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Synonyms:
GIPR antagonist 1
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | GIPR antagonist 1 is a GIPR inhibitor with an IC50 of 4.8 nM. It effectively suppresses the glucose-dependent insulinotropic polypeptide receptor signaling pathway. GIPR antagonist 1 is applicable in research related to type 2 diabetes and obesity. |
| In vitro | GIPR antagonist 1 (Compound 27) (10-100 nM, 6 h) effectively blocks human GIPR and inhibits downstream cAMP production in a concentration-dependent manner in CHO-K1 cells stably expressing human GIPR. |
| Molecular Weight | 504.55 |
| Formula | C28H29FN4O4 |
| Cas No. | 3059497-30-9 |
| Smiles | C(NC1=CC(F)=C(C(C)C)C=C1)(=O)N2[C@@H](C(NC3=CC=C(C=C3)C4=C(C)N=C(C(O)=O)C=C4)=O)CCC2 |
| 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.
| Size | Quantity | Unit Price | Amount | Operation |
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