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Proton Pump

Proton Pump相关产品(21)
货号 产品名 中文名称 产品描述
SJ-MA0035 Bafilomycin A1 (Baf-A1) 巴佛洛霉素A1

Bafilomycin A1 是特异性,可逆的 V-ATPase 抑制剂,IC50 值为 4-400 nmol/mg。Bafilomycin A1,大环内酯类抗生素, 是一种自噬晚期阶段抑制剂。Bafilomycin A1 阻断自噬体与溶酶体的融合,并抑制培养细胞溶酶体中的酸化和蛋白质降解。Bafilomycin A1 也诱导调亡。

SJ-MX1323 PF-3716556 PF-3716556 is a selective H+,K+-ATPase inhibitor (pIC50 = 6 in human recombinant ion-leaky assays).
SJ-MX2220A Esomeprazole sodium 埃索美拉唑钠盐 Esomeprazole Sodium (formerly 18-sodium; H199; 18 sodium; H-199; Nexium IV; S-Omeprazole sodium), the sodium salt of esomeprazole, is the S-isomer of omeprazole which is a potent PPI-proton pump inhibitor with an IC50 of 0.076 mg/kg. Esomeprazole Sodium has been approved for the short-term treatment of gastroesophageal reflux disease-GERD.
SJ-MX2220B Esomeprazole magnesium trihydrate 埃索美拉唑镁三水合物 Esomeprazole magnesium trihydrate (S-Omeprazole magnesium trihydrate) is a proton pump inhibitor (PPI) that is used to reduce gastric acid secretion. Esomeprazole Magnesium is the magnesium salt of esomeprazole, the S-isomer of omeprazole. In the acidic compartment of parietal cells, esomeprazole is protonated and converted into the active achiral sulphenamide; the active sulphenamide forms one or more covalent disulfide bonds with the proton pump hydrogen-potassium adenosine triphosphatase (H+/K+ ATPase), thereby inhibiting its activity and the parietal cell secretion of H+ ions into the gastric lumen.
SJ-MX2820 (R)-Lansoprazole 右旋兰索拉唑 (R)-Lansoprazole (formerly known as T168390; TAK390; Kapidex; Dexilant, R-Lansoprazole and TAK-390MR), the dextrorotatory or R-enantiomer of lansoprazole, is a proton pump inhibitor (PPI) formulated to have dual delayed-release properties by employing a novel release formulation that prolongs its absorption. Dexlansoprazole is used to treat non-erosive GERD (gastroesophageal reflux disease).
SJ-MX3632 Vonoprazan 沃诺拉赞 Vonoprazan (TAK-438 free base) 是一种质子泵抑制剂 (PPI),是高效的,具有口服活性的钾竞争性酸阻断剂 (potassium-competitive acid blocker, P-CAB),具有抗分泌活性。在 pH 为 6.5 时,Vonoprazan 抑制猪胃微粒体中的 H+,K+-ATPase 酶活性,IC50 值为 19 nM。Vonoprazan 被开发用于研究胃酸相关疾病,如胃食管反流病和消化性溃疡。
SJ-MX1219A Vonoprazan Fumarate 富马酸沃诺拉赞 Potassium-competitive acid blocker (P-CAB); reversibly inhibits gastric H+, K+-ATPase; TAK-438 exerts a longer and more potent antisecretory effect than lansoprazole as a result of its high accumulation and slow clearance from the gastric glands.
SJ-MX2221A Tenatoprazole sodium 泰妥拉唑钠 Tenatoprazole sodium (TU-199 sodium) 是质子泵抑制剂; 抑制猪胃H+/K+-ATPase酶活性的 IC50 值为6.2 μM。
SJ-MX2220 Esomeprazole magnesium 埃索美拉唑镁 Esomeprazole magnesium ((S)-Omeprazole magnesium) 是一种有效的具有口服活性 H+, K+-ATPase 抑制剂,可用于上消化道疾病和胃食管反流疾病的研究。Esomeprazole magnesium 是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。
SJ-MX2221 Tenatoprazole (TU-199) 泰妥拉唑 Tenatoprazole (TU-199) 是一种具有口服活性的,基于咪唑吡啶的质子泵 (proton pump) 抑制剂,能延长的血浆半衰期。Tenatoprazole 抑制猪胃 H+/K+-ATP 酶活性,IC50 值为 6.2 μM。Tenatoprazole 阻断泛素与 ESCRT-1 因子 Tsg101 的相互作用,抑制几种包膜病毒的产生,包括 EBV。
SJ-MX1846 Pantoprazole 泮托拉唑

