Weight | 402.585 g/mol |
---|---|
Formula | C21H26N2O2S2 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 0 |
Aromatic Rings | 2 |
Rotatable Bonds | 4 |
Sulforidazine (14759-06-9)
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- Greater potency of mesoridazine and sulforidazine compared with the parent compound, thioridazine, on striatal dopamine autoreceptors. (Journal of Pharmacology and Experimental Therapeutics, 1984)
- Comparative antidopaminergic properties of thioridazine, mesoridazine and sulforidazine on the corpus striatum. (Journal of Pharmacology and Experimental Therapeutics, 1989)
- Development of a radioimmunoassay procedure for sulforidazine and its comparison with a high-performance liquid chromatographic method. (Therapeutic Drug Monitoring, 1987)
- Comparative anticholinergic properties of thioridazine, mesoridazine and sulforidazine. (Journal of Pharmacology and Experimental Therapeutics, 1989)
- The metabolism of piperidine-type phenothiazine antipsychotic agents. I. Sulforidazine in the rat (Xenobiotica, 1992)
- Sensitive and specific high-performance liquid chromatographic assay for the quantification of sulforidazine and two diastereomeric sulforidazine-5-sulfoxide metabolites in plasma (Journal of Chromatography B: Biomedical Sciences and Applications, 1987)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1CCCCC1CCN2C3=CC=CC=C3SC4=C2C=C(C=C4)S(=O)(=O)C
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InChIKeyFLGCRGJDQJIJAW-UHFFFAOYSA-N
- Pubchem - Sulforidazine
- Wikipedia - sulforidazine
Sulforidazine (Imagotan, Psychoson, Inofal) a typical antipsychotic and a metabolite of thioridazine; it and mesoridazine are more potent than the parent compound, whose pharmacological effects are believed by some to be largely due to its metabolism into sulforidazine and mesoridazine.
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