or-s1

(R)-OR-S1 is a SAM-competitive, highly selective, orally bioavailable dual inhibitor of EZH1 2.

IMSs inhibitor S12 Perchlorate 有抗纤维化和抗癌作用。

KCC2 potentiators-1 (Compound 2) 是一种氯化钾共转运体-2 (KCC2) 增强剂，具有在神经系统疾病研究中的潜在应用价值。

PDE7 inhibitor S14 is a cell-permeable PDE7 inhibitor that acts by targeting the cyclic adenosine monophosphate (cAMP) cAMP-response element-binding protein (CREB) pathway.

NLRP3 modulators 1 (WO2017184746A1, compound 107) is a potent modulator of NLRP3, capable of agonizing or partially agonizing the activity of NLRP3. This compound proves valuable in investigating conditions, diseases, or disorders where a reduction in LRP3 activity plays a role in the pathology.

Protein Kinase Inhibitors 1 Hydrochloride effectively inhibits HIPK2, demonstrating high potency with IC50 values of 136 nM for HIPK1 and 74 nM for HIPK2, alongside a dissociation constant (Kd) of 9.5 nM for HIPK2.

Protein kinase inhibitors 1 是新型的 HIPK2 抑制剂，其 IC50=74 nM，Kd=9.5 nM。

Protein kinase inhibitors 1 hydrochlorid (Protein kinase inhibitors 1 hydrochlorid (1365986-44-2(free base))) 是一种新型 HIPK2 抑制剂，IC50 为 74 nM，Kd 为 9.5 nM。

BPH-1086 (compound 10) 是一种IspH 抑制剂。IspH 结构域通过与核糖体蛋白 (RPS1) 融合，能够结合 mRNA 或形成细菌核糖体。