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Home > Products
| Cat.No. | Product name | Product Description |
| R2101246 | BSJ-03-123 | BSJ-03-123 is a Selective Cdk6 degrader. BSJ-03-123 exploits protein-interface d |
| R2101247 | VH032-C10-NH2 dihydrochloride | (S,R,S)-AHPC-C10-NH2 dihydrochloride (VH032-C10-NH2 dihydrochloride) is a synthe |
| R2101248 | VH032-C4-NH2 | (S,R,S)-AHPC-C4-NH2 is a synthesized E3 ligase ligand-linker conjugate that inco |
| R2101249 | AT1 | BRD4 degrader AT1 is a highly selective Brd4 degrader based on PROTAC technology |
| R2101250 | dBET57 | dBET57 is heterobifunctional degrader of BRD4 based on the PROTAC technology, ex |
| R2101251 | (S)-AZD6738 | (S)-Ceralasertib is a potent and selective inhibitor of sulfoximine morpholinopy |
| R2101252 | MS4078 | MS4078 is an anaplastic lymphoma kinase (ALK) PROTAC. It has a Kd of 19 nM for b |
| R2101253 | (S)-JQ-35 | (S)-JQ-35 (TEN-010) is an inhibitor of the Bromodomain and Extra-Terminal (BET) |
| R2101254 | A1874 | A1874 is a nutlin-based and BRD4-degrading PROTAC which induces BRD4 degradation |
| R2101255 | TL13-112 | TL13-112 is a selective degrader of ALK-PROTAC and inhibits ALK activity (IC50: |
| R2101256 | CCT367766 | CCT367766 is the PROTAC-based pirin targeting protein degradation probe, deplete |
| R2101258 | MS1943 | MS1943 is a orally bioavailable EZH2 selective degrader(IC50 of 120 nM). |
| R2101259 | SGK3 degrader-1 | PROTAC SGK3 degrader-1 (SGK3-PROTAC1) is a PROTAC conjugate of the 308-R SGK inh |
| R2101260 | VH032-C4-NH2 dihydrochloride | (S,R,S)-AHPC-C4-NH2 dihydrochloride is a synthesized E3 ligase ligand-linker con |
| R2101261 | XZ739 | XZ739 is a CRBN-based PROTAC Bcl-XL decompressant, which acts on Molt-4 cells. A |
| R2101262 | INNO206 | |
| R2101263 | TL12-186 | TL12-186 is a CRBN-dependent multi-kinase PROTAC decompressor.Including CDK, BTK |
| R2101265 | TL13-12 | TL13-12 is a selective degrader of ALK-PROTAC and inhibits ALK activity (IC50: 0 |
| R2101266 | VH032-C5-COOH | (S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized E3 ligase ligand-linker co |
| R2101267 | TD-165 | TD-165 is a PROTAC-based cereblon (CRBN) degrader. TD-165 comprises a cereblon ( |
| R2101268 | BAY-1797 | BAY-1797 is an orally active and selective P2X4 antagonist (IC50: 211 nM against |
| R2101269 | Sparsentan | Sparsentan is a first-in-class orally active and highly potent dual endothelin A |
| R2101270 | Ripretinib | Ripretinib is an orally bioavailable inhibitor of KIT and PDGFRA. |
| R2101271 | Larotrectinib sulfate（LOXO101） | LOXO-101 is an oral active and specific ATP-competitive inhibitor of tropomyosin |
| R2101257 | UNC6852 | UNC6852 is a selective degrader that targets polycomb repressive complex 2 (PRC2 |
