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| 目录号 | 产品名称 | 产品描述 |
| R10736 | OAC-1 | OAC1是转录因子Oct4活化剂，提高iPSC的重编程效率和编程过程中的加速。 |
| R10737 | OAC2 | OAC2是Oct4激活化合物，其通过Oct4基因启动子激活表达。 |
| R10740 | Dihydroethidium | Dihydroethidium(Hydroethidine; PD-MY 003) is a superoxide indicator; exhibits bl |
| R10741 | Apilimod;STA5326 | Apilimod(STA 5326) is a potent IL-12/IL-23 inhibitor, IL-12 production in cultur |
| R10742 | Apilimod mesylate (STA 5326 mesylate) | Apilimod(STA 5326)甲磺酸盐是IL-12/IL-23抑制剂，能抑制IFN-γ/LPS刺激的人PBMC产生IL-12，IC50为10 nM。 |
| R10748 | C7280948 | C7280948 is an inhibitor of histone arginine methyltransferase PRMT1 with IC50 v |
| R10756 | trans-Tranilast | Tranilast (trans-) 是一种抗过敏药物, 用于治疗支气管哮喘, 过敏性鼻炎和特应性皮炎。 |
| R10757 | Bimiralisib (Synonyms: PQR309) | Bimiralisib (PQR309) 是一种有效的，可渗透脑的，PI3K/mTOR 抑制剂，抑制 PI3Kα, PI3Kδ, PI3Kβ, PI3Kγ 和 |
| R10758 | Tizoxanide | Tizoxanide is the active metabolite of Nitazoxanide, which is a thiazolide anti- |
| R10760 | BQU57 | BQU57选择性抑制Ral,选择性比Ras或Rho高, BQU57对H2122 和H358细胞的IC50值分别为 2.0 μM 和1.3 μM。 |
| 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 |
| 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 |
| R10789 | CPI-203 | CPI203 is a novel potent, selective and cell permeable inhibitor of the bromodom |
| R10808 | PTZ-343; phenothiazine sodium salt | PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi |
| R10809 | Golotimod; SCV 07 | Golotimod is an orally bioavailable synthetic peptide containing the amino acids |
| R10810 | Uramustine | Uramustine is a chemotherapy drug which belongs to the class of alkylating agent |
| R10822 | PTZ-343 | PTZ-343 is a phenothiazine derivative with chemical name: sodium 3-(10H-phenothi |
| R10833 | Lesinurad;RDEA594 | Lesinurad 是一种 URAT1 和 OAT 抑制剂，用作肾转运蛋白OAT1 和OAT3 的底物，Km值分别为 0.85 和 2 μM。 |
| R10836 | MS417 | |
| R10265 | ID8;ID-8 | ID-8是DYRK抑制剂，长时间培养可维持胚胎干细胞的自我更新。 |
| R10161 | GW4064 | GW 4064 是一种有效的 FXR 激动剂，EC50 为 65 nM。 |
| R10263 | Fexaramine | Fexaramine is a small molecule farnesoid X receptor (FXR) agonist with 100-fold |
| R10546 | Obeticholic acid; INT747 | Obeticholic acid (INT-747) 是口服有效的，选择性的法尼醇 X 受体 (FXR) 激动剂， EC50 值为 99 nM。 |
| R10169 | CP91149 | CP-91149 is a selective glycogen phosphorylase (GP) inhibitor with IC50 of 0.13 |
