NEW PRODUCTS
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 24042 | SPG-601 ( VSN-16R ) | 863713-78-4 | ≧98.0% |  |
| SPG-601 (formerly VSN-16R) is an orally available cannabinoid receptor agonist. | ||||
| 24043 | AZD-5462 | 2787501-83-9 | ≧98.0% |  |
| AZD5462 is a small molecule agonist of the RXFP1 relaxin receptor. | ||||
| 24048 | Sebetralstat free base | 1933514-13-6 | 98% Min. |  |
| Sebetralstat (KVD-900), an oral plasma kallikrein inhibitor. | ||||
| 24015 | ASX-173 | 2748800-08-8 | ≧98.0% |  |
| ASX-173 is a compound that inhibit the activity of asparagine synthetase (ASNS). | ||||
| 24057 | NDI-091143 | 2375840-87-0 | ≧97.0% |  |
| NDI-091143 is a novel potent inhibitor of human ATP-citrate lyase, indirectly disrupt | ||||
| 24069 | Tuvusertib | 1613200-51-3 | ≧98.0% |  |
| Tuvusertib, also known as M-1774 and ATR inhibitor 1, is a ATR inhibitor. M1774 selec | ||||
| 24066 | Lartesertib | 2495096-26-7 | 98% Min. |  |
| Lartesertib (M4076) is a potent inhibitor of serine/threonine protein kinase ATM. | ||||
| 24101 | Crelosidenib | 2230263-60-0 | 98% Min. |  |
| Crelosidenib is an isocitrate dehydrogenase 1 (IDH1) inhibitor. It is an antineoplast | ||||
| 24109 | CBR-5884 | 681159-27-3 | ≧98.0% |  |
| CBR 5884 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor which was able to inhi | ||||
| 24110 | VVD-130037 ( BAY-3605349 ) | 3034880-93-5 | ≧98.0% | _3034880-93-5.png) |
| VVD-130037 (BAY-3605349) is an oral, small-molecule activator of KEAP1 (INrf2). | ||||
| 24111 | PLX-4545 | 2892065-45-9 | ≧98.0% |  |
| PLX-4545 is an orally bioavailable molecular glue degrader of IKZF2 designed to desta | ||||
| 24112 | HC-5404-FU | 3034479-99-4 | ≧98.0% |  |
| HC-5404-FU is a novel, highly selective and potent PERK inhibitor. | ||||