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Levamlodipine Besylate is a powerful dihydropyridine calcium channel blocker possessing vasodilation properties and used in the treatment of hypertension and angina
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Amlodipine maleate is a dihydropyridine calcium channel blocker that acts as an orally active antianginal agent. It blocks voltage-dependent L-type calcium channels, inhibiting the initial influx of calcium. It can be used for the research of high blood pressure and cancer.
Calcium channel blocker
Orally active
Blocks voltage-dependent L-type calcium channels, inhibiting the initial influx of calcium
Used for research related to high blood pressure and cancer
High purity (99.87%)
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Mirogabalin besylate is a research-grade small molecule that acts as a selective, orally available ligand for the α2δ subunit of voltage-gated calcium channels. It is supplied as a high-purity solid with manufacturer documentation supporting identity, purity, and safe handling for laboratory research.
High purity (99.6%) suitable for research applications.
Molecular formula C18H25NO5S; molecular weight 367.46.
Solid powder formulation supplied in a 50 MG unit.
Store solid sealed at 4°C, away from moisture; in solution store at -80°C (6 months) or -20°C (1 month).
Documentation available: datasheet, certificate of analysis, and safety data sheet.
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Amlodipine (CAS 88150-42-9) is a dihydropyridine-based small molecule that functions as a long-acting calcium channel blocker It selectively inhibits L-type calcium channels on vascular smooth muscle and cardiac myocytes thereby reducing intracellular calcium influx This action leads to vasodilation and decreased vascular resistance Amlodipine is widely utilized in biomedical research to investigate calcium signaling pathways vascular tone modulation and cardiovascular pharmacology Its mechanistic profile also makes it a reference compound in studies evaluating novel antihypertensive or vasodilatory agents
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Cisatracurium Besylate (CAS 96946-42-8) is a non-depolarizing neuromuscular blocking agent that acts by competitively inhibiting acetylcholine at nicotinic receptors on the neuromuscular junction This inhibition prevents depolarization of the muscle cell membrane resulting in skeletal muscle relaxation Cisatracurium Besylate is utilized in biomedical research to study neuromuscular transmission skeletal muscle function and mechanisms underlying muscle paralysis It is also frequently used as an adjunct in anesthesia research to model conditions requiring controlled muscle relaxation such as intubation or mechanical ventilation
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PF-562271 Besylate is the benzenesulfonate salt of PF-562271 which is a potent ATP-competitive reversible inhibitor of FAK with IC50 of 1 5 nM 10-fold less potent for Pyk2 than FAK and 100-fold selectivity against other protein kinases except for some CDKs Phase 1
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NCC-149 is a selective histone deacetylase 8 (HDAC8) inhibitor used in research on neural differentiation and HDAC8-related signaling pathways. It is supplied as a high-purity solid for laboratory use and is commonly prepared as a DMSO stock for cellular and biochemical assays.
Selective HDAC8 inhibition for targeted epigenetic studies.
Suitable for neural differentiation experiments and mechanistic research.
High reported purity for reproducible experimental results.
Available in small milligram pack sizes for screening and assay development.
Soluble in DMSO for preparation of concentrated stock solutions.
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Amlodipine is an antianginal agent and an orally active dihydropyridine calcium channel blocker. It functions by blocking voltage-dependent L-type calcium channels, thereby inhibiting the initial influx of calcium. It can be used in the research of high blood pressure and cancer.
Functions as an antianginal agent
Orally active dihydropyridine calcium channel blocker
Blocks voltage-dependent L-type calcium channels
Inhibits initial influx of calcium
Suitable for research on high blood pressure
Suitable for research on cancer
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More