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Litorin is a bombesin derivative derived from amphibians and acts as a bombesin receptor agonist. It induces smooth muscle contraction, stimulates the secretion of gastrin, gastric acid, and pancreatic juice, and inhibits nutrient uptake in in vivo experiments.

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $56 | 4-6 weeks | 4-6 weeks | |
| 5 mg | $163 | 4-6 weeks | 4-6 weeks | |
| 10 mg | $247 | 4-6 weeks | 4-6 weeks | |
| 25 mg | $418 | 4-6 weeks | 4-6 weeks | |
| 50 mg | $595 | 4-6 weeks | 4-6 weeks |
| Description | Litorin is a bombesin derivative derived from amphibians and acts as a bombesin receptor agonist. It induces smooth muscle contraction, stimulates the secretion of gastrin, gastric acid, and pancreatic juice, and inhibits nutrient uptake in in vivo experiments. |
| Targets&IC50 | GRP:5.1 nM (Ki) |
| In vitro | Methods: The inhibitory effect of [D-Phe¹, Leu⁸,⁹] litorin on receptor binding in mouse Swiss 3T3 cells was determined. Results: [D-Phe¹, Leu⁸,⁹] litorin inhibited the binding of ¹²⁵I-[Tyr⁴] BN to mouse Swiss 3T3 cells, with a Ki value of 5.1 nM [2]. Methods: The effect of litorin on ³H-thymidine incorporation in mouse Swiss 3T3 cells was examined. Results: Litorin stimulated ³H-thymidine incorporation in mouse Swiss 3T3 cells, with an EC₅₀ value of 2.3 nM [2]. |
| In vivo | Methods: The application of ⁹⁹ᵐTc-litorin for tumor imaging was developed and evaluated. Results: ⁹⁹ᵐTc-litorin can be used for noninvasive imaging of tumors with high expression of gastrin-releasing peptide receptor (GRP-R) [1]. Methods: The regulatory effects of litorin on physiological functions related to the gastrointestinal tract and smooth muscle were investigated in vivo. Results: Litorin stimulated smooth muscle contraction, promoted the secretion of gastrin, gastric acid and pancreatic juice, and inhibited the absorption of nutrients in vivo [2]. |
| Molecular Weight | 1085.24 |
| Formula | C51H68N14O11S |
| Cas No. | 55749-97-8 |
| Smiles | C([C@H](NC([C@@H](NC(=O)[C@H]1NC(=O)CC1)CCC(N)=O)=O)C(N[C@H](C(N[C@H](C(NCC(N[C@@H](CC2=CN=CN2)C(N[C@@H](CC3=CC=CC=C3)C(N[C@@H](CCSC)C(N)=O)=O)=O)=O)=O)[C@H](C)C)=O)C)=O)C=4C=5C(NC4)=CC=CC5 |
| Relative Density. | 1.34 g/cm3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO: 80 mg/mL (73.72 mM), Sonication is recommended. H2O: 1 mg/mL (0.92 mM), Sonication is recommended. |
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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