Floramanoside D 是一种黄酮醇糖苷，其可抑制醛糖还原酶 (IC50为 2.2 μM)，并清除 2,2-二苯基-1-苦基肼 (2,2-diphenyl-1-picrylhydrazyl, DPPH) (SC50为 12.5 μM)。

Rhetsinine 是一种在 Evodia rutaecarpa 中发现的醛糖还原酶 (aldose reductase) 抑制剂，IC50 为 24.1 μM。在 100 μM 浓度下，Rhetsinine 显著抑制山梨醇积累，抑制率达 79.3%。Rhetsinine 可用于研究糖尿病并发症，如糖尿病神经病变和视网膜病变。

MK-386 is a potent and selective inhibitor of human type-1 5alpha-reductase.

Isobutyl-deoxynyboquinone (IB-DNQ) is a selective substrate for NAD(P)H: quinone oxidoreductase (NQO1) and is utilized in anticancer research.

Hydroxyevodiamine is a natural product

Danshenol A has strong aldose reductase (AR) inhibitory activity, has IC50 of 0.10 microM which is comparable to that of epalrestat in clinical use. Danshenol A also has antitumor activity in T-24, QGY, K562, Me180 and BIU87 cell lines, shows inhibited growth of K562 (IC50 = 0.53 μg/mL), T-24 (IC50 = 7.94 μg/mL), QGY (IC50 = 4.65 μg/mL) and Me180 (IC50 = 6.89 μg/mL) cell lines.

Tanshindiol B possesses a unique anti-cancer activity whose mechanism involves the inhibition of EZH2 activity and would provide chemically valuable information for designing a new class of potent EZH2 inhibitors. It also possesses the anti-angiogenic act

17alpha-Estradiol-2,4-d2 是 17alpha-Estradiol 的氘代化合物。17alpha-Estradiol 的 CAS 号为 57-91-0。17α-Estradiol 是一种雌性激素，可抑制5α-reductase，在雄原性脱发的研究中有潜力。

8-Lavandulylkaempferol exhibits significant inhibitory effects with IC(50) values of 7.10 and 8.11 microM for butyrylcholinesterase and acetylcholinesterase, respectively. It shows inhibitory activities against aldose reductase, with the the IC50 of 0.79 microM.