(±)-N-3-Benzylnirvanol是 (+) 和 (-) N-3-Benzylnirvanol 的外消旋混合物，显示出选择性 CYP2C19 抑制活性，适用于药物代谢和药物相互作用的研究。

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

Hypericin, a natural product isolated and purified from the herb of Hypericum perforatum L., is a photosensitive antiviral with anticancer and antidepressant agent derived from Hypericum perforatum.

Liarozole (R75251; R85246)是一种咪唑衍生物，作为口服有效的维甲酸 (RA) 代谢阻断剂 (RAMBA)，它抑制维甲酸依赖的细胞色素P450 (CYP26) 4-羟基化，IC50为7 μM，从而增加组织维甲酸水平，并具有抗肿瘤特性。

8-Geranyloxypsoralen, a natural product isolated and purified from the herbs of Seseli mairei Wolff., inhibits β-secretase (BACE1) activity in non-competitive manner, with the IC(50) values < 25.0 uM. 8-Geranyloxypsoralen possesses nematicidal activities, the median lethal concentrations (LC(50)) is 188.3 mg/ L against B. xylophilus and is 117.5 mg/L against P. redivivus.

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.

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

(+)-Cedrol是一种倍半萜，存在于雪松精油中，具有抗炎、抗痉挛和抗真菌活性。它还能抑制细胞色素P-450酶的活性，主要抑制 CYP2B6 和 CYP3A4，对 CYP2C8、CYP2C9 和 CYP2C19 的抑制作用较弱。对药物代谢有显著影响。

N-Desmethyl-Apalutamide是 Apalutamide 的活性代谢产物，作用力约为原药物的三分之一。它由 CYP2C8 和 CYP3A4 介导形成，具有中等至强的 CYP3A4 和 CYP2B6 诱导作用，且与血浆蛋白结合能力较强，适用于雄激素受体抑制剂代谢和药物相互作用的研究。

Nampt-IN-5是一种有效的烟酰胺磷酸核糖基转移酶 (NAMPT) 抑制剂，也能抑制 CYP3A4 活性。Nampt-IN-5 可抑制 A2780 和 COR-L23 细胞，IC50 值分别为 0.7 nM 和 3.9 nM。

Acetyl shikonin, a natural product isolated and purified from the roots of Lithosperraum erythrorhizon Sieb. et Zucc., inhibits the generation of NADPH oxidase complex in the activation of respiratory burst of PMNs, but does not directly inhibit the activity of NADPH oxidase already generated, and is a non-selective cytochrome P450 inhibitor.

Schisandrin A is a naturally occuring agonist of the adiponectin receptor 2 with an IC50 value of 3.5 µM.

Itraconazole-d3是 Itraconazole 的氘代物，常用于分析 itraconazole 在体内代谢的药物动力学研究，有助于理解其在治疗真菌感染中的药物代谢途径。

Rhapontigenin, a natural product isolated and purified from the rhizomes of Rheum undulatum with antioxidative, antihyperlipidemic, and antifungal activities, inhibits tyrosinase activity and melanin synthesis in B16F10 melanoma cells and HIF-1α accumulation and angiogenesis in PC-3 prostate cancer cells, suppresses breast cancer cell migration and invasion, which is involved in inhibiting the PI3K-dependent Rac1 signaling pathway.

Mephenytoin是一种抗惊厥药物，作为 CYP2C19 和 CYP2B6 的底物，在药物代谢研究中具有重要价值，适用于药物代谢和个体化治疗的研究。

Desmethylcitalopram hydrochloride是 Citalopram 的活性代谢物，具有抗抑郁作用，并能抑制细胞色素 P450-2D6 和 -2C19，其 IC50 值分别为 39.5 和 53.5 μM。

TP0472993是一种口服有效的细胞色素 P450 (CYP) 4A11 和 CYP4F2 的双抑制剂，IC₅₀ 值分别为 140 nM 和 40 nM，适用于肾脏疾病的研究。