Biological consequences of the incorporation of amphiphilic amino acids into opioid peptide sequences
✍ Scribed by Aleksandra Olma; Aleksandra Misicka; Dirk Tourwé; Andrzej W. Lipkowski
- Publisher
- Springer Netherlands
- Year
- 1998
- Tongue
- English
- Weight
- 163 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1573-3149
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
S)-ctMethyimethionine, (S)-ctMethylleucine, 2-aminoisobutyric acid and (S)-otMethylphenylalanine have been incorporated by solid phase peptide strategy in a peptide sequence. The coupling reactions of these Boc-ctMe amino acids and of the following residue in the sequence were readily achieved afte