Pantoprazole (BY1023) 是一种具有口服活性的,有效质子泵 (proton pump) 抑制剂 (PPI)。Pantoprazole 是一种取代的苯并咪唑,是一种有效的 H+/K+-ATPase 抑制剂,IC50 为 6.8 μM。Pantoprazo 可以改善 pH 值稳定性,并具有抗分泌,抗溃疡的作用。Pantoprazo 联合阿霉素 (Doxorubicin) 可显着增加肿瘤生长延迟。

SJ-MX1710 Lansoprazole (AG 1749) 兰索拉唑 Lansoprazole (AG 1749) 是质子泵抑制剂,能抑制胃酸生成。Lansoprazole (AG 1749) 是中性鞘磷脂酶 (N-SMase) 的抑制剂(外泌体抑制剂)。
SJ-MX1847 Rabeprazole (LY307640) 雷贝拉唑 Rabeprazole (LY307640) 是一种二代质子泵抑制剂 (pump inhibitor, PPI),不可逆地抑制胃 H+/K+-ATPase。Rabeprazole 诱导细胞凋亡 (apoptosis)。Rabeprazole 也抑制尿苷核苷核糖水解酶 (UNH) ,IC50 为 0.3 μM。Rabeprazole 可用于胃溃疡和胃食管反流的研究。
SJ-MX1847A Rabeprazole (LY307640) sodium 雷贝拉唑钠 Rabeprazole sodium (LY307640 sodium) 是一种二代质子泵抑制剂 (pump inhibitor, PPI),不可逆地抑制胃 H+/K+-ATPase。Rabeprazole sodium 诱导细胞凋亡 (apoptosis)。Rabeprazole sodium 也抑制尿苷核苷核糖水解酶 (UNH) ,IC50 为 0.3 μM。Rabeprazole sodium 可用于胃溃疡和胃食管反流的研究。
SJ-MX2040 Ilaprazole (IY-81149) 艾普拉唑 Ilaprazole (IY-81149),一种具有口服活性质子泵抑制剂,以剂量依赖性方式不可逆地抑制 H+/K+-ATPase,在兔壁细胞制剂中的 IC50 为 6 μM。Ilaprazole 用于胃溃疡的研究。Ilaprazole 也是一种有效的T细胞起源蛋白激酶 (TOPK) 抑制剂。
SJ-MX1219 Vonoprazan Fumarate 富马酸沃诺拉赞 Vonoprazan Fumarate (TAK-438)是一种新型P-CAB(钾离子竞争性酸抑制剂),可逆抑制H+/K+, ATPase,IC50为19 nM (pH 6.5),控制胃酸分泌。
SJ-MN0531 Abscisic Acid (Dormin) 脱落酸 Abscisic acid ((S)-(+)-Abscisic acid) 是一种口服有效的植物激素,存在于水果和蔬菜中,也是一种内源性的哺乳动物激素。Abscisic acid 是一种生长抑制剂,可以调节植物生长发育Abscisic acid 抑制质子泵 (H+-ATPase),并导致 Ca2+ 依赖性的质膜去极化。Abscisic acid 是 LANCL2 的天然配体,是一种有效的胰岛素敏感化合物,具有用于糖尿病前期,2 型糖尿病和代谢综合征研究的潜力。
SJ-MX1713 Omeprazole (H 16868) 奥美拉挫 Omeprazole (H 16868) 是一种质子泵 (proton pump) 抑制剂 (PPI),有潜力用于胃肠道疾病的研究。Omeprazole 竞争性抑制 CYP2C19 活性,Ki 为 2 到 6 μM。Omeprazole 还抑制革兰氏阳性菌和革兰氏阴性菌生长。Omeprazole 是中性鞘磷脂酶 (N-SMase) 的抑制剂(外泌体抑制剂)。
SJ-MX1947 EN6 EN6 是一种小分子体内自噬 (autophagy) 激活剂,其共价靶向溶酶体v-ATP 酶的 ATP6V1A 亚基中的半胱氨酸 277。EN6 介导的 ATP6V1A 修饰使 v-ATP 酶与 Rag 解偶联,导致 mTORC1 信号传导的抑制,溶酶体酸化增加和自噬激活。EN6 以溶酶体依赖性方式清除 TDP-43 聚集物,这是额颞叶痴呆的致病因子。
SJ-MN0834 Rabeprazole Sulfide Rabeprazole thioether is a major and  active metabolite of rabeprazole which is a novel, potent and 2nd-generation proton pump inhibitor (PPI) that is used as  an antiulcer drug. It irreversibly inactivates gastric H+/K+-ATPase and induces apoptosis. Rabeprazole acts as an uridine nucleoside ribohydrolase (UNH) inhibitor with an IC50 of 0.3 μM. Rabeprazole can be used for the research of gastric ulcerations and gastroesophageal reflux. It is a partially reversible gastric proton pump inhibitor and also an inhibitor of ATP4.