Xestospongin C 产品活性：Xestospongin C ((-)-Xestospongin C) 是一种选择性、可逆的肌醇 1,4,5-三磷酸受体 (IP3R) 抑制剂。Xestospongin C 是肌膜/内质网Ca2+ ATP 酶 (SERCA) 的抑制剂。Xestospongin C 阻断 IP3 诱导的 Ca2+ 从小脑微粒体释放，IC50 为 358 nM。Xestospongin C 是研究神经元和非神经元细胞中 IP3R 和 Ca2+ 信号的结构和功能的工具。 产品来源： https://www.medchemexpress.cn/xestospongin-c.html 研究领域：Membrane Transporter/Ion Channel | Neuronal Signaling | Apoptosis 作用靶点：Calcium Channel | Apoptosis 结构分类：生物碱 | 哌啶类生物碱 | 结构分类 In Vitro: Xestospongin C (XeC; 10 μM; 1 h before Aβ) pretreatment before Aβ1-42 (20 μM; 24 hours) application displays a significant decrease in the early apoptotic rate (9.87%) compared to the Aβ alone treated group (18.38%).? Xestospongin C (10 μM; 1 h before Aβ) and Aβ1-42 (20 μM; 100 s) has significant main effects on the peak value and average values of Ca2+ changes, as well as a significant interaction in primary cultured hippocampal neurons. In Vivo: Xestospongin C (3 μM; intracerebroventrical injection by a pump for four weeks) ameliorates the disinhibition-like behavior and long term spatial memory deficits of 8-month-old male APP/PS1 mice of Alzheimer's disease. 相关产品：MG-132 | Doxorubicin hydrochloride | Bafilomycin A1 | Tamoxifen | Y-27632 | LY294002 | Paclitaxel | Z-VAD-FMK | Acetylcysteine | Angiotensin II human | 2-Deoxy-D-glucose | Staurosporine | Actinomycin D | SB-431542 | 5-Fluorouracil | Bortezomib | Deferoxamine mesylate | Oxaliplatin | Trametinib | Sorafenib | Temozolomide | Gemcitabine | Decitabine | Mdivi-1 | Rotenone | Etoposide | Elesclomol | Ruxolitinib | Monomethyl auristatin E | DAPT 品牌介绍: MCE (MedChemExpress) 拥有数百种全球独家化合物，我们致力于为全球科研客户提供最新最全的高品质小分子活性化合物；10,000 多种高选择性抑制剂、激动剂涉及各热门信号通路及疾病领域；设有专业的实验中心和严格的质控、验证体系；提供 LC/MS、NMR、HPLC、手性分析、元素分析等各项质检报告，确保产品的高纯度、高品质；产品的生物活性多经各国客户实验验证；Nature, Cell, Science 等多种顶级期刊及制药专利收录了MCE客户的科研成果；专业团队跟踪最新的制药及生命科学研究进展，为您提供全球最新的活性化合物；与世界各大制药公司及知名科研机构建立了长期的合作。