Paxilline 产品活性：Paxilline 是一种来自 Penicillium paxilli 的吲哚生物碱霉菌毒素，通过封闭通道的阻断机制有效地抑制 BK 通道。 Paxilline 也能抑制肌质网 Ca2+ 刺激的 ATP 酶 (SERCA)，对不同亚型的 SERCA 作用的 IC50 值为介于 5 μM-50 μM 之间。 Paxilline 具有显着的抗惊厥活性。 产品来源： https://www.medchemexpress.cn/paxilline.html 研究领域：Membrane Transporter/Ion Channel | Neuronal Signaling 作用靶点：Potassium Channel | Calcium Channel 来源：植物 | 其他科 结构分类：生物碱 | 吲哚类生物碱 | 萜类 | 二萜 | 结构分类 相关产品：Natural Product Library Plus | Bioactive Compound Library Plus | Membrane Transporter/Ion Channel Compound Library | Neuronal Signaling Compound Library | Natural Product Library | Terpenoids Library | Anti-Alzheimer's Disease Compound Library | Neuroprotective Compound Library | Alkaloids Library | Neurodegenerative Disease-related Compound Library | Plant-Sourced Natural Product Library | Calcium Channel Blocker Library | Potassium Channel Compound Library | Human Metabolite Library | Antihypertensive Compound Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | Ion Channel Compound Library | Multi-Target Compound Library | Bioactive Compound Library Max | Nigericin sodium salt | Thapsigargin | Ionomycin | L-Ascorbic acid | Yoda 1 | BAPTA-AM | Minocycline hydrochloride | Verapamil | 2-Aminoethyl diphenylborinate | Acetylcholine chloride | GSK1016790A | Branaplam | Nifedipine | Rosuvastatin Calcium | Fasudil Hydrochloride | SCH-23390 hydrochloride | Ebselen | Halofuginone | Glibenclamide | Bay K 8644 | Quinidine (15% dihydroquinidine) | Carbamazepine | Tetrandrine | Ruthenium red | L-Phenylalanine | E-4031 | ISX-9 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。