| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 25175 | Nizubaglustat ( Synonyms: AZ-3102 ) | 1633666-49-5 | ≧98.0% | ![]() |
| Nizubaglustat (AZ-3102) is an oral small molecule which inhibits glucosylceramide syn | ||||
| 25192 | CBR-470-1 | 2416095-06-0 | ≧98.0% | ![]() |
| CBR-470-1 is an Inhibitor of the glycolytic enzyme PGK1that induces Nrf2 activity. | ||||
| 25191 | Z57346765 | 1016340-64-9 | ≧98.0% | ![]() |
| Z57346765 is a PGK1-specific inhibitor that reduces the activity of metabolic enzymes | ||||
| 25178 | DS-1001b | 1898207-64-1 | ≧98.0% | ![]() |
| DS-1001 is an oral brain-penetrant mutant IDH1 selective inhibitor. | ||||
| 25190 | QBS10072S | 1802735-28-9 | ≧98.0% | ![]() |
| QBS10072S isa blood-brain-barrier (BBB) penetrative agent composed of a cytotoxic che | ||||
| 186264 | MTX115325 | 2750895-97-5 | ≧98.0% | ![]() |
| MTX115325 is a potent, selective, brain-penetrant USP30 inhibitor with good drug-like | ||||
| 186269 | TAK-071 | 1820812-16-5 | ≧98.0% | ![]() |
| TAK-071 is a muscarinic M1 receptor positive allosteric modulator. | ||||
| 25200 | VT-3989 | 2506273-81-8 | ≧98.0% | ![]() |
| VT3989, a first-in-class potent oral TEAD palmitoylation inhibitor, disrupts YAP tran | ||||
| 25195 | Soclenicant (BNC-210 ; IW-2143) | 1020634-41-6 | ≧98.0% | ![]() |
| Soclenicant (BNC-210 ; IW-2143) is a novel α7 nicotinic acetylcholine receptor-negat | ||||
| 25196 | Rosolutamide ( AJ-201 ; ASC-JM17 ) | 1039760-91-2 , 2074613-88-8 [ALTERNATIVE] | ≧98.0% | ![]() |
| Rosolutamide (formerly known as AJ-201, ASC-JM-17 or ALZ-002) is a nuclear factor ery | ||||
| 25197 | Bexobrutideg ( NX-5948 ) | 2649400-34-8 | ≧98.0% | ![]() |
| Bexobrutideg (NX-5948) is a BTK degrader. | ||||
| 25198 | Bezuclastinib | 1616385-51-3 | ≧98.0% | ![]() |
| Bezuclastinib is an oral, small-molecule inhibitor of the kinase activity of the KIT | ||||
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