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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 01:27:37 UTC

Update Date

2021-09-26 22:58:25 UTC

HMDB ID

HMDB0248232

Secondary Accession Numbers

None

Metabolite Identification

Common Name

alpha-Methyl-m-tyrosine

Description

alpha-Methyl-m-tyrosine belongs to the class of organic compounds known as phenylpropanoic acids. Phenylpropanoic acids are compounds with a structure containing a benzene ring conjugated to a propanoic acid. Based on a literature review very few articles have been published on alpha-Methyl-m-tyrosine. This compound has been identified in human blood as reported by (PMID: 31557052 ). Alpha-methyl-m-tyrosine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically alpha-Methyl-m-tyrosine 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


  Mrv1652309112103272D          

 14 14  0  0  0  0            999 V2000
    1.0164    3.1895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    1.7605    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  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  4  9  1  0  0  0  0
  6 10  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  2 14  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0248232

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(N)(CC1=CC(O)=CC=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C10H13NO3/c1-10(11,9(13)14)6-7-3-2-4-8(12)5-7/h2-5,12H,6,11H2,1H3,(H,13,14)

> <INCHI_KEY>
CAHPJJJZLQXPKS-UHFFFAOYSA-N

> <FORMULA>
C10H13NO3

> <MOLECULAR_WEIGHT>
195.218

> <EXACT_MASS>
195.089543283

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
27

> <JCHEM_AVERAGE_POLARIZABILITY>
19.799569766845522

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-amino-3-(3-hydroxyphenyl)-2-methylpropanoic acid

> <ALOGPS_LOGP>
-1.89

> <JCHEM_LOGP>
-1.0558730812949533

> <ALOGPS_LOGS>
-1.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.242910475040464

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.065014051067446

> <JCHEM_PKA_STRONGEST_BASIC>
9.889081944066303

> <JCHEM_POLAR_SURFACE_AREA>
83.55

> <JCHEM_REFRACTIVITY>
51.810500000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.81e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
α-methyl-m-tyrosine

> <JCHEM_VEBER_RULE>
0

$$$$

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       1.897   5.954   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.001   6.930   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       3.437   3.286   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3   11   14                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    4                                                       
CONECT   10    6                                                            
CONECT   11    2   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    2                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   28    0
END

COMPND    HMDB0248232
HETATM    1  C1  UNL     1      -1.162   1.217   1.233  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.594   0.046   0.411  1.00  0.00           C  
HETATM    3  N1  UNL     1      -2.078   0.474  -0.868  1.00  0.00           N  
HETATM    4  C3  UNL     1      -0.552  -1.038   0.314  1.00  0.00           C  
HETATM    5  C4  UNL     1       0.707  -0.601  -0.289  1.00  0.00           C  
HETATM    6  C5  UNL     1       0.994  -0.649  -1.630  1.00  0.00           C  
HETATM    7  C6  UNL     1       2.199  -0.224  -2.152  1.00  0.00           C  
HETATM    8  C7  UNL     1       3.162   0.271  -1.311  1.00  0.00           C  
HETATM    9  C8  UNL     1       2.916   0.338   0.042  1.00  0.00           C  
HETATM   10  O1  UNL     1       3.905   0.843   0.885  1.00  0.00           O  
HETATM   11  C9  UNL     1       1.690  -0.099   0.541  1.00  0.00           C  
HETATM   12  C10 UNL     1      -2.767  -0.565   1.131  1.00  0.00           C  
HETATM   13  O2  UNL     1      -2.578  -1.011   2.275  1.00  0.00           O  
HETATM   14  O3  UNL     1      -4.019  -0.650   0.582  1.00  0.00           O  
HETATM   15  H1  UNL     1      -0.141   1.566   1.035  1.00  0.00           H  
HETATM   16  H2  UNL     1      -1.290   1.061   2.331  1.00  0.00           H  
HETATM   17  H3  UNL     1      -1.848   2.070   0.976  1.00  0.00           H  
HETATM   18  H4  UNL     1      -1.868   1.443  -1.114  1.00  0.00           H  
HETATM   19  H5  UNL     1      -2.017  -0.216  -1.617  1.00  0.00           H  
HETATM   20  H6  UNL     1      -1.016  -1.883  -0.233  1.00  0.00           H  
HETATM   21  H7  UNL     1      -0.343  -1.414   1.337  1.00  0.00           H  
HETATM   22  H8  UNL     1       0.264  -1.029  -2.308  1.00  0.00           H  
HETATM   23  H9  UNL     1       2.415  -0.267  -3.214  1.00  0.00           H  
HETATM   24  H10 UNL     1       4.105   0.601  -1.746  1.00  0.00           H  
HETATM   25  H11 UNL     1       3.749   0.903   1.884  1.00  0.00           H  
HETATM   26  H12 UNL     1       1.566  -0.016   1.621  1.00  0.00           H  
HETATM   27  H13 UNL     1      -4.398  -0.027  -0.117  1.00  0.00           H  
CONECT    1    2   15   16   17
CONECT    2    3    4   12
CONECT    3   18   19
CONECT    4    5   20   21
CONECT    5    6    6   11
CONECT    6    7   22
CONECT    7    8    8   23
CONECT    8    9   24
CONECT    9   10   11   11
CONECT   10   25
CONECT   11   26
CONECT   12   13   13   14
CONECT   14   27
END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
a-Methyl-m-tyrosine	Generator
Α-methyl-m-tyrosine	Generator
alpha-Methyl-m-tyrosine, (DL)-isomer	HMDB
alpha-Methyl-m-tyrosine, (L)-isomer	HMDB
alpha-Methyl-meta-tyrosine	HMDB

