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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2021-09-23 17:52:58 UTC

Update Date

2021-09-23 17:52:58 UTC

HMDB ID

HMDB0302451

Secondary Accession Numbers

None

Metabolite Identification

Common Name

4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol

Description

4alpha,14alpha,24-trimethyl-cholesta-8(24)-dien-3beta-ol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). 4alpha,14alpha,24-trimethyl-cholesta-8(24)-dien-3beta-ol can be found in a number of food items such as green bell pepper, yellow bell pepper, orange bell pepper, and pepper (c. annuum), which makes 4alpha,14alpha,24-trimethyl-cholesta-8(24)-dien-3beta-ol a potential biomarker for the consumption of these food products.

Structure

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


  Mrv0541 02241212342D          

 31 34  0  0  0  0            999 V2000
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  4 29  1  6  0  0  0
 15 30  1  6  0  0  0
 24 31  1  0  0  0  0
M  END

HMDB0302451
     RDKit          3D
4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol
 81 84  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv0541 02241212342D          

 31 34  0  0  0  0            999 V2000
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 21 23  1  0  0  0  0
 22 28  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
  4 29  1  6  0  0  0
 15 30  1  6  0  0  0
 24 31  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0302451

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@H](CCC(C)=C(C)C)C1CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)[C@@H](C)C1CC3

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O/c1-19(2)20(3)9-10-21(4)23-13-17-30(8)26-12-11-24-22(5)27(31)15-16-28(24,6)25(26)14-18-29(23,30)7/h21-24,27,31H,9-18H2,1-8H3/t21-,22+,23?,24?,27+,28+,29-,30+/m1/s1

> <INCHI_KEY>
GCZFZGBLBXBCJP-BGXCJGIWSA-N

> <FORMULA>
C30H50O

> <MOLECULAR_WEIGHT>
426.7174

> <EXACT_MASS>
426.386166222

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
55.10042226842239

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S,6S,11R,15R)-14-[(2R)-5,6-dimethylhept-5-en-2-yl]-2,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-ol

> <ALOGPS_LOGP>
6.85

> <JCHEM_LOGP>
7.572032942666667

> <ALOGPS_LOGS>
-5.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.95724607023405

