Synthesis and antibacterial activities of a novel alkylide: 3-O-(3-aryl-2-propargyl) and 3-O-(3-aryl-2-propenyl)clarithromycin derivatives-Reference-Cited by-同舟云学术

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Synthesis and antibacterial activities of a novel alkylide: 3-O-(3-aryl-2-propargyl) and 3-O-(3-aryl-2-propenyl)clarithromycin derivatives

Published:2010-05 Issue:9 Volume:20 Page:2880-2883
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Liang Jian-Hua,Wang Yue-Ying,Wang He,Li Xiao-Li,An Kun,Xu Ying-Chun,Yao Guo-Wei

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference32 articles.

1. Acid degradation of erythromycin A and erythromycin B

2. Chemical modification of erythromycins. IX. Selective methylation at the C-6 hydroxyl group of erythromycin a oxime derivatives and preparation of clarithromycin.

3. Chemical modification of erythromycins. III. In vitro and in vivo antibacterial activities of new semisynthetic 6-O-methylerythromycins A, TE-031 (clarithromycin) and TE-032.

4. Translation and Protein Synthesis: Macrolides

5. Synthesis and Antibacterial Activity of Ketolides (6-O-Methyl-3-oxoerythromycin Derivatives): A New Class of Antibacterials Highly Potent Against Macrolide-Resistant and -Susceptible Respiratory Pathogens

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1. Design and structure-activity relationships of ether-linked alkylides: Hybrids of 3-O-descladinosyl macrolides and quinolone motifs;Bioorganic Chemistry;2024-10

2. Design and synthesis of novel macrolones bridged with linkers from 11,12-positions of macrolides;Bioorganic & Medicinal Chemistry Letters;2022-07

3. Recent Advancements in Macrolide Hybrids against Staphylococcus aureus;Current Topics in Medicinal Chemistry;2021-12-08

4. Design, synthesis and antibacterial evaluation of novel C-11, C-9 or C-2′-substituted 3-O-descladinosyl-3-ketoclarithromycin derivatives;Bioorganic & Medicinal Chemistry Letters;2021-07

5. 14- and 15-membered lactone macrolides and their analogues and hybrids: structure, molecular mechanism of action and biological activity;European Journal of Medicinal Chemistry;2019-11

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