New Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 24012 | Zunsemetinib | 1640282-42-3 | ≧98.0% |  |
| Zunsemetinib is an investigational oral mitogen-activated protein kinase-activated pr | ||||
| 24013 | Ziftomenib ( KO-539 ) | 2134675-36-6 | ≧98.0% | _2134675-36-6.png) |
| Ziftomenib is an oral, potent, and selective small molecule inhibitor that targets th | ||||
| 24014 | Zelasudil | 2365193-22-0 | ≧98.0% |  |
| Zelasudil is a potent, highly selective and orally-active inhibitor that targets Rho- | ||||
| 24056 | proTAME | 1362911-19-0 | ≧95.0%+ |  |
| ProTAME is Small molecule inhibitors of the APC/C. | ||||
| 24020 | KB-0742 dihydrochloride | 2416874-75-2 | ≧98.0% |  |
| KB-0742 is a Potent, Selective, Orally Bioavailable Small Molecule Inhibitor of CDK9 | ||||
| 24018 | AM-9747 | 2691869-82-4 | ≧98.0% |  |
| AM-9747 is an MTA cooperative PRMT5 inhibitor. AM-9747 selectively inhibited the prol | ||||
| 20676 | KUS121 | 1357164-52-3 | ≧98.0% |  |
| KUS-121 is a small-molecule inhibitor of the transitional endoplasmic reticulum ATPas | ||||
| 20677 | UJN49930 ( UGT8-IN-1 ) | 2414349-93-0 | ≧98.0% | _2414349-93-0.png) |
| UJN49930 ( UGT8-IN-1 ) is an inhibitor of UDP-galactose ceramide galactosyltransferas | ||||
| 24021 | SY-008 | 1480443-32-0 | ≧98.0% |  |
| SY-008 is a sodium glucose transporter 1 (SGLT1) inhibitor. | ||||
| 24016 | SY-008 Acetate | 1878218-66-6 | ≧98.0% |  |
| SY-008 is a sodium glucose transporter 1 (SGLT1) inhibitor. | ||||
| 24024 | CVN-293 | 2815296-08-1 | ≧98.0% |  |
| CVN-293 is an oral, brain-penetrant, small-molecule inhibitor of KCNK13. | ||||
| 24025 | BIIB-129 | 2770960-52-4 | ≧98.0% |  |
| BIIB129 is a covalent, selective, small molecule inhibitor of Bruton's tyrosine k | ||||