Chemical Formula

C₁₀H₁₃NO₃

Average Molecular Weight

195.218

Monoisotopic Molecular Weight

195.089543283

IUPAC Name

2-amino-3-(3-hydroxyphenyl)-2-methylpropanoic acid

Traditional Name

α-methyl-m-tyrosine

CAS Registry Number

Not Available

SMILES

CC(N)(CC1=CC(O)=CC=C1)C(O)=O

InChI Identifier

InChI=1S/C10H13NO3/c1-10(11,9(13)14)6-7-3-2-4-8(12)5-7/h2-5,12H,6,11H2,1H3,(H,13,14)

InChI Key

CAHPJJJZLQXPKS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylpropanoic acids. Phenylpropanoic acids are compounds with a structure containing a benzene ring conjugated to a propanoic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Phenylpropanoic acids

Sub Class

Not Available

Direct Parent

Phenylpropanoic acids

Alternative Parents

Substituents

3-phenylpropanoic-acid
Alpha-amino acid
Alpha-amino acid or derivatives
Amphetamine or derivatives
Phenylpropane
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Monocyclic benzene moiety
Benzenoid
Amino acid or derivatives
Amino acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Carbonyl group
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Amine
Hydrocarbon derivative
Primary amine
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

monocarboxylic acid (CHEBI:10303 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (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	-1.9	ALOGPS
logP	-1.1	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	2.07	ChemAxon
pKa (Strongest Basic)	9.89	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	83.55 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	51.81 m³·mol⁻¹	ChemAxon
Polarizability	19.8 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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]+	138.565	30932474
DeepCCS	[M-H]-	135.556	30932474
DeepCCS	[M-2H]-	172.197	30932474
DeepCCS	[M+Na]+	147.735	30932474
AllCCS	[M+H]+	142.9	32859911
AllCCS	[M+H-H2O]+	138.8	32859911
AllCCS	[M+NH4]+	146.7	32859911
AllCCS	[M+Na]+	147.8	32859911
AllCCS	[M-H]-	142.4	32859911
AllCCS	[M+Na-2H]-	143.1	32859911
AllCCS	[M+HCOO]-	144.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
alpha-Methyl-m-tyrosine	CC(N)(CC1=CC(O)=CC=C1)C(O)=O	3074.0	Standard polar	33892256
alpha-Methyl-m-tyrosine	CC(N)(CC1=CC(O)=CC=C1)C(O)=O	1795.1	Standard non polar	33892256
alpha-Methyl-m-tyrosine	CC(N)(CC1=CC(O)=CC=C1)C(O)=O	2007.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
alpha-Methyl-m-tyrosine,3TMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(N[Si](C)(C)C)C(=O)O[Si](C)(C)C	1917.0	Semi standard non polar	33892256
alpha-Methyl-m-tyrosine,3TMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(N[Si](C)(C)C)C(=O)O[Si](C)(C)C	1935.6	Standard non polar	33892256
alpha-Methyl-m-tyrosine,3TMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2029.5	Standard polar	33892256
alpha-Methyl-m-tyrosine,3TMS,isomer #2	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2122.2	Semi standard non polar	33892256
alpha-Methyl-m-tyrosine,3TMS,isomer #2	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2004.5	Standard non polar	33892256
alpha-Methyl-m-tyrosine,3TMS,isomer #2	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2258.2	Standard polar	33892256
alpha-Methyl-m-tyrosine,3TMS,isomer #3	CC(CC1=CC=CC(O)=C1)(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2104.7	Semi standard non polar	33892256
alpha-Methyl-m-tyrosine,3TMS,isomer #3	CC(CC1=CC=CC(O)=C1)(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2082.1	Standard non polar	33892256
alpha-Methyl-m-tyrosine,3TMS,isomer #3	CC(CC1=CC=CC(O)=C1)(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2193.1	Standard polar	33892256
alpha-Methyl-m-tyrosine,4TMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2139.9	Semi standard non polar	33892256
alpha-Methyl-m-tyrosine,4TMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2068.4	Standard non polar	33892256