> <JCHEM_PKA_STRONGEST_BASIC>
-1.067900568879626

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
134.4286

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.54e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5S,6S,11R,15R)-14-[(2R)-5,6-dimethylhept-5-en-2-yl]-2,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0302451
     RDKit          3D
4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol
 81 84  0  0  0  0  0  0  0  0999 V2000
    7.4483   -0.5134    1.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8176    0.5036    0.2862 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3327    1.8904    0.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7872    0.1456   -0.4990 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2028    1.2062   -1.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2878   -1.2441   -0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9264   -1.4712   -0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7765   -0.8280   -0.7638 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6787   -1.2711   -2.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5616   -1.1068    0.0756 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8391   -0.4612    1.4363 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5908    0.3245    1.7943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4531   -0.4217    1.0179 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7043   -1.7440    1.6775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6791    0.3144    0.7417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3734    0.0861   -0.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9211   -0.8738   -1.4031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6250   -1.5511   -1.0752 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2666   -0.5759   -0.3388 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2432    0.7722   -0.9731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6387    0.8044   -0.5802 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2811    2.1979   -1.1175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4596    0.1616   -1.6971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8635    0.7760   -1.5785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5092    0.0553   -0.3983 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.6731    0.7458   -0.0938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5681   -0.0214    0.7818 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0830   -1.4199    0.9367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4414    0.9878    0.6536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6819    1.0696    1.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872    1.3337    1.6839 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1901   -0.0647    1.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6835   -1.0106    1.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.3030    0.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5205    2.6276    0.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8003    2.1734    1.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1379    1.9491   -0.5000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7233    0.7517   -2.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5688    1.9319   -0.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0609    1.8216   -1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4792   -1.6076   -1.5675 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0416   -1.8530    0.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7807   -2.6037    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9113   -1.2148    1.0630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9459    0.2653   -0.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1274   -2.2210   -2.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7349   -1.3627   -2.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2065   -0.4978   -2.7850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5049   -2.2229    0.1591 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6469    0.3013    1.3680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0793   -1.2125    2.1999 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4020    0.3032    2.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6850    1.3891    1.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7454   -1.5374    2.7880 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0518   -2.5081    1.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7450   -2.0656    1.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6999   -1.6915   -1.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9504   -0.4362   -2.4288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8728   -2.4111   -0.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1892   -2.0126   -1.9555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282    1.5861   -0.3155 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2154    1.1392   -1.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4407    0.8127   -1.8723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7848    2.9922   -0.4928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5937    2.3387   -2.1654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2165    2.4203   -1.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5305   -0.9339   -1.5930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0502    0.4593   -2.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7559    1.8296   -1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4668    0.5811   -2.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8007   -0.9506   -0.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4046    1.6825    0.1162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1481    0.2628    1.6845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6592   -2.0861    0.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0051   -1.5438    0.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2646   -1.8279    1.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9910    1.9843    0.5588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8195    0.1612    2.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0045    1.9219    2.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0841    2.3645    1.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7162    1.2569    2.6894 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
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 16 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 30 31  1  0
 19 10  1  0
 29 21  1  0
 19 13  1  0
 31 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  5 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  6
  9 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 20 61  1  0
 20 62  1  0
 20 63  1  0
 22 64  1  0
 22 65  1  0
 22 66  1  0
 23 67  1  0
 23 68  1  0
 24 69  1  0
 24 70  1  0
 25 71  1  6
 26 72  1  0
 27 73  1  1
 28 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 30 78  1  0
 30 79  1  0
 31 80  1  0
 31 81  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      -4.036  -0.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.369  -1.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.369  -2.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.036  -3.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.702  -2.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.702  -1.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.368  -0.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.368  -3.700   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.035  -2.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.035  -1.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.035   1.690   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.368   0.920   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.633   1.690   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.299   0.920   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.299  -0.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.966  -0.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.966   0.920   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -6.703  -3.700   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.702   0.150   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.299   2.460   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.966   4.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.633   3.230   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.300   3.230   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.634   4.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.967   3.230   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.301   4.000   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.967   1.690   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.299   4.000   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.036  -5.240   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.368  -2.107   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.634   5.540   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5   29                                                  
CONECT    5    4    6    8                                                  
CONECT    6    1    5    7   19                                             
CONECT    7    6   12   10                                                  
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    7    9   15                                                  
CONECT   11   12   14                                                       
CONECT   12    7   11                                                       
CONECT   13   14   22   17                                                  
CONECT   14   11   13   15   20                                             
CONECT   15   10   14   16   30                                             
CONECT   16   15   17                                                       
CONECT   17   13   16                                                       
CONECT   18    3                                                            
CONECT   19    6                                                            
CONECT   20   14                                                            
CONECT   21   22   23                                                       
CONECT   22   13   21   28                                                  
CONECT   23   21   24                                                       
CONECT   24   23   25   31                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   22                                                            
CONECT   29    4                                                            
CONECT   30   15                                                            
CONECT   31   24                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

