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Home > Products
| Cat.No. | Product name | Product Description |
| R2030153 | Pifithrin-β (hydrobromide) | Pifithrin-β hydrobromide (PFT β hydrobromide) is a potent p53 inhibitor with an |
| R2030154 | YL0919 hydrochloride;YL-0919hydrochloride | YL0919, a novel antidepressant candidate with dual activity as a 5-HT1A receptor |
| R2030155 | YM-58483(BTP2) | YM-58483 is the first selective and potent inhibitor of CRAC channels and subseq |
| R2030156 | KRIBB11 | KRIBB11 is an inhibitor of Heat shock factor 1 (HSF1), with IC50 of 1.2 μM. |
| R2030157 | MX-69 | MX69 is an inhibitor of MDM2/XIAP, used for cancer treatment. |
| R2030158 | 10074-G5 | 10074-G5 is an inhibitor of c-Myc-Max dimerization with an IC50 of 146 μM. |
| R2030159 | BIA 10-2474 | BIA 10-2474 is an inhibitor of fatty acid amide hydrolase (FAAH) with IC50 value |
| R2030160 | S107 | S107 is an orally available, blood brain barrier-permeable compound, which stabi |
| R2030161 | S49076 hydrochloride;S-49076 hydrochloride | S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 val |
| R2030162 | Thiomyristoyl | Thiomyristoyl is a potent and specific SIRT2 inhibitor with an IC50 of 28 nM. |
| R2030163 | UK-371804 | UK-371804 is a urokinase-type plasminogen activator (uPA) inhibitor with a Ki of |
| R2030164 | LW6 (HIF-1α inhibitor; LW8) | LW6 (HIF-1α inhibitor) is a novel HIF-1 inhibitor with an IC50 of 4.4 μM. LW6 de |
| R2030165 | FIN56 | FIN56 is a specific inducer of ferroptosis. |
| R2030167 | Bay 41-4109 racemate | BAY 41-4109 racemate is the racemate of BAY 41-4109. BAY 41-4109 is a potent inh |
| R2030169 | GJ103 | GJ103 is an active analog of the read-through compound GJ072. |
| R2030170 | ISCK03 | ISCK03 is a specific SCF/c-Kit inhibitor. |
| R2030171 | HSP70-IN-1 | HSP70-IN-1 is a heat shock protein (HSP) inhibitor; inhibits the growth of Kasum |
| R2030172 | PD-166866；PD166866 | PD166866 is a selective FGFR1 tyrosine kinase inhibitor with an IC50 of 52.4 nM. |
| R2030173 | GW506033X;PKR-IN-C16 | PKR-IN-C16 is a specific protein kinase (PKR) inhibitor. PKR-IN-C16 is able to i |
| R2030174 | s49076 | S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 val |
| R2030176 | Nodinitib-1 (ML130; CID-1088438) | Nodinitib-1 (ML130;CID-1088438) is a NOD1 inhibitor with an IC50 of 0.56 μM.&nbs |
| R2030178 | Sugammadex | Sugammadex sodium is a synthetic γ-cyclodextrin derivative, and acts as a new re |
| R2030179 | XL019 | XL019 is a potent，orally active, and selective JAK2 inhibitor, with IC50s o |
| R2030182 | Amuvatinib (MP470; HPK 56) | Amuvatinib (MP470) is an orally bioavailable multi-targeted tyrosine kinase inhi |
| R2030183 | PHT 427 | PHT-247 is an inhibitor of the pleckstrin homology (PH) domain of Akt, and it is |
