CAS |
No.65-29-2 |
中文名称 |
加拉碘铵 |
英文名称 |
Gallamine Triethiodide |
别名 |
Flaxedil;Benzkurin;三碘季胺酚 |
分子式 |
C30H60I3N3O3 |
分子量 |
891.53 |
溶解性 |
Soluble in Water/DMSO(Need ultrasonic) |
纯度 |
≥98% |
外观(性状) |
White to yellow Solid |
储存条件 |
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year |
EC |
EINECS 200-605-1 |
MDL |
MFCD00011832 |
SMILES |
CC[N+](CC)(CC)CCOC1=C(C(=CC=C1)OCC[N+](CC)(CC)CC)OCC[N+](CC)(CC)CC.[I-].[I-].[I-] |
InChIKey |
REEUVFCVXKWOFE-UHFFFAOYSA-K |
InChI |
InChI=1S/C30H60N3O3.3HI/c1-10-31(11-2,12-3)22-25-34-28-20-19-21-29(35-26-23-32(13-4,14-5)15-6)30(28)36-27-24-33(16-7,17-8)18-9;;;/h19-21H,10-18,22-27H2,1-9H3;3*1H/q+3;;;/p-3 |
PubChem CID |
6172 |
靶点 |
AChR |
通路 |
Neuronal Signaling |
背景说明 |
是一种胆碱能受体抑制剂。 |
生物活性 |
Gallamine Triethiodide 是一种胆碱受体抑制剂,IC50为68.0μM。[1] |
IC50 |
AChR: 68.0μM(IC50)[1] |
In Vitro |
Gallamine Triethiodide has effect on [3H]QNB dissociation was biphasic,being higher at their low(10(-6)to 10(-5)M)than at their high concentrations(10(-4)to 10(-3)and that at high concentrations strongly inhibited the dissociation of [3H]QNB receptor complexes elicited by the excess of atropine.[1] |
数据来源文献 |
[1]. Nedoma J,et al. Stabilization of antagonist binding to cardiac muscarinic acetylcholine receptors by gallamine and other neuromuscular blocking drugs. J Pharmacol Exp Ther. 1986 Jan;236(1):219-23. |
规格 |
100mg 500mg |
单位 |
瓶 |