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FT827

Catalog No.GC32917 Copy One-Click Copy Product Info

FT827 es un inhibidor selectivo y covalente de la proteasa 7 específica de ubiquitina (USP7) (Ki=4.2 ?M). FT827 se une al dominio catalítico USP7 (USP7CD; residuos 208-560) con un valor aparente de Kd de 7.8 ?M.

Products are for research use only. Not for human use. We do not sell to patients.

FT827 Chemical Structure

Cas No.: 1959537-86-0

Tamaño Precio Disponibilidad Cantidad
1mg
177,00 $
Disponible
5mg
420,00 $
Disponible
10mg
513,00 $
Disponible
25mg
672,00 $
Disponible
50mg
828,00 $
Disponible
100mg
1.090,00 $
Disponible
200mg
1.480,00 $
Disponible

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Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.



Description of FT827

FT827 is a selective, covalent ubiquitin-specific protease 7 (USP7; Ki=4.2µM, Kd=7.8µM) inhibitor. FT827 can be used in cancer-related research[1-2].

In vitro, FT827 (0.1-2µM) treated MCF7 breast cancer cells for 60 minutes. FT827 specifically inhibited USP7 activity in cells and did not affect other DUBs including USP47 and USP10[2].

References:
[1] El-Hamaky AA, El-Hamamsy MH, El-Moselhy TF, et al. Therapeutic targeting of ubiquitin-specific protease 7 (USP7): Mechanistic insights, dysregulation, and advances in drug discovery. Eur J Med Chem. 2025 Oct 15;296:117872.
[2] Turnbull AP, Ioannidis S, Krajewski WW, et al. Molecular basis of USP7 inhibition by selective small-molecule inhibitors. Nature. 2017 Oct 26;550(7677):481-486.

Protocol of FT827

Cell experiment [1]:

Cell lines

MCF7 cells (human breast cancer cell line)

Preparation Method

Intact MCF7 breast cancer cells were incubated with FT827, followed by incubation with the ubiquitin active site suicide probe haemagglutinin (HA)-tagged ubiquitin bromoethyl (HA-UbC2Br).

Reaction Conditions

0.1μM; 60min

Applications

FT827 inhibited USP7 probe reactivity with IC50 of 0.1-2µM. FT827 only affected USP7, but not other deubiquitinases (DUBs) including USP47 and USP10

References:
[1] Turnbull AP, Ioannidis S, Krajewski WW, et al. Molecular basis of USP7 inhibition by selective small-molecule inhibitors. Nature. 2017 Oct 26;550(7677):481-486.

Chemical Properties of FT827

Cas No. 1959537-86-0 SDF
Canonical SMILES C=CS(=O)(NC1=CC=CC=C1C2=CC=C(C(N3CCC(O)(CN(C=NC4=C5C=NN4C)C5=O)CC3)=O)C=C2)=O
Formula C27H28N6O5S M.Wt 548.61
Solubility DMSO : 125 mg/mL (227.85 mM) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of FT827

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 1.8228 mL 9.1139 mL 18.2279 mL
5 mM 364.6 μL 1.8228 mL 3.6456 mL
10 mM 182.3 μL 911.4 μL 1.8228 mL
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In vivo Formulation Calculator (Clear solution) of FT827

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL saline, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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3. All of the above co-solvents are available for purchase on the GlpBio website.

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Review for FT827

Average Rating: 5 ★★★★★ (Based on Reviews and 4 reference(s) in Google Scholar.)

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