peptic ulcers

Anisotropine Methylbromide 是一种抗胆碱能药物，已用于缓解胃肠道痉挛和抑制胃酸分泌。

Abeprazan hydrochloride (Fexuprazan hydrochloride) 是一种有效的、可逆的、具有口服活性的potassium-competitive acid 阻滞剂，通过竞争性的与钾离子结合抑制 H+，K+- ATPase，而无需酸激活。Abeprazan hydrochloride 是一种质子泵抑制剂(PPI)，通过减少胃酸的产生而起作用，可用于治疗胃酸相关疾病，如胃食管反流病(GERD)和消化性溃疡。

AGN-201904 是质子泵抑制剂，是一种奥美拉唑前药，可延缓衰老，可用于预防和治疗消化性溃疡。

Linetastine (TMK-688) 是一种 5-脂氧合酶抑制剂(5-LOX)，能抑制白三烯的产生，并能拮抗组胺的作用。Linetastine可用于研究哮喘、动脉粥样硬化和消化性溃疡。

Betahistine mesylate (Extovyl) 是可口服的组胺 H1 受体激动剂和 H3 受体的拮抗剂，可用作血管扩张剂，用于类风湿性关节炎的研究。

DL-methionine methylsulfonium chloride 是天然的蛋氨酸衍生物。它能够有效保护胃粘膜，避免其受到乙醇诱导的损伤。

IKs124是 KCNE2/KCNQ1 钾通道阻滞剂，IC50=8 nM，同时对KCNE1和KCNE3的IC50分别为370 nM和440 nM，可用于研究消化性溃疡。

Siltenzepine is an agent of anti-acid agent,and used in the treatment of peptic ulcers.

Urease-IN-12 (compound 5e) 是一种竞争性脲酶抑制剂，具有 IC50: 0.35 μM 的活性，可能用于抑制幽门螺杆菌导致的胃炎和消化性溃疡。

Oxyphencyclimine is a muscarinic receptor antagonist (MRA) anticholinergic drug used to treat peptic ulcers.

Aprofene (Aprophen) is an antagonist of muscarinic and nicotinic acetylcholine receptors. It may be used in the therapy of peptic ulcers, endarteritis (inflammation of the inner shell of the artery), cholecystitis (inflammation of the gallbladder), and sp

Isopropamide (R5) is a long-acting anticholinergic drug. It is used to treat peptic ulcers and other gastrointestinal disorders involving excess gastric acid (gastrointestinal acidosis) and hyperactivity.

Methantheline Bromide is a synthetic spasmolytic used to relieve cramps or spasms of the stomach, bowel, and bladder. It is also useful for intestinal or gastric ulcers (peptic ulcer disease), intestinal problems, pancreatitis, gastritis, biliary dysmotil

Nordoxepin hydrochloride (Desmethyldoxepin hydrochloride) 具有抗抑郁活性，可用于研究抑郁症和消化性溃疡病。

Betahistine (Vasomotal) 是可口服的组胺 H1 受体激动剂和 H3 受体的拮抗剂，可用作血管扩张剂，用于类风湿性关节炎的研究。

Isopropamide iodide 是长效季铵盐抗胆碱能药物。它用于研究消化性溃疡和其他胃肠道疾病，尤其是胃酸过多和运动过度。

Pirenzepine (LS 519 free base) is a selective antagonist of the M1 muscarinic acetylcholine receptor (mAChR). It effectively inhibits gastric acid secretion and reduces muscle spasm, making it a valuable compound for investigating peptic ulcers. Additionally, Pirenzepine exhibits anti-proliferative activity against cancer cells [1] [2].

Arbortristoside A is an anti-inflammatory and antinociceptive. This activity may be due to the inhibiting effect of prostaglandin, histamine and serotonin. Arbortristoside A has also been shown to act on ulcerations and may facilitate healing of peptic ulcers.

Arbaprostil is a synthetic prostaglandin E analog that protects gastric mucosa, prevents ulceration, and promotes healing of peptic ulcers. The protective effect is independent of acid inhibition. It is also a potent inhibitor of pancreatic function and can inhibit the growth of experimental tumors. Arbaprostil is a prodrug for the potent PGE2.

Urease-IN-6为一种高效Urease抑制剂，IC50值为14.2 μM，适用于消化性溃疡和胃溃疡研究。

Urease-IN-7 (Compound 5k)，作为竞争性Urease抑制剂，具有IC50为3.33 μM和Ki值为3.62μM。该化合物可用于消化性溃疡和胃溃疡研究。

Urease-IN-8 (Compound 5e) 为一竞争性脲酶 (Urease) 抑制剂，具IC50值为3.51 μM，Ki值为3.11 μM，主要用于消化性溃疡与胃溃疡研究。

Bisfentidine 是一种H2受体拮抗剂，能够阻断胃壁细胞上的H2受体以减少胃酸分泌。它能够与肝脏微粒体中的细胞色素 P-450 结合，从而影响药物代谢。Bisfentidine 可用于研究药物代谢过程、脂质过氧化过程和消化性溃疡等疾病。

Nordoxepin hydrochloride (Standard) 是一种可用于分析的标准物质，通常用作 Nordoxepin hydrochloride 的研究和分析中参考的标准样品。Nordoxepin hydrochloride (Desmethyldoxepin hydrochloride) 具有抗抑郁活性，可用于研究抑郁症和消化性溃疡病。