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| Cat.No. | Product name | Product Description |
| 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 |
| R2030184 | NQDI-1 | NQDI 1, an inhibitor of ASK1(apoptosis signal-regulating kinase 1), attenua |
| R2030185 | EMD534085 | EMD534085 is a potent and selective inhibitor of the mitotic kinesin-5 with an I |
| R2030186 | Ly2584702 tosylate | LY-2584702 tosylate salt is a selective ATP competitive inhibitor of p70S6K with |
| R2030187 | SHP099 hydrochloride | SHP099 hydrochloride is a potent, selective and orally available SHP2 inhibitor |
| R2030188 | PIM447 (LGH447) | PIM447 (LGH447) is a potent, orally available, and selective pan-PIM kinase inhi |
| R2030189 | Palonosetron | Palonosetron is a 5-HT3 antagonist used in the prevention and treatment of chemo |
| R2030190 | ASP5878 | ASP5878 is an oral active inhibitor of FGFR 1, 2, 3, and 4, with IC50 values of |
| R2030191 | Allitinib (AST-1306; ALS 1306) | Allitinib (AST-1306) is an orally active and irreversible EGFR and ErbB2 inhibit |
| R2030192 | Methylphenidate hydrochloride | |
| R2030193 | Isofraxidin | sofraxidin, a coumarin component from Acanthopanax senticosus, inhibits MMP-7 ex |
| R2030194 | MLN0905 | MLN0905 is a potent PLK1 inhibitor, with an IC50 of 2 nM. |
| R2030197 | Palonosetron Hydrochloride | Palonosetron Hcl is a 5-HT3 antagonist used in the prevention and treatment of c |
| R2030198 | PIM-447 dihydrochloride (LGH447 dihydrochloride) | PIM447 dihydrochloride (LGH447 dihydrochloride) is a potent, orally available, a |
