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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.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
7-oxodehydroabietic acid (CAS 18684-55-4) is a diterpene resin acid used in natural product research and studies of insect endocrine-disrupting activity. It is supplied as a white to off-white solid with high reported purity for laboratory research applications.
High purity: 99.7% as supplied on the COA.
White to off-white solid suitable for analytical and preparative work.
Molecular formula C20H26O3 and molecular weight 314.42 g·mol⁻1.
Available in small milligram pack sizes for research use.
Certificate of analysis and safety data sheet available for quality and safety verification.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Podophyllotoxone is a lignan-class tubulin inhibitor isolated from the roots of Dysosma versipellis. It exhibits antiproliferative activity by inhibiting tubulin polymerization and is supplied as a research-grade small-molecule reagent for in vitro studies of microtubule dynamics and antimitotic effects.
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.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More