Search Ontology: 
        
        ChEBI
            L-tyrosine
- Term ID
 - CHEBI:17895
 - Synonyms
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- (-)-alpha-amino-p-hydroxyhydrocinnamic acid
 - (2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid
 - (S)-(-)-Tyrosine
 - (S)-2-Amino-3-(p-hydroxyphenyl)propionic acid
 - (S)-3-(p-Hydroxyphenyl)alanine
 - (S)-alpha-amino-4-hydroxybenzenepropanoic acid
 - (S)-Tyrosine
 - 4-hydroxy-L-phenylalanine
 - L-Tyrosin
 - L-tyrosine
 - Tyr
 - Tyrosine
 - Y
 
 - Definition
 - An optically active form of tyrosine having L-configuration.
 - References
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- CAS:60-18-4
 - DrugBank:DB00135
 - Drug_Central:2786
 - ECMDB:ECMDB00158
 - Gmelin:50929
 - HMDB:HMDB0000158
 - KEGG:C00082
 - KEGG:D00022
 - KNApSAcK:C00001397
 - MetaCyc:TYR
 - PDBeChem:TYR
 - PMID:15171683
 - PMID:22360849
 - PMID:22402312
 - Reaxys:392441
 - UM-BBD_compID:c0234
 - Wikipedia:Tyrosine
 - YMDB:YMDB00364
 
 - Ontology
 - ChEBI ( EBI )
 
                
                    
                        Phenotype 
                    
                    
                
                
            
        
        
    
        
            
            
    
    
    
    
                
                    
                        Phenotype resulting from L-tyrosine
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype where environments contain L-tyrosine
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype modified by environments containing L-tyrosine
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype affecting L-tyrosine
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Human Disease Model