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JTT 551 can be used in the research of type 2 diabetes mellitus. JTT 551 is selective a protein tyrosine phosphatase 1B (PTP1B) inhibitor, with Kis of 0.22 μM and 9.3 μM for PTP1B and TCPTP (T-cell protein tyrosine phosphatase), respectively.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,970 | 8-10 weeks | 8-10 weeks | |
| 50 mg | $2,580 | 8-10 weeks | 8-10 weeks | |
| 100 mg | $3,400 | 8-10 weeks | 8-10 weeks |
| Description | JTT 551 can be used in the research of type 2 diabetes mellitus. JTT 551 is selective a protein tyrosine phosphatase 1B (PTP1B) inhibitor, with Kis of 0.22 μM and 9.3 μM for PTP1B and TCPTP (T-cell protein tyrosine phosphatase), respectively. |
| Targets&IC50 | PTP1B:0.22 μM , TCPTP:9.3 μM |
| In vitro | JTT-551 exhibits low affinity for CD45 protein tyrosine phosphatase (CD45) and leucocyte common antigen-related (LAR) protein tyrosine phosphatase, with dissociation constants (Kis) greater than 30 μM for both. Simultaneously, it enhances insulin-induced deoxyglucose uptake in a dose-dependent manner at concentrations of 10 and 30 μM. Primarily, JTT-551 acts as a selective inhibitor of protein tyrosine phosphatase 1B (PTP1B), demonstrating Kis of 0.22 μM for PTP1B and 9.3 μM for T-cell protein tyrosine phosphatase (TCPTP), thereby indicating its specificity and potential therapeutic utility in modulating insulin sensitivity. |
| In vivo | JTT 551 effectively lowers triglyceride (TG) levels at a dosage of 30 mg/kg by Day 7, without impacting insulin and total cholesterol (TC) levels. Additionally, at dosages of 3 mg/kg and 30 mg/kg administered orally (p.o.), this compound demonstrates a dose-dependent reduction in blood glucose levels in db/db mice across multiple time points, specifically on Days 7, 14, and 28. |
| Molecular Weight | 605.85 |
| Formula | C34H43N3O3S2 |
| Cas No. | 776309-04-7 |
| Smiles | CCCC(CCC)c1ccc(OCc2ccc(cc2)-c2csc(CN(CC(O)=O)Cc3ncc(s3)C(C)(C)C)n2)cc1 |
| Relative Density. | 1.174 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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