H Sinzinger, P Fitscha
Index: J. Cardiovasc. Pharmacol. 19 Suppl 3 , S29-31, (1992)
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Isradipine, a calcium antagonist of the dihydropyridine type, shows antiatherosclerotic actions that interfere with all three main mechanisms of atherosclerosis. These actions are mediated by the release of prostaglandin I2 and endothelium-derived relaxing factor, and the subsequent elevation of intracellular adenosine-3',5'-cyclic phosphate and 3',5'-guanosine monophosphate, respectively. These mechanisms have been proven in vitro and in animal models. Preliminary data in humans suggest that these mechanisms have clinical relevance in the long-term treatment of patients as well.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
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Isradipine
CAS:75695-93-1 |
C19H21N3O5 |
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Cav1.3 channels control D2-autoreceptor responses via NCS-1 ...
2014-08-01 [Brain 137(Pt 8) , 2287-302, (2014)] |
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Analysis of responses to the TRPV4 agonist GSK1016790A in th...
2014-01-01 [Am. J. Physiol. Heart Circ. Physiol. 306(1) , H33-40, (2014)] |
|
L-type calcium channel blockade alleviates molecular and rev...
2013-01-15 [Behav. Brain Res. 237 , 190-9, (2013)] |
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Felodipine and isradipine: new calcium-channel-blocking agen...
1993-04-01 [Clin. Pharm. 12(4) , 261-75, (1993)] |
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Experimental and clinical effects of isradipine relevant to ...
1994-07-01 [Am. J. Hypertens. 7(7 Pt 2) , 30S-34S, (1994)] |
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