(3S,6S,9S,12R,15S,18S,21S,24S,30S,33S,34R)-30-ethyl-34-((R,E)-hex-4-en-2-yl)-6,9,18,24-tetraisobutyl-3,21-diisopropyl-4,7,10,12,15,19,25,28-octamethyl-33-(methylamino)-1-oxa-4,7,10,13,16,19,22,25,28,31-decaazacyclotetratriacontan-2,5,8,11,14,17,20,23,26,29,32-undecaone; (2S,3R,4R,6E)-3-Hydroxy-4-methyl-2-(methylamino)-6-octenoyl-(2S)-2-aminobutanoyl-N-methylglycyl-N-methyl-L-leucyl-L-valyl-N-methyl-L-leucyl-L-alanyl-D-alanyl-N-methyl-L-leucyl-N-methyl-L-leucyl-N-methyl-L-valine (111)-Lactone
Cyclosporin EP Impurity C (Iso Cyclosporin A) is a fully characterized chemical compound used as a reference standard of API Cyclosporine. The standard offered is compliant with regulatory guidelines. Cyclosporin EP Impurity C (Iso Cyclosporin A) is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 59865-16-6
