Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
24043 | AZD-5462 | 2787501-83-9 | ≧98.0% | ![]() |
AZD5462 is a small molecule agonist of the RXFP1 relaxin receptor. | ||||
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 | ||||
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% | ![]() |
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 | ||||
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 |
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