Sugar amino acid based 24-membered macrocycliC C-2-symmetric cationic peptides were designed and synthesized. The cationic group was introduced in the sugar amino acids. The conformation of these cyclic compounds was ascertained through NMR techniques, which proved they were amphipathic in nature. All the compounds were bacteriolytic, showed good activity against the Gr(+v)e and Gr(-ve) bacteria, and exhibited low hemolytic activity.
机构:
Sichuan Univ, Key Lab Drug Targeting, Minist Educ, W China Sch Pharm, Chengdu 610041, Peoples R ChinaSichuan Univ, Key Lab Drug Targeting, Minist Educ, W China Sch Pharm, Chengdu 610041, Peoples R China
He Gu
Guo Li
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机构:Sichuan Univ, Key Lab Drug Targeting, Minist Educ, W China Sch Pharm, Chengdu 610041, Peoples R China
Guo Li
Ma Li-Fang
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机构:Sichuan Univ, Key Lab Drug Targeting, Minist Educ, W China Sch Pharm, Chengdu 610041, Peoples R China
Ma Li-Fang
Wang Qian-Qian
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机构:Sichuan Univ, Key Lab Drug Targeting, Minist Educ, W China Sch Pharm, Chengdu 610041, Peoples R China
Wang Qian-Qian
He Ze-Chao
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机构:Sichuan Univ, Key Lab Drug Targeting, Minist Educ, W China Sch Pharm, Chengdu 610041, Peoples R China