 9999.9734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 23 19  1  0  0  0  0
 23 22  1  0  0  0  0
 18 20  1  0  0  0  0
 20  5  1  6  0  0  0
 15 19  1  0  0  0  0
 19  4  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0006845

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@]1(CC[C@@]2([H])C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)[C@@H](C)[C@]1([H])CC3)[C@H](C)CCC(=C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C29H48O/c1-18(2)19(3)8-9-20(4)23-12-13-25-22-10-11-24-21(5)27(30)15-17-29(24,7)26(22)14-16-28(23,25)6/h18,20-21,23-25,27,30H,3,8-17H2,1-2,4-7H3/t20-,21+,23-,24+,25+,27+,28-,29+/m1/s1

> <INCHI_KEY>
QLDNWJOJCDIMKK-XLFBYWHPSA-N

> <FORMULA>
C29H48O

> <MOLECULAR_WEIGHT>
412.6908

> <EXACT_MASS>
412.370516158

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
53.45054455315034

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S,6S,7S,11R,14R,15R)-2,6,15-trimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-5-ol

> <ALOGPS_LOGP>
6.64

> <JCHEM_LOGP>
7.373577317666668

> <ALOGPS_LOGS>
-5.78

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.95724607071678

> <JCHEM_PKA_STRONGEST_BASIC>
-1.0679005686684793

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
129.14759999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.90e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5S,6S,7S,11R,14R,15R)-2,6,15-trimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0006845
     RDKit          3D
4alpha-Methylfecosterol
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.2082    0.2731   -1.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6268   -0.6100   -0.9916 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6977   -1.4606   -0.2662 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2852   -1.0555   -0.0829 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0100    0.0887    0.8598 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6379    1.3789    0.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5850    0.1027    1.3112 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2918    1.2020    2.2819 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0505    1.9098    1.6899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6222    0.6975    1.1591 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7997    0.8860    0.3222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2624   -0.1277   -0.3731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3479   -1.2047   -0.7816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0080   -1.2158   -0.1430 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5143    0.1236    0.2841 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6348    1.0018   -0.8827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7057   -0.1636   -0.7323 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9141    0.5280   -2.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2315   -1.5636   -0.7526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6743   -1.5726   -1.1151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4645   -0.4311   -0.5847 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8862    0.4629   -1.5895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8398    0.3407    0.5118 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2471   -0.3021    1.8447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3767    0.5762    0.4221 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9962    2.0357    0.4717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5394    2.1826    0.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1099   -0.7115   -0.7443 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6081   -2.1042   -1.0840 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4733   -0.4207    0.6758 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9691    0.8847   -2.3926 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1532    0.4074   -2.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7785   -2.5441   -0.5898 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1251   -1.5283    0.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8976   -0.7813   -1.0939 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7585   -1.9735    0.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5816   -0.2438    1.8047 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7625    1.2481    0.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4453    1.8485   -0.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4735    2.1606    1.3553 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4135   -0.8717    1.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8835    0.7967    3.2565 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0697    1.8783    2.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5415    2.3761    2.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3514    2.6629    0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7390   -0.0271    1.9805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8774   -2.1686   -0.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1945   -1.1718   -1.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7021   -1.7024   -0.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0801   -1.9026    0.7519 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1165    1.9645   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4234    1.2510   -1.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0428    0.5058   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9098    0.6868   -2.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4770   -0.0983   -2.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3759    1.5098   -1.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6881   -2.1664   -1.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0567   -2.0089    0.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7930   -1.5685   -2.2380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0913   -2.5742   -0.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4316   -0.8622   -0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8116    0.7380   -1.4908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3373    1.3552    0.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0402   -1.0463    1.7104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3409   -0.8431    2.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4779    0.4650    2.6058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9180    0.1197    1.3515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6379    2.6631   -0.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1866    2.3927    1.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968    2.5446   -0.8299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0597    2.9538    0.8495 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6459   -0.0077   -1.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6907   -2.1110   -0.8897 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1264   -2.8066   -0.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3567   -2.2795   -2.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1505    0.4722    0.7779 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5763   -0.1791    1.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9976   -1.2652    1.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 12 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
  2 28  1  0
 28 29  1  0
 28 30  1  0
 15  7  1  0
 25 17  1  0
 15 10  1  0
 27 11  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  1
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  1
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 16 51  1  0
 16 52  1  0
 16 53  1  0
 18 54  1  0
 18 55  1  0
 18 56  1  0
 19 57  1  0
 19 58  1  0
 20 59  1  0
 20 60  1  0
 21 61  1  1
 22 62  1  0
 23 63  1  1
 24 64  1  0
 24 65  1  0
 24 66  1  0
 25 67  1  1
 26 68  1  0
 26 69  1  0
 27 70  1  0
 27 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
 30 76  1  0
 30 77  1  0
 30 78  1  0
M  END

