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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 01:27:30 UTC

Update Date

2022-11-23 21:42:16 UTC

HMDB ID

HMDB0248230

Secondary Accession Numbers

None

Metabolite Identification

Common Name

alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin

Description

alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin, also known as alpha-methyl-5-HT or alpha-methyl-5-hydroxytryptamine, belongs to the class of organic compounds known as serotonins. Serotonins are compounds containing a serotonin moiety, which consists of an indole that bears an aminoethyl a position 2 and a hydroxyl group at position 5. Based on a literature review a significant number of articles have been published on alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin. This compound has been identified in human blood as reported by (PMID: 31557052 ). Alpha-methyl-5-hydroxytryptamine; alpha-methylserotonin is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0248230
     RDKit          3D
alpha-Methyl-5-HT
 28 29  0  0  0  0  0  0  0  0999 V2000
   -1.8858    1.4623    0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4930    0.3578   -0.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0171   -0.6119    0.4106 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -0.2728   -1.5175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3615   -0.8755   -0.8814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2876   -2.2386   -0.5476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8952   -2.4315    0.0349 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6068   -1.3098    0.1120 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8699   -0.9748    0.6034 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3185    0.3252    0.5089 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5328    1.3022   -0.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0660    2.5829   -0.1192 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2994    0.9780   -0.5467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8293   -0.3194   -0.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7359    1.9210    0.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1301    1.0895    0.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5197    2.2496   -0.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4186    0.7450   -1.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2260   -0.8325    1.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8080   -0.1191    0.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1660    0.4431   -2.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0869   -1.0686   -2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0848   -2.9714   -0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2591   -3.3529    0.4040 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4605   -1.7671    1.0492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3131    0.5641    0.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6097    3.3747   -0.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117    1.7502   -0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14  5  1  0
 14  8  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  7 24  1  0
  9 25  1  0
 10 26  1  0
 12 27  1  0
 13 28  1  0
M  END


  Mrv1652309112103272D          

 14 15  0  0  0  0            999 V2000
   -1.4604    1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2054    0.9256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.7541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7575    0.3126    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
 10 13  1  0  0  0  0
  2 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0248230

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(N)CC1=CNC2=C1C=C(O)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C11H14N2O/c1-7(12)4-8-6-13-11-3-2-9(14)5-10(8)11/h2-3,5-7,13-14H,4,12H2,1H3

> <INCHI_KEY>
LYPCGXKCQDYTFV-UHFFFAOYSA-N

> <FORMULA>
C11H14N2O

> <MOLECULAR_WEIGHT>
190.246

> <EXACT_MASS>
190.110613079

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
21.086308977369992

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(2-aminopropyl)-1H-indol-5-ol

> <ALOGPS_LOGP>
1.01

> <JCHEM_LOGP>
0.8447161339862828

> <ALOGPS_LOGS>
-2.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
18.191071325767094

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.382781216754472

> <JCHEM_PKA_STRONGEST_BASIC>
10.159194400097645

> <JCHEM_POLAR_SURFACE_AREA>
62.03999999999999

> <JCHEM_REFRACTIVITY>
56.7726

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.49e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
α-methyl-5-hydroxytryptamine

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0248230
     RDKit          3D
alpha-Methyl-5-HT
 28 29  0  0  0  0  0  0  0  0999 V2000
   -1.8858    1.4623    0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4930    0.3578   -0.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0171   -0.6119    0.4106 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -0.2728   -1.5175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3615   -0.8755   -0.8814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2876   -2.2386   -0.5476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8952   -2.4315    0.0349 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6068   -1.3098    0.1120 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8699   -0.9748    0.6034 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3185    0.3252    0.5089 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5328    1.3022   -0.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0660    2.5829   -0.1192 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2994    0.9780   -0.5467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8293   -0.3194   -0.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7359    1.9210    0.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1301    1.0895    0.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5197    2.2496   -0.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4186    0.7450   -1.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2260   -0.8325    1.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8080   -0.1191    0.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1660    0.4431   -2.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0869   -1.0686   -2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0848   -2.9714   -0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2591   -3.3529    0.4040 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4605   -1.7671    1.0492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3131    0.5641    0.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6097    3.3747   -0.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117    1.7502   -0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14  5  1  0
 14  8  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  7 24  1  0
  9 25  1  0
 10 26  1  0
 12 27  1  0
 13 28  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -2.726   3.192   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.250   1.728   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.744   1.408   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.268  -0.057   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -0.268  -2.549   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.864  -0.533   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.864  -2.073   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.198   0.237   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0      -3.281   0.583   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    4    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11    7                                                       
CONECT   13   10                                                            
CONECT   14    2                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   30    0
END

