{"chebi_id":"1784","chebi_name":"biphenyl-4-amine","chebi_synonyms":["p-aminodiphenyl","4-Aminobiphenyl","paraaminodiphenyl","p-xenylamine","p-phenylaniline","biphenyl-4-ylamine","4-biphenylamine","4-aminodiphenyl","4-amino-1,1'-biphenyl","p-biphenylamine","[1,1'-biphenyl]-4-amine"],"diffprof_id_observed":["MTBLS2406_0002_00000009","MTBLS3916_0001_00000001"],"diffprof_id_var_observed":[],"inchikey":"DMVOXQPQNTYEKQ-UHFFFAOYSA-N","inn_name":"","iupac_name":"[1,1'-biphenyl]-4-amine","num_study_observed":2,"reactome_ids":["R-HSA-1430728","R-HSA-211859","R-HSA-211897","R-HSA-211945","R-HSA-211957","R-HSA-211981"],"reactome_names":["Metabolism","Biological oxidations","Cytochrome P450 - arranged by substrate type","Phase I - Functionalization of compounds","Aromatic amines can be N-hydroxylated or N-dealkylated by CYP1A2","Xenobiotics"],"study_id_observed":["MTBLS2406","MTBLS3916"],"study_id_var_observed":[],"synonym_name":"4-Aminobiphenyl"}