Fadolmidine HCl - CAS 189353-32-0
Catalog number: 189353-32-0
Category: Inhibitor
Not Intended for Therapeutic Use. For research use only.
Fadolmidine Hydrochloride, is a novel α2-adrenoceptor (α2-AR) agonist, having antinociception properties. It can be used for the control of inflammatory, postoperative and neuropathic pain.
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Fadolmidine; MPV-2426.
1.Histamine in the locus coeruleus promotes descending noradrenergic inhibition of neuropathic hypersensitivity.
Wei H1, Jin CY1, Viisanen H1, You HJ2, Pertovaara A3. Pharmacol Res. 2014 Dec;90:58-66. doi: 10.1016/j.phrs.2014.09.007. Epub 2014 Oct 7.
Among brain structures receiving efferent projections from the histaminergic tuberomammillary nucleus is the pontine locus coeruleus (LC) involved in descending noradrenergic control of pain. Here we studied whether histamine in the LC is involved in descending regulation of neuropathic hypersensitivity. Peripheral neuropathy was induced by unilateral spinal nerve ligation in the rat with a chronic intracerebral and intrathecal catheter for drug administrations. Mechanical hypersensitivity in the injured limb was assessed by monofilaments. Heat nociception was assessed by determining radiant heat-induced paw flick. Histamine in the LC produced a dose-related (1-10μg) mechanical antihypersensitivity effect (maximum effect at 15min and duration of effect 30min), without influence on heat nociception. Pretreatment of LC with zolantidine (histamine H2 receptor antagonist), but not with pyrilamine (histamine H1 receptor antagonist), and spinal administration of atipamezole (an α2-adrenoceptor antagonist), prazosine (an α1-adrenoceptor antagonist) or bicuculline (a GABAA receptor antagonist) attenuated the antihypersensitivity effect of histamine.
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CAS 189353-32-0 Fadolmidine HCl

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