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。

Transketolase-IN-2（化合物4w）是一种强效的Transketolase抑制剂，对Digitaria sanguinalis和Amaranthus retroflexus展现出显著的抑制效果（200 mg/L浓度下抑制率超过90%，100 mg/L浓度下抑制率约为80%）。该化合物适用于研究杂草防治。

N3PT is a potent and selective inhibitor of transketolase(TK) with IC50 of 22 nM for Apo-TK)

Transketolase-IN-3为有效的转酮酶(TK)抑制剂，展现出杰出的除草活性，并对血红木(DS)及苋菜(AR)显示出抑制效果，适用于研究除草剂。

Oxythiamine diphosphate is a competitivethiamine pyrophosphate inhibitor(Ki of 30 nM).