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| 目录号 | 产品名称 | 产品描述 |
| R10764 | BMH-21 | BMH-21 is a DNA intercalator, which binds ribosomal DNA and inhibits RNA polymer |
| R10766 | SC-202671 | JNK inhibitor IX is a selective and potent JNK inhibitor with pIC50 of 6.5 and 6 |
| R10767 | MPEP hydrochloride | MPEP is a potent, highly selective non-competitive antagonist at the mGlu5a rece |
| R10768 | KU-60019 | KU-60019 is an improved analogue of KU-55933, with IC50 of 6.3 nM for ATM in cel |
| R10769 | O4I2 | O4I2 is a potent Oct3/4 inducer in various human cell lines including human fibr |
| R10771 | O4I1 | O4I1 is as a potent Oct3/4 inducer.Target: Oct3/4 |
| R10774 | TG6-10-1 | TG6-10-1 是一种 EP2 拮抗剂, 低纳摩尔下有效作用于 EP2, 比作用于人 EP3, EP4 和 IP 受体选择性高 300, EP1 受体选择性高 |
| R10775 | B7/CD28 interaction inhibitor 1 | B7/CD28 interaction inhibitor 1 (copmound 6b) 是一种有效的 B7.1-CD28 相互作用抑制剂，IC50 为 50 |
| R10776 | 4-Keto13-cis-Retinoic Acid | |
| R10778 | Pimelic diphenylamide 106; TC-H106 | Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I HDAC (HD |
| R10779 | UF010 | UF010是一种有效的选择性HADC抑制剂, 作用于HDACs 3, 2, 1 和 8, IC50值分别为 0.06μM, 0.1μM, 0.5μM, 和1.5 |
| R10780 | KC7F2 | KC7F2 是一种有效的缺氧诱导因子 HIF-1 通道抑制剂，在 LN229-HRE-AP 细胞中 IC50 值为 20 μM，可用作癌症治疗剂。 |
| R10781 | WDR50103 | WDR5-0103 is a potent and selective WD repeat-containing protein 5 (WDR5) antago |
| R10782 | Losartan Carboxylic Acid (E-3174) | Losartan Carboxylic Acid (E-3174) 是 Losartan 的活性羧酸代谢产物，是血管紧张素 Ⅱ 受体 1 型 (AT1 |
| R10783 | vorapaxar intermediate 1 | |
| R10784 | vorapaxar intermediate 2 | |
| R10785 | Savolitinib (Volitinib; HMPL-504; AZD-6094) | volitinib (AZD-6094) 是一种高效选择性、口服生物利用度 c-Met 抑制剂，对 c-Met 和 p-Met 的 IC50 分别为 5 nM |
| R10786 | FMK | FMK is a RSK2 kinase inhibitor. |
| R10789 | CPI-203 | CPI203 is a novel potent, selective and cell permeable inhibitor of the bromodom |
| R10790 | 2-(2,6-dimethylphenylamino)-N- (7-(hydroxyamino)-7-oxoheptyl)pyrimidine-5-carboxamide | |
| R10793 | (-)-JQ1 | The bromodomain and extra terminal domain (BET) family of proteins, including BR |
| R10794 | Capadenoson; BAY 68-4986 | Capadenoson (BAY 68-4986) is a new adenosine A1 receptor agonist. |
| R10797 | CWHM-12 | CWHM-12是αV整联蛋白的有效抑制剂，抑制αvβ8，αvβ3，αvβ6和αvβ1的 IC50 值分别为0.2，0.8，1.5，1.8 nM。 |
| R10799 | LCL161 Enantiomer | LCL161 is an orally bioavailable second mitochondrial-derived activator of caspa |
| R10801 | Deltarasin | Deltarasin is a small molecular inhibitor of KRAS-PDEδ interaction with Kd of 38 |
