Epothilone B是微管稳定剂，Ki 为0.71 μM。 它通过与αβ-微管蛋白异二聚体亚基结合而起作用，导致αβ-微管蛋白解离的减少。

Adenosine Amine Congener is shown to be an aqueous-soluble Adenosine A1-R agonist.

AB928 is an orally bioavailable, selective dual adenosine receptor (A2aR/A2bR) antagonist with immunomodulatory activity.

AM-92016 hydrochloride 是整流钾电流 (IK) 的特异性阻断剂。 AM-92016 hydrochloride 延迟整流钾通道，使膜复极化，从而限制神经冲动的持续时间。

c-di-AMP (Cyclic diadenylate) 是 STING 激动剂，其与 STING 结合，从而激活 TBK3-IRF3 信号传导途径，随后引发 I 型 IFN 和 TNF 产生。c-di-AMP (Cyclic diadenylate) 是一种细菌第二信使，主要在革兰氏阳性细菌中，可调节细胞生长，存活以及毒力。c-di-AMP (Cyclic diadenylate) 也调节宿主免疫反应。c-di-AMP (Cyclic diadenylate) 可作为一种有效的粘膜佐剂，刺激体液和细胞

Cyclic-di-GMP 是 STING 的激动剂也是一个可以调节不同细菌物种的生物膜形成，运动性和毒力的第二信使。

DS-6051b is a potent and selective ROS1 and TRK family inhibitor with IC50 of 0.207 nM, 0.622 nM and 0.980 nM against ROS1, NTRK1 and NTRK3. DS-6051b especially inhibits ROS1 G2032R and other crizotinib-resistant ROS1 mutants.

EMI1 (EGFR MaMTH Inhibitor 1) is a novel EGFR ex19del/T790M/C797S inhibitor.

Enpp-1-IN-1 是一种有效的选择性 enpp-1 (核苷酸焦磷酸酶-磷酸二酯酶 1) 抑制剂，详细信息请参考专利文献 WO2019046778 中的例 55。

GS-441524 对猫传染性腹膜炎病毒 (FIPV) 有较强的抑制作用，对应的 EC50 值为 0.78 μM。

JA2131 is a selective bioavailable poly(ADP-ribose) glycohydrolase (RARG) inhibitor with IC50 of 0.4 μM.

MS1943 是一种一流的，具有口服生物活性的 EZH2 选择性降解剂，其IC50 为 120 nM。MS1943 显著降低了许多三阴性乳腺癌和其他癌及非癌细胞系中的EZH2蛋白水平。MS1943 有效地阻止了多个三阴性乳腺癌和其他癌细胞系的增殖。

An inhibitor that is useful for affinity chromatography

TCMDC-135051 是一种高选择性和有效性的蛋白激酶 PfCLK3 抑制剂，具有低的靶外毒性。TCMDC-135051 可以防止滋养体到裂殖体的转变，破坏转录并减少向蚊子载体的传播。TCMDC-135051 具有抗寄生虫活性 (EC50=320 nM)。

The compound (Akt-I-1,2) inhibited both Akt1 and Akt2 with IC50 values of 2.7 and 21 μM respectively.

Telaprevir (VX-950) is an HCV NS3-4A serine protease inhibitor with IC50 of 0.35 μM.

Nelfinavir(AG-1341) is a potent and orally bioavailable human immunodeficiency virus HIV-1 protease inhibitor (Ki=2 nM) and is widely prescribed in combination with HIV reverse transcriptase inhibitors for the treatment of HIV infection.

Sitravatinib (MGCD516) is a novel small molecule inhibitor targeting multiple RTKs involved in driving sarcoma cell growth, including c-Kit, PDGFRβ, PDGFRα, c-Met, and Axl.

ATH686 (ATH-686) is a potent and selective, second-generation inhibitor of mutant FLT3 protein kinase.

Danicopan (ACH-4471,) is a highly potent, orally active Factor D inhibitor with Kd of 0.54 nM.

Tavapadon is a potent, orally-bioavailable, selective partial agonist of the dopamine D1 and D5 receptors.

Hoechst染料是DNA蓝色荧光染料，Hoechst 33342是其中一种。