icotinib

Icotinib (Conmana) 是一种口服的基于喹唑啉的表皮生长因子受体 (EGFR) 抑制剂，IC50值为5 nM，具有潜在的抗肿瘤活性。

Icotinib Hydrochloride (BPI-2009H) 是一种口服的基于喹唑啉的表皮生长因子受体 (EGFR) 抑制剂，IC50值为5 nM，具有潜在的抗肿瘤活性。

Icotinib-d4 是 Icotinib 的氘代化合物。

Edicotinib (JNJ-527) 是能够透过血脑屏障的、口服具有活性的、选择性的CSF-1R 抑制剂 (IC50值为3.2 nM)，对 KIT (IC50值为20 nM) 和 FLT3 (IC50值为190 nM) 的抑制作用较小。Edicotinib (JNJ-527) 能够阻断小胶质细胞的增殖并减弱神经退行性变，可用于研究阿尔茨海默病和类风湿性关节炎。

Pimicotinib hydrochloride 是一种CSF1R抑制剂，具有抗肿瘤活性。

Edicotinib, also known as JNJ-40346527, is a small molecule and orally available inhibitor of colony-stimulating factor-1 receptor (CSF1R; FMS) with potential antineoplastic activity. FMS tyrosine kinase inhibitor JNJ-40346527 blocks the receptor-ligand interaction between FMS and its ligand CSF1, thereby preventing autophosphorylation of FMS. As a result, unphosphorylated FMS cannot activate FMS-mediated signaling pathways, thus potentially inhibiting cell proliferation in FMS-overexpressed tumor cells.

Pimicotinib (ABSK021) 为一种有效的 CSF1R 抑制剂，具抗肿瘤活性，可用于研究晚期实体瘤。

R 93274 is a radioiodinated 5-HT2A receptor antagonist.