所有图片(1)
别名:
1-(2,3-二氯苯甲酰基)-5-甲氧基-2-甲基-(3-(吗啉-4-基)乙基)-1H-吲哚 盐酸盐, 242 盐酸盐, L-768, L-768242 盐酸盐, L768242 盐酸盐, ML-SI1盐酸盐
经验公式（希尔记法）:
C23H24Cl2N2O3 · HCl
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质量水平
检测方案
≥98% (HPLC)
形式
solid
药品控制
regulated under CDSA - not available from Sigma-Aldrich Canada
储存条件
desiccated
颜色
white to pink
溶解性
DMSO: soluble >10 mg/mL
H2O: insoluble <2 mg/mL
储存温度
2-8°C
SMILES字符串
Cl.COc1ccc2n(c(C)c(CCN3CCOCC3)c2c1)C(=O)c4cccc(Cl)c4Cl
InChI
1S/C23H24Cl2N2O3.ClH/c1-15-17(8-9-26-10-12-30-13-11-26)19-14-16(29-2)6-7-21(19)27(15)23(28)18-4-3-5-20(24)22(18)25;/h3-7,14H,8-13H2,1-2H3;1H
InChI key
JIQYDHDVNNFPMU-UHFFFAOYSA-N
应用
GW405833盐酸盐被用作溶酶体瞬时受体电位粘脂素1 (TRPML1)特异性抑制剂，以验证TRPML1是否介导神经元中tau蛋白的释放，并验证其是否介导溶酶体tau蛋白的释放。也用作TRPML通道阻断剂，以研究粘脂素瞬时受体电位阳离子通道3 (MCOLN3/TRPML3)功能和运输对海拉细胞自噬的影响。
生化/生理作用
GW405833是一种选择性的大麻素CB2受体激动剂；止痛药。 GW405833可以高亲和力结合人和大鼠CB2受体（Ki′s 3.9和3.6 nM）；充当部分激动剂（与完全激动剂CP55，940相比，对福司可林刺激的cAMP形成的抑制率为50％）。GW405833在炎性、神经性和切口疼痛的大鼠模型中具有有效的镇痛作用；缺乏CB1激动剂常见的CNS效应。
GW405833盐酸盐，又称ML-SI1，是一种细胞可渗透溶酶体瞬时受体电位阳离子通道、粘脂素亚家族(TRPML)阻断剂。
警示用语：
Danger
危险声明
危险分类
Acute Tox. 3 Oral - Aquatic Chronic 4
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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