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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:04:03 UTC

Update Date

2022-03-07 02:54:22 UTC

HMDB ID

HMDB0035123

Secondary Accession Numbers

HMDB35123

Metabolite Identification

Common Name

3-Epimoretenol

Description

3-Epimoretenol belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30). 3-Epimoretenol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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


  Mrv0541 02241208162D          

 31 35  0  0  0  0            999 V2000
   -1.7008   -1.1619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9858   -1.5743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3437   -1.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2707   -0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3121   -0.9199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7008    0.4881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7008   -0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4144    0.0755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1294   -0.3368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1294   -1.1619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8445   -1.5743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9294    0.1073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2707    1.3130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4847    1.4519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5475    0.4963    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
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
M  END

HMDB0035123
     RDKit          3D
3-Epimoretenol
 81 85  0  0  0  0  0  0  0  0999 V2000
    6.7135   -0.1210   -0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
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 31 79  1  0
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 31 81  1  0
M  END


  Mrv0541 02241208162D          

 31 35  0  0  0  0            999 V2000
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 25 26  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  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035123

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(=C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O/c1-19(2)20-11-15-27(5)21(20)12-17-29(7)23(27)9-10-24-28(6)16-14-25(31)26(3,4)22(28)13-18-30(24,29)8/h20-25,31H,1,9-18H2,2-8H3

> <INCHI_KEY>
LFPVZIIPFONRSW-UHFFFAOYSA-N

> <FORMULA>
C30H50O

> <MOLECULAR_WEIGHT>
426.7174

> <EXACT_MASS>
426.386166222

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
54.09484979913826

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,2,9,14,18,18-hexamethyl-6-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-ol

> <ALOGPS_LOGP>
6.26

> <JCHEM_LOGP>
7.448046480999999

> <ALOGPS_LOGS>
-6.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.48943339017772

