Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C24H33N.ClH |
| Molecular Weight | 371.986 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(CC1CCCCC1)NCCC(C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChIKey=HDIWDSZQIUBDFT-UHFFFAOYSA-N
InChI=1S/C24H33N.ClH/c1-20(19-21-11-5-2-6-12-21)25-18-17-24(22-13-7-3-8-14-22)23-15-9-4-10-16-23;/h3-4,7-10,13-16,20-21,24-25H,2,5-6,11-12,17-19H2,1H3;1H
Droprenilamine hydrochloride is coronary vasodilator. It is a secondary amine structurally related to the antianginal drug prenylamine. It increases coronary flow in the isolated guinea-pig heart and partially inhibits pitressin-induced ST-segment changes in anaesthetized rats. Droprenilamine hydrochloride also elevated coronary blood flow in the anaesthetized greyhound and reduced the incidence of cardiac dysrhythmias, which result from acute ligation of the anterior descending branch of the left coronary artery. Droprenilamine hydrochloride only reduced heart rate when administered after coronary artery occlusion, a fact, which may be related to the effects of the drug on the increased sympatho-adrenal outflow produced by myocardial ischemia.
Approval Year
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59182-63-7
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65471
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m1125
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admin on Mon Mar 31 22:42:12 GMT 2025 , Edited by admin on Mon Mar 31 22:42:12 GMT 2025
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OG73JS161X
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DTXSID40974615
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admin on Mon Mar 31 22:42:12 GMT 2025 , Edited by admin on Mon Mar 31 22:42:12 GMT 2025
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ACTIVE MOIETY
SUBSTANCE RECORD