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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.
NVR 3-778 is a first-in-class, orally bioavailable hepatitis B virus (HBV) capsid assembly modulator of the sulfamoylbenzamide class. It inhibits HBV capsid assembly and viral replication, shows pan-genotypic antiviral activity in preclinical models, and has advanced into clinical evaluation. Supplied as a high-purity research-grade compound for in vitro and in vivo HBV studies.
High purity (99.9%).
Orally bioavailable in preclinical models.
Pan-genotypic antiviral activity against HBV.
Mechanism: capsid assembly modulation.
Available in multiple small pack sizes for research flexibility.
Stable as powder at -20°C for up to 3 years.
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Demecolcine is a colchicine-derivative mitotic inhibitor used in research to disrupt microtubule polymerization and to study cell division, apoptosis, and cytoskeleton-related pathways. It is supplied as a research-grade small molecule with defined storage recommendations for powder and solution states.
Potent tubulin inhibitor (IC50 ≈ 2.4 μM).
Useful for cell cycle and apoptosis studies.
Available in small research pack sizes (e.g., 10 MG).
Powder stable at -20°C for extended storage; solution stability specified for frozen storage.
Datasheet provides CAS, formula, molecular weight, and handling guidance.
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NVR 3-778 is a research-stage hepatitis B virus (HBV) capsid assembly modulator (CAM) belonging to the sulfamoylbenzamide class. It is orally bioavailable and has demonstrated antiviral activity in preclinical and clinical studies; the compound is supplied as a solid powder or as a DMSO solution for use in in vitro and in vivo research.
Reported purity 99.88%.
Molecular formula C18H16F4N2O4S and molecular weight 432.39 g·mol-1.
CAS number 1445790-55-5.
Available in small research quantities and as a 10 mM solution in DMSO.
Used for mechanism-of-action, antiviral efficacy, and pharmacokinetic studies.
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FK706 is a potent, slow-binding, competitive inhibitor of human neutrophil elastase used in biochemical and cellular research to study elastase activity and inflammation-related pathways. It is selective versus other serine proteases and has reported anti-inflammatory effects.
Potent inhibitor of human neutrophil elastase (IC50 83 nM; Ki 4.2 nM).
Active against mouse and porcine elastase (IC50s 22 nM and 100 nM).
Selective versus other serine proteases such as trypsin, chymotrypsin, and cathepsin G.
High purity (99.12%) and solid, white to off-white appearance.
Soluble ≥100 mg/mL in water and 115 mg/mL in DMSO (sonication may be required).
Molecular weight 592.54 g/mol; formula C26H32F3N4NaO7.
Store sealed away from moisture; in solution: -80°C (6 months), -20°C (1 month).
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AR-420626 is a selective agonist of free fatty acid receptor 3 (FFAR3/GPR41) used as a research tool to probe FFAR3-mediated signaling. It exhibits an IC50 of 117 nM, is supplied as a solid 10 mg quantity with reported purity of 98.29%, and is intended for research use only.
Selective FFAR3 agonist with an IC50 of 117 nM.
Reported purity 98.29%.
Molecular formula C21H18Cl2N2O3; molecular weight 417.29 g/mol.
Supplied as a 10 MG solid suitable for in vitro studies.
Recommended storage: powder -20°C (up to 3 years).
For research use only; not for human or diagnostic use.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More