TIELVETICA CHIMICA ACTA ting of the CBO-protecting group ha; been condensed with N-CBO-S-benzyl-I<cysteinyl-L-tyrosyl-L-isoleucyl-azide. Cleavage of the protecting groups of the resulting nonapeptide with sodium in liquid ammonia, oxidation with air in dilute aqueous solution and purification by cou
Synthèse d'homologues de la lysine-vasopressine et de l'oxytocine contenant une séquence His-Sér ou Sér-His en position N-terminale
✍ Scribed by S. T. Guttmann; R. A. Boissonnas
- Publisher
- John Wiley and Sons
- Year
- 1962
- Tongue
- German
- Weight
- 822 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
(His‐Ser‐Cys)^1^‐lysine‐vasopressin, (Ser‐His‐Cys)^1^‐lysine‐vasopressin, (His‐Ser‐Cys)^1^‐oxytocin and (Ser‐His‐Cys)^1^‐oxytocin have been synthesized by condensing dipeptide azides with nonapeptides. The first peptide was also prepared by reacting a pentapeptide azide with an hexapeptide. It exhibits a noteworthy ACTH‐releasing activity in vivo and a better specificity than lysine‐vasopressin.
📜 SIMILAR VOLUMES
## Abstract The synthesis of branched‐chain sugars of the __gem__‐hydroxy‐formyl and the __gem__‐hydroxy‐hydroxymethyl types is described. A 5‐deoxy‐1,2‐O‐isopropylidene‐furanos‐3‐ulose is treated with cyanomethylene‐triphenyl‐phosphorane, yielding the two geometrical isomers of the corresponding b