FTI-2153 is a potent and highly selective farnesyltransferase (FTase) inhibitor (IC50: 1.4 nM). FTI-2153 is >3000-fold more potent at blocking H-Ras (IC50, 10 nM) than Rap1A processing.

Prenyl-IN-1 是一种具有有效性和选择性的 prenylation 抑制剂，对香叶烯基转移酶 (geranylgeranyltransferase) 或法尼基转移酶 (farnesyltransferase) 具有抑制作用。Prenyl-IN-1 在帕金森模型中显示出抗氧化应激作用。

BMS961 is a potent and selective retinoic acid receptor gamma (RARγ) agonist (IC50: 30 nM).

VU0155069 hydrochloride (CAY10593 hydrochloride) 为一种高效选择性磷脂酶 D (PLD) 抑制剂，对PLD1和PLD2展示出不同的抑制活性，IC50值分别为46 nM和933 nM。此外，VU0155069 hydrochloride 能够抑制人类及小鼠乳腺癌细胞系的迁移。

Entacapone sodium salt inhibits catechol-O-methyltransferase(COMT) with similar IC50 in different tissues including live, duodenum, kidney and lung, but entacapone is more active than tolcapone in those tissues. Entacapone (< 100 μM) is a potent inhibitor of α-syn and β-amyloid (Aβ) oligomerization and fibrillogenesis, and also protects against extracellular toxicity induced by the aggregation of both proteins in PC12 cells.Entacapone sodium salt is a specific, potent, peripherally acting catechol-O-methyltransferase (COMT) inhibitor with IC50 of 151 nM for PD treatment.

Levamisole hydrochloride ((-)-Tetramisole hydrochloride) 是驱虫剂和免疫调节剂。它对HSV 病毒有明显抗病毒作用。

Doxercalciferol (TSA 840) 是一种维生素 D2 类似物，是一种维生素 D 受体激活剂，能够阻碍肾病的进程。

Zaragozic acid A trisodium 是真菌的代谢产物，具有作为角鲨烯合成酶可逆竞争性抑制剂的功能。

G43-C3-TEG为糖基转移酶抑制剂，其作用机制在于降低EPS（细胞外多糖）的生成，进而减少生物膜形成。