RAAS

Enalapril Maleate (MK-421 Maleate) 一种是血管紧张素转化酶（ACE）抑制剂。

Angiotensin II (3-8), human 是活性稍弱的血管紧张素AT1受体激动剂。

Angiotensin amide, an octapeptide amide, can be used to increase blood pressure by vasoconstriction.

TRV055 is a Gq-biased ligand of the angiotensin II receptor type 1 (AT1R). TRV055 is efficacious in stimulating cellular Gq-mediated signaling. TRV055 can be used to develop the Gq-biased AT1R agonists.

Theasinensin C 是从红茶水中提起得到的化合物，对肾素活性的 IC50 值为40.21 μM。

L162441 is an antagonist of Angiotensin type 1 receptor.

Aliskiren (CGP 60536; CGP60536B; SPP 100) hydrochloride 是一种选择性的、口服具有活力的、肾素 (renin) 抑制剂 (IC50: 1.5 nM)。Aliskiren hydrochloride 能够用于研究高血压、心血管疾病和癌症恶病质。

Benzyl benzoate (Benzoic acid benzyl ester) 是化妆品中的香料成分，可研究疥疮和蠕形螨相关的炎症性皮肤病。

Renin FRET Substrate I is a specific compound that functions as a substrate for human renin. It is specifically designed to contain the exact cleavage site found in the N-terminal peptide of human angiotensinogen.

VTP-27999 TFA 是烷基胺肾素抑制剂(IC50:0.47 nM)。

Angiotensin I/II (1-5) 是由血管紧张素 I/II 肽转化而来，有 1-5 个氨基酸组成的多肽。血管紧张素 I 是由肾素对血管紧张素原的作用形成的，血管紧张素 I 可产生血管紧张素 II 。血管紧张素 II 用于高血压、特发性膜性肾病和肾素-血管紧张素系统的研究。

Perindoprilat (Perindoprilate) 是一种血管紧张素转换酶抑制剂。

Aliskiren (CGP 60536) D6 Hydrochloride is a deuterium-labeled Aliskiren. Aliskiren hemifumarate is a direct and orally active renin inhibitor (IC50: 1.5 nM).

diuretic and antihypertensive

Competitive non-selective angiotensin II antagonist.

Tasosartan (WAY-ANA 756) 是长效血管紧张素 II 受体拮抗剂。

Irbesartan-d4 (Irbesartan D4) 是 Irbesartan 的氘代化合物，是血管紧张素受体阻滞剂，可用于研究心血血管疾病。

Bopindolol ((±)-Bopindolol) fumarate 是一种具有部分激动剂活性的、口服具有活力的 β-肾上腺素受体 (ARs) 拮抗剂，对 β1- 和 β2-ARs 无选择性，对 β3-AR 亚型亲和力低。Bopindolol fumarate 是 Pindolol 的前体药物，能够用于研究原发性和肾血管性高血压。

Irbesartan (SR-47436) 是一种 1 型血管紧张素 II 受体拮抗剂，IC50为1.3 nM。

Sinapinic Acid (Synapoic acid) 是从 Hydnophytum formicarumJack. 根中分离到的酚类，是HDAC 抑制剂，对ACE-I 的活性也有抑制作用。它有抗肿瘤活性，诱导肿瘤细胞凋亡，具有抗氧化、抗糖尿病的作用。

Olmesartan impurity, a compound related to Olmesartan, is an angiotensin II receptor (AT1R) antagonist utilized in the study of high blood pressure. Olmesartan (RNH-6270) is the parent compound with similar properties and functions as an AT1R antagonist.

1-Methyl-2-[(4Z,7Z)-4,7-tridecadienyl]-4(1H)-quinolone，为喹诺酮类生物碱，作用为二酰基甘油酰基转移酶抑制剂与血管紧张素II受体阻断剂，其IC50值依次为20.1 μM与34.1 μM。此化合物亦展现对幽门螺杆菌的有效抗活性，MIC值达10 μg/mL。

PD 134922 is a HIV-1 protease inhibitors. Inactivation of the protease prevents infectious virion formation.

L-159282 is an orally active and nonpeptide angiotensin II receptor antagonist. It also has anti-hypertensive activity.

E-4177 是一种血管紧张素II-1型受体(AT1R)拮抗剂，可用于研究心血管疾病。

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。

Azilsartan mepixetil is a potent angiotensin II receptor antagonist with enhanced efficacy and prolonged duration of action. It exhibits more prominent and sustained effects in lowering blood pressure and heart rate, while maintaining a high level of safety. Furthermore, Azilsartan mepixetil demonstrates optimal protective efficacy for cardiovascular and renal functions. Hence, it holds promise for the research and treatment of hypertension, chronic heart failure, and diabetic nephropathy.

Olmesartan Medoxomil (Benicar) 是血管紧张素 (angiotensin AT1) 受体选择性抑制剂(IC50:66.2 μM)。

Camellianin A 是从 A. nitida 和 茶叶中提取得到的类黄酮列化合物，具有抗癌活性，抑制血管紧张素转换酶 (ACE) 活性，促进 Hep G2 和 MCF-7 细胞凋亡。Camellianin A 可预防CCl4-通过施加抗氧化应激、抗炎和抗细胞凋亡诱导肝损伤。

Olmesartan D4 is the deuterium labeled Olmesartan. Olmesartan is an antagonist of angiotensin II receptor (AT1R) used to treat high blood pressure.

Ditekiren is a renin inhibitor with orally active.

PD 123177 is an inhibitor of Nonpeptide angiotensin AII-2.

Milfasartan is a potent, selective antagonist of AT1 receptor with oral activity. It markedly lowers the blood-pressure in conscious renal and spontaneously hypertensive rats.

Zankiren is a renin inhibitor. Zankiren can reduce blood pressure, plasma renin activity, and angiotension II.

SC 46944 is a highly potent human renin inhibitor.