COMPND    HMDB0248230
HETATM    1  C1  UNL     1      -1.886   1.462   0.218  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.493   0.358  -0.570  1.00  0.00           C  
HETATM    3  N1  UNL     1      -3.017  -0.612   0.411  1.00  0.00           N  
HETATM    4  C3  UNL     1      -1.551  -0.273  -1.518  1.00  0.00           C  
HETATM    5  C4  UNL     1      -0.361  -0.876  -0.881  1.00  0.00           C  
HETATM    6  C5  UNL     1      -0.288  -2.239  -0.548  1.00  0.00           C  
HETATM    7  N2  UNL     1       0.895  -2.432   0.035  1.00  0.00           N  
HETATM    8  C6  UNL     1       1.607  -1.310   0.112  1.00  0.00           C  
HETATM    9  C7  UNL     1       2.870  -0.975   0.603  1.00  0.00           C  
HETATM   10  C8  UNL     1       3.319   0.325   0.509  1.00  0.00           C  
HETATM   11  C9  UNL     1       2.533   1.302  -0.067  1.00  0.00           C  
HETATM   12  O1  UNL     1       3.066   2.583  -0.119  1.00  0.00           O  
HETATM   13  C10 UNL     1       1.299   0.978  -0.547  1.00  0.00           C  
HETATM   14  C11 UNL     1       0.829  -0.319  -0.461  1.00  0.00           C  
HETATM   15  H1  UNL     1      -2.736   1.921   0.810  1.00  0.00           H  
HETATM   16  H2  UNL     1      -1.130   1.089   0.942  1.00  0.00           H  
HETATM   17  H3  UNL     1      -1.520   2.250  -0.459  1.00  0.00           H  
HETATM   18  H4  UNL     1      -3.419   0.745  -1.066  1.00  0.00           H  
HETATM   19  H5  UNL     1      -2.226  -0.832   1.052  1.00  0.00           H  
HETATM   20  H6  UNL     1      -3.808  -0.119   0.885  1.00  0.00           H  
HETATM   21  H7  UNL     1      -1.166   0.443  -2.296  1.00  0.00           H  
HETATM   22  H8  UNL     1      -2.087  -1.069  -2.106  1.00  0.00           H  
HETATM   23  H9  UNL     1      -1.085  -2.971  -0.750  1.00  0.00           H  
HETATM   24  H10 UNL     1       1.259  -3.353   0.404  1.00  0.00           H  
HETATM   25  H11 UNL     1       3.460  -1.767   1.049  1.00  0.00           H  
HETATM   26  H12 UNL     1       4.313   0.564   0.901  1.00  0.00           H  
HETATM   27  H13 UNL     1       2.610   3.375  -0.505  1.00  0.00           H  
HETATM   28  H14 UNL     1       0.712   1.750  -0.996  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3    4   18
CONECT    3   19   20
CONECT    4    5   21   22
CONECT    5    6    6   14
CONECT    6    7   23
CONECT    7    8   24
CONECT    8    9    9   14
CONECT    9   10   25
CONECT   10   11   11   26
CONECT   11   12   13
CONECT   12   27
CONECT   13   14   14   28
END

HMDB0248230
     RDKit          3D
alpha-Methyl-5-HT
 28 29  0  0  0  0  0  0  0  0999 V2000
   -1.8858    1.4623    0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4930    0.3578   -0.5704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0171   -0.6119    0.4106 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5508   -0.2728   -1.5175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3615   -0.8755   -0.8814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2876   -2.2386   -0.5476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8952   -2.4315    0.0349 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6068   -1.3098    0.1120 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8699   -0.9748    0.6034 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3185    0.3252    0.5089 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5328    1.3022   -0.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0660    2.5829   -0.1192 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2994    0.9780   -0.5467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8293   -0.3194   -0.4615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7359    1.9210    0.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1301    1.0895    0.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5197    2.2496   -0.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4186    0.7450   -1.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2260   -0.8325    1.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8080   -0.1191    0.8855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1660    0.4431   -2.2963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0869   -1.0686   -2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0848   -2.9714   -0.7504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2591   -3.3529    0.4040 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4605   -1.7671    1.0492 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3131    0.5641    0.9012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6097    3.3747   -0.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7117    1.7502   -0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14  5  1  0
 14  8  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  7 24  1  0
  9 25  1  0
 10 26  1  0
 12 27  1  0
 13 28  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
alpha-Methyl-5-HT	ChEBI
alpha-Methyl-5-hydroxytryptamine	ChEBI
a-Methyl-5-HT	Generator
Α-methyl-5-HT	Generator
a-Methyl-5-hydroxytryptamine	Generator
Α-methyl-5-hydroxytryptamine	Generator
a-Methyl-5-hydroxytryptamine; a-methylserotonin	Generator
Α-methyl-5-hydroxytryptamine; α-methylserotonin	Generator
a-Methylserotonin	HMDB
Α-methylserotonin	HMDB
alpha-Methyl-5-HT maleate	HMDB
alpha-Methylserotonin	HMDB
alpha-Methylserotonin, (Z)-2-butenedioate	HMDB

