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| 目录号 | 产品名称 | 产品描述 |
| R10555 | PF-06687859; RG-3039 | RG3039 (PF-06687859) 是具有口服活性，可渗透大脑的 DcpS 抑制剂， IC50 值为 0.069 nM。 |
| R10586 | Tiplaxtinin;PAI-039 | Tiplaxtinin(PAI-039) is an orally efficacious and selective plasminogen activato |
| R10594 | CID2011756 | CID-2011756 is a cell-active ATP competitive and specific PKD1 inhibitor that in |
| R10600 | Ampalex; CX-516 | Ampalex (Ampakine CX516; CX516; BDP 12) is an ampakine and nootropic that acts a |
| R10611 | PD169316 | PD 169316 是一种高效，细胞透过的，有选择性的 p38 MAP kinase 抑制剂，IC50 值为 89 nM。PD169316 选择性地抑制磷酸化 |
| R10612 | RKI-1313 | |
| R10613 | 1246535-95-4 | |
| R10614 | HPGDS inhibitor 1 | HPGDS inhibitor 1 is a novel and selective Hematopoietic Prostaglandin D Synthas |
| R10619 | AT-56 | AT-56 is am orally active inhibitor of lipocalin-type prostaglandin D synthase ( |
| R10620 | ML161 | ML-161 is an allosteric inhibitor of PAR1 with IC50 of 0.26 μM. |
| R10623 | Etofenamate | Etofenamate is an anti-inflammatory, anti-arrhythmic amino acid. |
| R10625 | NSI-189 | NSI-189 is a nootropic and neurogenic research chemical derived from nicotinamid |
| R10627 | ICILIN | Icilin is a cooling agent that activates the novel cold receptors TRPM8 (CMR1) a |
| R10630 | Siramesine Hydrochloride | Siramesine Hydrochloride is a selective sigma-2 receptor agonist, which has been |
| R10631 | SiramesineLu-28-179 | Anti-cancer agent siramesine is a lysosomotropic detergent that induces cytoprot |
| R10634 | Betrixaban | Betrixaban 是一种口服有效的选择性 factor Xa (fXa) 抑制剂，IC50 为 1.5 nM。 |
| R10637 | Methylisoindigotin | Meisoindigo, a derivative of Indigo naturalis, is a promising agent with in vitr |
| R10643 | VGX-1027 | VGX-1027 is an orally active immunomodulator. Phase 1. |
| R10644 | Y320 | Y-320是免疫调节剂，能抑制IL-15刺激CD4 T细胞后的IL-17生成，IC50为20到60 nM。 |
| R10645 | Atglistatin | Atglistatin 是一种选择性的脂肪甘油三酯脂酶 (ATGL) 抑制剂，体外抑制脂解作用，IC50 为 0.7 μM。 |
| R10646 | Ametantrone ;NSC196473 | Ametantrone (AM) is a synthetic 9,10-anthracenedione bearing two (hydroxyethylam |
| R10649 | P7C3 | P7C3 is a potent proneurogenic and neuroprotective chemical that targets NAMPT e |
| R10656 | CP-640186;CP640186 | CP-640186 是一种有效且可透过细胞的 乙酰辅酶A羧化酶 (ACC) 抑制剂，抑制大鼠肝脏 ACC1 和大鼠骨骼肌 ACC2 的 IC50为 53 nM |
| R10657 | CID797718 | |
| R10662 | TTP22 | TTP 22 is a high affinity, casein kinase 2 (CK2) inhibitor (IC50= 0.1uM, Ki= 40n |
