Opevesostat是一种胆固醇侧链裂解酶（CYP11A1）的抑制剂。

Polygalaxanthone III抑制CYP450酶，并抑制CYP2E1催化的chlorzoxazone 6-羟基化，其IC50为50.56μM。

Bergaptol 是一种抑制 CYP3A4 酶去甲基化活性的抑制剂，IC50 为 24.92 μM。最近的研究表明其具有抗增殖和抗癌特性。

Oteseconazole (VT-1161) 是一种有效的口服抗真菌药物。它强力结合并抑制白色念珠菌的细胞色素 P45051 (CYP51) 活性，其 Kd 值小于 39 nM，而不影响人类 CYP51。

Itraconazole (R51211) 是一种三唑类抗真菌剂和强效、口服活性的 Hedgehog (Hh) 信号通路拮抗剂，IC50 约为 800 nM。Itraconazole 强效抑制羊毛甾醇 14α-脱甲基酶（细胞色素 P450 酶），从而阻止羊毛甾醇向麦角甾醇的氧化转化。Itraconazole 具有抗癌和抗血管生成作用，是一种氧甾醇结合蛋白 (OSBP) 抑制剂。

ε-Viniferin (epsilon-Viniferin) 可从葡萄属 (Vitis vinifera) 中提取，是白藜芦醇（Resveratrol ）的二聚体，有效抑制 CYP 家族，Ki 值介于 0.5-20 μM。ε-Viniferin具有强大的抗氧化、抗炎、抗糖尿病和抗神经退行性疾病活性。

Cobicistat是一种有效的选择性CYP3A抑制剂，IC50为30-285 nM。

Dihydromethysticin 是来自卡瓦（kava）的一种卡瓦内酯，诱导CYP3A23活性。

1-Ethynylnaphthalene is a selective inhibitor of cytochrome P450 1B1.

Orteronel is a highly selective inhibitor of human 17,20-lyase with IC50 of 38 nM, and exhibits > 1000-fold selectivity over other CYPs such as 11-hydroxylase and CYP3A4.

Curcumenol inhibits NF-κB activation by suppressing the nuclear translocation of the NF-κB p65 subunit and blocking IκBα phosphorylation and degradation.

Dazoxiben hydrochloride is a potent, orally active thromboxane (TX) synthase inhibitor that reduces the formation of blood clots.

5-Methoxypsoralen, a naturally occurring linear furocoumarin, has been successfully used in combination with ultraviolet (UV) A irradiation [psoralen plus UV (PUVA)] to manage psoriasis and vitiligo and inhibits proliferation in the human hepatocellular carcinoma cell line.

Ramatroban is a thromboxane A(2) (TxA(2)) antagonist marketed for allergic rhinitis.

Benzbromarone is a CYP2C9 inhibitor with Ki of 19.3 nM.

Naringin dihydrochalcone is a sweetening agent and an artificial sweetener derived from naringin and also an inhibitor of CYP enzymes.

Tetrahydropiperine is a cyclohexyl analogue of piperine that inhibits the cytochrome P450 (CYP) isoform CYP1A1/arylhydrocarbon hydroxylase (AHH; IC50=23 µM).