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IUPAC Name : 6-((1-(2-Chloro-4-(furan-2-yl)benzyl)-4-hydroxypiperidin-4-yl)methyl)-3-(4-fluorophenyl)-2-methyl-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one
| Price And Availability | ||||
|---|---|---|---|---|
| Pack Size | Price in USD | Add To Shopping Cart | Availability | Shipping Status |
| 5MG | Request A Quote | Back Order | Estimated to ship on 04 October 2026 | |
| 10MG | Request A Quote | Back Order | Estimated to ship on 04 October 2026 | |
| 25MG | Request A Quote | Back Order | Estimated to ship on 04 October 2026 | |
| 50MG | Request A Quote | Back Order | Estimated to ship on 04 October 2026 | |
| 100MG | Request A Quote | Back Order | Estimated to ship on 04 October 2026 | |
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| Chemical Properites | |
|---|---|
Mol. Formula : C29H27ClFN5O3 | Mol. Weight : 548.02 |
Appearance : Solid | Melting Point : Not available |
| For Laboratory research use only, not for drug, household or other uses. | |
Applications : This is a potent and selective USP7 inhibitor from a series of N‑benzylpiperidinol derivatives, featuring nanomolar USP7 inhibition (X20 and X26: IC50 = 7.6 and 8.2 nM) with a distinct binding mode confirmed by crystallography. Among them, X36 shows good oral PK in rats (F = 40.8%, t1/2= 3.5 h) and delivers significant antitumor efficacy in the MC38 colon cancer syngeneic model. Its activity is associated with enhanced infiltration of CD8⁺ T cells, NK cells, and NKT cells, along with reduced Tregs and MDSCs, indicating immune‑microenvironment modulation. Overall, this series—especially X36—supports the development of USP7 inhibitors as promising cancer immunotherapy agents.
References : Li X. et al.: J. Med. Chem., 65(24), 16622-16639, 2022.
Storage : Keep container tightly closed under nitrogen or argon and refrigerate for long-term shelf life.
Caution : In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical advice. Wear suitable protective clothing and gloves.
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