## Abstract The synthesis of the C‐14 labeled isotopomer of LY300502, a potent 5α‐reductase inhibitor has been accomplished in four radiochemical steps. The route involves the synthesis of LY300502‐[^14^C] from LY300502 __via__ a circuitous route; the label was introduced with ethyl chloroformate‐[
Hypotensive effect induced by a cyclic dopamine analog, trans-4-methyl-7,8-dihydroxy-1,2,3,4,4a,5,6,10b- octahydrobenzo[f]quinoline
✍ Scribed by Fouad M. Sharabi; John P. Long; Joseph G. Cannon
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 383 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0022-3549
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✦ Synopsis
The antihypertensive effects of trans-4-methyl-7,8-dihydroxy-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinoline, a dopamine agonist, were investigated in dogs and spontaneous hypertensive rats. Intravenous administration of low doses of this cyclic analog of dopamine (0.25--1.00 microgram/kg) consistently reduced blood pressure and heart rate, concurrently recorded in the dog. This effect was antagonized by haloperidol, a specific dopamine antagonist. The dopamine analog also reduced systolic blood pressure of spontaneous hypertensive rats. This study confirmed the possibility that the decrease in blood pressure and heart rate elicited by the dopamine analog is attributable to an effect on specific dopaminergic receptors.
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