TRV120055, a Gq-biased agonist, demonstrates a 10-fold higher molecular efficacy when tested against the AT1R-Gq fusion protein in comparison to the AT1R-βarr2 fusion protein.

Chymase 是一种蛋白质消化酶，主要定位于肥大细胞 (MC)、成纤维细胞和血管内皮细胞。在炎症信号、组织损伤和细胞应激的情况下，Chymase 会释放到胞外间质中。它还参与血管紧张素 II (Ang II) 的生成，是心血管疾病研究的关键成分。

Chlorothiazide (Standard) 是 Chlorothiazide 的标准品，适用于定量分析、质量控制及生化实验等相关研究。Chlorothiazide (Diuril) 是噻嗪类利尿剂，其作用和用途与氢氯噻嗪相似，能够抗高血压，其IC50为3.8 mM。

Angiotensin AT2 receptor agonist

Aclerastide is an angiotensin receptor agonist. Administration of Aclerastide reduced fibrosis and scarring in the healing wounds. This action was more pronounced with longer administration of the peptide after injury. The action of this peptide was block

BMS-248360 is a potent and orally active dual antagonist of both angiotensin II receptor (AT1) and endothelin A (ETA) receptor. With Kis of 10 nM and 1.9 nM for hAT1 and hETA receptor, respectively. BMS-248360 shows hypertensive effects[1].

Olmesartan medoxomil impurity C is an Olmesartan medoxomil impurity. Olmesartan medoxomil is a potent and selective angiotensin AT1 receptor inhibitor with IC50 of 66.2 μM. [1]. Senda A, et al. Effects of Angiotensin II Receptor Blockers on Metabolism of Arachidonic Acid via CYP2C8. Biol Pharm Bull. 2015;38(12):1975-9. [2]. Shah S, et al. Simultaneous Quantitative Analysis of Olmesartan Medoxomil and Amlodipine Besylate in Plasma by High-performance Liquid Chromatography Technique. J Young Pharm. 2012 Apr;4(2):88-94.

TRV056 is a Gq-biased agonist of the angiotensin II type 1 receptor (AT1R), demonstrating efficacy in stimulating Gq-mediated cellular signaling. It can serve as a foundation for the development of Gq-biased AT1R agonists.

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