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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
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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, inhibiting the initial influx of calcium. This compound is used in research for its effects on high blood pressure and cancer.
Orally active dihydropyridine calcium channel blocker
Blocks voltage-dependent L-type calcium channels
Utilized in research for high blood pressure
Utilized in research for cancer
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PF-562271 besylate is an ATP-competitive, reversible inhibitor of focal adhesion kinase (FAK) and Pyk2 that exhibits low-nanomolar potency and is used in biochemical and cellular research to probe FAK/Pyk2 signaling pathways.
Potent inhibition of FAK and Pyk2 with IC50s of 1.5 nM and 13 nM.
High purity suitable for research applications.
Chemical formula C27H26F3N7O6S2; molecular weight 665.66 g·mol⁻¹.
Available in multiple package sizes, including 100 mg.
Storage: sealed at 4°C; in solvent: -80°C (6 months), -20°C (1 month).
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Also available in 1 mL, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Harmaline hydrochloride (Harmidine hydrochloride) is a fluorescent indole alkaloid from the group of harmala alkaloids and beta-carbolines. It is the partially hydrogenated form of harmine.Harmaline produces a generalized tremor in normal rats by inducing rhythmic firing of inferior olivary neurons Purity 99.53%
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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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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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