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Organic compounds that contain one or more carbonyl (a carbon atom with a double bond to an oxygen atom) functional groups. Includes compounds with functional groups that contain a carbonyl in their structure such as ketones, aldehydes, and others.
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N-trans-Feruloyltyramine (CAS 66648-43-9) is a naturally occurring alkaloid recognized for its antioxidant properties Mechanistically it reduces intracellular reactive oxygen species (ROS) levels and mitigates apoptosis in response to oxidative agents such as hydrogen peroxide Through its modulation of oxidative stress pathways N-trans-Feruloyltyramine is of interest in studies exploring the pathogenesis and intervention of neurodegenerative disorders and cancer associated with oxidative damage This compound thus serves as a useful tool for investigating oxidative stress and its cellular effects in biomedical research
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A tetracyclic diterpene found in croton oil; has been used in the semisynthesis of inhibitors of the HIV-1-induced cytopathic effect on MT-4 cells and 4a-phorbol esters
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trans-PX20606 (trans-PX-102) is a small-molecule agonist of the farnesoid X receptor (FXR) for research use. It exhibits low-nanomolar potency in FXR functional assays and is supplied as a 10 mM solution in DMSO or as solid quantities for biochemical and cellular studies.
Low-nanomolar FXR agonist activity with reported EC50s around 32-34 nM.
Available as 10 mM solution in DMSO and as solid quantities (2 mg, 5 mg, 10 mg).
High chemical purity, typically ≥99.2% by HPLC.
Molecular weight approximately 554.85 g·mol⁻¹ and formula C29H22Cl3NO4.
Intended for in vitro research applications; not for human or veterinary use.
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(R)-Propranolol hydrochloride is the less active enantiomer of propranolol, a nonselective β-adrenergic receptor (βAR) antagonist. Propranolol exhibits high affinity for both β1AR and β2AR. The (R)-enantiomer can prevent adrenaline-induced cardiac arrhythmias in animals, though it requires a significantly higher dose compared to its (-)-enantiomer. It is suitable for research use.
Less active enantiomer of a β-adrenoceptor antagonist.
Nonselective antagonist with affinity for β1AR and β2AR.
Demonstrates ability to prevent adrenaline-induced cardiac arrhythmias.
Can reverse ouabain-induced ventricular tachycardia.
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