COMPND    HMDB0302451
HETATM    1  C1  UNL     1       7.448  -0.513   1.169  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.818   0.504   0.286  1.00  0.00           C  
HETATM    3  C3  UNL     1       7.333   1.890   0.284  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.787   0.146  -0.499  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.203   1.206  -1.356  1.00  0.00           C  
HETATM    6  C6  UNL     1       5.288  -1.244  -0.526  1.00  0.00           C  
HETATM    7  C7  UNL     1       3.926  -1.471  -0.040  1.00  0.00           C  
HETATM    8  C8  UNL     1       2.777  -0.828  -0.764  1.00  0.00           C  
HETATM    9  C9  UNL     1       2.679  -1.271  -2.192  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.562  -1.107   0.076  1.00  0.00           C  
HETATM   11  C11 UNL     1       1.839  -0.461   1.436  1.00  0.00           C  
HETATM   12  C12 UNL     1       0.591   0.325   1.794  1.00  0.00           C  
HETATM   13  C13 UNL     1      -0.453  -0.422   1.018  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.704  -1.744   1.678  1.00  0.00           C  
HETATM   15  C15 UNL     1      -1.679   0.314   0.742  1.00  0.00           C  
HETATM   16  C16 UNL     1      -2.373   0.086  -0.359  1.00  0.00           C  
HETATM   17  C17 UNL     1      -1.921  -0.874  -1.403  1.00  0.00           C  
HETATM   18  C18 UNL     1      -0.625  -1.551  -1.075  1.00  0.00           C  
HETATM   19  C19 UNL     1       0.267  -0.576  -0.339  1.00  0.00           C  
HETATM   20  C20 UNL     1       0.243   0.772  -0.973  1.00  0.00           C  
HETATM   21  C21 UNL     1      -3.639   0.804  -0.580  1.00  0.00           C  
HETATM   22  C22 UNL     1      -3.281   2.198  -1.118  1.00  0.00           C  
HETATM   23  C23 UNL     1      -4.460   0.162  -1.697  1.00  0.00           C  
HETATM   24  C24 UNL     1      -5.863   0.776  -1.578  1.00  0.00           C  
HETATM   25  C25 UNL     1      -6.509   0.055  -0.398  1.00  0.00           C  
HETATM   26  O1  UNL     1      -7.673   0.746  -0.094  1.00  0.00           O  
HETATM   27  C26 UNL     1      -5.568  -0.021   0.782  1.00  0.00           C  
HETATM   28  C27 UNL     1      -5.083  -1.420   0.937  1.00  0.00           C  
HETATM   29  C28 UNL     1      -4.441   0.988   0.654  1.00  0.00           C  
HETATM   30  C29 UNL     1      -3.682   1.070   1.922  1.00  0.00           C  
HETATM   31  C30 UNL     1      -2.187   1.334   1.684  1.00  0.00           C  
HETATM   32  H1  UNL     1       8.190  -0.065   1.838  1.00  0.00           H  
HETATM   33  H2  UNL     1       6.684  -1.011   1.811  1.00  0.00           H  
HETATM   34  H3  UNL     1       7.953  -1.303   0.589  1.00  0.00           H  
HETATM   35  H4  UNL     1       6.520   2.628   0.031  1.00  0.00           H  
HETATM   36  H5  UNL     1       7.800   2.173   1.246  1.00  0.00           H  
HETATM   37  H6  UNL     1       8.138   1.949  -0.500  1.00  0.00           H  
HETATM   38  H7  UNL     1       4.723   0.752  -2.232  1.00  0.00           H  
HETATM   39  H8  UNL     1       4.569   1.932  -0.808  1.00  0.00           H  
HETATM   40  H9  UNL     1       6.061   1.822  -1.793  1.00  0.00           H  
HETATM   41  H10 UNL     1       5.479  -1.608  -1.567  1.00  0.00           H  
HETATM   42  H11 UNL     1       6.042  -1.853   0.071  1.00  0.00           H  
HETATM   43  H12 UNL     1       3.781  -2.604   0.002  1.00  0.00           H  
HETATM   44  H13 UNL     1       3.911  -1.215   1.063  1.00  0.00           H  
HETATM   45  H14 UNL     1       2.946   0.265  -0.758  1.00  0.00           H  
HETATM   46  H15 UNL     1       2.127  -2.221  -2.343  1.00  0.00           H  
