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SUN B8155

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Catalog No. T23406Cas No. 345893-91-6
Alias SUN-B 8155

SUN B8155 is a calcitonin (CT) receptor agonist that selectively mimics the biological effects of calcitonin and induces cAMP formation in cells expressing recombinant human CT receptor.

SUN B8155

SUN B8155

🥰Excellent
Purity: 99.38%
Catalog No. T23406Alias SUN-B 8155Cas No. 345893-91-6
SUN B8155 is a calcitonin (CT) receptor agonist that selectively mimics the biological effects of calcitonin and induces cAMP formation in cells expressing recombinant human CT receptor.
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Purity:99.38%
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Product Introduction

Bioactivity
Description
SUN B8155 is a calcitonin (CT) receptor agonist that selectively mimics the biological effects of calcitonin and induces cAMP formation in cells expressing recombinant human CT receptor.
Targets&IC50
cAMP:21 μM (EC50)
In vitro
SUN B8155 (1-1000 μM, 1 hr treatment) promoted intracellular cAMP production in a concentration-dependent manner in T47D cells, with cAMP levels increasing approximately 42-fold at the highest concentration. The compound also increased cAMP production in the UMR106-06 cell line derived from rat osteogenic sarcoma. In CHO/hPTHR or CHO parental cells, SUN B8155 was unable to trigger cAMP production. However, in CHO/hCTR cells, SUN B8155 significantly enhanced cAMP generation in a concentration-dependent manner with an EC50 of 21 μM. [1]
In vivo
Intraperitoneal injection of SUN B8155 (100 mg/kg) resulted in a significant decrease in serum calcium concentration of approximately 9% at 30 minutes post-dose.[1]
AliasSUN-B 8155
Chemical Properties
Molecular Weight273.29
FormulaC14H15N3O3
Cas No.345893-91-6
SmilesO=C1C=C(C(=C(O)N1O)C(=NC=2C=CC=CC2N)C)C
Relative Density.1.34 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 80 mg/mL (292.73 mM), Sonication is recommended
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.6591 mL18.2956 mL36.5912 mL182.9558 mL
5 mM0.7318 mL3.6591 mL7.3182 mL36.5912 mL
10 mM0.3659 mL1.8296 mL3.6591 mL18.2956 mL
20 mM0.1830 mL0.9148 mL1.8296 mL9.1478 mL
50 mM0.0732 mL0.3659 mL0.7318 mL3.6591 mL
100 mM0.0366 mL0.1830 mL0.3659 mL1.8296 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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