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Tegoprazan {[allProObj[0].p_purity_real_show]}

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。

Tegoprazan 化学结构 CAS号:942195-55-3
Tegoprazan 化学结构
CAS号:942195-55-3
Tegoprazan 3D分子结构
CAS号:942195-55-3
Tegoprazan 化学结构 CAS号:942195-55-3
Tegoprazan 3D分子结构 CAS号:942195-55-3
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Tegoprazan 纯度/质量文件 产品仅供科研

货号:A1177296 标准纯度: {[allProObj[0].p_purity_real_show]}
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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。

Tegoprazan 细胞实验

Cell Line
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.

Tegoprazan 动物实验

Species
Animal Model
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

Tegoprazan 实验方案

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

Tegoprazan 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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
方案 一
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方案 三
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