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Home > Products
| Cat.No. | Product name | Product Description |
| R10763 | Kevetrin hydrochloride; NSC525990 | Kevetrin hydrochloride is a small molecule and activator of the tumor suppressor |
| 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 |
| R10770 | 1016535-83-3 | |
| R10771 | O4I1 | O4I1 is as a potent Oct3/4 inducer.Target: Oct3/4 |
| R10773 | 220904-99-4 | |
| R10774 | TG6-10-1 | TG6-10-1 is an EP2 antagonist, shows low-nanomolar antagonist activity against o |
| R10775 | B7/CD28 interaction inhibitor 1 | B7/CD28 interaction inhibitor 1 (copmound 6b) is a potent B7.1-CD28 interaction |
| R10776 | 4-Keto13-cis-Retinoic Acid | CAS NO.：71748-57-7Product Name：4-Keto 13-cis-Retinoic Acid Methyl EsterSynonyms： |
| R10778 | Pimelic diphenylamide 106; TC-H106 | Pimelic diphenylamide 106 is a slow, tight-binding inhibitor of class I HDAC (HD |
| R10779 | UF010 | UF010 is a potent and selective HADC inhibitor with IC50 ~0.06 μM, 0.1 μM, 0.5 μ |
| R10780 | KC7F2 | KC7F2 is a potent HIF-1 pathway inhibitor and that its potential as a cancer the |
| R10781 | WDR50103 | WDR5-0103 is a potent and selective WD repeat-containing protein 5 (WDR5) antago |
| R10782 | EXP-3174 | Losartan Carboxylic Acid (E-3174), an active carboxylic acid metabolite of Losar |
| R10783 | vorapaxar intermediate 1 | |
| R10784 | vorapaxar intermediate 2 | |
| R10785 | Savolitinib (Volitinib; HMPL-504; AZD-6094) | Savolitinib(Volitinib; AZD-6094; Volitinib) is an orally bioavailable inhibitor |
| 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. |
