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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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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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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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Tigulixostat is an orally active, non-purine selective xanthine oxidase inhibitor used in preclinical and biochemical research to investigate uric acid metabolism and potential treatments for gout and hyperuricemia. It is provided as a solid suitable for preparation of stock solutions for in vitro and in vivo studies.
High purity (99.2%).
Non-purine selective xanthine oxidase inhibitor.
Suitable for biochemical and preclinical research applications.
Provided as a solid for solution preparation.
Available in small research pack sizes for convenience.
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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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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool<|a>
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool<|a>
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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.
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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DSM502 is a pyrrole-based dihydroorotate dehydrogenase (DHODH) inhibitor selective for Plasmodium DHODH. It shows nanomolar potency in enzyme and cell assays, and has demonstrated in vivo antimalarial efficacy in mouse models. Supplied as a high-purity solid or DMSO solution, it is intended for research use.
Pyrrole-based DHODH inhibitor selective for Plasmodium enzymes.
Nanomolar potency in enzyme and cell-based assays.
Demonstrated efficacy in mouse infection models.
High purity suitable for biochemical studies.
Soluble at high concentration in DMSO for in vitro use.
Stable when stored as powder at -20°C for long-term storage.
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