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My Cart> Small Molecule Compounds > Inhibitors & Antagonists & Agonists > Neuronal Signal Pathway > Umeclidinium BromideCAS：869113-09-7
Molecular Formula：C29H34BrNO2
Molecular Weight：508.49
Storage：Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year
Purity：≥98%
Appearance：White to off-white Solid
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| CAS | 869113-09-7 |
| Name | Umeclidinium Bromide |
| Molecular Formula | C29H34BrNO2 |
| Molecular Weight | 508.49 |
| Solubility | Soluble in DMSO(Need ultrasonic) |
| Purity | ≥98% |
| Appearance | White to off-white Solid |
| Storage | Powder:2-8℃，2 years;Insolvent(Mother Liquid):-20℃，6 months;-80℃，1 year |
| MDL | MFCD27976798 |
| SMILES | C1C[N+]2(CCC1(CC2)C(C3=CC=CC=C3)(C4=CC=CC=C4)O)CCOCC5=CC=CC=C5.[Br-] |
| InChIKey | PEJHHXHHNGORMP-UHFFFAOYSA-M |
| InChI | InChI=1S/C29H34NO2.BrH/c31-29(26-12-6-2-7-13-26，27-14-8-3-9-15-27)28-16-19-30(20-17-28，21-18-28)22-23-32-24-25-10-4-1-5-11-25;/h1-15，31H，16-24H2;1H/q+1;/p-1 |
| PubChem CID | 11519069 |
| Target Point | mAChR |
| Passage | Neuronal Signaling;GPCR & G Protein |
| Background | It is a mAChR antagonist. |
| Biological Activity | Umeclidinium bromide 是一种新型 mAChR 拮抗剂，对克隆的人类 M1-M5 mAChRs 的亲和力（Ki）为 0.05 至 0.16 nM。[1] |
| Data Literature Source | [1]. Salmon M，et al. Pharmacological characterization of GSK573719 (umeclidinium): a novel，long-acting，inhaled antagonist of the muscarinic cholinergic receptors for treatment of pulmonary diseases. J Pharmacol Exp Ther. 2013 May;345(2):260-70. [2]. Calzetta L，et al. Pharmacological characterization of the interaction between umeclidinium and vilanterol in human bronchi. Eur J Pharmacol. 2017 Oct 5;812:147-154. |
| Unit | Bottle |
| Specification | 2mg 5mg |
Remark：These protocols are for reference only. Solarbio does not independently validate these methods.
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