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0    8662.6338666.617   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8661.3038661.210   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0    8658.6368662.754   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0    8666.6228668.943   0.000  0.00  0.00           C+0
HETATM    5  H   UNK     0    8666.6228664.313   0.000  0.00  0.00           H+0
HETATM    6  H   UNK     0    8662.6338661.985   0.000  0.00  0.00           H+0
HETATM    7  C   UNK     0    8661.3028665.841   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8659.9688665.071   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8659.9688663.531   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8661.3028662.761   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8662.6308665.071   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8662.6308663.531   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8663.9648662.761   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8665.2978663.531   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8665.2948668.166   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8663.9608667.396   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8663.9608665.856   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8665.2948665.086   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8666.6278667.396   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8666.6278665.856   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8668.0928665.380   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8668.9978666.626   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    8668.0928667.872   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0    8668.0928669.412   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    8669.4288670.178   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0    8666.7608670.178   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0    8670.7608669.412   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0    8672.0968670.178   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0    8673.4328669.412   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0    8672.0968671.718   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0    8674.7648670.178   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0    8673.4328667.872   0.000  0.00  0.00           C+0
HETATM   33  H   UNK     0    8669.4288668.638   0.000  0.00  0.00           H+0
CONECT    1   11                                                            
CONECT    2   10                                                            
CONECT    3    9                                                            
CONECT    4   19                                                            
CONECT    5   20                                                            
CONECT    6   12                                                            
CONECT    7    8   11                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10    3                                                  
CONECT   10    9    2   12                                                  
CONECT   11   12    7    1   17                                             
CONECT   12   11   13   10    6                                             
CONECT   13   12   14                                                       
CONECT   14   13   18                                                       
CONECT   15   16   19                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   11                                                  
CONECT   18   17   14   20                                                  
CONECT   19   20   23   15    4                                             
CONECT   20   19   21   18    5                                             
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   24   33   19   22                                             
CONECT   24   23   25   26                                                  
CONECT   25   24   27                                                       
CONECT   26   24                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28   31   32                                                  
CONECT   30   28                                                            
CONECT   31   29                                                            
CONECT   32   29                                                            
CONECT   33   23                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