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351218351362649

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
130.90829999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.95e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,2,9,14,18,18-hexamethyl-6-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HMDB0035123
     RDKit          3D
3-Epimoretenol
 81 85  0  0  0  0  0  0  0  0999 V2000
    6.7135   -0.1210   -0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6593    0.1817   -1.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8064    1.4420   -2.1052 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5071   -0.6626   -1.2787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6955   -1.9678   -0.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3412   -2.2549    0.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9218   -0.8415    0.4761 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7049   -0.3832    1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2007   -0.2038   -0.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7867    1.2109   -0.9619 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7617    1.6894   -0.0112 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9586    0.6747    0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9762    1.1604    2.2129 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4275   -0.7233    0.6264 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7913   -1.5799    1.6390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6796   -1.6511    1.2183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3339   -0.3218    1.0384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6940   -0.5714    0.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7791   -1.9748   -0.1586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7281   -0.6223    1.6003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9189    0.2115    1.3568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5273    0.1504   -0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2922   -1.0208   -0.2058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4920    0.3371   -1.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6229   -0.6008   -2.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7817    1.7406   -1.6830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1492    0.4973   -0.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1473    0.9251   -1.4847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7260    0.6103   -1.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5308    0.7416    0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9588    2.1345    0.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6212    0.5531   -0.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8776   -0.9422    0.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0165    1.4880   -2.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9590    2.3404   -1.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7653    1.3169   -2.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3822   -0.9681   -2.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7929   -2.8347   -1.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4170   -2.0340    0.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6387   -2.6589   -0.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4863   -2.8696    1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6894    0.7042    1.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7719   -0.6494    1.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3733   -0.9834    2.5160 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4578   -0.7587   -1.5257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4047    1.4355   -2.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7019    1.8438   -0.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0243    2.3890   -0.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2822    2.4281    0.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0056    1.3075    2.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4747    2.1741    2.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5546    0.5282    2.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0330   -1.1000   -0.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9178   -1.3727    2.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1926   -2.6284    1.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1765   -2.1800    2.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6482   -2.2533    0.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4953    0.0630    2.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1741   -2.1144   -1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8281   -2.1922   -0.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5803   -2.7041    0.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0329   -1.6359    1.8645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2267   -0.2166    2.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7680    1.2892    1.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7145   -0.1391    2.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3172    0.9631   -0.0157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2875   -1.5992    0.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7070   -1.0995   -2.5610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0352   -0.1303   -3.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4469   -1.3337   -1.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8766    1.7977   -1.7741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3536    1.7597   -2.7066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4161    2.5275   -1.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3221    1.4027    0.2068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2605    2.0140   -1.7203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3521    0.4219   -2.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0910    1.2454   -1.7459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5342   -0.4302   -1.4631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0914    2.7733    1.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6158    2.1164    1.6992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3681    2.7395   -0.0428 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
  9  4  1  0
 30 12  1  0
 14  7  1  0
 30 17  1  0
 27 18  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
 10 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 13 50  1  0
 13 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 19 59  1  0
 19 60  1  0
 19 61  1  0
 20 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 22 66  1  0
 23 67  1  0
 25 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 26 73  1  0
 27 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 31 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      -3.175  -2.169   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.840  -2.939   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.642  -2.163   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.505  -0.629   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.583  -1.717   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.175   0.911   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.175  -0.629   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.507   0.141   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.842  -0.629   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.842  -2.169   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -7.176  -2.939   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.735   0.200   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.840   1.681   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.505   2.451   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.826   1.681   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.826   0.141   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.826  -1.399   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.498  -4.120   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.507  -2.939   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.519  -4.120   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.161  -0.629   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.493   0.141   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.493   1.681   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.638   2.710   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.012   4.120   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.482   3.958   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.161   2.451   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.914   3.357   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.176   3.537   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.145   2.392   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.622   0.926   0.000  0.00  0.00           C+0
CONECT    1    2    7   19                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   12   16                                             
CONECT    5    4                                                            
CONECT    6    7                                                            
CONECT    7    1    6    8   12                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10                                                            
CONECT   12    4    7   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   27                                                  
CONECT   16    4   15   17   21                                             
CONECT   17   16                                                            
CONECT   18   19                                                            
CONECT   19    1   10   18   20                                             
CONECT   20   19                                                            
CONECT   21   16   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   15   23   26   28                                             
CONECT   28   27                                                            
CONECT   29   30                                                            
CONECT   30   24   29   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

