Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 121804 | APD597 | 897732-93-3 | 98% |  |
| APD597 is a potent and selective GPR119 agonist, which is potential useful for the tr | ||||
| 121434 | AT-101 | 90141-22-3 | 98% |  |
| AT-101 is the orally bioavailable the R-(-) enantiomer of gossypol with potential ant | ||||
| 120701 | 4-Aminobenzeneboronic Acid Hydrochloride | 80460-73-7 | 98% |  |
| Coming soon! | ||||
| 120409 | Alendronate sodium trihydrate | 121268-17-5 | 98% |  |
| Coming soon! | ||||
| 120408 | Ambroxol hydrochloride | 23828-92-4 | 98% |  |
| Coming soon! | ||||
| 120110 | Actinomycin D | 50-76-0 | 98% |  |
| Actinomycin D is the most significant member of actinomycines, which are a class of p | ||||
| 120104 | Altiratinib | 1345847-93-9 | 98% |  |
| Altiratinib is a novel c-MET/TIE-2/VEGFR inhibitor; effectively reduce tumor burden i | ||||
| 120103 | AGI-5198 | 1355326-35-0 | 98% |  |
| AGI-5198 is a novel R132H-IDH1 inhibitor, identified through a high-throughput screen | ||||
| 120102 | Acotiamide HCl | 773092-05-0 | 98% |  |
| Acotiamide is a drug approved in Japan for the treatment of postprandial fullness, up | ||||
| 120101 | A66 | 1166227-08-2 | 98% |  |
| A66 is a potent and specific p110 inhibitor with IC50 of 32 nM, >100 fold selectiv | ||||
| 112101 | AV-412 | 451492-95-8 | 99.38% |  |
| AV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth fact | ||||
| 111913 | AR-12 | 742112-33-0 | 98% |  |
| AR-12 is an orally available, targeted anti-cancer agent that has been shown in pre-c | ||||
| 110909 | AR 231453 | 733750-99-7 | 98% |  |
| AR231453 is a potent and selective small molecule agonist of GPR119 that enhances glu | ||||
| 110906 | AZD6738 | 1352226-88-0 | 97% |  |
| AZD6738 is an orally available morpholino-pyrimidine-based inhibitor of ataxia telang | ||||
| 110217 | 3-Amino-2,6-dibromopyridine | 39856-57-0 | 98% |  |
| Coming soon! | ||||
| 110214 | 2-Amino-4-(trifluoromethyl)pyridine | 106447-97-6 | 98% | pyridine-cas-106447-97-6.png) |
| Coming soon! | ||||
| 110211 | 1-aminocyclopropanecarboxylic acid | 22059-21-8 | 98% |  |
| Coming soon! | ||||
| 110207 | 3-Amino-1-propanesulfonic acid | 3687-18-1 | 98% |  |
| Coming soon! | ||||
| 102702 | Alda 1 | 349438-38-6 | 98% |  |
| Alda 1 is a cell-permeable benzamide compound that selectively enhances the activity | ||||
| 102619 | ACTB-1003 | 939805-30-8 | 98% |  |
| ACTB-1003 is a potent inhibitor of FGFR1 with IC50 <10 nM in FGFR-1 biochemical as | ||||
| 102613 | ABT-751 | 141430-65-1 | 98% |  |
| ABT-751 is a novel bioavailable tubulin-binding and antimitotic sulfonamide agent wit | ||||
| 102604 | AZD1981 | 802904-66-1 | 98% |  |
| AZD1981 is a potent and selective CRTh2 antagonist; displaces radio-labelled PGD2 fro | ||||
| 101921 | AL 082D06 | 256925-03-8 | 98% |  |
| AL 082D06(D-06) is the first selective, nonsteroidal glucocorticoid receptor (GR) ant | ||||
| 101910 | ANA-12 | 219766-25-3 | 98% |  |
| ANA-12 is aTrkB receptor antagonist, which showed direct and selective binding to Trk | ||||
| 91823 | (3aR,5S)-3a,4,5,7-tetrahydro-5-methyl-3H-pyrano[3,4-c]isoxazole | 1613393-51-3 | 98% | -3a457-tetrahydro-5-methyl-3H-pyrano[34-c]isoxazole-cas-1613393-51-3.png) |
| Coming soon! | ||||
| 91803 | (3aR,5R)-3a,4,5,7-tetrahydro-5-methyl-3H-pyrano[3,4-c]isoxazole | 1220327-45-6 | 98% | -3a457-tetrahydro-5-methyl-3H-pyrano[34-c]isoxazole-cas-1220327-45-6.png) |
| Coming soon! | ||||
| 91411 | Amoxanox | 68302-57-8 | 98% |  |
| Amlexanox inhibits mast cell release of allergic mediators, which is also an antialle | ||||
| 91404 | (3aR,4S,7R,7aS)-Hexahydro-4,7-methanoisobenzofuran-1,3-dione | 14166-28-0 | 98% | -Hexahydro-47-methanoisobenzofuran-13-dione-cas-14166-28-0.png) |
| The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3 | ||||
| 91401 | (3aR,4S,7R,7aS)-Hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione | 14805-29-9 | 98% | -Hexahydro-1H-47-methanoisoindole-13(2H)-dione-cas-14805-29-9.png) |
| The related APILurasidone hydrochlorideThe related intermediates4-(1,2-Benzothiazol-3 | ||||
| 901301 | AZD3759 | 1626387-80-1 | ≧99.0% |  |
| AZD3759 isan orally available inhibitor of the epidermal growth factor receptor (EGFR | ||||