HETATM   47  H16 UNL     1       3.735  -1.363  -2.583  1.00  0.00           H  
HETATM   48  H17 UNL     1       2.207  -0.498  -2.785  1.00  0.00           H  
HETATM   49  H18 UNL     1       1.505  -2.223   0.159  1.00  0.00           H  
HETATM   50  H19 UNL     1       2.647   0.301   1.368  1.00  0.00           H  
HETATM   51  H20 UNL     1       2.079  -1.213   2.200  1.00  0.00           H  
HETATM   52  H21 UNL     1       0.402   0.303   2.892  1.00  0.00           H  
HETATM   53  H22 UNL     1       0.685   1.389   1.514  1.00  0.00           H  
HETATM   54  H23 UNL     1      -0.745  -1.537   2.788  1.00  0.00           H  
HETATM   55  H24 UNL     1       0.052  -2.508   1.544  1.00  0.00           H  
HETATM   56  H25 UNL     1      -1.745  -2.066   1.427  1.00  0.00           H  
HETATM   57  H26 UNL     1      -2.700  -1.692  -1.436  1.00  0.00           H  
HETATM   58  H27 UNL     1      -1.950  -0.436  -2.429  1.00  0.00           H  
HETATM   59  H28 UNL     1      -0.873  -2.411  -0.383  1.00  0.00           H  
HETATM   60  H29 UNL     1      -0.189  -2.013  -1.955  1.00  0.00           H  
HETATM   61  H30 UNL     1      -0.128   1.586  -0.315  1.00  0.00           H  
HETATM   62  H31 UNL     1       1.215   1.139  -1.353  1.00  0.00           H  
HETATM   63  H32 UNL     1      -0.441   0.813  -1.872  1.00  0.00           H  
HETATM   64  H33 UNL     1      -3.785   2.992  -0.493  1.00  0.00           H  
HETATM   65  H34 UNL     1      -3.594   2.339  -2.165  1.00  0.00           H  
HETATM   66  H35 UNL     1      -2.216   2.420  -1.065  1.00  0.00           H  
HETATM   67  H36 UNL     1      -4.531  -0.934  -1.593  1.00  0.00           H  
HETATM   68  H37 UNL     1      -4.050   0.459  -2.677  1.00  0.00           H  
HETATM   69  H38 UNL     1      -5.756   1.830  -1.310  1.00  0.00           H  
HETATM   70  H39 UNL     1      -6.467   0.581  -2.475  1.00  0.00           H  
HETATM   71  H40 UNL     1      -6.801  -0.951  -0.765  1.00  0.00           H  
HETATM   72  H41 UNL     1      -7.405   1.682   0.116  1.00  0.00           H  
HETATM   73  H42 UNL     1      -6.148   0.263   1.684  1.00  0.00           H  
HETATM   74  H43 UNL     1      -5.659  -2.086   0.265  1.00  0.00           H  
HETATM   75  H44 UNL     1      -4.005  -1.544   0.666  1.00  0.00           H  
HETATM   76  H45 UNL     1      -5.265  -1.828   1.972  1.00  0.00           H  
HETATM   77  H46 UNL     1      -4.991   1.984   0.559  1.00  0.00           H  
HETATM   78  H47 UNL     1      -3.819   0.161   2.542  1.00  0.00           H  
HETATM   79  H48 UNL     1      -4.005   1.922   2.584  1.00  0.00           H  
HETATM   80  H49 UNL     1      -2.084   2.365   1.329  1.00  0.00           H  
HETATM   81  H50 UNL     1      -1.716   1.257   2.689  1.00  0.00           H  
CONECT    1    2   32   33   34
CONECT    2    3    4    4
CONECT    3   35   36   37
CONECT    4    5    6
CONECT    5   38   39   40
CONECT    6    7   41   42
CONECT    7    8   43   44
CONECT    8    9   10   45
CONECT    9   46   47   48
CONECT   10   11   19   49
CONECT   11   12   50   51
CONECT   12   13   52   53
CONECT   13   14   15   19
CONECT   14   54   55   56
CONECT   15   16   16   31
CONECT   16   17   21
CONECT   17   18   57   58
CONECT   18   19   59   60
CONECT   19   20
CONECT   20   61   62   63
CONECT   21   22   23   29
CONECT   22   64   65   66
CONECT   23   24   67   68
CONECT   24   25   69   70
CONECT   25   26   27   71
CONECT   26   72
CONECT   27   28   29   73
CONECT   28   74   75   76
CONECT   29   30   77
CONECT   30   31   78   79
CONECT   31   80   81
END