COMPND    HMDB0035123
HETATM    1  C1  UNL     1       6.714  -0.121  -0.567  1.00  0.00           C  
HETATM    2  C2  UNL     1       5.659   0.182  -1.294  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.806   1.442  -2.105  1.00  0.00           C  
HETATM    4  C4  UNL     1       4.507  -0.663  -1.279  1.00  0.00           C  
HETATM    5  C5  UNL     1       4.696  -1.968  -0.581  1.00  0.00           C  
HETATM    6  C6  UNL     1       3.341  -2.255   0.129  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.922  -0.842   0.476  1.00  0.00           C  
HETATM    8  C8  UNL     1       3.705  -0.383   1.617  1.00  0.00           C  
HETATM    9  C9  UNL     1       3.201  -0.204  -0.853  1.00  0.00           C  
HETATM   10  C10 UNL     1       2.787   1.211  -0.962  1.00  0.00           C  
HETATM   11  C11 UNL     1       1.762   1.689  -0.011  1.00  0.00           C  
HETATM   12  C12 UNL     1       0.959   0.675   0.752  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.976   1.160   2.213  1.00  0.00           C  
HETATM   14  C14 UNL     1       1.428  -0.723   0.626  1.00  0.00           C  
HETATM   15  C15 UNL     1       0.791  -1.580   1.639  1.00  0.00           C  
HETATM   16  C16 UNL     1      -0.680  -1.651   1.218  1.00  0.00           C  
HETATM   17  C17 UNL     1      -1.334  -0.322   1.038  1.00  0.00           C  
HETATM   18  C18 UNL     1      -2.694  -0.571   0.461  1.00  0.00           C  
HETATM   19  C19 UNL     1      -2.779  -1.975  -0.159  1.00  0.00           C  
HETATM   20  C20 UNL     1      -3.728  -0.622   1.600  1.00  0.00           C  
HETATM   21  C21 UNL     1      -4.919   0.212   1.357  1.00  0.00           C  
HETATM   22  C22 UNL     1      -5.527   0.150  -0.001  1.00  0.00           C  
HETATM   23  O1  UNL     1      -6.292  -1.021  -0.206  1.00  0.00           O  
HETATM   24  C23 UNL     1      -4.492   0.337  -1.090  1.00  0.00           C  
HETATM   25  C24 UNL     1      -4.623  -0.601  -2.223  1.00  0.00           C  
HETATM   26  C25 UNL     1      -4.782   1.741  -1.683  1.00  0.00           C  
HETATM   27  C26 UNL     1      -3.149   0.497  -0.460  1.00  0.00           C  
HETATM   28  C27 UNL     1      -2.147   0.925  -1.485  1.00  0.00           C  
HETATM   29  C28 UNL     1      -0.726   0.610  -1.122  1.00  0.00           C  
HETATM   30  C29 UNL     1      -0.531   0.742   0.361  1.00  0.00           C  
HETATM   31  C30 UNL     1      -0.959   2.135   0.799  1.00  0.00           C  
HETATM   32  H1  UNL     1       7.621   0.553  -0.597  1.00  0.00           H  
HETATM   33  H2  UNL     1       6.878  -0.942   0.086  1.00  0.00           H  
HETATM   34  H3  UNL     1       5.017   1.488  -2.880  1.00  0.00           H  
HETATM   35  H4  UNL     1       5.959   2.340  -1.516  1.00  0.00           H  
HETATM   36  H5  UNL     1       6.765   1.317  -2.696  1.00  0.00           H  
HETATM   37  H6  UNL     1       4.382  -0.968  -2.401  1.00  0.00           H  
HETATM   38  H7  UNL     1       4.793  -2.835  -1.283  1.00  0.00           H  
HETATM   39  H8  UNL     1       5.417  -2.034   0.216  1.00  0.00           H  
HETATM   40  H9  UNL     1       2.639  -2.659  -0.601  1.00  0.00           H  
HETATM   41  H10 UNL     1       3.486  -2.870   1.016  1.00  0.00           H  
HETATM   42  H11 UNL     1       3.689   0.704   1.820  1.00  0.00           H  
HETATM   43  H12 UNL     1       4.772  -0.649   1.505  1.00  0.00           H  
HETATM   44  H13 UNL     1       3.373  -0.983   2.516  1.00  0.00           H  
HETATM   45  H14 UNL     1       2.458  -0.759  -1.526  1.00  0.00           H  
