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| Cat.No. | Product name | Product Description |
| R2101233 | acivicin；AT-125; U-42126 | Acivicin (AT-125), a natural product produced by Streptomyces sviceus, is a γ−gl |
| R2101234 | Cenicriviroc(mesylate) | Cenicriviroc Mesylate is a dual CCR2/CCR5 antagonist, also inhibits both HIV-1 a |
| R2101235 | AZD4573 | AZD4573 is an effective and selective CDK9 inhibitor (IC50: <4 nM). It enable |
| R2101236 | WYE-354 | WYE-354(IC50=5 nM) is an effective, selective and ATP-competitive mTOR inhibitor |
| R2101237 | ML-SA1 | activator of TRPML channels. |
| R2101238 | Fezolinetant | Fezolinetant is an antagonist of the neurokinin 3 receptor (NK3R). It is used fo |
| R2101239 | AZD-4320 | AZD4320 is an inhibitor of BH3-mimicking dual BCL2/BCLxL. For KPUM-MS3, KPUM-UH1 |
| R2101240 | RTA 405 | CDDO-EA is an activator of NF-E2 related factor 2/antioxidant response element ( |
| R2101241 | BDTX-189 | BDTX-189 is an orally bioavailable, irreversible, selective, small-molecule inhi |
| R2101242 | E3 Ligase Ligand-Linker Conjugates 2 | E3 Ligase Ligand-Linker Conjugates 2 is a synthesized E3 ligase ligand-linker co |
| R2101243 | E3 ligase Ligand-Linker Conjugates 28 | (S,R,S)-AHPC-C4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conju |
| R2101244 | E3 Ligase Ligand-Linker Conjugates 20 | Thalidomide-O-amido-C8-NH2 (Cereblon Ligand-Linker Conjugates 2), a synthesized |
| R2101245 | E3 ligase Ligand-Linker Conjugates 7 | (S,R,S)-AHPC-PEG4-NH2 hydrochloride is a synthesized E3 ligase ligand-linker con |
| 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). |
