The syntheses of the chain‐homologues of hypertensin, H · Arg‐Val‐Tyr‐Val‐His‐Pro‐Phe · OH, H · Asp(NH~2~)‐Arg‐Val‐Tyr‐Val‐His‐Pro · OH, and H · Asp(R)‐Arg‐Val‐Tyr‐Tyr‐Val‐His‐Pro‐Phe · OH (R −OH and −NH~2~), are described in detail. A system for the nomenclature of such analogues is proposed. The
Synthetische Analoge des Hypertensins. III. Gly1, II, Val5-Hypertensin II, Orn2, Val5-Hypertensin II, Phe4, Val5-Hypertensin II, und Derivate
✍ Scribed by B. Riniker; R. Schwyzer
- Book ID
- 102854547
- Publisher
- John Wiley and Sons
- Year
- 1961
- Tongue
- German
- Weight
- 503 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
The syntheses of the five hypertensin analogues, H · Gly‐Arg‐Val‐Tyr‐Val‐His‐Pro‐Phe · OH (II), H · Asp(R)‐Orn‐Val‐Tyr‐Val‐His‐Pro‐Phe · OH (II, R −OH; IIIa, R −NH~2~), and H · Asp(R)‐Arg‐Val‐Phe‐Val‐His‐Pro‐Phe · OH (IV, R −OH; IVa, R −NH~2~), are described in detail (schemes 1, 2 and 3).
📜 SIMILAR VOLUMES
The syntheses of H · Asp(NH~2~)‐Arg(NO~2~)‐Val‐Tyr‐Val‐His‐Pro‐Phe·OH (I) and of H · Asp(NH~2~)‐Arg‐Val‐Tyr‐Val‐His‐Pro‐Phe · NH~2~ (II), functional derivatives of hypertensin II (angiotensin II), are described. On total acid hydrolysis, nitroarginine and peptides thereof are degraded to arginine an
## Abstract The synthesis of two octapeptides, H · Asp(β‐NH~2~)‐Arg‐Val‐Tyr‐Val‐His‐Pro‐Phe · OH and H · Asp(β‐OH)‐Arg‐Val‐Tyr‐Val‐His‐Pro‐Phe · OH, is described in detail (preliminary communications see footnote 3). The products show a very strong hypertensive activity, and may be identical with t