HETATM   46  H15 UNL     1       2.405   1.435  -2.007  1.00  0.00           H  
HETATM   47  H16 UNL     1       3.702   1.844  -0.919  1.00  0.00           H  
HETATM   48  H17 UNL     1       1.024   2.389  -0.514  1.00  0.00           H  
HETATM   49  H18 UNL     1       2.282   2.428   0.682  1.00  0.00           H  
HETATM   50  H19 UNL     1      -0.006   1.307   2.645  1.00  0.00           H  
HETATM   51  H20 UNL     1       1.475   2.174   2.302  1.00  0.00           H  
HETATM   52  H21 UNL     1       1.555   0.528   2.879  1.00  0.00           H  
HETATM   53  H22 UNL     1       1.033  -1.100  -0.373  1.00  0.00           H  
HETATM   54  H23 UNL     1       0.918  -1.373   2.686  1.00  0.00           H  
HETATM   55  H24 UNL     1       1.193  -2.628   1.494  1.00  0.00           H  
HETATM   56  H25 UNL     1      -1.177  -2.180   2.058  1.00  0.00           H  
HETATM   57  H26 UNL     1      -0.648  -2.253   0.276  1.00  0.00           H  
HETATM   58  H27 UNL     1      -1.495   0.063   2.094  1.00  0.00           H  
HETATM   59  H28 UNL     1      -2.174  -2.114  -1.039  1.00  0.00           H  
HETATM   60  H29 UNL     1      -3.828  -2.192  -0.431  1.00  0.00           H  
HETATM   61  H30 UNL     1      -2.580  -2.704   0.681  1.00  0.00           H  
HETATM   62  H31 UNL     1      -4.033  -1.636   1.865  1.00  0.00           H  
HETATM   63  H32 UNL     1      -3.227  -0.217   2.531  1.00  0.00           H  
HETATM   64  H33 UNL     1      -4.768   1.289   1.639  1.00  0.00           H  
HETATM   65  H34 UNL     1      -5.714  -0.139   2.080  1.00  0.00           H  
HETATM   66  H35 UNL     1      -6.317   0.963  -0.016  1.00  0.00           H  
HETATM   67  H36 UNL     1      -6.287  -1.599   0.582  1.00  0.00           H  
HETATM   68  H37 UNL     1      -3.707  -1.099  -2.561  1.00  0.00           H  
HETATM   69  H38 UNL     1      -5.035  -0.130  -3.171  1.00  0.00           H  
HETATM   70  H39 UNL     1      -5.447  -1.334  -1.963  1.00  0.00           H  
HETATM   71  H40 UNL     1      -5.877   1.798  -1.774  1.00  0.00           H  
HETATM   72  H41 UNL     1      -4.354   1.760  -2.707  1.00  0.00           H  
HETATM   73  H42 UNL     1      -4.416   2.528  -1.023  1.00  0.00           H  
HETATM   74  H43 UNL     1      -3.322   1.403   0.207  1.00  0.00           H  
HETATM   75  H44 UNL     1      -2.260   2.014  -1.720  1.00  0.00           H  
HETATM   76  H45 UNL     1      -2.352   0.422  -2.476  1.00  0.00           H  
HETATM   77  H46 UNL     1      -0.091   1.245  -1.746  1.00  0.00           H  
HETATM   78  H47 UNL     1      -0.534  -0.430  -1.463  1.00  0.00           H  
HETATM   79  H48 UNL     1      -0.091   2.773   1.146  1.00  0.00           H  
HETATM   80  H49 UNL     1      -1.616   2.116   1.699  1.00  0.00           H  
HETATM   81  H50 UNL     1      -1.368   2.739  -0.043  1.00  0.00           H  
CONECT    1    2    2   32   33
CONECT    2    3    4
CONECT    3   34   35   36
CONECT    4    5    9   37
CONECT    5    6   38   39
CONECT    6    7   40   41
CONECT    7    8    9   14
CONECT    8   42   43   44
CONECT    9   10   45
CONECT   10   11   46   47
CONECT   11   12   48   49
CONECT   12   13   14   30
CONECT   13   50   51   52
CONECT   14   15   53
CONECT   15   16   54   55
CONECT   16   17   56   57
CONECT   17   18   30   58
CONECT   18   19   20   27
CONECT   19   59   60   61
CONECT   20   21   62   63
CONECT   21   22   64   65
CONECT   22   23   24   66
CONECT   23   67
CONECT   24   25   26   27
CONECT   25   68   69   70
CONECT   26   71   72   73
CONECT   27   28   74
CONECT   28   29   75   76
CONECT   29   30   77   78
CONECT   30   31
CONECT   31   79   80   81
END

