✦ LIBER ✦

Synthesis of14C-phenazepam and its potential metabolites

✍ Scribed by L. N. Yakubovskaya; A. V. Bogatskii; S. A. Andronati; V. G. Zin'kovskii; N. Ya. Golovenko

Book ID: 112408729
Publisher: Springer
Year: 1979
Tongue: English
Weight: 314 KB
Volume: 13
Category: Article
ISSN: 0091-150X
DOI: 10.1007/bf00780535

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Intrahepatic circulation of14C-phenazepa

Intrahepatic circulation of14C-phenazepam and its metabolites in albino rats

✍ A. V. Bogatskii; N. Ya. Golovenko; V. G. Zin'kovskii 📂 Article 📅 1980 🏛 Springer US 🌐 English ⚖ 283 KB

Synthesis of14C-hydrogenated analog of p

Synthesis of14C-hydrogenated analog of phenazepam

✍ V. A. Sozinov; O. P. Rudenko; V. G. Zin'kovskii; N. Ya. Golovenko; A. I. Lisitsy 📂 Article 📅 1984 🏛 Springer 🌐 English ⚖ 412 KB

Modulation of GABAAreceptor-mediated cur

Modulation of GABAAreceptor-mediated currents by phenazepam and its metabolites

✍ Maksim V. Kopanitsa, Olga V. Zhuk, Volodymyr G. Zinkovsky, Oleg A. Krishtal 📂 Article 📅 2001 🏛 Springer-Verlag 🌐 English ⚖ 133 KB

Synthesis of [14C] - and [13C6]-labeled

Synthesis of [14C] - and [13C6]-labeled tipranavir and its potential hydroxyl metabolite and the glucuronide conjugate

✍ Bachir Latli; Matt Hrapchak; John A. Easter; Wayne T. Stolle; Karl Grozinger; Dh 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 French ⚖ 185 KB

## Abstract Tipranavir or Aptivus^®^ is a non‐peptidic protease inhibitor approved for the combination treatment with ritonavir of HIV infection. Tipranavir labeled with radioactive and stable isotopes of carbon was required for drug metabolism (excretion, distribution, and absorption) studies and

Synthesis of two 14C-labeled forms of pr

Synthesis of two 14C-labeled forms of prinomide, a potential anti-inflammatory compound and its hydroxy metabolite, labeled with 14C

✍ Naba K. Chaudhuri; Bohdan Markus 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 French ⚖ 298 KB

## Abstract The synthesis of two ^14^C‐labeled forms of prinomide, compounds 7 and 10, and the synthesis of a ^14^C‐labeled form of its hydroxy metabolite are described. Compound 7 was synthesized by the reaction of phenyl isocyanate and 1‐methyl‐β‐oxo‐pyrrole‐2‐propanenitrile‐carbonyl‐^14^C (6), w

A short synthesis of [14C]-labelled leva

A short synthesis of [14C]-labelled levamisole and its major metabolite

✍ Cor G.M. Janssen; Jos B.A. Thijssen; Willy L.M. Verluyten 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 109 KB

## Abstract Levamisole (**I**) is the __levo__ isomer of tetramisole. It is a broad spectrum anthelmintic which is used extensively as a veterinary drug for food producing animals. Metabolism and environmental studies necessitated the synthesis of ^14^C‐labelled levamisole (**6**) and of its major