HMDB0302451
     RDKit          3D
4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol
 81 84  0  0  0  0  0  0  0  0999 V2000
    7.4483   -0.5134    1.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8176    0.5036    0.2862 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3327    1.8904    0.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7872    0.1456   -0.4990 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2028    1.2062   -1.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2878   -1.2441   -0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9264   -1.4712   -0.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7765   -0.8280   -0.7638 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6787   -1.2711   -2.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5616   -1.1068    0.0756 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8391   -0.4612    1.4363 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5908    0.3245    1.7943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4531   -0.4217    1.0179 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7043   -1.7440    1.6775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6791    0.3144    0.7417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3734    0.0861   -0.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9211   -0.8738   -1.4031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6250   -1.5511   -1.0752 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2666   -0.5759   -0.3388 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2432    0.7722   -0.9731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6387    0.8044   -0.5802 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2811    2.1979   -1.1175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4596    0.1616   -1.6971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8635    0.7760   -1.5785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5092    0.0553   -0.3983 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.6731    0.7458   -0.0938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5681   -0.0214    0.7818 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0830   -1.4199    0.9367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4414    0.9878    0.6536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6819    1.0696    1.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872    1.3337    1.6839 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1901   -0.0647    1.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6835   -1.0106    1.8111 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9534   -1.3030    0.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5205    2.6276    0.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8003    2.1734    1.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1379    1.9491   -0.5000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7233    0.7517   -2.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5688    1.9319   -0.8083 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0609    1.8216   -1.7925 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4792   -1.6076   -1.5675 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0416   -1.8530    0.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7807   -2.6037    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9113   -1.2148    1.0630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9459    0.2653   -0.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1274   -2.2210   -2.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7349   -1.3627   -2.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2065   -0.4978   -2.7850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5049   -2.2229    0.1591 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6469    0.3013    1.3680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0793   -1.2125    2.1999 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4020    0.3032    2.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6850    1.3891    1.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7454   -1.5374    2.7880 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0518   -2.5081    1.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7450   -2.0656    1.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6999   -1.6915   -1.4365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9504   -0.4362   -2.4288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8728   -2.4111   -0.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1892   -2.0126   -1.9555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1282    1.5861   -0.3155 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2154    1.1392   -1.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4407    0.8127   -1.8723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7848    2.9922   -0.4928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5937    2.3387   -2.1654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2165    2.4203   -1.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5305   -0.9339   -1.5930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0502    0.4593   -2.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7559    1.8296   -1.3100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4668    0.5811   -2.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8007   -0.9506   -0.7647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4046    1.6825    0.1162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1481    0.2628    1.6845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6592   -2.0861    0.2654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0051   -1.5438    0.6663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2646   -1.8279    1.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9910    1.9843    0.5588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8195    0.1612    2.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0045    1.9219    2.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0841    2.3645    1.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7162    1.2569    2.6894 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
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 16 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 30 31  1  0
 19 10  1  0
 29 21  1  0
 19 13  1  0
 31 15  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  5 38  1  0
  5 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  7 44  1  0
  8 45  1  6
  9 46  1  0
  9 47  1  0
  9 48  1  0
 10 49  1  0
 11 50  1  0
 11 51  1  0
 12 52  1  0
 12 53  1  0
 14 54  1  0
 14 55  1  0
 14 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 20 61  1  0
 20 62  1  0
 20 63  1  0
 22 64  1  0
 22 65  1  0
 22 66  1  0
 23 67  1  0
 23 68  1  0
 24 69  1  0
 24 70  1  0
 25 71  1  6
 26 72  1  0
 27 73  1  1
 28 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 30 78  1  0
 30 79  1  0
 31 80  1  0
 31 81  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
4a,14a,24-Trimethyl-cholesta-8(24)-dien-3b-ol	Generator
4Α,14α,24-trimethyl-cholesta-8(24)-dien-3β-ol	Generator

