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Synthesis of Salmon Calcitonin Analogs Using Fmoc-based Chemistry on MBHA Resins
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作者 Bin YANG Zhen Kai DING +1 位作者 Zong Jin HAN Qi Kai ZHANG(Beijing Institute of Pharmacology and Toxicology, Beijing 100850) 《Chinese Chemical Letters》 SCIE CAS CSCD 1999年第7期549-552,共4页
Peptide analogs of salmon calcitonin (sCT) were synthesized by using Fmoc-based chemistry on MBHA resins. Salmon calcitonin was modified by 1) cysteines at positions 1 and 7 were replaced by valine and alanine respect... Peptide analogs of salmon calcitonin (sCT) were synthesized by using Fmoc-based chemistry on MBHA resins. Salmon calcitonin was modified by 1) cysteines at positions 1 and 7 were replaced by valine and alanine respectively to result in open chain analogs, 2) the glycine at position 30 was replaced by alanine, D-alanine and sarcosine respectively, and 3) some residues were deleted besides the above two modifications. A modified two-step deprotection / cleavage procedure, in which a solvent of TFA / TMSBr / thioanisole / EDT / m-cresol combines with HF cleavage, was adopted in SPPS. 展开更多
关键词 salmon calcitonin analogs fmoc-based SPPS MBHA resin the two-Step deprotection/cleavage procedure
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