178181-74-3Relevant articles and documents
Preparation of a glycopeptide analogue of type II collagen - Use of acid labile protective groups for carbohydrate moieties in solid phase synthesis of O-linked glycopeptides
Broddefalk, Johan,Bergquist, Karl-Erik,Kihlberg, Jan
, p. 3011 - 3014 (1996)
A glycopeptide analogue of the immunodeficient T cell epitope on type II collagen has been prepared by solid phase synthesis. Preparation of a glycosylated amino acid from two monosaccharide units that carried silyl and isopropylidene protective groups and Fmoc 5-hydroxynorvaline was essential for the synthesis. After assembly of the glycopeptide the carbohydrate protective groups were removed simultaneously with acid catalyzed cleavage from the solid phase.
ANTI-BACTERIAL PEPTIDE MACROCYCLES AND USE THEREOF
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Page/Page column 97, (2018/11/10)
The present invention relates to compounds of formula (I) wherein X1 to X8 and R1 to R8 are as described herein, as well as pharmaceutically acceptable salts thereof for the use in the treatment or prevention of infections and resulting diseases caused by Pseudomonas aeruginosa.
PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII
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Page/Page column 316; 317, (2017/06/01)
The present invention provides compounds of formula (I) wherein X1 to X8 and R1 to R8 are as described herein, as well as pharmaceutically acceptable salts thereof. Further the present invention is concerned with the manufacture of the compounds of formula (I), pharmaceutical compositions comprising them and their use as medicaments for the treatment of diseases and infections caused by Acinetobacter baumannii.