Chemical Formula

C₃₀H₅₀O

Average Molecular Weight

426.7174

Monoisotopic Molecular Weight

426.386166222

IUPAC Name

(2S,5S,6S,11R,15R)-14-[(2R)-5,6-dimethylhept-5-en-2-yl]-2,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-ol

Traditional Name

(2S,5S,6S,11R,15R)-14-[(2R)-5,6-dimethylhept-5-en-2-yl]-2,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-5-ol

CAS Registry Number

Not Available

SMILES

C[C@H](CCC(C)=C(C)C)C1CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)[C@@H](C)C1CC3

InChI Identifier

InChI=1S/C30H50O/c1-19(2)20(3)9-10-21(4)23-13-17-30(8)26-12-11-24-22(5)27(31)15-16-28(24,6)25(26)14-18-29(23,30)7/h21-24,27,31H,9-18H2,1-8H3/t21-,22+,23?,24?,27+,28+,29-,30+/m1/s1

InChI Key

GCZFZGBLBXBCJP-BGXCJGIWSA-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
14-alpha-methylsteroid
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

Not Available

Ontology

Not Available

Not Available

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	6.85	ALOGPS
logP	7.57	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	4	ChemAxon
Refractivity	134.43 m³·mol⁻¹	ChemAxon
Polarizability	55.1 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
AllCCS	[M+H]+	213.248	32859911
AllCCS	[M+H-H2O]+	211.366	32859911
AllCCS	[M+Na]+	215.473	32859911
AllCCS	[M+NH4]+	214.979	32859911
AllCCS	[M-H]-	213.372	32859911
AllCCS	[M+Na-2H]-	215.567	32859911
AllCCS	[M+HCOO]-	218.136	32859911
DeepCCS	[M-2H]-	246.631	30932474
DeepCCS	[M+Na]+	221.456	30932474

Predicted Kovats Retention Indices

Not Available

Spectra

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 10V, Positive-QTOF	splash10-0a6r-1004900000-49f9468ee0d62f9a117b	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 20V, Positive-QTOF	splash10-00o0-4129200000-b94768668a1a17a3bd25	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 40V, Positive-QTOF	splash10-00lr-9288200000-eb65e98028ecb3ea620c	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 10V, Negative-QTOF	splash10-004i-0000900000-4986ef9ac4d6e87dec4e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 20V, Negative-QTOF	splash10-004i-0000900000-3f4fd20224efb4916099	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 40V, Negative-QTOF	splash10-0a4i-3009600000-863a247f5c8ce8682915	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 10V, Positive-QTOF	splash10-001i-9147200000-9d8beb129bac2189a3ff	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 20V, Positive-QTOF	splash10-001i-9211000000-57fbee7a072f59ecb201	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 40V, Positive-QTOF	splash10-001i-9521000000-1b87e1287c4206599e88	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 10V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 20V, Negative-QTOF	splash10-004i-0000900000-43e99e872292ca648e72	2021-10-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol 40V, Negative-QTOF	splash10-00di-0003900000-dbd181142f6017eece54	2021-10-21	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

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

FDB004626

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

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

Showing metabocard for 4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol (HMDB0302451)

MOL for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

3D MOL for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

3D SDF for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

3D-SDF for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

PDB for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

3D PDB for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

SMILES for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

INCHI for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

Structure for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

3D Structure for HMDB0302451 (4alpha,14alpha,24-Trimethyl-cholesta-8(24)-dien-3beta-ol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

MS/MS Spectra