## Abstract 2‐Propyl‐8‐oxo‐1‐[(2′‐(1H‐tetrazole‐5‐yl) biphenyl‐4‐yl)methyl]‐4, 5, 6, 7‐tetrahydrocyclohept imidazole (KT3‐671), which has been found to be a potent and selective angiotesin II receptor antagonist, was synthesized in ^14^C‐labelled form by using potassium[^14^C]‐cyanide. [^14^C](KT3‐
✦ LIBER ✦
Synthesis of [Sar1, Val5, (4′-Azido-3′,5′-ditritio)Phe8] Angiotensin II, a Photoaffinity Label for the Isolation of Angiotensin II Receptors Communication 1
✍ Scribed by Michel Bernier; Emannuel Escher
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- German
- Weight
- 219 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The synthesis of [Sar^1^, Val^5^, (4′‐azido‐3′,5′‐ditritio)Phe^8^] angiotensin II from a iodinated precursor peptide is described. The principal problems of this synthesis and their resolution are discussed: (i) The β‐induced autophotolysis of the highly tritiated (73 Ci/mmol) and photosensitive label, and (ii) the absorption problems encountered during the purification of microgramm quantities. Such photoaffinity labels are being used for specific labeling and isolation of peptide hormone receptors.
📜 SIMILAR VOLUMES
Synthesis of [14C]KT3-671, 2-Propyl-8-ox
✍
Naoto Ueyama; Takashi Yanagisawa; Tsuyoshi Tomiyama
📂
Article
📅
1995
🏛
John Wiley and Sons
🌐
French
⚖ 263 KB