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| 目录号 | 产品名称 | 产品描述 |
| R2101053 | ML298 | ML298 (CID53393915) is a potent, specific inhibitor of Phospholipase D2 (PLD2) w |
| R2101054 | SW155246 | SW155246 is a potent and selective DNMT1 (DNA methyltransferase 1) inhibitor wit |
| R2101055 | ML-299 | ML299 (VU0463568) is a dual inhibitor of PLD1 and PLD2 with IC50 of 6 nM and 20 |
| R2101056 | VUF11418 | VUF11418 is a nonpeptidomimetic agonist of the G protein-coupled chemokine recep |
| R2101057 | CGS-15943 | CGS15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor |
| R2101058 | NSC177223 | API-1 (NSC 177223) is a potent inhibitor of Akt that induces GSK3-dependent, β-T |
| R2101059 | ML162 | 一种小分子探针，选择性杀死诱导表达突变RAS的细胞；抑制BJeLR（表达HRAS G12V）细胞系，IC50为25 nM，显示出比BJeH LT（不含HRAS |
| R2101060 | GSK-843 | GSK-843 是一种受体相互作用蛋白激酶 3 (RIP3 or RIPK3) 抑制剂，高亲和力结合 RIP3 激酶结构域，IC50 值为 8.6 nM，并抑制 |
| R2101061 | Imidazenil | Imidazenil is a GABA-A modulator that blocks the sedative effects without loweri |
| R2101062 | FIT-039 | FIT-039 是一种选择性，ATP 竞争性且具有口服活性的 CDK9 抑制剂，对 CKD9/cyclin T1 的 IC50 为 5.8 μM。FIT-039 |
| R2101063 | SR8278 | SR8278 是一种竞争性核血红素受体 REV-ERB 合成拮抗剂。SR8278 抑制 REV-ERBα 转录活性，EC50 为 0.47 μM。SR8278 |
| R2101064 | VPC23019 | VPC23019，一种含芳基酰胺的鞘氨醇 1-磷酸 (S1P) receptor 调节剂，S1P1 和 S1P3 受体的竞争性拮抗剂 (pKis=7.86 和 |
| R2101065 | HS-1793 | HS-1793 is a stable resveratrol analog that protects cardiac against mitochondri |
| R2101066 | Mycro3 | Mycro 3 是一种有效的选择性 c-Myc 抑制剂。 |
| R2101067 | RBC10 | RBC10 is an inhibitor of Ral binding to RALBP1 (the effector). |
| R2101068 | PD089828 | PD-089828 是 ATP 竞争性 FGFR-1、PDGFR-β 和 EGFR (IC50 分别为 0.15, 1.76, 5.47 µM) 抑制剂和 c- |
| R2101069 | CRANAD-28 | CRANAD-28, a blood brain barrier (BBB) penetrable two-photon imaging probe, acts |
| R2101070 | BPU-11 | BPU-11 is a HCN4 CLP ligand. It acts by modulating channel function and complete |
| R2101071 | CE3F4 | CE3F4 是一种选择性的 Epac1 拮抗剂，对 Epac1 和 Epac2(B) 的 IC50 值分别为 10.7 μM 和 66 μM。 |
| R2101072 | NIBR-0213 | A potent, selective, orally active S1P1 antagonist with IC50 of 2.5 nM Ca2+ mobi |
| R2101073 | BDP5290 | BDP5290 是 ROCK 和 MRCK 的有效抑制剂，对于 ROCK1，ROCK2，MRCKα 和 MRCKβ 的 IC50 值分别为 5 nM，50 nM |
| R2101074 | PH-064 | PH-064 (BIM-46187) 是摘自专利FR 2879460 A1中的钠离子通道抑制剂。 |
| R2101075 | ry785;Kv2-IN-A1 | Kv2-IN-A1 is a Kv2.1 and Kv2.2 inhibitor. |
| R2101076 | DD1 | DD1 is a proteasome inhibitor that induces human myeloid tumor-selective apoptos |
| R2101077 | AEM1 | NRF2抑制剂AEM1是癌细胞中NRF2转录活性的特异性小分子抑制剂，对一组>100种激酶（包括PI3K，AKT和PKC的同种型）没有活性；广泛降低NRF |
