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| Cat.No. | Product name | Product Description |
| 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 |
| R21042801 | Bexarotene | Bexarotene is a selective retinoid X receptor (RXR) agonist used to treat cutane |
| R21042802 | Pentoxyverine Citrate | Carbetapentane citrate has a selective inhibitory effect on the cough center, wi |
| R21042804 | HISPIDIN | Hispidin is a PKC inhibitor, a phenolic compound from Phelinus linteus that has |
| R21042805 | Dexpramipexole | Dexpramipexole(KNS-760704), also known as R-(+) -pramipexole, is a neuroprotecti |
| R21042806 | Efaproxiral sodium | Efaproxiral sodium is an allosteric regulator of hemoglobin (Hb) synthesis that |
| R21042807 | Trandolaprilat | Trandolaprilat is a non-sulfhydryl angiotensin-converting enzyme inhibitor. |
| R21042808 | naltrexone | A potent, competitive antagonist for μ, κ, δ, and σ-opioid receptors with Ki of |
| R21042809 | ROCAGLAMIDE | Rocaglamide is a potent inhibitor of NF-κB activation. |
| R21042810 | MSA-2 | MSA-2 is an oral nonnucleotide STING agonist with an EC50 of 8.3 μM for human ST |
| R21042811 | LY-2183240 | LY2183240 is a highly active cannabinoid absorbance blocker with an IC50 of 270 |
| R21042812 | DS-1206b | |
| R21042813 | Phthalazinone pyrazole | Phthalazinone pyrazole is a potent inhibitor of Aurora A kinase with IC50 of 31 |