Chemical Formula

C₁₁H₁₄N₂O

Average Molecular Weight

190.246

Monoisotopic Molecular Weight

190.110613079

IUPAC Name

3-(2-aminopropyl)-1H-indol-5-ol

Traditional Name

α-methyl-5-hydroxytryptamine

CAS Registry Number

Not Available

SMILES

CC(N)CC1=CNC2=C1C=C(O)C=C2

InChI Identifier

InChI=1S/C11H14N2O/c1-7(12)4-8-6-13-11-3-2-9(14)5-10(8)11/h2-3,5-7,13-14H,4,12H2,1H3

InChI Key

LYPCGXKCQDYTFV-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as serotonins. Serotonins are compounds containing a serotonin moiety, which consists of an indole that bears an aminoethyl a position 2 and a hydroxyl group at position 5.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Tryptamines and derivatives

Direct Parent

Serotonins

Alternative Parents

Substituents

Serotonin
Hydroxyindole
3-alkylindole
Indole
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Substituted pyrrole
Benzenoid
Pyrrole
Heteroaromatic compound
Azacycle
Amine
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

tryptamines (CHEBI:48295 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

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	1.01	ALOGPS
logP	0.84	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	9.38	ChemAxon
pKa (Strongest Basic)	10.16	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	62.04 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	56.77 m³·mol⁻¹	ChemAxon
Polarizability	21.09 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	142.793	30932474
DeepCCS	[M-H]-	140.162	30932474
DeepCCS	[M-2H]-	176.123	30932474
DeepCCS	[M+Na]+	151.661	30932474
AllCCS	[M+H]+	144.9	32859911
AllCCS	[M+H-H2O]+	140.8	32859911
AllCCS	[M+NH4]+	148.6	32859911
AllCCS	[M+Na]+	149.7	32859911
AllCCS	[M-H]-	144.0	32859911
AllCCS	[M+Na-2H]-	144.4	32859911
AllCCS	[M+HCOO]-	145.1	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	9.3319 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	3.7 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	818.6 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	276.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	94.6 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	152.2 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	108.9 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	290.5 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	240.0 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	457.1 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	636.5 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	203.9 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	774.7 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	220.0 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	204.1 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	572.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	411.3 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	190.6 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
alpha-Methyl-5-HT	CC(N)CC1=CNC2=C1C=C(O)C=C2	3237.4	Standard polar	33892256
alpha-Methyl-5-HT	CC(N)CC1=CNC2=C1C=C(O)C=C2	1947.7	Standard non polar	33892256
alpha-Methyl-5-HT	CC(N)CC1=CNC2=C1C=C(O)C=C2	2192.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
alpha-Methyl-5-HT,2TMS,isomer #1	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)N[Si](C)(C)C	2126.4	Semi standard non polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #1	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)N[Si](C)(C)C	2194.7	Standard non polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #1	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)N[Si](C)(C)C	2384.0	Standard polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #2	CC(N)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12	2103.4	Semi standard non polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #2	CC(N)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12	2217.9	Standard non polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #2	CC(N)CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12	2452.2	Standard polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #3	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)N[Si](C)(C)C	2217.0	Semi standard non polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #3	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)N[Si](C)(C)C	2269.6	Standard non polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #3	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)N[Si](C)(C)C	2423.1	Standard polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #4	CC(CC1=C[NH]C2=CC=C(O)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2326.9	Semi standard non polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #4	CC(CC1=C[NH]C2=CC=C(O)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2359.3	Standard non polar	33892256
alpha-Methyl-5-HT,2TMS,isomer #4	CC(CC1=C[NH]C2=CC=C(O)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2577.1	Standard polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #1	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)N[Si](C)(C)C	2180.4	Semi standard non polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #1	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)N[Si](C)(C)C	2228.3	Standard non polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #1	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)N[Si](C)(C)C	2278.8	Standard polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #2	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2318.7	Semi standard non polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #2	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2361.0	Standard non polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #2	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2357.8	Standard polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #3	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2377.3	Semi standard non polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #3	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2464.4	Standard non polar	33892256
