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化驗
≥95% (HPLC)
品質等級
形狀
powder
顏色
white
溶解度
ethanol: 20 mg/mL
儲存溫度
−20°C
SMILES 字串
[H]C(=O)[C@H](CCSC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(C)=O
InChI
1S/C19H35N3O4S/c1-12(2)9-16(20-14(5)24)19(26)22-17(10-13(3)4)18(25)21-15(11-23)7-8-27-6/h11-13,15-17H,7-10H2,1-6H3,(H,20,24)(H,21,25)(H,22,26)/t15-,16-,17-/m0/s1
InChI 密鑰
RJWLAIMXRBDUMH-ULQDDVLXSA-N
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應用
钙蛋白酶抑制剂 II 已用于蛋白质印迹。此外,它还用于研究Spy1A(一类细胞周期蛋白)在细胞周期中的降解机制。
钙蛋白酶抑制剂II是一种细胞透过性肽,可限制钙蛋白酶、组织蛋白酶 L 和组织蛋白酶 B 的活性。钙蛋白酶抑制剂 II 还可以防止甲基汞诱导的大鼠小脑神经元细胞死亡。
生化/生理作用
钙蛋白酶是在神经系统中表达的半胱氨酸蛋白酶。钙蛋白酶表现出钙依赖性酶活性。在小鼠模型中,抑制钙蛋白酶可防止血管紧张素II诱导的白细胞浸润,并减轻血管周围炎症。
其他說明
以前为 CAS# 136632-32-1
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
Bioorganic & medicinal chemistry letters, 21(19), 5944-5947 (2011-08-23)
In this study, 22 new betulinic acid (BA) derivatives were synthesized and tested for their inhibition of the chymotrypsin-like activity of 20S proteasome. From the SAR study, we concluded that the C-3 and C-30 positions are the pharmacophores for increasing
The cyclin-dependent kinase activator, Spy1A, is targeted for degradation by the ubiquitin ligase NEDD4
The Journal of Biological Chemistry, 284(5), 2617-2627 (2009)
Bioorganic & medicinal chemistry letters, 21(7), 1926-1928 (2011-03-11)
A new class of proteasome inhibitors was synthesized using lithocholic acid as a scaffold. Modification at the C-3 position of lithocholic acid with a series of acid acyl groups yielded compounds with a range of potency on proteasome inhibition. Among
Spontaneous epileptiform discharges in a mouse model of Alzheimer's disease are suppressed by antiepileptic drugs that block sodium channels
Epilepsy Research (2011)
Aneurysm: New Insights for the Healthcare Professional, 56-57 (2013)
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