COMPND    HMDB0006845
HETATM    1  C1  UNL     1       5.208   0.273  -1.882  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.627  -0.610  -0.992  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.698  -1.461  -0.266  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.285  -1.056  -0.083  1.00  0.00           C  
HETATM    5  C5  UNL     1       3.010   0.089   0.860  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.638   1.379   0.532  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.585   0.103   1.311  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.292   1.202   2.282  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.051   1.910   1.690  1.00  0.00           C  
HETATM   10  C10 UNL     1      -0.622   0.697   1.159  1.00  0.00           C  
HETATM   11  C11 UNL     1      -1.800   0.886   0.322  1.00  0.00           C  
HETATM   12  C12 UNL     1      -2.262  -0.128  -0.373  1.00  0.00           C  
HETATM   13  C13 UNL     1      -1.348  -1.205  -0.782  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.008  -1.216  -0.143  1.00  0.00           C  
HETATM   15  C15 UNL     1       0.514   0.124   0.284  1.00  0.00           C  
HETATM   16  C16 UNL     1       0.635   1.002  -0.883  1.00  0.00           C  
HETATM   17  C17 UNL     1      -3.706  -0.164  -0.732  1.00  0.00           C  
HETATM   18  C18 UNL     1      -3.914   0.528  -2.049  1.00  0.00           C  
HETATM   19  C19 UNL     1      -4.232  -1.564  -0.753  1.00  0.00           C  
HETATM   20  C20 UNL     1      -5.674  -1.573  -1.115  1.00  0.00           C  
HETATM   21  C21 UNL     1      -6.464  -0.431  -0.585  1.00  0.00           C  
HETATM   22  O1  UNL     1      -6.886   0.463  -1.589  1.00  0.00           O  
HETATM   23  C22 UNL     1      -5.840   0.341   0.512  1.00  0.00           C  
HETATM   24  C23 UNL     1      -6.247  -0.302   1.845  1.00  0.00           C  
HETATM   25  C24 UNL     1      -4.377   0.576   0.422  1.00  0.00           C  
HETATM   26  C25 UNL     1      -3.996   2.036   0.472  1.00  0.00           C  
HETATM   27  C26 UNL     1      -2.539   2.183   0.207  1.00  0.00           C  
HETATM   28  C27 UNL     1       7.110  -0.711  -0.744  1.00  0.00           C  
HETATM   29  C28 UNL     1       7.608  -2.104  -1.084  1.00  0.00           C  
HETATM   30  C29 UNL     1       7.473  -0.421   0.676  1.00  0.00           C  
HETATM   31  H1  UNL     1       5.969   0.885  -2.393  1.00  0.00           H  
HETATM   32  H2  UNL     1       4.153   0.407  -2.135  1.00  0.00           H  
HETATM   33  H3  UNL     1       4.779  -2.544  -0.590  1.00  0.00           H  
HETATM   34  H4  UNL     1       5.125  -1.528   0.800  1.00  0.00           H  
HETATM   35  H5  UNL     1       2.898  -0.781  -1.094  1.00  0.00           H  
HETATM   36  H6  UNL     1       2.759  -1.974   0.297  1.00  0.00           H  
HETATM   37  H7  UNL     1       3.582  -0.244   1.805  1.00  0.00           H  
HETATM   38  H8  UNL     1       4.763   1.248   0.627  1.00  0.00           H  
HETATM   39  H9  UNL     1       3.445   1.848  -0.419  1.00  0.00           H  
HETATM   40  H10 UNL     1       3.473   2.161   1.355  1.00  0.00           H  
HETATM   41  H11 UNL     1       1.413  -0.872   1.874  1.00  0.00           H  
HETATM   42  H12 UNL     1       0.883   0.797   3.257  1.00  0.00           H  
HETATM   43  H13 UNL     1       2.070   1.878   2.560  1.00  0.00           H  
HETATM   44  H14 UNL     1      -0.542   2.376   2.514  1.00  0.00           H  
HETATM   45  H15 UNL     1       0.351   2.663   0.953  1.00  0.00           H  
HETATM   46  H16 UNL     1      -0.739  -0.027   1.980  1.00  0.00           H  
HETATM   47  H17 UNL     1      -1.877  -2.169  -0.594  1.00  0.00           H  
HETATM   48  H18 UNL     1      -1.194  -1.172  -1.905  1.00  0.00           H  
HETATM   49  H19 UNL     1       0.702  -1.702  -0.864  1.00  0.00           H  
HETATM   50  H20 UNL     1      -0.080  -1.903   0.752  1.00  0.00           H  
HETATM   51  H21 UNL     1       1.116   1.965  -0.783  1.00  0.00           H  
HETATM   52  H22 UNL     1      -0.423   1.251  -1.216  1.00  0.00           H  
HETATM   53  H23 UNL     1       1.043   0.506  -1.813  1.00  0.00           H  
HETATM   54  H24 UNL     1      -2.910   0.687  -2.541  1.00  0.00           H  
HETATM   55  H25 UNL     1      -4.477  -0.098  -2.787  1.00  0.00           H  
HETATM   56  H26 UNL     1      -4.376   1.510  -1.986  1.00  0.00           H  
HETATM   57  H27 UNL     1      -3.688  -2.166  -1.534  1.00  0.00           H  
HETATM   58  H28 UNL     1      -4.057  -2.009   0.253  1.00  0.00           H  
HETATM   59  H29 UNL     1      -5.793  -1.569  -2.238  1.00  0.00           H  
HETATM   60  H30 UNL     1      -6.091  -2.574  -0.809  1.00  0.00           H  
HETATM   61  H31 UNL     1      -7.432  -0.862  -0.187  1.00  0.00           H  
HETATM   62  H32 UNL     1      -7.812   0.738  -1.491  1.00  0.00           H  
HETATM   63  H33 UNL     1      -6.337   1.355   0.537  1.00  0.00           H  
HETATM   64  H34 UNL     1      -7.040  -1.046   1.710  1.00  0.00           H  
HETATM   65  H35 UNL     1      -5.341  -0.843   2.197  1.00  0.00           H  
HETATM   66  H36 UNL     1      -6.478   0.465   2.606  1.00  0.00           H  
HETATM   67  H37 UNL     1      -3.918   0.120   1.351  1.00  0.00           H  
HETATM   68  H38 UNL     1      -4.638   2.663  -0.177  1.00  0.00           H  
HETATM   69  H39 UNL     1      -4.187   2.393   1.512  1.00  0.00           H  
HETATM   70  H40 UNL     1      -2.397   2.545  -0.830  1.00  0.00           H  
HETATM   71  H41 UNL     1      -2.060   2.954   0.849  1.00  0.00           H  
HETATM   72  H42 UNL     1       7.646  -0.008  -1.391  1.00  0.00           H  
HETATM   73  H43 UNL     1       8.691  -2.111  -0.890  1.00  0.00           H  
HETATM   74  H44 UNL     1       7.126  -2.807  -0.395  1.00  0.00           H  
HETATM   75  H45 UNL     1       7.357  -2.279  -2.150  1.00  0.00           H  
HETATM   76  H46 UNL     1       8.150   0.472   0.778  1.00  0.00           H  
HETATM   77  H47 UNL     1       6.576  -0.179   1.282  1.00  0.00           H  
HETATM   78  H48 UNL     1       7.998  -1.265   1.167  1.00  0.00           H  
CONECT    1    2    2   31   32
CONECT    2    3   28
CONECT    3    4   33   34
CONECT    4    5   35   36
CONECT    5    6    7   37
CONECT    6   38   39   40
CONECT    7    8   15   41
CONECT    8    9   42   43
CONECT    9   10   44   45
CONECT   10   11   15   46
CONECT   11   12   12   27
CONECT   12   13   17
CONECT   13   14   47   48
CONECT   14   15   49   50
CONECT   15   16
CONECT   16   51   52   53
CONECT   17   18   19   25
CONECT   18   54   55   56
CONECT   19   20   57   58
CONECT   20   21   59   60
CONECT   21   22   23   61
CONECT   22   62
CONECT   23   24   25   63
CONECT   24   64   65   66
CONECT   25   26   67
CONECT   26   27   68   69
CONECT   27   70   71
CONECT   28   29   30   72
CONECT   29   73   74   75
CONECT   30   76   77   78
END

