Lisinopril specified impurity F is a reference standard used in pharmaceutical analysis. It is a chemically defined compound related to the active pharmaceutical ingredient lisinopril, serving as a quality control tool for impurity profiling.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 1132650-67-9
(1R,2S,6R,7S)-4-[[(1R,2R)-2-[[4-(1,2-benzothiazol-3-yl)-2,2,3,3,5,5,6,6-octadeuteriopiperazin-1-yl]methyl]cyclohexyl]methyl]-4-azatricyclo[5.2.1.02,6]decane-3,5-dione
pharmaceutical raw material
5'-Deoxy-5-fluoro-N-{[(²H₁₁)pentyloxy]carbonyl}cytidine
pharmaceutical raw material
N-[(1R)-1-Borono-3-methylbutyl]-Nalpha-(pyrazine-2-carbonyl)-D-phenylalaninamide
pharmaceutical raw material
Hirudin
pharmaceutical raw material
(2S)-1-((2S)-2-(((1S)-3-cyclohexyl-1-(ethoxycarbonyl)propyl)amino)propanoyl)pyrrolidine-2-carboxylic acid
research compound
(2S)-1-[(2S)-6-amino-2-[[(1S)-1-carboxy-3-cyclohexylpropyl]amino]hexanoyl]pyrrolidine-2-carboxylic acid
QYSKCMYFYQRFSL-BZSNNMDCSA-N
C1CCC(CC1)CC[C@@H](C(=O)O)N[C@@H](CCCCN)C(=O)N2CCC[C@H]2C(=O)O