HMDB0035123
     RDKit          3D
3-Epimoretenol
 81 85  0  0  0  0  0  0  0  0999 V2000
    6.7135   -0.1210   -0.5675 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6593    0.1817   -1.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8064    1.4420   -2.1052 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5071   -0.6626   -1.2787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6955   -1.9678   -0.5810 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3412   -2.2549    0.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9218   -0.8415    0.4761 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7049   -0.3832    1.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2007   -0.2038   -0.8526 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7867    1.2109   -0.9619 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7617    1.6894   -0.0112 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9586    0.6747    0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9762    1.1604    2.2129 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4275   -0.7233    0.6264 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7913   -1.5799    1.6390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6796   -1.6511    1.2183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3339   -0.3218    1.0384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6940   -0.5714    0.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7791   -1.9748   -0.1586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7281   -0.6223    1.6003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9189    0.2115    1.3568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5273    0.1504   -0.0010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2922   -1.0208   -0.2058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4920    0.3371   -1.0895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6229   -0.6008   -2.2228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7817    1.7406   -1.6830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1492    0.4973   -0.4598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1473    0.9251   -1.4847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7260    0.6103   -1.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5308    0.7416    0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9588    2.1345    0.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6212    0.5531   -0.5969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8776   -0.9422    0.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0165    1.4880   -2.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9590    2.3404   -1.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7653    1.3169   -2.6961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3822   -0.9681   -2.4007 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7929   -2.8347   -1.2828 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4170   -2.0340    0.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6387   -2.6589   -0.6013 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4863   -2.8696    1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6894    0.7042    1.8203 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7719   -0.6494    1.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3733   -0.9834    2.5160 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4578   -0.7587   -1.5257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4047    1.4355   -2.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7019    1.8438   -0.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0243    2.3890   -0.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2822    2.4281    0.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0056    1.3075    2.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4747    2.1741    2.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5546    0.5282    2.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0330   -1.1000   -0.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9178   -1.3727    2.6864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1926   -2.6284    1.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1765   -2.1800    2.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6482   -2.2533    0.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4953    0.0630    2.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1741   -2.1144   -1.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8281   -2.1922   -0.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5803   -2.7041    0.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0329   -1.6359    1.8645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2267   -0.2166    2.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7680    1.2892    1.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7145   -0.1391    2.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3172    0.9631   -0.0157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2875   -1.5992    0.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7070   -1.0995   -2.5610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0352   -0.1303   -3.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4469   -1.3337   -1.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8766    1.7977   -1.7741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3536    1.7597   -2.7066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4161    2.5275   -1.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3221    1.4027    0.2068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2605    2.0140   -1.7203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3521    0.4219   -2.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0910    1.2454   -1.7459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5342   -0.4302   -1.4631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0914    2.7733    1.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6158    2.1164    1.6992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3681    2.7395   -0.0428 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
  9  4  1  0
 30 12  1  0
 14  7  1  0
 30 17  1  0
 27 18  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  0
  5 39  1  0
  6 40  1  0
  6 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  0
 10 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 13 50  1  0
 13 51  1  0
 13 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 19 59  1  0
 19 60  1  0
 19 61  1  0
 20 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 22 66  1  0
 23 67  1  0
 25 68  1  0
 25 69  1  0
 25 70  1  0
 26 71  1  0
 26 72  1  0
 26 73  1  0
 27 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  0
 29 78  1  0
 31 79  1  0
 31 80  1  0
 31 81  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
3-Epi-moretenol	HMDB

