Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 2091204 | 5-hydroxy-2,4-dimethylpyrimidine | 412003-95-3 | ≧96.0% |  |
| 2,4-dimethylpyrimidin-5-ol is a key intermidiate ofLemborexant. Kg scale may be provi | ||||
| 24101 | Crelosidenib | 2230263-60-0 | ≧98.0% |  |
| Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor. | ||||
| 25076 | HC-7366 | 2803470-63-3 | ≧98.0% |  |
| HC-7366 is a potent and selective activator of the general control nonderepressible 2 | ||||
| 41788 | CB-6644 | 2316817-88-4 | 96.33% |  |
| CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL | ||||
| 21075 | 1-cyanocyclohexyl 4-methylbenzenesulfonate | 90775-01-2 | ≧98.0% |  |
| 1-cyanocyclohexyl 4-methylbenzenesulfonate (CAS 90775-01-2 ) is an important building | ||||
| 25079 | Sevabertinib ( BAY-2927088 ) | 2521285-05-0 | ≧98.0% |  |
| Sevabertinib ( BAY-2927088 ) is a oral, non-covalent, tyrosine kinase receptor inhibi | ||||
| 171653 | 4-Bromo-6-methylpyridine-2-carbonitrile | 886372-53-8 | ≧95.0% |  |
| 4-Bromo-6-methylpyridine-2-carbonitrile, CAS 886372-53-8 | ||||
| 20633 | STX-478 | 2883540-92-7 | ≧98.0% |  |
| STX-478 is a second generation, mutant-selective, oral PI3Ka small molecule allosteri | ||||
| 25148 | Atebimetinib | 2669009-92-9 | ≧98.0% |  |
| Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1 | ||||
| 21253 | indole-4-boronic acid pinacol ester | 388116-27-6 | ≧95.0% |  |
| indole-4-boronic acid pinacol ester, CAS 388116-27-6, is an important intermeidate. | ||||
| 24084 | Iclepertin (BI-425809) | 1421936-85-7 | ≧98.0% | _1421936-85-7.png) |
| Iclepertin (BI-425809) is an oral, small-molecule inhibitor of GlyT-1for the treatmen | ||||
| 25075 | LLL12 | 1260247-42-4 | ≧97.0% |  |
| LLL12 is a potent STAT3 inhibitor. | ||||