NEW PRODUCTS
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 122919 | Tenapanor | 1234423-95-0 | 98% |  |
| Tenapanoris an inhibitor of the sodium-proton exchanger NHE3. Thisantiporter protein | ||||
| 52003 | Zosuquidar trihydrochloride | 167465-36-3 | 99% |  |
| zosuquidar trihydrochloride is adifluorocyclopropyl quinoline. Zosuquidar trihydrochl | ||||
| 6111110 | Nastorazepide | 209219-38-5 | 98% |  |
| Nastorazepide (Z-360) is a selective, orally available, 1,5-benzodiazepine-derivative | ||||
| 111891 | ONC206 | 1638178-87-6 | 98% Min. |  |
| ONC206 is a chemical analogue of ONC201. ONC206 is a benzyl-flurobenzyl imipridone th | ||||
| 52002 | K-7174 dihydrochloride | 191089-60-8 | 98% |  |
| K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of | ||||
| 512193 | ITI-214(phosphate) | 1642303-38-5 | 98% Min. |  |
| ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic | ||||
| 2017889 | Roluperidone ( CYR-101 ) | 359625-79-9 | 98.0% |  |
| Roluperidone, also known as MIN-101, CYR-101, and MT-210, is a 5-HT2A and sigma 2 rec | ||||
| 52019 | GSK 2656157 | 1337532-29-2 | 98% |  |
| GSK2656157 is an ATP-competitive and highly selective inhibitor ofPERKwithIC50of 0.9 | ||||
| 77821 | ACY-775 | 1375466-18-4 | 98.0% by HPLC |  |
| ACY-775 is a potent and selective HDAC6 inhbiitor. ACY-775 inhibits HDAC6 with low na | ||||
| 2051515 | Asapiprant | 932372-01-5 | 98% Min. |  |
| Asapiprant is a potent and selective DP1 receptor antagonist, with a Ki of 0.44 nM. A | ||||
| 102703 | AZD-8835 | 1620576-64-8 | ≧98.0% |  |
| AZD8835 is a potent and selective inhibitor of PI3Kalpha and PI3Kdelata with excellen | ||||
| 112591 | U-73343 | 142878-12-4 | 98% Min. |  |
| U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p | ||||