Tolbutamide NEW
| Price | $41 |
| Package | 500mg |
| Supply Ability: | 10g |
| Update Time: | 2026-05-11 |
Product Details
| Product Name: Tolbutamide | CAS No.: 64-77-7 |
| Purity: 99.80% | Supply Ability: 10g |
| Release date: 2026/05/11 |
Product Introduction
Bioactivity
| Name | Tolbutamide |
| Description | Tolbutamide (HLS 831) is a sulphonylurea hypoglycemic agent with actions and uses similar to those of CHLORPROPAMIDE. |
| Cell Research | C6 glioma cells are incubated in serum-free DMEM at 37 °C for at least 24 hours before each experiment. Tolbutamide (400 μM) is incubated for 24 hours in serum-free medium. Incubations are performed at 37 °C in an atmosphere of 95% air/5% CO2 with 90–95% humidity. (Only for Reference) |
| Kinase Assay | cAMP kinase assay: Diced epididymal fat pads from fed Wistar rats (175-225 gm) are obtained after decapitation and incubated at 37 °C for two hours in Krebs-bicarbonate buffer containing 1.27 mM CaCl2. When added, Tolbutamide is present only during the incubation. After incubation fat pads are rinsed and sonicated in cold Krebs-bicarbonate buffer. The aqueous supematants from centrifugation at 50,000 × g for 30 minutes at 4 °C contained 0.75 to 1.25 mg protein per mL and are assayed for cyclic AMP-stimulated protein kinase activity. The assay is performed in 0.2 mL with these additions, 10 μmoles sodium glycerofiosphate pH 7.0, 2 μmoles sodium fluoride, 0.4 μmoles theophylline, 0.1 μmoles ethylene glyool bis (β-aminoethyl ether)-N, N'-tetraaoetic acid, 3 μmoles magnesium chloride, 0.3 mg mixed histone, 2 nmoles (γ- 32P) ATP, 1 nmoles cyclic AMP when indicated, and 0.05 ml of supernatant. |
| In vitro | Daily treatment of cells with 450 mg/kg of Tolbutamide for seven consecutive days significantly increases the binding of insulin to adipocytes. The binding curve suggests an increase in the number of receptor sites rather than an increased affinity. This effect is associated with an enhanced insulin response in adipose tissue. Compared to the control group, adipocytes from Tolbutamide-treated animals show a notable increase in the conversion of glucose to fat in the presence of insulin. While low doses of Tolbutamide can elicit a metabolic effect by stimulating insulin secretion, they do not augment the number of insulin binding sites. An increase in insulin binding sites occurs only in the presence of high doses of Tolbutamide, which, at such levels, reduces overall insulin, including its pancreatic secretion and serum levels. |
| In vivo | Tolbutamide is effective only in patients who can normally produce insulin, as it helps to lower blood glucose levels. The compound inhibits the activity of both basal protein kinase and cyclic AMP-activated protein kinase, with an IC50 concentration of 4 mM. It dose-dependently inhibits the phosphorylation of bifunctional proteins induced by glucagon. In the presence of 10(-9) M glucagon, adding 2 mM Tolbutamide reduces the activity of 6-phosphofructokinase and enhances the activity of fructose-2,6-bisphosphatase. Additionally, Tolbutamide inhibits the activity of free and membrane-bound proteases in canine cardiac tissue. Its inhibitory effect on cyclic AMP-dependent protein kinase activity in adipose tissue may account for its antilipolytic action. Tolbutamide also inhibits the proliferation of C6 glioma cells by increasing the concentration of Cx43, which is associated with reduced phosphorylation of pRb due to upregulation of the cyclin-dependent kinase inhibitors p21 and p27. |
| 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 : 247.5 mg/mL (915.48 mM), Sonication is recommended. Ethanol : 50 mg/mL (184.95 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (7.4 mM), Sonication is recommended. |
| Keywords | Tolbutamide | PotassiumChannel | Potassium Channel | KcsA | Inhibitor | inhibit | HLS-831 | HLS831 | Autophagy |
| Inhibitors Related | Stavudine | Aceglutamide | Hemin | Tamoxifen | Cysteamine hydrochloride | Guanidine hydrochloride | Hydroxychloroquine | Enzalutamide | Paeonol | Naringin | Alginic acid | Sildenafil citrate |
| Related Compound Libraries | Failed Clinical Trials Compound Library | Bioactive Compound Library | Pain-Related Compound Library | Membrane Protein-targeted Compound Library | Anti-Cancer Clinical Compound Library | Drug Repurposing Compound Library | FDA-Approved Drug Library | Anti-Cancer Approved Drug Library | Anti-Aging Compound Library | Bioactive Compounds Library Max | Ion Channel Targeted Library | Anti-Cancer Drug Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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