HMDB0006845
     RDKit          3D
4alpha-Methylfecosterol
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.2082    0.2731   -1.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6268   -0.6100   -0.9916 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6977   -1.4606   -0.2662 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2852   -1.0555   -0.0829 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0100    0.0887    0.8598 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6379    1.3789    0.5322 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5850    0.1027    1.3112 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2918    1.2020    2.2819 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0505    1.9098    1.6899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6222    0.6975    1.1591 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7997    0.8860    0.3222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2624   -0.1277   -0.3731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3479   -1.2047   -0.7816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0080   -1.2158   -0.1430 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5143    0.1236    0.2841 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6348    1.0018   -0.8827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7057   -0.1636   -0.7323 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9141    0.5280   -2.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2315   -1.5636   -0.7526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6743   -1.5726   -1.1151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4645   -0.4311   -0.5847 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8862    0.4629   -1.5895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8398    0.3407    0.5118 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2471   -0.3021    1.8447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3767    0.5762    0.4221 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9962    2.0357    0.4717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5394    2.1826    0.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1099   -0.7115   -0.7443 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6081   -2.1042   -1.0840 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4733   -0.4207    0.6758 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9691    0.8847   -2.3926 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1532    0.4074   -2.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7785   -2.5441   -0.5898 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1251   -1.5283    0.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8976   -0.7813   -1.0939 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7585   -1.9735    0.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5816   -0.2438    1.8047 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7625    1.2481    0.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4453    1.8485   -0.4194 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4735    2.1606    1.3553 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4135   -0.8717    1.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8835    0.7967    3.2565 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0697    1.8783    2.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5415    2.3761    2.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3514    2.6629    0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7390   -0.0271    1.9805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8774   -2.1686   -0.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1945   -1.1718   -1.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7021   -1.7024   -0.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0801   -1.9026    0.7519 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1165    1.9645   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4234    1.2510   -1.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0428    0.5058   -1.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9098    0.6868   -2.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4770   -0.0983   -2.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3759    1.5098   -1.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6881   -2.1664   -1.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0567   -2.0089    0.2532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7930   -1.5685   -2.2380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0913   -2.5742   -0.8087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4316   -0.8622   -0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8116    0.7380   -1.4908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3373    1.3552    0.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0402   -1.0463    1.7104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3409   -0.8431    2.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4779    0.4650    2.6058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9180    0.1197    1.3515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6379    2.6631   -0.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1866    2.3927    1.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968    2.5446   -0.8299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0597    2.9538    0.8495 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6459   -0.0077   -1.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6907   -2.1110   -0.8897 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1264   -2.8066   -0.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3567   -2.2795   -2.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1505    0.4722    0.7779 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5763   -0.1791    1.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9976   -1.2652    1.1666 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  6
 12 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
  2 28  1  0
 28 29  1  0
 28 30  1  0
 15  7  1  0
 25 17  1  0
 15 10  1  0
 27 11  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  1
  6 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  1
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  1
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 16 51  1  0
 16 52  1  0
 16 53  1  0
 18 54  1  0
 18 55  1  0
 18 56  1  0
 19 57  1  0
 19 58  1  0
 20 59  1  0
 20 60  1  0
 21 61  1  1
 22 62  1  0
 23 63  1  1
 24 64  1  0
 24 65  1  0
 24 66  1  0
 25 67  1  1
 26 68  1  0
 26 69  1  0
 27 70  1  0
 27 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
 30 76  1  0
 30 77  1  0
 30 78  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
4alpha-Methylfecosterol	HMDB
4 alpha-Methyl-5 alpha-ergosta-8,24(28)-dien-3 beta-ol	MeSH, HMDB
4a-Methylfecosterol	Generator
4Α-methylfecosterol	Generator, HMDB
(3beta,4alpha,5alpha)-4-Methylergosta-8,24(28)-dien-3-ol	HMDB
(3β,4α,5α)-4-Methylergosta-8,24(28)-dien-3-ol	HMDB
24,25-Dihydro-4alpha-methyl-24-methylenezymosterol	HMDB
24,25-Dihydro-4α-methyl-24-methylenezymosterol	HMDB
4α-Methylfecosterol	HMDB

