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Devazepide is a competitive, selective, orally available non-peptide CCK1 (cholecystokinin 1) receptor antagonist that inhibits bladder cancer cell proliferation and migration while inducing apoptosis and cell cycle arrest.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $68 | 5 days | 5 days | |
| 5 mg | $128 | 7-10 days | 7-10 days | |
| 1 mL x 10 mM (in DMSO) | $152 | 7-10 days | 7-10 days |
| Description | Devazepide is a competitive, selective, orally available non-peptide CCK1 (cholecystokinin 1) receptor antagonist that inhibits bladder cancer cell proliferation and migration while inducing apoptosis and cell cycle arrest. |
| Targets&IC50 | CCK receptor (rat pancreas):45 pM, CCK receptor (guinea pig brain):245 nM, CCK receptor (bovine gallbladder):81 pM |
| In vivo | Oral gavage administration of Devazepide (4 mg/kg, twice daily) significantly accelerated cholesterol crystal formation, crystal growth until developing into microlithiasis, and promoted gallstone formation in mice [2]. Intraperitoneal injection of Devazepide (0.1–1 mg/kg) exerted opposing regulatory effects on the basal spontaneous activity of mice and the hypokinesia induced by caerulein and apomorphine [3]. |
| Synonyms | MK-329, MK329, L-364,718, L364,718 |
| Molecular Weight | 408.45 |
| Formula | C25H20N4O2 |
| Cas No. | 103420-77-5 |
| Smiles | N(C(=O)C1=CC=2C(N1)=CC=CC2)[C@H]3N=C(C=4C(N(C)C3=O)=CC=CC4)C5=CC=CC=C5 |
| Relative Density. | 1.31 g/cm3 (Predicted) |
| Storage | keep away from moisture,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 160 mg/mL (391.72 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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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