(±)10(11)-DiHDPA is produced from cytochrome P450 epoxygenase action on docosahexaenoic acid . It has been shown to inhibit VEGF-induced angiogenesis in mice and may have additional anti-inflammatory and anti-tumor effects.

Reduced haloperidol is an active metabolite of haloperidol . It is formed via reduction of haloperidol by ketone reductase. Reduced haloperidol inhibits radioligand binding to sigma-1 and dopamine D2 receptors (Kis = 1.4 and 31 nM, respectively) and stimulates brain-derived neurotrophic factor (BDNF) secretion from CCF-SSTG1 and U87MG astrocytic glial cells. It also inhibits norepinephrine, dopamine, and serotonin (5-HT) reuptake (Kis = 21, 25, and 33 μM, respectively, in COS-7 cells expressing the human transporters). Reduced haloperidol (0.5 mg/kg) increases latency to paw withdrawal in mouse models of capsaicin- but not force-induced mechanical hypersensitivity.

(Rac)-3′-Hydroxy simvastatin 是一种 Simvastatin 代谢物。Simvastatin 是一种竞争性的 HMG-CoA 还原酶抑制剂，Ki 值为 0.2 nM。

Quetiapine sulfoxide dihydrochloride is a main Quetiapinem metabolite. Quetiapine is a agonist of 5-HT receptors and a antagonist of dopamine receptor.Quetiapine is a second-generation antipsychotic.

Mono(5-carboxy-2-ethylpentyl) phthalate (MECPP)是Di-(2-ethylhexyl) phthalate (DEHP)的一种代谢产物，后者为硬质聚氯乙烯(PVC)中添加的主要增塑剂，以提升其柔韧性、耐温性、光学透明性、强度和抗扭结性。

Venetoclax N-oxide 是 Venetoclax 的杂质。Venetoclax (ABT-199; GDC-0199) 是一种高效，选择性的和口服有效的Bcl-2抑制剂，Ki 小于0.01 nM。