ANTIPAIN HYDROCHLORIDE DIHYDRATE

N2-[[(1-Carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-L-valinamide PHE-ARG-VAL-ARG-CHO Antipain research grade 4-((aminoiminomethyl)amino)-1-formylbutyl)- ANTIPAIN HYDROCHLORIDE DIHYDRATE N2-[[(1-carboxyphenethyl)amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-L-valinamide ANTIPAIN ~10000 U/MG Nα-[N2-[[(1-Carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl]-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]-L-valinamide Nα-[Nα-[[(1-Carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl]-N-(1-formyl-4-guanidinobutyl)-L-valinamide Aids006469 Aids-006469 L-Valinamide, N(sup 2)-(((1-carboxy-2-phenylethyl)amino)carbonyl)-L-arginyl-N-(4-((aminoiminomethyl)amino)-1-formylbutyl)- Phe-co-Arg-Val-L-Arg-h L-Valinamide, N2-[[(1-carboxy-2-phenylethyl)amino]carbonyl]-L-arginyl-N-[4-[(aminoiminomethyl)amino]-1-formylbutyl]- ANTIPAIN HYDROCHLORIDE DIHYDRATE USP/EP/BP 37691-11-5 C27H44N10O6HCl C27H49ClN10O8 C27H44N10O6 A - K Aldehydes Antibacterial Antibiotics A to Z Antibiotics Antibiotics A-F Antibiotics by Application Antineoplastic and Immunosuppressive Antibiotics Building Blocks C13-C60 Carbonyl Compounds Chemical Structure Class Chemical Synthesis Inhibits an Enzyme Mechanism of Action Organic Building Blocks Peptides Spectrum of Activity Pepetides