TCS 21311 (NIBR3049) 是一种高选择性JAK3抑制剂，IC50为 8 nM，它的选择性是 JAK1、JAK2 和 TYK2 的100倍以上，还抑制PKCα、PKCθ和GSK3β，IC50值分别为 13、68 和 3 nM。

NAMI-A 是一种钌基化合物，具有抗肿瘤转移的选择性活性。NAMI-A 可抑制癌细胞粘附和迁移。

Meclofenamic acid sodium (Movens) 是一种非甾体抗炎药，可用于治疗关节炎 、缓解疼痛、痛经和严重月经失血。它是一种非选择性的缝隙连接阻断剂，是一种高选择性的脂肪和肥胖相关酶抑制剂。

N6-Cyclohexyladenosine (CHA) 是一种选择性腺苷 A1 受体激动剂，EC50 为 8.2 nM。

Gap19 是一种衍生自 Cx43 细胞质环九个氨基酸的肽，是选择性连接蛋白 43 半通道阻滞剂。它可以防止 C 末端与 CL 的分子内相互作用，具有保护心肌作用。

Bryostatin 3 is a protein kinase C activator.

3'-Demethylnobiletin 是样一种存在于柑橘类水果中的多甲氧基黄酮类化合物，是一种 Nobiletin 的衍生物。N 其中 obiletin 能够调节 Src，FAK 和 STAT3 信号传导来抗肿瘤，并能够抑制肿瘤血管生成。

Bisindolylmaleimide VIII acetate (Ro 31-7549 acetate) 是一种选择性蛋白激酶 C 抑制剂。它促进 Fas 介导的细胞凋亡，并抑制 T 细胞介导的自身免疫性疾病。

para-amino-Blebbistatin is a more water-soluble form of (S)-4'-nitro-blebbistatin , which is a more stable and less phototoxic form of (-)-blebbistatin .1,2,3 (-)-Blebbistatin is a selective cell-permeable inhibitor of non-muscle myosin II ATPases that rapidly and reversibly inhibits Mg-ATPase activity and in vitro motility of non-muscle myosin IIA and IIB for several species (IC50s = 0.5-5 μM), while poorly inhibiting smooth muscle myosin (IC50 = 80 μM).2,3,4 Through these effects, it blocks apoptosis-related bleb formation, directed cell migration, and cytokinesis in vertebrate cells. However, prolonged exposure to blue light (450-490 nm) results in degradation of blebbistatin to an inactive product via cytotoxic intermediates, which may be problematic for its use in fluorescent live cell imaging applications.5,6 The addition of a 4'-amino group increases its water solubility, decreases the inherent fluorescence, stabilizes the molecule to circumvent its degradation by prolonged blue