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Results for "

dihydropyridine ca

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    9
    TargetMol | Activity
Felodipine
T014572509-76-3
Felodipine (CGH-869) is a longlasting 1, 4-dihydropyridine calcium channel repressor.
  • $47
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Cilnidipine
T0388132203-70-4
Cilnidipine (FRC-8653)(FRC8653) is a dual L- and N-type calcium channel blocker and displays antihypertensive, sympatholytic and neuroprotective activity.
  • $41
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Amlodipine
T138588150-42-9
Amlodipine (UK-48340) is a synthetic dihydropyridine and a calcium channel blocker with antihypertensive and antianginal properties.
  • $45
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Amlodipine Besylate
T0231111470-99-6
Amlodipine Besylate(Amlodipine benzenesulfonate) is a long-lasting calcium channel blocker.
  • $33
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Nimodipine
T034366085-59-4
Nimodipine (BAY-e 9736), a 1, 4-dihydropyridine calcium channel blocker, acts primarily on vascular smooth muscle cells.
  • $40
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Isradipine
T095775695-93-1
Isradipine (PN 200-110) is a dihydropyridine calcium channel blocker with antihypertensive and vasodilator activities. Isradipine blocks calcium entry through calcium ion channels in coronary and peripheral vascular smooth muscle, dilating coronary arteries and peripheral arterioles. This action increases oxygen delivery by enhancing blood flow and decreases oxygen requirements by reducing total peripheral resistance.
  • $33
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Darodipine
T1505372803-02-2
Darodipine (PY-108068) is a dihydropyridine type Ca+2 antagonist.
  • $55
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Oxodipine
T6812390729-41-2In house
Oxodipine, a dihydropyridine-type calcium antagonist, inhibited KCl-induced aortic contraction in rabbits and reduced cardiac force in less potent rat ventricular test-paper contractions. In rat cultured neonatal ventricular myocytes, Oxodipine reduced L-type Ca currents (I) with an IC of 0.24 μM, and against T-type Ca currents (I) with an IC of 0.41 μM. Oxodipine causes constipation in mice and gingival hyperplasia in dogs.
  • $76
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UK-59811 hydrochloride
T397702250025-89-7
UK-59811 hydrochloride is a potent inhibitor of the Ca V Ab voltage-gated calcium channels in bacterial homotetrameric models. It is derived from Br-dihydropyridine, possessing significant inhibitory properties with an IC 50 of 194 nM.
  • $970
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