Bioorganic & Medicinal Chemistry Letters 1998-12-01

Design and synthesis of new potent, silent 5-HT1A antagonists by covalent coupling of aminopropanol derivatives with selective serotonin reuptake inhibitors.

M Perez, P J Pauwels, I Pallard-Sigogneau, C Fourrier, P Chopin, C Palmier, V Colovray, S Halazy

Index: Bioorg. Med. Chem. Lett. 8(23) , 3423-8, (1998)

Full Text: HTML

Abstract

Hybrid molecules built up by covalent coupling of aminopropanol derivatives (especially pindolol) with antidepressant drugs like fluoxetine, paroxetine or milnacipran were found to be potent and silent 5-HT1A antagonists (KB < 1 nM for 7c and 9a).


Related Compounds

  • Penbutolol sulfate

Related Articles:

5-HT receptor subtypes involved in the spinal antinociceptive effect of acetaminophen in rats.

2001-11-30

[Eur. J. Pharmacol. 432(1) , 1-7, (2001)]

Autoreceptors remain functional after prolonged treatment with a serotonin reuptake inhibitor.

1999-07-24

[Brain Res. 835(2) , 224-8, (1999)]

Affinity of (+/-)-pindolol, (-)-penbutolol, and (-)-tertatolol for pre- and postsynaptic serotonin 5-HT(1A) receptors in human and rat brain.

2000-08-01

[J. Neurochem. 75(2) , 755-62, (2000)]

The antiaggressive potency of (-)-penbutolol involves both 5-HT1A and 5-HT1B receptors and beta-adrenoceptors.

1996-02-15

[Eur. J. Pharmacol. 297(1-2) , 1-8, (1996)]

High-performance liquid chromatography with chemiluminescence detection of penbutolol and its hydroxylated metabolite in rat plasma.

2001-06-15

[J. Chromatogr. B. Biomed. Sci. Appl. 757(2) , 229-35, (2001)]

More Articles...