Moenomycin analogues with long-chain amine lipid parts from reductive aminations

Autor:	Lothar Hennig, Matthias Findeisen, Maxime Lampilas, Sabine Giesa, Peter Welzel, Stefan Vogel, Katherina Stembera, Claire Tillier, Christian Bonhomme
Rok vydání:	2001
Předmět:	Membrane Chemistry Moenomycin A Organic Chemistry Drug Discovery Aldehyde degradation Organic chemistry Amine gas treating Chromophore Biochemistry Reductive amination Long chain
Zdroj:	Tetrahedron. 57:4147-4160
ISSN:	0040-4020
DOI:	10.1016/s0040-4020(01)00306-4
Popis:	From a moenomycin A glycolic aldehyde degradation product lacking the chromophore unit and most of the lipid part, a number of amines were prepared by reductive amination. Their interaction with artificial membranes as well as their transglycosylase inhibiting and antibiotic properties were studied.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::75bbda01b5f0a9e2028c6bb675a57aa5 https://doi.org/10.1016/s0040-4020(01)00306-4 Zobrazit plný text záznamu Full Text from ScienceDirect