Cat. No. | Product Name | Target | Signaling Pathways |
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T22371 |
Mivacurium dichloride
米库氯铵,Mivacurium chloride,二氯美维库铵 |
AChR | Neuroscience |
Mivacurium dichloride (Mivacurium chloride) 是苄基异喹啉衍生物,可与 nAChR 偶联,以减少或抑制乙酰胆碱对肌肉细胞末端盘的去极化作用。它也是非去极化短效的神经肌肉阻滞剂和骨骼肌松弛剂。 | |||
T6397 |
Atracurium besylate
Tracrium,51W89,BW-33A,苯磺酸阿曲库铵 |
AChR | Neuroscience |
Atracurium besylate (51W89) 是一种神经肌肉阻断剂,ED95为0.2 mg/kg。 | |||
T1594 |
Vecuronium bromide
ORG NC 45,维库溴铵 |
AChR | Neuroscience |
Vecuronium bromide (ORG NC 45) 是一种合成的中效单季铵盐类固醇和非去极化神经肌肉阻滞剂,具有肌肉松弛活性。 | |||
T0156 |
Rocuronium bromide
ORG 9426,罗库溴铵,ORG 9426 (Bromide) |
AChR | Neuroscience |
Rocuronium bromide (ORG 9426) 是一种氨基甾体类的、非去极化的神经肌肉受体抑制剂,也是一种肌肉松弛剂。 | |||
T12748 |
Rocuronium
罗库铵,Org-9426 |
Others | Others |
Rocuronium is an blocker of aminosteroid non-depolarizing neuromuscular. | |||
T29846 |
Alcuronium free base
Alcuronium,Alcuronum,Diallylnortoxiferine,Alcuronium kation,Alloferine |
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Alcuronium free base is a non-depolarizing skeletal muscle relaxant similar to Tubocurarine. It is used as an anesthesia adjuvant. | |||
T25636 |
Laudexium
Laudexium ion,Laudexium cation |
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Laudexium is a neuromuscular blocking drug or skeletal muscle relaxant in the category of non-depolarizing neuromuscular-blocking drugs. It is used adjunctively in surgical anesthesia to facilitate endotracheal intubation and to provide skeletal muscle re | |||
T33638 |
Neostigmine Iodide
SB 24,SB24,TL1321,TL 1321,TL-1321,SB-24 |
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Neostigmine Iodide is a parasympathic compound used as a reversible acetylcholinesterase inhibitor to improve muscle tone in patients with myasthenia gravis and in routine anesthesia to reverse the effects of non-depolarizing muscle relaxants such as rocu | |||
T70269 |
Hexamethonium chloride dihydrate
|
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Hexamethonium chloride dihydrate is a non-depolarizing NMJ blocker and nAChR antagonist. It has previously been used to treat hypertension. It inhibits sympathetic nervous system activity and acts as a skeletal muscle relaxant. | |||
T68645 |
Hexamethonium monotartrate
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Hexamethonium monotartrate is a non-depolarizing NMJ blocker and nAChR antagonist. It has previously been used to treat hypertension. It inhibits sympathetic nervous system activity and acts as a skeletal muscle relaxant. | |||
T69161 |
Hexamethonium bromide dihydrate
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Hexamethonium bromide dihydrate is a non-depolarizing NMJ blocker and nAChR antagonist. It has previously been used to treat hypertension. It inhibits sympathetic nervous system activity and acts as a skeletal muscle relaxant. | |||
T68811 | Trimetaphan camsilate | ||
Trimetaphan camsilate is a drug that counteracts cholinergic transmission at the ganglion type of nicotinic receptors of the autonomic ganglia and therefore blocks both the sympathetic nervous system and the parasympathetic nervous system. It acts as a non-depolarizing competitive antagonist at the nicotinic acetylcholine receptor, is short-acting, and is given intravenously. | |||
T75283 | Atracurium | ||
Atracurium (BW-33A free acid)为高效的竞争性非去极化神经肌肉阻滞剂,兼具AChR受体拮抗作用。该化合物能够诱导支气管收缩及实现神经肌肉阻滞,并促进星形胶质细胞分化[5]。 | |||
T37702 |
Pancuronium (bromide hydrate)
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Pancuronium is an aminosteroid antagonist of muscle-type nicotinic acetylcholine receptors (nAChRs) with an IC50value of 14.8 nM using patch clamp electrophysiology in BOSC23 cells expressing mouse nAChRs.1It acts as a non-depolarizing neuromuscular blocking agent.2Pancuronium enhances anesthesia induced by isoflurane , reducing immobilization with an ED50value of 1.62 μg/kg.3 1.Liu, M., and Dilger, J.P.Site selectivity of competitive antagonists for the mouse adult muscle nicotinic acetylcholin... |