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Synthesized from the 5-carbon precursors isopentenyl diphosphate and dimethylallyl diphosphate; includes the carotenoids, which are precursors of vitamin A and also possess antioxidant effects.
Goserelin acetate is a synthetic GnRH (gonadotropin-releasing hormone) agonist peptide supplied for research use in studies of hormone-dependent cancers and reproductive biology. The acetate salt is formulated for laboratory assays and preclinical work where a defined GnRH receptor agonist is required.
High reported purity (99.87%) suitable for research applications.
Well-characterized molecular formula and weight for identity confirmation.
Supplied in small milligram quantities for laboratory experiments.
Appropriate for in vitro and preclinical cancer biology studies.
Datasheet and handling instructions available for proper storage and use.
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Tanshinone IIA (CAS 568-72-9) is a diterpene quinone extracted from the medicinal plant Salvia miltiorrhiza (Danshen) It modulates cellular signaling by inhibiting the binding of transcription factors NF- B and AP-1 to DNA thereby regulating gene expression associated with inflammation and proliferation Tanshinone IIA has demonstrated the capacity to suppress -amyloid aggregation and protect neuronal PC12 cells against -amyloid-induced apoptosis It exhibits both antioxidant and anti-inflammatory properties supporting its use in studies related to oncology neurodegeneration and inflammation
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An iridoid glycoside with diverse biological activities; reduces exudate volume and nitrite levels in a rat model of carrageenan-induced air pouch inflammation at 0.1 mg/pouch; prevents prevents carrageenan-induced paw edema in rats at 100 mg/kg, p.o.; reduces serum levels of ALT and AST and hepatic levels of MDA as well as decreases in hepatic levels of SOD and GPX in a rat model of high-fat diet-induced NASH at 50 and 100 mg/kg; prevents increases in apoptosis and decreases in the number of dopaminergic neurons in the substantia nigra in a mouse model of MPTP-induced Parkinson's disease at 100 mg/kg; improves motor coordination in the rotarod and swim tests in a rat model of Parkinson's disease
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
rel-VU6021625 is the relative stereochemical isomer of VU6021625, a potent and selective antagonist of the muscarinic acetylcholine receptor M4. It is supplied as a white to off-white solid intended for research use only; reported activity includes IC50 = 0.44 nM (human M4) and 57 nM (rat M4). Chemical identifiers include formula C25H32N6O, molecular weight 432.56, CAS 2307718-96-1, and high purity (~99.7%).
Selective mAChR M4 antagonist with nanomolar potency.
Intended for research use only.
White to off-white solid with high purity (~99.7%).
Chemical formula C25H32N6O; molecular weight 432.56.
Available in 10 MG quantities.
Storage: powder at -20°C for long term; in solvent store at -80°C for extended periods.
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A derivative of betulin; active against E. aerogenes, E. coli, E. faecalis, P. aeruginosa, S. aureus, and C. albicans, as well as L. donovani amastigotes, at 50 µM; is cytotoxic to Huh7 hepatocellular carcinoma cells at 50 µM
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More