SAHO是一种儿茶酚 - O - 甲基转移酶(COMT)抑制剂，其 IC50 数值为 860 μM，可应用于甲基化反应调控剂相关的研究工作。

Lipiferolide is an inhibitor of farnesyl protein transferase(FPTase), it inhibits the FPTase activity in a dose-dependent manner, and shows cell growth inhibitory activity against several tumor cells, it possesses cytotoxic activity against KB cells. Liriodenine also has antiplasmodial activity.

7beta-Methoxyrosmanol inhibited acyl CoA:diacylglycerol acyltransferase (DGAT)1 activity, with the IC50 values ranging from 39.5 ± 0.6 to 144.2 ± 3.1 μM.

PG 34 是 OSMI-1 的结构类似物，也是 O-GlcNAc 转移酶 (OGT) 的弱抑制剂，其 IC50 值为 68 μM。

Lith-O-Asp是一种竞争性、高选择性的唾液酸转移酶抑制剂 (ST3Gal III/I Ki = 1.3 μM)。它通过降低细胞表面唾液酰化水平抑制肿瘤细胞的粘附、迁移和侵袭，用于癌症转移机制研究。

FTI 276 TFA is effective against plasmodium falciparum and humans.It is a protein-based nikyltransferase (PFT) inhibitor with an IC50s of 0.9 nM and 0.5 nM, respectively.

alpha-2,6-Sialyltransferase (Pd26ST) 能够催化末端和内部半乳糖及N-乙酰半乳糖胺的唾液酸化，形成末端α2,6-唾液酸苷。

Ibiglustat (Venglustat) succinate is an orally active, brain-penetrant inhibitor of glucosylceramide synthase (GCS). It is utilized in the investigation of Gaucher disease type 3, Parkinson's disease associated with GBA mutations, Fabry disease, GM2 gangliosidosis, and autosomal dominant polycystic kidney disease.

Transketolase-IN-4 是一种转酮酶抑制剂 ，IC50值为3.9 μM。Transketolase-IN-4 对结核分枝杆菌 DXS 有抑制作用，IC50 为 114.1 μM。 Transketolase-IN-4 抑制 SW620、LS174T 和 MIA PaCa-2 的肿瘤细胞增殖。