Dehydroandrographolide succinate 是从中药穿心莲中提取的一种天然产物，具有免疫刺激、抗感染和抗炎作用，有潜力研究病毒性肺炎和病毒性上呼吸道感染。

A 286982是高效的LFA-1/ICAM-1相互作用变构抑制剂，在LFA-1/ICAM-1结合和LFA-1介导的细胞粘附实验中，其IC50分别为44和35 nM。

ALK inhibitor 1 是嘧啶类 ALK 的有效抑制剂。它是一种睾丸特异性丝氨酸/苏氨酸激酶 2 (TSSK2;IC50=31 nM) 和粘着斑激酶 (FAK;IC50=2 nM) 抑制剂。

UCN-02 (7-epi-Hydroxystaurosporine) 是一种由链霉菌属 N-126 菌株产生，具有选择性和高效性的蛋白激酶 C (PKC) 抑制剂，抑制 PKA。UCN-02 具有抗肿瘤活性。

Larazotide is an octapeptide paracellular permeability inhibitor whose structure is derived from a protein (zonula occludens toxin) secreted by Vibrio cholerae for treatment of Coeliac disease.

PF-04577806 is a potent, selective, and ATP competitive inhibitor of the protein kinase C (PKC). It exhibits significant inhibitory activity against various isoforms of PKC, including PKCα, PKCβI, PKCβII, PKCγ, and PKCθ, with IC50 values of 2.4 nM, 8.1 nM, 6.9 nM, 45.9 nM, and 29.5 nM, respectively. Furthermore, PF-04577806 has the ability to reverse retinal vascular leakage in diabetic rats.