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AHFS/Drugs.com | International Drug Names |
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.020.285 ![]() |
Chemical and physical data | |
Formula | C30H35F2N3O |
Molar mass | 491.627 g·mol−1 |
3D model (JSmol) | |
Melting point | 159 to 161 °C (318 to 322 °F) |
Solubility in water | Almost insoluble in water(<0.01%); Very soluble in chloroform(>50%); mg/mL (20 °C) |
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Lidoflazine is a piperazine calcium channel blocker. It is a coronary vasodilator with some antiarrhythmic action.[1] Lidoflazine was discovered at Janssen Pharmaceutica in 1964.
Extracted from[1]
Solvent | 0.01
N |
0.1
N | ||
% | pH | % | pH | |
Hydrochloric Acid | 0.4 | 3.0 | 0.7 | 1.9 |
Tartaric Acid | 0.3 | 3.1 | 1.0 | 2.5 |
Citric Acid | 0.3 | 3.1 | 0.5 | 2.5 |
Lactic Acid | 0.2 | 3.4 | 0.7 | 2.9 |
Acetic Acid | 0.1 | 3.5 | 0.4 | 3.8 |
((cite journal))
: CS1 maint: DOI inactive as of February 2022 (link)Simple piperazines (no additional rings) | |
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Phenylpiperazines |
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Benzylpiperazines | |
Diphenylalkylpiperazines (benzhydrylalkylpiperazines) |
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Pyrimidinylpiperazines | |
Pyridinylpiperazines | |
Benzo(iso)thiazolylpiperazines | |
Tricyclics (piperazine attached via side chain) |
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Others/Uncategorized |