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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

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✦ 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.


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✍ Naoto Ueyama; Takashi Yanagisawa; Tsuyoshi Tomiyama 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 French ⚖ 263 KB

## 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‐