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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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Tigulixostat (LC350189) is an orally active non-purine selective xanthine oxidase inhibitor. It is used in the research of gout and hyperuricemia by effectively reducing serum uric acid levels. It also promotes M2 macrophage polarization and can alleviate hyperuricemic nephropathy in urate oxidase knockout (Uox-KO) mice.
Orally active non-purine selective xanthine oxidase inhibitor
Effectively reduces serum uric acid levels
Used in the research of gout and hyperuricemia
Promotes M2 macrophage polarization
Alleviates hyperuricemic nephropathy in Uox-KO mice
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Gallic acid (Standard) is the analytical standard of Gallic acid, intended for research and analytical applications. It is a natural polyhydroxyphenolic compound and a free radical scavenger that inhibits cyclooxygenase-2 (COX-2).
Gallic acid has various activities, including antimicrobial, antioxidant, anti-inflammatory, and anticancer activities.
The compound is an analytical standard, used as a reference standard assay.
Commonly used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
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Daphnin is a coumarin bioactive component with antibacterial activity, isolated from the whole herb of Daphne odora (Thunb.), which is traditionally used in Chinese folk medicine for fever relief.
Antibacterial activity
Purity: 99.85%
Available in various quantities for research use
Provided with data sheet
Certificate of analysis (COA)
Safety data sheet (SDS)
Handling instructions
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Thymopentin is a biologically active peptide primarily secreted by the epithelial cells of the thymic cortex and medulla. It acts as an effective immunomodulatory agent.
Effective immunomodulatory agent.
Short plasma half-life of 30 seconds.
Enhances the generation of T-cell lineage.
Supports T-cell lineage derived from human embryonic stem cells.
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NVR 3-778 is a first-in-class, orally bioavailable hepatitis B virus (HBV) capsid assembly modulator (CAM) of the sulfamoylbenzamide chemical class used in research to inhibit HBV replication and the generation of infectious viral particles. It has been characterized in preclinical and clinical studies and is supplied for research use with high reported purity and defined physicochemical properties.
First-in-class capsid assembly modulator with demonstrated antiviral activity.
Orally bioavailable small molecule suitable for preclinical assays.
Pan-genotypic inhibition of HBV replication in cell-based models.
Solid, white to off-white material with reported solubility in DMSO and ethanol.
High reported purity appropriate for research applications.
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Tegoprazan is a potassium-competitive acid blocker (P-CAB) provided as a high-purity research reagent for studies of gastric acid regulation and related pharmacology. It is intended for in vitro assays and preclinical investigations and is supplied with analytical characterization to support research use.
High-purity reference compound for biochemical and cellular assays.
Potassium-competitive acid blocker mechanism relevant to acid suppression studies.
Suitable for in vitro and preclinical pharmacology investigations.
Comes with analytical documentation including purity and structural identifiers.
Stable solid form convenient for handling and storage.
Available in small research quantities for dose-ranging experiments.
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VLX600 is a small-molecule oxidative phosphorylation (OxPhos) inhibitor and iron chelator used in cancer and mitochondrial metabolism research. It impairs mitochondrial respiration, induces autophagy, and shows selective cytotoxicity in quiescent or nutrient-starved tumor cells. Molecular formula C17H15N7; molecular weight 317.35; CAS 327031-55-0.
Inhibits mitochondrial oxidative phosphorylation.
Functions as an iron chelator.
Induces autophagy and promotes tumor cell death under nutrient limitation.
Useful as a reference compound for cancer metabolism studies.
Crystalline solid with reported DMSO solubility around 25 mg/mL.
Recommended storage at -20°C as a powder.
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Maohuoside A is a single compound isolated from E. koreanum that potently promotes osteogenesis. It enhances the osteogenesis of bone marrow-derived mesenchymal stem cells via bone morphogenetic protein (BMP) and MAPK signaling pathways.
For research use only
Not sold to patients
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DDD85646 (IMP-366) is an orally active inhibitor of N-myristoyltransferase (NMT) with potent enzymatic activity against Trypanosoma brucei (TbNMT IC50 = 2 nM) and measurable activity versus human NMT (hNMT IC50 = 4 nM). It is supplied as a high-purity research compound for in vitro and in vivo pharmacology studies targeting NMT.
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Gallic acid (CAS 149-91-7) is a naturally occurring polyphenolic compound widely distributed in the plant kingdom with substantial levels identified in sources such as gallnuts grapes tea hops and oak bark It exerts biological effects primarily through antioxidant and anti-inflammatory mechanisms including scavenging free radicals and modulating cellular oxidative stress pathways Gallic acid has been investigated for its capacity to inhibit enzymes involved in inflammation and carcinogenesis influencing cell proliferation and apoptosis in various in vitro models Due to these properties it serves as a valuable tool for studies on oxidative damage inflammation and cancer biology
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AR420626 is a selective agonist of free fatty acid receptor 3 (FFAR3/GPR41) used in receptor pharmacology and signaling research. It is supplied as an off-white to light yellow solid with reported purity ≥98% and a molecular weight of 417.29 g·mol⁻¹. Recommended storage and handling conditions depend on form (powder or solution) to preserve stability.
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