| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 25205 | AF710B | N/A | ≧98.0% ; EE≧98.0% | ![]() |
| AF710B is a highly selective and potent allosteric agonist for M1 muscarinic and σ1 | ||||
| 25206 | MA242 TFA | 1049704-18-8 | ≧98.0% | ![]() |
| MA242 isMDM2 and NFAT1 dual inhibitorthat induces MDM2 auto-ubiquitination and degrad | ||||
| 25208 | MK256 | 2271348-04-8 | ≧98.0% | ![]() |
| MK256 is a novel CDK8 inhibitor with potent antitumor activity in AML through downreg | ||||
| 26A032 | Mutant IDH1/NAMPT-IN-1 | 3040122-14-0 | ≧98.0% | ![]() |
| Mutant IDH1/NAMPT-IN-1 ( compound 23h ) has excellent and balanced inhibitory activit | ||||
| 26A029 | Vps34-PIK-III | 1383716-40-2 | ≧98.0% | ![]() |
| Vps34-PIK-III is a selective inhibitor of VPS34 that binds a unique hydrophobic pocke | ||||
| 26A030 | NEO-811 | 3084635-78-6 | ≧98.0% | ![]() |
| NEO-811 is an investigational molecular glue degrader designed to induce targeted deg | ||||
| 26A043 | BI 44370 | 866086-05-7 | ≧98.0% | ![]() |
| BI 44370 was developed as a calcitonin gene-related peptide(CGRP)receptor antagonist | ||||
| 26A044 | Gridegalutamide | 2446929-86-6 | ≧98.0% | ![]() |
| gridegalutamide is an orally bioavailable androgen receptor (AR) degrader, with poten | ||||
| 26A047 | BH-30643 | 3062177-59-4 | ≧98.0% | ![]() |
| BH-30643 is a novel, orally available, non-covalent, macrocyclic, mutant selective OM | ||||
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