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Various organic compounds consisting of carbon, hydrogen, and oxygen atoms that are found in foods and living tissues; typically broken down to release energy; includes sugars, sugar alcohols, sugar acids and derivatives, glycosyl compounds, and more.
Beta-Eudesmol (CAS No 473-15-4) is a sesquiterpenoid alcohol commonly researched for its pharmacological properties Originating from plants like Atractylodes lancea it targets various biochemical pathways notably influencing neurological and inflammatory responses Studies indicate that its in vitro activity often falls in the nanomolar to low micromolar range showing potential in modulating cellular processes It is frequently utilized in cell models such as neuronal and cancer cell lines and has been the subject of animal studies to explore its therapeutic potential Beta-Eudesmol is valuable in drug screening due to its diverse biological effects Experimental concentrations typically depend on the specific research design
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α-Glucosidase-IN-22 (compound 7i), a benzimidazole, is a potent α-glucosidase inhibitor with an IC50 of 0.64 μM. It is a potent anti-diabetic agent and has potential for type 2 diabetes mellitus (T2DM) research.
Potent α-glucosidase inhibitor with an IC50 of 0.64 μM.
Potent anti-diabetic agent.
Has potential for type 2 diabetes mellitus (T2DM) research.
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HyperTrap Heparin FF Column is an affinity chromatography medium designed for the purification of heparin-binding biomolecules The column exploits the strong ionic and specific interactions between immobilized heparin and target proteins such as growth factors coagulation factors and certain enzymes enabling selective retention and efficient separation from complex biological mixtures This tool is widely utilized in the isolation and characterization of heparin-binding proteins investigation of protein glycosaminoglycan interactions and purification of bioactive factors for downstream functional assays and structural analyses
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D-3263 hydrochloride is an enteric-coated, orally bioavailable agonist of transient receptor potential melastatin member 8 (TRPM8). It binds and activates TRPM8, modulates calcium and sodium flux, and has been investigated for potential antineoplastic effects and modulation of androgen-related pathways.
Orally bioavailable TRPM8 agonist suitable for in vivo studies.
Enteric-coated formulation for improved gastrointestinal stability.
High purity (98.0%) supports reproducible experimental results.
Soluble in DMSO and formulatable for common in vivo vehicles.
Stable when stored sealed at 4°C; solvent stability at -80°C for extended storage.
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BET-IN-19 is a potent small-molecule BET bromodomain inhibitor for research use. It inhibits hIL-6 mRNA transcription and c-myc activity in AML MV4-11 cells (IC50 ≤ 0.3 μM). The compound has molecular formula C19H19N5O, molecular weight 333.39, and reported purity ≈99.7%; it is supplied as a powder and is typically stored at -20°C (powder) or at -80°C in solvent for longer term.
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