Chemical Formula

C₃₀H₅₀O

Average Molecular Weight

426.7174

Monoisotopic Molecular Weight

426.386166222

IUPAC Name

1,2,9,14,18,18-hexamethyl-6-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-ol

Traditional Name

1,2,9,14,18,18-hexamethyl-6-(prop-1-en-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicosan-17-ol

CAS Registry Number

18610-71-4

SMILES

CC(=C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C

InChI Identifier

InChI=1S/C30H50O/c1-19(2)20-11-15-27(5)21(20)12-17-29(7)23(27)9-10-24-28(6)16-14-25(31)26(3,4)22(28)13-18-30(24,29)8/h20-25,31H,1,9-18H2,2-8H3

InChI Key

LFPVZIIPFONRSW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Hopanoids

Direct Parent

Hopanoids

Alternative Parents

Substituents

Triterpenoid
Hopane-skeleton
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

Not Available

Fats and oils (FooDB: FOOD00864)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	223 - 224 °C	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	0.0002 g/L	ALOGPS
logP	6.26	ALOGPS
logP	7.45	ChemAxon
logS	-6.3	ALOGPS
pKa (Strongest Acidic)	19.49	ChemAxon
pKa (Strongest Basic)	-0.84	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	1	ChemAxon
Refractivity	130.91 m³·mol⁻¹	ChemAxon
Polarizability	54.09 Å³	ChemAxon
Number of Rings	5	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]+	196.225	31661259
DarkChem	[M-H]-	192.581	31661259
DeepCCS	[M-2H]-	238.108	30932474
DeepCCS	[M+Na]+	213.335	30932474
AllCCS	[M+H]+	214.9	32859911
AllCCS	[M+H-H2O]+	213.1	32859911
AllCCS	[M+NH4]+	216.6	32859911
AllCCS	[M+Na]+	217.1	32859911
AllCCS	[M-H]-	212.5	32859911
AllCCS	[M+Na-2H]-	214.3	32859911
AllCCS	[M+HCOO]-	216.5	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
3-Epimoretenol	CC(=C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C	2522.7	Standard polar	33892256
3-Epimoretenol	CC(=C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C	3275.1	Standard non polar	33892256
3-Epimoretenol	CC(=C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O)C(C)(C)C3CCC12C	3464.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
3-Epimoretenol,1TMS,isomer #1	C=C(C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O[Si](C)(C)C)C(C)(C)C3CCC21C	3439.8	Semi standard non polar	33892256
3-Epimoretenol,1TBDMS,isomer #1	C=C(C)C1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCC(O[Si](C)(C)C(C)(C)C)C(C)(C)C3CCC21C	3655.5	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 - 3-Epimoretenol GC-MS (Non-derivatized) - 70eV, Positive	splash10-03dj-0119400000-544f7e1713d3a6d84864	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Epimoretenol GC-MS (1 TMS) - 70eV, Positive	splash10-0089-1011900000-3c17465681cc9ce54ea0	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 3-Epimoretenol 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 - 3-Epimoretenol 10V, Positive-QTOF	splash10-0a6r-0001900000-7ed7943a0548f9d20870	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 20V, Positive-QTOF	splash10-0a6r-0579800000-da2f645e2bea2350cd5d	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 40V, Positive-QTOF	splash10-00ks-1697100000-cc12ba84ff173c841e73	2016-08-02	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 10V, Negative-QTOF	splash10-004i-0000900000-a151356599ecdae79709	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 20V, Negative-QTOF	splash10-004i-0000900000-a6f39d6620a2c9c38b31	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 40V, Negative-QTOF	splash10-0a4l-1009500000-8651e3fe7de80e2e7fe4	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 10V, Positive-QTOF	splash10-004i-0022900000-e54dbad7ce217020c8b9	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 20V, Positive-QTOF	splash10-0019-5679100000-3abf35750488962582ab	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 40V, Positive-QTOF	splash10-017i-9310000000-cbd005c466d95ca44c06	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 10V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 20V, Negative-QTOF	splash10-004i-0000900000-590c9e4adfdd12b64d93	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 3-Epimoretenol 40V, Negative-QTOF	splash10-004i-0000900000-a98e2193ee7d0d5f9b51	2021-09-23	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

FDB013756

KNApSAcK ID

C00036122

Chemspider ID

525874

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

604951

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

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 3-Epimoretenol (HMDB0035123)

MOL for HMDB0035123 (3-Epimoretenol)

3D MOL for HMDB0035123 (3-Epimoretenol)

3D SDF for HMDB0035123 (3-Epimoretenol)

3D-SDF for HMDB0035123 (3-Epimoretenol)

PDB for HMDB0035123 (3-Epimoretenol)

3D PDB for HMDB0035123 (3-Epimoretenol)

SMILES for HMDB0035123 (3-Epimoretenol)

INCHI for HMDB0035123 (3-Epimoretenol)

Structure for HMDB0035123 (3-Epimoretenol)

3D Structure for HMDB0035123 (3-Epimoretenol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra