
PRE-084 hydrochloride
CAS No. 75136-54-8
PRE-084 hydrochloride ( —— )
产品货号. M22600 CAS No. 75136-54-8
PRE-084 盐酸盐是 σ1 的选择性激动剂(IC50:44 nM)。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥300 | 有现货 |
![]() ![]() |
10MG | ¥478 | 有现货 |
![]() ![]() |
25MG | ¥996 | 有现货 |
![]() ![]() |
50MG | ¥1766 | 有现货 |
![]() ![]() |
100MG | ¥3151 | 有现货 |
![]() ![]() |
200MG | ¥4820 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称PRE-084 hydrochloride
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述PRE-084 盐酸盐是 σ1 的选择性激动剂(IC50:44 nM)。
-
产品描述PRE-084 hydrochloride is a selective agonist of σ1(IC50:44 nM, in the sigma receptor assay).
-
体外实验PRE-084 hydrochloride (0.1-100 μM; 24 h) protects cultured cortical neurons against β-amyloid toxicity (maximally neuroprotective at 10 μM) and reduces the levels of proapoptotic protein Bax at 10 μM. Cell Viability AssayCell Line:Cortical cells (βAP(25-35)-induced neurotoxicity model)Concentration:0.1-100 μM Incubation Time:24 h Result:Reduced neuronal toxicity in a bell shaped-manner and is maximally neuroprotective at 10 μM.Western Blot Analysis Cell Line:Cortical cells (βAP(25-35)-induced neurotoxicity model)Concentration:10 μM Incubation Time:24 hResult:Reduced the levels of proapoptotic protein Bax in cortical neurons induced by βAP(25-35).
-
体内实验PRE-084 hydrochloride (0.25 mg/kg; i.p.; 3 times a week for 8 weeks) displays beneficial effects on motor performance (improves motor neuron survival, ameliorates paw abnormality and grip strength performance) in wobbler mice, and shows neuroprotective effects (increases the levels of BDNF in the gray matter).PRE-084 hydrochloride (1 mg/kg; i.p.; single) protects the heart by activating the Akt eNOS pathway in myocardial infarction model. Animal Model:Wobbler mice (4-week-old).Dosage:0.25 mg/kg Administration:Intraperitoneal injection; 3 times a week for 8 weeks.Result:Significantly improved ameliorated paw abnormality from week 4, and notably improved paw grip strength at week 5.Reduced the number of reactive astrocytes whereas increased the number of pan-macrophage marker CD68-positive cells and CD206+ cells involved in tissue restoration.Animal Model:Adult male Sprague?Dawley rats (220-250 g; myocardial infarction model).Dosage:1 mg/kg Administration:Intraperitoneal injection; single.Result:Significantly decreased the degree of myocardial apoptosis.Led to significantly increased expression of p?Akt and p?eNOS.
-
同义词——
-
通路Autophagy
-
靶点Sigma receptor
-
受体σ1
-
研究领域——
-
适应症——
化学信息
-
CAS Number75136-54-8
-
分子量353.88
-
分子式C19H28ClNO3
-
纯度>98% (HPLC)
-
溶解度DMSO:31 mg/mL (87.6mM)
-
SMILESCl.O=C(OCCN1CCOCC1)C1(CCCCC1)c1ccccc1
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Peviani M, et al. Neuroprotective effects of the Sigma-1 receptor (S1R) agonist PRE-084, in a mouse model of motor neuron disease not linked to SOD1 mutation. Neurobiol Dis. 2014 Feb;62:218-232.
产品手册




关联产品
-
KB-5492 free base
KB-5492 free base 是一种有效的和选择性的 sigma 受体抑制剂,抑制 [3H]1,3-di(2-tolyl)guanidine (DTG) 与 sigma 受体结合,IC50 值为 3.15 μM。KB-5492 free base 是一种抗溃疡剂。
-
BD1047.2HBr
BD-1047 dihydrobromide 是 sigma 受体的选择性功能拮抗剂。
-
MS-377
MS-377 是一种有效的选择性 sigma-1 受体配体,Kd 为 15.2 nM。