antihypertensive effect

Urapidil hydrochloride (Urapidil HCl) 是α1-肾上腺素受体拮抗剂和5-HT1A 受体激动剂。

N,N'-Dicyclohexylurea (AURORA KA-3582) 是一种可溶性环氧化物水解酶 (sEH) 抑制剂。

Dixyrazine（UCB 3412） 具有短暂的降压作用，可预防注射硫酸鱼精蛋白引起的脑水肿，可用于研究与神经系统相关的疾病。

Peimisine (Ebeiensine) 非竞争性拮抗气管平滑肌 M 受体，抑制 Ach 引起的平滑肌收缩。它兴奋 β 受体和拮抗内钙释放，促进一氧化氮释放，可舒张气管平滑肌，有平喘作用。

Alacepril (DU-1219) 是一种具有口服活性血管紧张素转换酶 (ACE) 抑制剂，具有长效抗高血压作用。

Nanofin (Lupetidine) 是一种神经性阻断药，具有降压作用，可用于轻中度高血压的研究。

(R)-SCH 42495 is the less active enantiomer of SCH 42495. SCH 42495 is an orally active inhibitor of neutral metalloendopeptidase (NEP), with antihypertensive effect.

SCH 42495 racemate is the racemate of SCH 42495. SCH 42495 is an orally active neutral inhibitor of metalloendopeptidase (NEP), with antihypertensive effect.

Imarikiren（又名TAK-272）是一种高效、选择性强且可口服的直接肾素抑制剂，主要用于治疗糖尿病肾病。在hPRA检测中，TAK-272对人肾素的抑制活性极强（IC50 = 2.1 nM），并且对其他天冬酰胺蛋白酶如胃蛋白酶（IC50 > 10 μM）和组织蛋白酶D（IC50 > 10 μM）具有优异的选择性。在大鼠中，TAK-272展示了显著改善的PK形态（F = 25.2%）。通过口服给药（3 和 10 mg kg），TAK-272展现了剂量依赖性的强效持久的降压效果。目前，TAK-272 HCl正处于人类临床试验阶段。

Eprosartan (SKF-108566J free base) 是一种具有选择性和竞争性的非肽类血管紧张素II受体拮抗剂，对AT1受体亚型具有高亲和力，可用作降压剂。Eprosartan 对血管紧张素 II 受体有抑制作用，在大鼠和人类肾上腺皮质膜中的 IC50 值分别为 9.2 nM 和 3.9 nM。

A-80b is a synthesized pyridazino[4,5-b]indole derivate with potent and long-lasting antihypertensive activity. The decrease in diastolic pressure was greater than the decrease in systolic pressure and cardiac frequency was not modified significantly. A-8

Fenquizone (M.G. 13054) 是一种噻嗪样利尿剂，具有慢性抗高血压作用。Fenquizone 可用于水肿和高血压的研究。

Alamandine can be formed from angiotensin A by action of ACE-2 or directly from angiotensin-(1-7) by decarboxylation of its aspartate residue. The angiotensin A analog produces effects resembling those of Ang II (1-7). However, it acts independently of the two known vasodilators receptors of the RAS (Mas and angiotensin II type 2). To produce its effects, alamandine binds to the Mas-related receptor, MrgD. A novel orally active formulation of alamandine produced a long-term antihypertensive effect in spontaneously hypertensive rats and cardioprotective effects. These novel findings will be helpful for developing a new understanding of the RAS, a key regulator of blood pressure and fluid balance. The heptapeptide could serve as a model peptide, e.g. in the development and evaluation of analytical methods.

Trichlormethiazide sodium 是口服有效的噻嗪类利尿剂，显示降压活性。在急性肾功能衰竭大鼠中，Trichlormethiazide sodium 可增加尿量、Na 和 K 排泄，并有改善肌酐清除率 (CCRE)。

CB096 is a novel inhibitor of RAN translation. specifically binds to a repeating 1 × 1 GG internal loop structure, 5'CGG 3'GGC, that is formed when r(G4C2)exp folds, also acting as a potent vasorelaxant agent, showing antihypertensive effect.

Azilsartan mepixetil potassium (QR-01019K)，是一种高效安全的血管紧张素 II 受体拮抗剂，展现出卓越的持久降压效应以及显著且持续的降心率功能，有望用于治疗高血压、慢性心力衰竭和糖尿病肾病。

Isomartynoside has inhibition against the angiotensin converting enzyme (ACE) activities, the IC 50 value is 505±26.7μg ml, it may have antihypertensive effect. Isomartynoside also shows obvious anti-fatigue activity.

Serpentinine may have antihypertensive effect.