Tiotropium Bromide hydrate
(Synonyms:噻托溴铵;噻托溴胺;(1R,2R,4S,5S,7S)-7-[2-羟基-2,2-二(2-噻吩基)乙酰氧]-9,9-二甲基-3-环氧-9-氮阳离子三环辛烷[3.3.1.02.4]壬烷溴化物;(1Α,2Β,4Β,5Α,7Β-7-[(羟基二-2-噻吩基乙酰基)氧]-9,9-二甲基-3-氧杂-9-氮阳离子三环[3.3.1.0^<2,4>^]壬烷溴化物;Tiotropium Bromide 噻托溴铵;噻托溴铵噻托溴铵一水合物;噻托溴铵一水合物;增强噻托溴铵对系统适应性 EP标准品;增强噻托溴铵溴铵一水 EP标准品;噻托溴铵一水合物(1R,2R,4S,5S,7S)-7-[2-羟基-2,2-二(2-噻吩基)乙酰氧]-9,9-二甲基-3-环氧-9-氮阳离子三环辛烷[3.3.1.02.4]壬烷溴化物;泰乌托品;(1R,2R,4S,5S,7S)-7-[2-羟基-2,2-二(2-噻吩基)乙酰氧]-9,9-二甲基-3-环氧-9-氮阳离子三环辛烷[3.3.1.02.4]壬烷溴化物一水合物)
目录号 : KG11970
CAS No. : 139404-48-1
纯度 : 98%
Tiotropium Bromide hydrate is an anticholinergic and bronchodilator and a muscarinic receptor antagonist.Target: mAChRTiotropium bromide (Ba 679 BR) is a novel potent and long-lasting muscarinic antagonist that has been developed for the treatment of chronic obstructive airways disease (COPD). Binding studies with [3H]tiotropium bromide in human lung have confirmed that this is a potent muscarinic antagonist with equal affinity for M1-, M2- and M3-receptors and is approximately 10-fold more potent than ipratropium bromide. In vitro tiotropium bromide has a potent inhibitory effect against cholinergic nerve-induced contraction of guinea-pig and human airways, that has a slower onset than atropine or ipratropium bromide. tiotropium bromide dissociates slowly from M3-receptors (on airway smooth muscle) but rapidly from M2 autoreceptors (on cholinergic nerve terminals) . Tiotropium bromide is a quaternary ammonium derivative that binds to muscarinic receptors. However, although tiotropium binds with high affinity to muscarinic receptors of M1-, M2- and M3-subtypes, it dissociates very slowly from M1- and M3-receptors but more rapidly from M2-receptors, thereby giving it a unique kinetic selectivity .
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| 分子式 |
C19H22NO4S2.Br.XH2O
|
| 分子量 |
490.43
|
| CAS号 |
139404-48-1
|
| 中文名称 |
噻托溴铵
|
| 储存方式 |
| Powder |
-20°C |
3 years |
| |
4°C |
2 years |
| In solvent |
-80°C |
6 months |
| |
-20°C |
1 month |
|