153029-91-5

Upstream product

• 153029-79-9 (2S,3S,4R,6S)-3-Benzyloxy-6-ethoxy-4-methoxy-2,4-dimethyl-tetrahydro-pyran 
• 153029-63-1 (2S,3S,4R,6S)-6-Ethoxy-4-methoxy-2,4-dimethyl-tetrahydro-pyran-3-ol 
• 114-07-8 erythromycin 
• 100-39-0 benzyl bromide 
• 2127-03-9 2,2'-dipyridyldisulphide 

Downstream Products

• 153030-02-5 C₄₆H₆₉NO₁₄ 

Relevant academic research and scientific papers

Cladinose analogues of sixteen-membered macrolide antibiotics: I. Synthesis of 4-O-Alkyl-L-cladinose analogues via glycosylation

The synthesis and biological evaluation of sixteen-membered macrolides possessing a 4-O-alkyl-α-L-cladinosyl moiety as the neutral sugar are described. The nine novel derivatives have been synthesized by glycosylation with l-thio sugars. The most active derivative of them showed prolonged antibacterial activity in rat plasma in vitro and improved pharmacokinetics.