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Fast conventional Fmoc solid-phase peptide synthesis with HCTU.
Authors:Christina A Hood  German Fuentes  Hirendra Patel  Karen Page  Mahendra Menakuru  Jae H Park
Institution:Department of Chemistry, Protein Technologies Inc., Tucson, Arizona, 4675 South Coach Drive, Tucson, Arizona 85714, USA.
Abstract:1H-Benzotriazolium 1-bis(dimethyl-amino)methylene]-5-chloro-hexafluorophosphate (1-),3-oxide (HCTU) is a nontoxic, nonirritating and noncorrosive coupling reagent. Seven biologically active peptides (GHRP-6, (65-74)ACP, oxytocin, G-LHRH, C-peptide, hAmylin(1-37), and beta-amyloid(1-42)) were synthesized with reaction times reduced to deprotection times of 3 min or less and coupling times of 5 min or less using HCTU as the coupling reagent. Expensive coupling reagents or special techniques were not used. Total peptide synthesis times were dramatically reduced by as much as 42.5 h (1.8 days) without reducing the crude peptide purities. It was shown that HCTU can be used as an affordable, efficient coupling reagent for fast Fmoc solid-phase peptide synthesis.
Keywords:HCTU  fast Fmoc SPPS  human amylin (1–37)  oxytocin  β‐amyloid
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