| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 24111 | PLX-4545 | 2892065-45-9 | ≧98.0% | ![]() |
| PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta | ||||
| 25001 | HC-5404 | 2247396-91-2 | ≧98.0% | ![]() |
| HC-5404 is a novel, highly selective and potent PERK inhibitor. | ||||
| 25016 | MD-43 | ≧98.0% | ![]() | |
| MD-43 is a potent and selective degrader of MCT4. | ||||
| 25032 | BMS-466442 | 1598424-76-0 | ≧98.0% | ![]() |
| BMS-466442 is a small molecule inhibitor of asc-1. | ||||
| 25033 | Azeliragon | 603148-36-3 | ≧98.0% | ![]() |
| Azeliragon (TTP488) is an orally bioavailable small molecule inhibitor of the recepto | ||||
| 25052 | Lazertinib mesylate | 2247995-37-3 | ≧98.0% | ![]() |
| Lazertinib is a an orally available third-generation, selective inhibitor of certain | ||||
| 25062 | GP130 modulator-1 | 2375779-31-8 | ≧98.0% | ![]() |
| GP130 modulator-1 (compound A33) is agp130signaling pathway modulator. GP130 modulato | ||||
| 25063 | Seladelpar sodium salt | 3026272-26-1 | ≧98.0% | ![]() |
| Seladelpar is a PPAR-delta agonist. | ||||
| 25065 | Ecopipam ( SCH 39166 ) | 112108-01-7 | ≧98.0% | ![]() |
| Ecopipam ( SCH 39166 ) is a Selective Dopamine Receptor D1/D5 Antagonist used in the | ||||
| 24058 | NST-628 | 3002056-30-3 | ≧98.0% | ![]() |
| NST-628 is a potent pan-RAF-MEK molecular glue that prevents the phosphorylation and | ||||
| 25088 | Tonabersat ( SB-220453 ) | 175013-84-0 | ≧98.0% | ![]() |
| Tonabersat, also known as SB-220453, is gap-junction modulator for the prevention of | ||||
| 25089 | Irpagratinib | 2230974-62-4 | ≧98.0% | ![]() |
| Irpagratinib is an orally bioavailable, selective inhibitor of human fibroblast growt | ||||
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