货号:A1177296
同义名:
CJ-12420; RQ-00000004
Tegoprazan是一种钾竞争性酸阻滞剂,专门针对胃酸分泌。它通过高选择性抑制 H+/K+-ATP酶,有效缓解胃酸过多及相关胃肠道症状,对胃食管反流病和胃溃疡有潜在治疗价值。
规格 | 价格 | 会员价 | 库存 | 数量 | |||
---|---|---|---|---|---|---|---|
{[ item.pr_size ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解
产品名称 | Proton Pump ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Zinc pyrithione | ✔ | 98+% | |||||||||||||||||
PF 03716556 |
++++
H+/K+-ATPase, pIC50: ~6.5 |
99% | |||||||||||||||||
Lansoprazole | ✔ | 98% | |||||||||||||||||
Esomeprazole Magnesium | ✔ | 98%+ | |||||||||||||||||
Rabeprazole | ✔ | 99%+ | |||||||||||||||||
Ilaprazole | ✔ | TOPK | 97% | ||||||||||||||||
Bafilomycin A1 |
++++
H+-ATPase, IC50: 0.44 nM |
99% | |||||||||||||||||
Pantoprazole sodium | ✔ | 98% | |||||||||||||||||
(R)-Lansoprazole | ✔ | 98% | |||||||||||||||||
Tenatoprazole | ✔ | 99%+ | |||||||||||||||||
Omeprazole | ✔ | 98% | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
Concentration | Treated Time | Description | References | |
Bone-marrow-derived macrophages (BMMs) | 0.5, 1, 10, 100 µg/mL | 24 hours | To evaluate the effects of Tegoprazan on cytotoxicity and NO production in BMMs. Results showed that TEGO significantly inhibited NO production at 100 µg/mL concentration, with cell viability exceeding 80%. | Int J Mol Sci. 2023 Sep 26;24(19):14589 |
HT-29 | 10 µM | 3 days | To evaluate the mitigating effect of Tegoprazan on indomethacin-induced inhibition of cell proliferation. Results showed that Tegoprazan significantly alleviated the inhibition of cell proliferation induced by indomethacin in HT-29 cells. | Sci Rep. 2024 Nov 8;14(1):27173 |
Caco-2 | 10-100 µM | 3 days | To evaluate the mitigating effect of Tegoprazan on indomethacin-induced inhibition of cell proliferation. Results showed that Tegoprazan significantly alleviated the inhibition of cell proliferation induced by indomethacin in Caco-2 cells. | Sci Rep. 2024 Nov 8;14(1):27173 |
HIEC-6 | 1-100 µM | 3 days | To evaluate the mitigating effect of Tegoprazan on indomethacin-induced inhibition of cell proliferation. Results showed that Tegoprazan significantly alleviated the inhibition of cell proliferation induced by indomethacin in HIEC-6 cells. | Sci Rep. 2024 Nov 8;14(1):27173 |
Caco-2 | 1.0 mM and 3.0 mM | 48 hours | Evaluated the protective effect of Tegoprazan on intestinal epithelial barrier function, showing that Tegoprazan significantly suppressed TNF-a-induced reduction in TEER levels and reduced FITC-dextran flux. | Front Immunol. 2022 May 25;13:870817 |
Het-1A cells | 30 µM | 6 hours | To evaluate the effect of Tegoprazan on HCl-induced inflammatory responses. Tegoprazan significantly inhibited HCl-induced pro-inflammatory cytokines (IL-6, IL-8, IL-1β, and TNF-α) but did not significantly affect pyroptosis rate. | Front Immunol. 2024 Dec 16;15:1410904. |
Administration | Dosage | Frequency | Description | References | ||
C57BL/6 mice | DNBS and DSS-induced colitis models | Oral | 30 mg/kg | Twice daily, throughout the experiment | Evaluated the protective effect of Tegoprazan on colitis, showing that Tegoprazan significantly improved symptoms of DNBS and DSS-induced colitis, including weight loss, colon shortening, and inflammatory cell infiltration. | Front Immunol. 2022 May 25;13:870817 |
Healthy male subjects | Healthy male subjects | Oral | 50 mg | Once daily for 7 days | To evaluate the pharmacokinetics and safety of Tegoprazan when co-administered with atorvastatin. Results showed no significant changes in the systemic exposure of atorvastatin when co-administered with Tegoprazan. | Front Pharmacol. 2021 Nov 11;12:754849 |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.58mL 0.52mL 0.26mL |
12.91mL 2.58mL 1.29mL |
25.81mL 5.16mL 2.58mL |
CAS号 | 942195-55-3 |
分子式 | C20H19F2N3O3 |
分子量 | 387.38 |
SMILES Code | FC1=C2[C@H](CCOC2=CC(F)=C1)OC3=C4NC(C)=NC4=CC(C(N(C)C)=O)=C3 |
MDL No. | MFCD30533430 |
别名 | CJ-12420; RQ-00000004; LXI-15028; K-CAB; IN-A001 |
运输 | 蓝冰 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
溶解方案 |
DMSO: 105 mg/mL(271.05 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
|