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Gallic acid is a naturally-occurring trihydroxybenzoic acid. Available in various quantities, it is an astringent, a cyclooxygenase 2 inhibitor, an antioxidant, an antineoplastic agent, a weak carbonic anhydrase inhibitor, an apoptosis inducer, etc.
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Furobufen is an anti-inflammatory research compound reported to produce antiarthritic and antipyretic effects and to provide analgesia in inflamed tissue. Supplied for research use only, it is documented with solubility and storage recommendations for laboratory handling.
Has CAS number 38873-55-1.
Chemical formula C16H12O4 and molecular weight 268.26 g·mol⁻¹.
Supplied as a powder and may be prepared in solvent for experiments.
Soluble in DMSO at 100 mg/mL; ultrasonic assistance recommended.
Storage: powder at -20°C (stable for 3 years) or 4°C (2 years); in solvent at -80°C (2 years) or -20°C (1 year).
Intended for research use only; not for diagnostic or therapeutic procedures.
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Furobufen is an anti-inflammatory research compound (CAS 38873-55-1) used as an analytical standard and reagent. It produces antiarthritic and antipyretic effects and has an analgesic effect in inflamed tissue. The compound is supplied as a powder and includes solubility and storage guidance for both in vitro and in vivo use.
Anti-inflammatory agent with antiarthritic and antipyretic effects.
Suitable as an analytical standard for research applications.
Supplied as a powder for ease of handling and long-term storage.
High solubility in DMSO; formulation guidance provided for in vivo studies.
Molecular formula C16H12O4 and molecular weight 268.26 g/mol.
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AR420626 is a research small molecule that functions as a selective agonist of free fatty acid receptor 3 (FFAR3/GPR41). It is used in preclinical studies to probe FFAR3-mediated signaling and biological effects, including anti-inflammatory, antidiabetic, and anticancer responses. Supplied as an off-white to light yellow solid in research-scale quantities.
Selective FFAR3 agonist with reported nanomolar activity.
Shown to modulate inflammatory and metabolic pathways in preclinical models.
Available in small pack sizes suitable for in vitro and in vivo studies.
Off-white to light yellow solid appearance for easy handling and verification.
Recommended storage: keep powder at -20°C for long-term stability.
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CDK12-IN-E9 is a research-grade small-molecule inhibitor that covalently inhibits CDK12 and has non-covalent activity against CDK9. Supplied as a white to off-white solid powder, it is intended for biochemical and cellular studies of cell cycle and DNA damage pathways. Solubility and storage data support use in both in vitro and in vivo formulations.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
AR420626 is a research compound that acts as a selective agonist of free fatty acid receptor 3 (FFAR3/FFA3). It is used in vitro and in vivo to investigate FFAR3-mediated signaling, inflammatory responses, and metabolic or cancer-related pathways. Reported activity values support its use in pharmacology and cell-based assays.
Selective FFAR3 agonist with reported IC50 ≈117 nM.
High purity suitable for biological assays and pharmacology studies.
Available as a solid or as a DMSO solution for convenient dosing.
Multiple package sizes support screening and follow-up studies.
Compatible with in vitro and in vivo experimental workflows.
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