4-amino-6-methoxy-1-phenylpyridazin-1-ium methyl sulfate
Amezinium mesylate
CAS: 30578-37-1
Molecular Formula: C12H15N3O5S
4-amino-6-methoxy-1-phenylpyridazin-1-ium methyl sulfate - Names and Identifiers
| Name | Amezinium mesylate |
| Synonyms | Tenfortan Supratonin 30578-37-1 REGULTON (KNOLL) Amezinium mesylate RISUMIC (DAINIPPON) Amezinium Methylsulfate SUPRATONIN (GRUNENTHAL) AMEZINIUM METHYL SULFATE 4-amino-6-methoxy-1-phenyl-pyridaziniumethylsulfate 6-methoxy-1-phenylpyridazin-1-ium-4-amine methylsulfate 4-amino-6-methoxy-1-phenylpyridazin-1-ium methyl sulfate |
| CAS | 30578-37-1 |
| EINECS | 250-248-0 |
| InChI | InChI=1/C11H11N3O.CH4O4S/c1-15-11-7-9(12)8-13-14(11)10-5-3-2-4-6-10;1-5-6(2,3)4/h2-8,12H,1H3;1H3,(H,2,3,4) |
4-amino-6-methoxy-1-phenylpyridazin-1-ium methyl sulfate - Physico-chemical Properties
| Molecular Formula | C12H15N3O5S |
| Molar Mass | 313.33 |
| Melting Point | 176° (dec) |
| Appearance | powder to crystal |
| Color | White to Light yellow |
| Merck | 14,394 |
| Storage Condition | Inert atmosphere,Room Temperature |
4-amino-6-methoxy-1-phenylpyridazin-1-ium methyl sulfate - Risk and Safety
| RTECS | UR6066500 |
| Toxicity | LD50 in mice, rats (mg/kg): 1630, 1410 orally; 40.4, 45.5 i.v. (Teschendorf) |
4-amino-6-methoxy-1-phenylpyridazin-1-ium methyl sulfate - Preparation solution concentration reference
| 1mg | 5mg | 10mg | |
|---|---|---|---|
| 1 mM | 3.192 ml | 15.958 ml | 31.915 ml |
| 5 mM | 0.638 ml | 3.192 ml | 6.383 ml |
| 10 mM | 0.319 ml | 1.596 ml | 3.192 ml |
| 5 mM | 0.064 ml | 0.319 ml | 0.638 ml |
Last Update：2024-01-02 23:10:35
4-amino-6-methoxy-1-phenylpyridazin-1-ium methyl sulfate - Reference Information
| biological activity | Amezinium is a sympathomimetic drug that has the effect of pressurizing blood vessels in the treatment of hypotension. It is a MAO inhibitor that antagonizes the reactivity of tyramine and prevents the uptake of norepinephrine by neurons. |
| Uses | A MAO inhibitor that antagonizes the reactivity of tyramine and prevents the uptake of norepinephrine by neurons. |
Last Update：2024-04-09 20:52:54
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