alpha-Methyl-m-tyrosine,4TMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C)=C1)(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2028.8	Standard polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2617.8	Semi standard non polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2536.4	Standard non polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2396.5	Standard polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #2	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2833.0	Semi standard non polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #2	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2608.2	Standard non polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #2	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2528.0	Standard polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #3	CC(CC1=CC=CC(O)=C1)(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2786.3	Semi standard non polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #3	CC(CC1=CC=CC(O)=C1)(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2676.8	Standard non polar	33892256
alpha-Methyl-m-tyrosine,3TBDMS,isomer #3	CC(CC1=CC=CC(O)=C1)(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2457.3	Standard polar	33892256
alpha-Methyl-m-tyrosine,4TBDMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3022.7	Semi standard non polar	33892256
alpha-Methyl-m-tyrosine,4TBDMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2805.1	Standard non polar	33892256
alpha-Methyl-m-tyrosine,4TBDMS,isomer #1	CC(CC1=CC=CC(O[Si](C)(C)C(C)(C)C)=C1)(C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2437.3	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-m-tyrosine GC-MS (Non-derivatized) - 70eV, Positive	splash10-052f-5900000000-c6f8f309c18987748d3b	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine 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-m-tyrosine 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-m-tyrosine 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-m-tyrosine GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine 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-m-tyrosine 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-m-tyrosine GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - alpha-Methyl-m-tyrosine GC-MS (TBDMS_2_4) - 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-m-tyrosine 10V, Positive-QTOF	splash10-0udj-0900000000-680e750da448421c2d6f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-m-tyrosine 20V, Positive-QTOF	splash10-053r-1900000000-927aa901807a808fc350	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-m-tyrosine 40V, Positive-QTOF	splash10-056r-9300000000-63e127e848af85cc764d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-m-tyrosine 10V, Negative-QTOF	splash10-052f-0900000000-7b87609000cd020b0e43	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-m-tyrosine 20V, Negative-QTOF	splash10-001i-1900000000-5ba8671f02bb36e0b8cb	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - alpha-Methyl-m-tyrosine 40V, Negative-QTOF	splash10-001i-4900000000-63290c67e5211864eba0	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	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

2026

KEGG Compound ID

C11820

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

2110

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

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-m-tyrosine (HMDB0248232)

MOL for HMDB0248232 (alpha-Methyl-m-tyrosine)

3D MOL for HMDB0248232 (alpha-Methyl-m-tyrosine)

3D SDF for HMDB0248232 (alpha-Methyl-m-tyrosine)

3D-SDF for HMDB0248232 (alpha-Methyl-m-tyrosine)

PDB for HMDB0248232 (alpha-Methyl-m-tyrosine)

3D PDB for HMDB0248232 (alpha-Methyl-m-tyrosine)

SMILES for HMDB0248232 (alpha-Methyl-m-tyrosine)

INCHI for HMDB0248232 (alpha-Methyl-m-tyrosine)

Structure for HMDB0248232 (alpha-Methyl-m-tyrosine)

3D Structure for HMDB0248232 (alpha-Methyl-m-tyrosine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra