Synthesis of novel lincomycin derivatives and their in vitro antibacterial activities

スポンサーリンク

概要

論文の詳細を見る
2013-03-25

著者

関連論文

Efficient Synthesis of Cyclic RGD Pseudopeptide with (E)-Alkene Dipeptide Isostere and Its Biological Activity
A New 5-HT_3 Receptor Ligand. II. Structure-Activity Analysis of 5-HT_3 Receptor Agonist Action in the Gut
PF1163A and B, New Antifungal Antibiotics Produces by Penicilium sp. II. Physico-chemical Properties and Structure Elucidation
PF1163A and B, New Antifungal Antibiotics Produced by Penicilium sp. : II. Physico-chemical Properties and Structure Elucidation
Discovery of 4-Pyridone Derivatives as Specific Inhibitors of Enoyl-Acyl Carrier Protein Reductase (FabI) with Antibacterial Activity against Staphylococcus aureus
Novel Azalides Derived from Sixteen-Membered Macrolides : I. Isolation of the Mobile Dialdehyde and Its One-Pot Macrocyclization with an Amine
Synthesis and Biological Evaluation of Novel Leucomycin Analogues Modified at the C-3 Position I. Epimerization and Methylation of the 3-Hydroxyl Group
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics VI. Synthesis of metabolically Programmed, Highly Potent Analogues of Sixteen-membered Macrolide Antibiotics
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics V. Preparation of Unsubstituted L-Cladinose Analogues: Effect of Methylation of a 3''-Hydroxyl Group on the Bioactivity
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics IV. Improved Therapeutic Effects of 4-O-Acyl-L-cladinose Analogues of Sixteen-membered Macrolide Antibiotics
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics II. Preparation of Pharmacokinetically Improved Analogues via Biotransformation
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics I. Synthesis of 4-O-Alkyl-L-cladinose Analogues via Glycosylation
Model Study for Preparation of asymmetric N, N'-Disubstituted piperazine Library:Efficient Synthesis of Aryl Piperazine and Benzyl Piperazine Derivatives on the Solid Support
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics III. Efficient Synthesis of 4-0-Alkyl-L-cladinose Analogues: Improved Antibacterial Activities Compatible with Pharmacokinetics
A Novel Synthesis of 2,3-Disubstituted-4-pyridones from 4-Methoxypyridine
ME3221, a Surmountable Angiotensin AT_1-Receptor Antagonist, Prevents Hypertensive Complications in Aged Stroke-Prone Spontaneously Hypertensive Rats
Synthesis of Potent α_vβ_3/α_β_3 Dual Antagonists Tricyclic Pharmacophore-based Molecules and Their Selectivity Control
Correlation of the antimicrobial activity of ME1036 with its binding affinities to the penicillin-binding proteins from Streptococcus pneumoniae strains
Effects of Chronic Treatment with ME3221 on Blood Pressure and Hypertensive Complications in Aged Stroke-Prone Spontaneously Hypertensive Rats
Synthesis of novel lincomycin derivatives and their in vitro antibacterial activities

もっと見る

スポンサーリンク