alpha-Methyl-5-HT,3TMS,isomer #3	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2386.6	Standard polar	33892256
alpha-Methyl-5-HT,4TMS,isomer #1	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2419.9	Semi standard non polar	33892256
alpha-Methyl-5-HT,4TMS,isomer #1	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2390.8	Standard non polar	33892256
alpha-Methyl-5-HT,4TMS,isomer #1	CC(CC1=CN([Si](C)(C)C)C2=CC=C(O[Si](C)(C)C)C=C12)N([Si](C)(C)C)[Si](C)(C)C	2281.3	Standard polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #1	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N[Si](C)(C)C(C)(C)C	2665.1	Semi standard non polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #1	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N[Si](C)(C)C(C)(C)C	2619.3	Standard non polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #1	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N[Si](C)(C)C(C)(C)C	2591.6	Standard polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #2	CC(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12	2581.9	Semi standard non polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #2	CC(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12	2611.1	Standard non polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #2	CC(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12	2602.9	Standard polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #3	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)N[Si](C)(C)C(C)(C)C	2687.7	Semi standard non polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #3	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)N[Si](C)(C)C(C)(C)C	2699.5	Standard non polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #3	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)N[Si](C)(C)C(C)(C)C	2588.1	Standard polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #4	CC(CC1=C[NH]C2=CC=C(O)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2808.1	Semi standard non polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #4	CC(CC1=C[NH]C2=CC=C(O)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2779.0	Standard non polar	33892256
alpha-Methyl-5-HT,2TBDMS,isomer #4	CC(CC1=C[NH]C2=CC=C(O)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2677.3	Standard polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #1	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N[Si](C)(C)C(C)(C)C	2880.2	Semi standard non polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #1	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N[Si](C)(C)C(C)(C)C	2849.2	Standard non polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #1	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N[Si](C)(C)C(C)(C)C	2600.3	Standard polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #2	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3041.1	Semi standard non polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #2	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2991.5	Standard non polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #2	CC(CC1=C[NH]C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2644.7	Standard polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #3	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3032.7	Semi standard non polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #3	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3070.4	Standard non polar	33892256
alpha-Methyl-5-HT,3TBDMS,isomer #3	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2640.9	Standard polar	33892256
alpha-Methyl-5-HT,4TBDMS,isomer #1	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3268.2	Semi standard non polar	33892256
alpha-Methyl-5-HT,4TBDMS,isomer #1	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3139.4	Standard non polar	33892256
alpha-Methyl-5-HT,4TBDMS,isomer #1	CC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2642.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-9500000000-3345670903104e99ae53	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-03	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 - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin 10V, Positive-QTOF	splash10-00di-0900000000-d62df09edbf84c9220c7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin 20V, Positive-QTOF	splash10-00ea-0900000000-16ba4926531d55be43e9	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin 40V, Positive-QTOF	splash10-0pc1-2900000000-f3316cb900f31070f4d7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin 10V, Negative-QTOF	splash10-000i-0900000000-d7d8df022571c838b83c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin 20V, Negative-QTOF	splash10-001i-0900000000-4335ab67f5fb947dafc0	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin 40V, Negative-QTOF	splash10-0f8c-2900000000-4eccc5842ab87f46925b	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

2023

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Alpha-Methylserotonin

METLIN ID

Not Available

PubChem Compound

2107

PDB ID

Not Available

ChEBI ID

48295

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin (HMDB0248230)

MOL for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

3D MOL for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

3D SDF for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

3D-SDF for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

PDB for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

3D PDB for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

SMILES for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

INCHI for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

Structure for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

3D Structure for HMDB0248230 (alpha-Methyl-5-hydroxytryptamine; alpha-Methylserotonin)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra