MiMeDB: Showing metabocard for 2Î²,20Î±-dimethyltetrahymanol (MMDBc0011904)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 03:35:54 UTC

Update Date

2022-08-31 06:33:44 UTC

Metabolite ID

MMDBc0011904

Metabolite Identification

Common Name

2Î²,20Î±-dimethyltetrahymanol

Description

2beta,20alpha-Dimethyltetrahymanol belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on 2beta,20alpha-Dimethyltetrahymanol.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152105352D          

 40 44  0  0  1  0            999 V2000
    6.4895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8522   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9337   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907   -1.1225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    1.8414    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230    1.1270    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270   -0.3020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230   -0.3020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 20  1  1  6  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21  2  1  1  0  0  0
 21 19  1  0  0  0  0
 22 13  1  0  0  0  0
 23 14  1  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 21  1  0  0  0  0
 27  3  1  0  0  0  0
 27  4  1  0  0  0  0
 27 17  1  0  0  0  0
 27 22  1  0  0  0  0
 28  5  1  0  0  0  0
 28  6  1  0  0  0  0
 28 23  1  0  0  0  0
 28 26  1  0  0  0  0
 29  7  1  6  0  0  0
 29 18  1  0  0  0  0
 29 22  1  0  0  0  0
 29 24  1  0  0  0  0
 30  8  1  1  0  0  0
 30 19  1  0  0  0  0
 30 23  1  0  0  0  0
 30 25  1  0  0  0  0
 31  9  1  6  0  0  0
 31 15  1  0  0  0  0
 31 24  1  0  0  0  0
 32 10  1  1  0  0  0
 32 16  1  0  0  0  0
 32 25  1  0  0  0  0
 32 31  1  0  0  0  0
 26 33  1  1  0  0  0
 20 34  1  1  0  0  0
 21 35  1  6  0  0  0
 22 36  1  1  0  0  0
 23 37  1  6  0  0  0
 24 38  1  1  0  0  0
 25 39  1  6  0  0  0
 26 40  1  6  0  0  0
M  END


  Mrv1652305152105352D          

 40 44  0  0  1  0            999 V2000
    6.4895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8522   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9337   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907   -1.1225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    1.8414    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230    1.1270    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270   -0.3020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5230   -0.3020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  1  0  0  0  0
 20  1  1  6  0  0  0
 20 17  1  0  0  0  0
 20 18  1  0  0  0  0
 21  2  1  1  0  0  0
 21 19  1  0  0  0  0
 22 13  1  0  0  0  0
 23 14  1  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 21  1  0  0  0  0
 27  3  1  0  0  0  0
 27  4  1  0  0  0  0
 27 17  1  0  0  0  0
 27 22  1  0  0  0  0
 28  5  1  0  0  0  0
 28  6  1  0  0  0  0
 28 23  1  0  0  0  0
 28 26  1  0  0  0  0
 29  7  1  6  0  0  0
 29 18  1  0  0  0  0
 29 22  1  0  0  0  0
 29 24  1  0  0  0  0
 30  8  1  1  0  0  0
 30 19  1  0  0  0  0
 30 23  1  0  0  0  0
 30 25  1  0  0  0  0
 31  9  1  6  0  0  0
 31 15  1  0  0  0  0
 31 24  1  0  0  0  0
 32 10  1  1  0  0  0
 32 16  1  0  0  0  0
 32 25  1  0  0  0  0
 32 31  1  0  0  0  0
 26 33  1  1  0  0  0
 20 34  1  1  0  0  0
 21 35  1  6  0  0  0
 22 36  1  1  0  0  0
 23 37  1  6  0  0  0
 24 38  1  1  0  0  0
 25 39  1  6  0  0  0
 26 40  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0011904

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(C)CC(C)(C)[C@]2([H])CC[C@]3(C)[C@]([H])(CC[C@]4([H])[C@@]5(C)C[C@]([H])(C)[C@]([H])(O)C(C)(C)[C@]5([H])CC[C@@]34C)[C@@]2(C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H56O/c1-20-17-27(3,4)22-13-15-31(9)24(29(22,7)18-20)11-12-25-30(8)19-21(2)26(33)28(5,6)23(30)14-16-32(25,31)10/h20-26,33H,11-19H2,1-10H3/t20-,21+,22+,23+,24-,25-,26+,29+,30+,31-,32-/m1/s1

> <INCHI_KEY>
IRRPBKNYCQPNRU-SDPCAQMASA-N

> <FORMULA>
C32H56O

> <MOLECULAR_WEIGHT>
456.799

> <EXACT_MASS>
456.433116423

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
58.624468323279444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4aR,6aR,6bR,8aS,11R,12aS,12bR,14aR,14bR)-2,4,4,6a,6b,9,9,11,12a,14b-decamethyl-docosahydropicen-3-ol

> <ALOGPS_LOGP>
6.74

> <JCHEM_LOGP>
8.46071223833333

> <ALOGPS_LOGS>
-7.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5740638612723145

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
140.07750000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.44e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4aR,6aR,6bR,8aS,11R,12aS,12bR,14aR,14bR)-2,4,4,6a,6b,9,9,11,12a,14b-decamethyl-hexadecahydropicen-3-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      12.114   3.437   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.206   3.437   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.791  -1.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.076  -2.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.264   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.954  -1.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.023  -2.095   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.034  -1.897   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.494  -1.897   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0      10.574   3.437   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.976   2.104   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      10.574   0.770   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.334   0.770   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       8.264  -0.564   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.644  -0.564   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.976  -0.564   0.000  0.00  0.00           H+0
CONECT    1   20                                                            
CONECT    2   21                                                            
CONECT    3   27                                                            
CONECT    4   27                                                            
CONECT    5   28                                                            
CONECT    6   28                                                            
CONECT    7   29                                                            
CONECT    8   30                                                            
CONECT    9   31                                                            
CONECT   10   32                                                            
CONECT   11   12   24                                                       
CONECT   12   11   25                                                       
CONECT   13   15   22                                                       
CONECT   14   16   23                                                       
CONECT   15   13   31                                                       
CONECT   16   14   32                                                       
CONECT   17   20   27                                                       
CONECT   18   20   29                                                       
CONECT   19   21   30                                                       
CONECT   20    1   17   18   34                                             
CONECT   21    2   19   26   35                                             
CONECT   22   13   27   29   36                                             
CONECT   23   14   28   30   37                                             
CONECT   24   11   29   31   38                                             
CONECT   25   12   30   32   39                                             
CONECT   26   21   28   33   40                                             
CONECT   27    3    4   17   22                                             
CONECT   28    5    6   23   26                                             
CONECT   29    7   18   22   24                                             
CONECT   30    8   19   23   25                                             
CONECT   31    9   15   24   32                                             
CONECT   32   10   16   25   31                                             
CONECT   33   26                                                            
CONECT   34   20                                                            
CONECT   35   21                                                            
CONECT   36   22                                                            
CONECT   37   23                                                            
CONECT   38   24                                                            
CONECT   39   25                                                            
CONECT   40   26                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   88    0
END

Synonyms

Value	Source
2b,20a-Dimethyltetrahymanol	Generator
2Β,20α-dimethyltetrahymanol	Generator

Molecular Formula

C₃₂H₅₆O

Average Mass

456.799

Monoisotopic Mass

456.433116423

IUPAC Name

(2S,3S,4aR,6aR,6bR,8aS,11R,12aS,12bR,14aR,14bR)-2,4,4,6a,6b,9,9,11,12a,14b-decamethyl-docosahydropicen-3-ol

Traditional Name

(2S,3S,4aR,6aR,6bR,8aS,11R,12aS,12bR,14aR,14bR)-2,4,4,6a,6b,9,9,11,12a,14b-decamethyl-hexadecahydropicen-3-ol

CAS Registry Number

Not Available

SMILES

[H][C@@]1(C)CC(C)(C)[C@]2([H])CC[C@]3(C)[C@]([H])(CC[C@]4([H])[C@@]5(C)C[C@]([H])(C)[C@]([H])(O)C(C)(C)[C@]5([H])CC[C@@]34C)[C@@]2(C)C1

InChI Identifier

InChI=1S/C32H56O/c1-20-17-27(3,4)22-13-15-31(9)24(29(22,7)18-20)11-12-25-30(8)19-21(2)26(33)28(5,6)23(30)14-16-32(25,31)10/h20-26,33H,11-19H2,1-10H3/t20-,21+,22+,23+,24-,25-,26+,29+,30+,31-,32-/m1/s1

InChI Key

IRRPBKNYCQPNRU-SDPCAQMASA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	2.4e-05 g/L	ALOGPS
logP	6.74	ALOGPS
logP	8.46	ChemAxon
logS	-7.3	ALOGPS
pKa (Strongest Basic)	-0.57	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	0	ChemAxon
Refractivity	140.08 m³·mol⁻¹	ChemAxon
Polarizability	58.62 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

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Proteobacteria	2	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78437629

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101124568

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for 2Î²,20Î±-dimethyltetrahymanol (MMDBc0011904)

MOL for #<Metabolite:0x0000559d01a653a8>

3D MOL for #<Metabolite:0x0000559d01a653a8>

3D SDF for #<Metabolite:0x0000559d01a653a8>

3D-SDF for #<Metabolite:0x0000559d01a653a8>

PDB for #<Metabolite:0x0000559d01a653a8>

3D PDB for #<Metabolite:0x0000559d01a653a8>

SMILES for #<Metabolite:0x0000559d01a653a8>

INCHI for #<Metabolite:0x0000559d01a653a8>

Structure for #<Metabolite:0x0000559d01a653a8>

3D Structure for #<Metabolite:0x0000559d01a653a8>