Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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The evolution of substrate discrimination in macrolide antibiotic resistance enzymes.Synthesis and Antibacterial Evaluation of a Series of 11,12-Cyclic Carbonate Azithromycin-3-O-descladinosyl-3-O-carbamoyl Glycosyl Derivatives.

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Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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2016 nî lūn-bûn

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2016年論文

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2016年論文

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name

Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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P1476

Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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P2093

David Pereira

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Evan Martens

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Prabhavathi Fernandes

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P275

Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

P2860

Molecular characterization of off-target activities of telithromycin: a potential role for nicotinic acetylcholine receptors

Binding and action of CEM-101, a new fluoroketolide antibiotic that inhibits protein synthesis

Fidaxomicin: A novel agent for the treatment of Clostridium difficile infection

Structural Insight into the Antibiotic Action of Telithromycin against Resistant Mutants

From Erythromycin to Azithromycin and New Potential Ribosome-Binding Antimicrobials.

A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes

Asymmetric total synthesis of erythromcin. 1. Synthesis of an erythronolide A secoacid derivative via asymmetric induction

Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides.

Recent developments on ketolides and macrolides.

Pharmacokinetics of solithromycin (CEM-101) after single or multiple oral doses and effects of food on single-dose bioavailability in healthy adult subjects.

P2888

ja.2016.137

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527-533

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scholarly article

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10.1038/JA.2016.137

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2017-05-01T00:00:00Z

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polycyclic compound

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biomedical investigative technique

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Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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P2860

P2860

Nature nurtures the design of new semi-synthetic macrolide antibiotics.

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