Chemical Formula

C₂₉H₄₈O

Average Molecular Weight

412.6908

Monoisotopic Molecular Weight

412.370516158

IUPAC Name

(2S,5S,6S,7S,11R,14R,15R)-2,6,15-trimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-5-ol

Traditional Name

(2S,5S,6S,7S,11R,14R,15R)-2,6,15-trimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-5-ol

CAS Registry Number

17757-07-2

SMILES

[H][C@@]1(CC[C@@]2([H])C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)[C@@H](C)[C@]1([H])CC3)[C@H](C)CCC(=C)C(C)C

InChI Identifier

InChI=1S/C29H48O/c1-18(2)19(3)8-9-20(4)23-12-13-25-22-10-11-24-21(5)27(30)15-17-29(24,7)26(22)14-16-28(23,25)6/h18,20-21,23-25,27,30H,3,8-17H2,1-2,4-7H3/t20-,21+,23-,24+,25+,27+,28-,29+/m1/s1

InChI Key

QLDNWJOJCDIMKK-XLFBYWHPSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergosterols and derivatives

Alternative Parents

Substituents

Ergosterol-skeleton
3-beta-hydroxysteroid
Hydroxysteroid
3-hydroxysteroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

ergostanoid (CHEBI:80094 )
Ergosterols and C24-methyl derivatives (C15776 )
Ergosterols and C24-methyl derivatives (LMST01031019 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0006845)
Membrane (HMDB: HMDB0006845)

Source

Exogenous

Exogenous (HMDB: HMDB0006845)

Food

Cereal and cereal product

Cereal product

Breakfast cereal (FooDB: FOOD00270)

Cereal

Wheat (FooDB: FOOD00561)

Cereals and cereal products (FooDB: FOOD00858)

Endogenous

Endogenous (HMDB: HMDB0006845)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Steroid Biosynthesis (PathBank: SMP0121236)

