Chemistry:Lubeluzole
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Formula | C22H25F2N3O2S |
Molar mass | 433.52 g·mol−1 |
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Lubeluzole (Prosynap) is a drug which acts as an indirect NMDA antagonist. It inhibits the release of glutamate, inhibits nitric oxide synthesis, and blocks calcium and sodium gated ion channels.[1] It has neuroprotective effects particularly in hypoxic conditions,[2][3] and was developed for the treatment of stroke.[4] Trials showed it to be safe, effective and well tolerated at low doses, but unfortunately higher doses produced the dangerous cardiac side effect of lengthening the QTc interval,[5][6] which could potentially lead to heart failure, and so this meant that subsequent trials were limited to using only the low dose range.[7] Animal studies had shown lubeluzole to produce neuroprotective effects when administered for prolonged periods, but the aim of its developers was to produce a drug that would be effective for preventing damage from acute stroke, and so ultimately it failed to show sufficient efficacy in trials and development for medical use was halted.[8]
References
- ↑ "Lubeluzole protects hippocampal neurons from excitotoxicity in vitro and reduces brain damage caused by ischemia". European Journal of Pharmacology 342 (2–3): 193–201. January 1998. doi:10.1016/s0014-2999(97)01499-4. PMID 9548385.
- ↑ "Altered Na(+)-channel function as an in vitro model of the ischemic penumbra: action of lubeluzole and other neuroprotective drugs". Brain Research 745 (1–2): 210–21. January 1997. doi:10.1016/s0006-8993(96)01094-3. PMID 9037412.
- ↑ "Neuroprotection of lubeluzole is mediated through the signal transduction pathways of nitric oxide". Journal of Neurochemistry 68 (2): 710–4. February 1997. doi:10.1046/j.1471-4159.1997.68020710.x. PMID 9003060.
- ↑ "Lubeluzole treatment of acute ischemic stroke. The US and Canadian Lubeluzole Ischemic Stroke Study Group". Stroke 28 (12): 2338–46. December 1997. doi:10.1161/01.str.28.12.2338. PMID 9412611.
- ↑ "The safety and tolerability of single intravenous doses of lubeluzole (Prosynap) in healthy volunteers". International Journal of Clinical Pharmacology and Therapeutics 35 (11): 491–5. November 1997. PMID 9401829.
- ↑ "N-methyl-D-aspartate antagonists for stroke and head trauma". Expert Opinion on Investigational Drugs 6 (4): 389–97. April 1997. doi:10.1517/13543784.6.4.389. PMID 15989606.
- ↑ "Cardiovascular safety of lubeluzole (Prosynap(R)) in patients with ischemic stroke". Cerebrovascular Diseases 8 (5): 247–54. 1998. doi:10.1159/000015861. PMID 9712921.
- ↑ "Lubeluzole for acute ischaemic stroke". The Cochrane Database of Systematic Reviews (1): CD001924. 2002. doi:10.1002/14651858.CD001924. PMID 11869612.
![]() | Original source: https://en.wikipedia.org/wiki/Lubeluzole.
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