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00069 g/L	ALOGPS
logP	6.64	ALOGPS
logP	7.37	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	18.96	ChemAxon
pKa (Strongest Basic)	-1.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	129.15 m³·mol⁻¹	ChemAxon
Polarizability	53.45 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	202.844	31661259
DarkChem	[M-H]-	200.248	31661259
DeepCCS	[M-2H]-	248.867	30932474
DeepCCS	[M+Na]+	223.215	30932474
AllCCS	[M+H]+	209.3	32859911
AllCCS	[M+H-H2O]+	207.3	32859911
AllCCS	[M+NH4]+	211.1	32859911
AllCCS	[M+Na]+	211.6	32859911
AllCCS	[M-H]-	207.6	32859911
AllCCS	[M+Na-2H]-	209.7	32859911
AllCCS	[M+HCOO]-	212.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
4alpha-Methylfecosterol	[H][C@@]1(CC[C@@]2([H])C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)[C@@H](C)[C@]1([H])CC3)[C@H](C)CCC(=C)C(C)C	2637.5	Standard polar	33892256
4alpha-Methylfecosterol	[H][C@@]1(CC[C@@]2([H])C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)[C@@H](C)[C@]1([H])CC3)[C@H](C)CCC(=C)C(C)C	3279.2	Standard non polar	33892256
4alpha-Methylfecosterol	[H][C@@]1(CC[C@@]2([H])C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)[C@@H](C)[C@]1([H])CC3)[C@H](C)CCC(=C)C(C)C	3253.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
4alpha-Methylfecosterol,1TMS,isomer #1	C=C(CC[C@@H](C)[C@H]1CC[C@H]2C3=C(CC[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C)[C@@H](C)[C@@H]1CC3)C(C)C	3306.2	Semi standard non polar	33892256
4alpha-Methylfecosterol,1TBDMS,isomer #1	C=C(CC[C@@H](C)[C@H]1CC[C@H]2C3=C(CC[C@@]21C)[C@@]1(C)CC[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](C)[C@@H]1CC3)C(C)C	3545.9	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 - 4alpha-Methylfecosterol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0032-0019000000-6f8c8cd8a7d225a3048f	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4alpha-Methylfecosterol GC-MS (1 TMS) - 70eV, Positive	splash10-06di-2004900000-8877055f754f2b4ac001	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 4alpha-Methylfecosterol 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 - 4alpha-Methylfecosterol 10V, Positive-QTOF	splash10-03dj-1019400000-5a5687b63ecb5002e1c0	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 20V, Positive-QTOF	splash10-03gj-5029100000-c5c21496ecefaf5c6379	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 40V, Positive-QTOF	splash10-001i-6069000000-672d03b792b2837c1872	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 10V, Negative-QTOF	splash10-03di-0002900000-02f9c4807c829d504e2a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 20V, Negative-QTOF	splash10-03di-0004900000-cb8bcbf4d9a655149a7b	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 40V, Negative-QTOF	splash10-000t-1009000000-1ac1e40e61ccf477c8bb	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 10V, Negative-QTOF	splash10-03di-0000900000-363450e12a0ea926276e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 20V, Negative-QTOF	splash10-03di-0000900000-363450e12a0ea926276e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 40V, Negative-QTOF	splash10-0a4i-0001900000-02f5c43e79de8082e487	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 10V, Positive-QTOF	splash10-03xs-0049400000-b3d2f15911af4078abf4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 20V, Positive-QTOF	splash10-066r-9278100000-93d1a3b37109728cc23e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha-Methylfecosterol 40V, Positive-QTOF	splash10-053u-8930000000-e82c5a534a1740fa5cf3	2021-09-22	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

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

193524

PDB ID

Not Available

ChEBI ID

80094

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Enzymes

Enzyme Details

1. Delta(14)-sterol reductase

General function:: Involved in delta14-sterol reductase activity
Specific function:: Involved in the conversion of lanosterol to cholesterol.
Gene Name:: TM7SF2
Uniprot ID:: O76062
Molecular weight:: 46405.345

Reactions

delta8,14-Sterol + NADPH + Hydrogen Ion → 4alpha-Methylfecosterol + NADP	details

Enzyme Details

2. 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase

General function:: Involved in cholestenol delta-isomerase activity
Specific function:: Catalyzes the conversion of Delta(8)-sterols to their corresponding Delta(7)-isomers.
Gene Name:: EBP
Uniprot ID:: Q15125
Molecular weight:: 26352.615

Reactions

4alpha-Methylfecosterol → 24-Methylenelophenol	details

Showing metabocard for 4alpha-Methylfecosterol (HMDB0006845)

MOL for HMDB0006845 (4alpha-Methylfecosterol)

3D MOL for HMDB0006845 (4alpha-Methylfecosterol)

3D SDF for HMDB0006845 (4alpha-Methylfecosterol)

3D-SDF for HMDB0006845 (4alpha-Methylfecosterol)

PDB for HMDB0006845 (4alpha-Methylfecosterol)

3D PDB for HMDB0006845 (4alpha-Methylfecosterol)

SMILES for HMDB0006845 (4alpha-Methylfecosterol)

INCHI for HMDB0006845 (4alpha-Methylfecosterol)

Structure for HMDB0006845 (4alpha-Methylfecosterol)

3D Structure for HMDB0006845 (4alpha-Methylfecosterol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

Reactions

Reactions