|
![]() |
|
|
Thioridazine
drug data and news
Thioridazine drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.
|
| Generic name | Thioridazine | ||
| Brand Names/Synonyms | Aldazine; Mallorol; Malloryl; Meleril; Mellaril; Mellaril Hydrochloride; Mellaril-S; Mellarit; Mellerets; Mellerette; Melleretten; Melleril; Metlaril; Novoridazine; Orsanil; Ridazin; Ridazine; Sonapax; Sonapax Hydrochloride; Stalleril; TP-21; Thioridazin; Thioridazine; Thioridazine Chloride; Thioridazine Hcl; Thioridazine Hcl Intensol; Thioridazine Hydrochloride; Thioridazine Hydrochloride [Jan]; Thioridazine, Prolongatum; Thioridazinhydrochlorid; Thoridazine Hydrochloride; Tioridazin; Usaf Sz-3; Usaf Sz-B | ||
| Indication | For the treatment of schizophrenia, and generalised anxiety disorder | ||
| Sponsored links | Description | Not Available | |
| Pharmacology | Thioridazine is a trifluoro-methyl phenothiazine derivative intended for the management of schizophrenia and other psychotic disorders. Thioridazine has not been shown effective in the management of behaviorial complications in patients with mental retardation. | ||
| Mechanism Of Action | Thioridazine blocks postsynaptic mesolimbic dopaminergic D1 and D2 receptors in the brain; blocks alpha-adrenergic effect, depresses the release of hypothalamic and hypophyseal hormones and is believed to depress the reticular activating system thus affecting basal metabolism, body temperature, wakefulness, vasomotor tone, and emesis. | ||
| Thioridazine News (When available) |
Lilly Submits Cymbalta Supplemental New Drug Application for ... May 9, 2006 | ||
| Dosage Forms | SUSPENSION; TABLET | ||
| Drug_Category | Antipsychotics; Dopamine Antagonists; Phenothiazines; ATC:N05AC02 | ||
| Absorption | 60% | ||
| Interactions |
-->Interactions for Thioridazine: Reduced cytochrome P450 2D6 isozyme activity, drugs which inhibit this isozyme (e.g., fluoxetine and paroxetine), and certain other drugs (e.g., fluvoxamine, propranolol, and pindolol) appear to appreciably inhibit the metabolism of thioridazine. The resulting elevated levels of thioridazine would be expected to augment the prolongation of the QTc interval associated with Mellaril and may increase the risk of serious, potentially fatal, cardiac arrhythmias, such as torsade de pointes-type arrhythmias. Such an increased risk may result also from the additive effect of co-administering Mellaril with other agents that prolong the QTc interval. Therefore, Mellaril is contraindicated with these drugs as well as in patients, comprising about 7% of the normal population, who are known to have a genetic defect leading to reduced levels of activity of P450 2D6. Drugs that Inhibit Cytochrome P450 2D6 In a study of 19 healthy male subjects, which included 6 slow and 13 rapid hydroxylators of debrisoquin, a single 25 mg oral dose of thioridazine produced a 2.4-fold higher Cmax and a 4.5- fold higher AUC for thioridazine in the slow hydroxylators compared to rapid hydroxylators. The rate of debrisoquin hydroxylation is felt to depend on the level of cytochrome P450 2D6 isozyme activity. Thus, this study suggests that drugs that inhibit P450 2D6 or the presence of reduced activity levels of this isozyme will produce elevated plasma levels of thioridazine. Therefore, the co-administration of drugs that inhibit P450 2D6 with Mellaril and the use of Mellaril in patients known to have reduced activity of P450 2D6 are contraindicated. Drugs that Reduce the Clearance of Mellaril® through Other Mechanisms Fluvoxamine: The effect of fluvoxamine (25 mg b.i.d. for one week) on thioridazine steady state concentration was evaluated in 10 male in-patients with schizophrenia. Concentrations of thioridazine and its two active metabolites, mesoridazine and sulforidazine, increased three-fold following co-administration of fluvoxamine. Fluvoxamine and Mellaril should not be co-administered. Propranolol: Concurrent administration of propranolol (100-800 mg daily) has been reported to produce increases in plasma levels of thioridazine (approximately 50%-400%) and its metabolites (approximately 80%-300%). Propranolol and Mellaril should not be co-administered. Pindolol: Concurrent administration of pindolol and thioridazine have resulted in moderate, dose-related increases in the serum levels of thioridazine and two of its metabolites, as well as higher than expected serum pindolol levels. Pindolol and Mellaril should not be co-administered. Drugs That Prolong the QTc Interval There are no studies of the co-administration of Mellaril and other drugs that prolong the QTc interval. However, it is expected that such co-administration would produce additive prolongation of the QTc interval and, thus, such use is contraindicated. | ||
| Toxicity | LD50=956-1034 mg/kg (Orally in rats); Agitation, blurred vision, coma, confusion, constipation, difficulty breathing, dilated or constricted pupils, diminished flow of urine, dry mouth, dry skin, excessively high or low body temperature, extremely low blood pressure, fluid in the lungs, heart abnormalities, inability to urinate, intestinal blockage, nasal congestion, restlessness, sedation, seizures, shock | ||
| Organisms Affected | Humans and other mammals | ||
| Chemical IUPAC Name | 10-[2-(1-methyl-2-piperidyl)ethyl]-2-methylsulfanyl-phenothiazine | ||
| Chemical Formula | C21H26N2S2 | ||
| Molecular Weight | 370.577 g/mol | ||
| Smiles String | CN1CCCCC1CCN2C3=CC=CC=C3SC4=C2C=C(C=C4)SC | ||
| Melting Point | 73 °C | ||
| Water Solubility | 0.0336 mg/L | ||
| State | Solid | ||
| LogP/Hphobicity | 6.552 | ||
| Isoelectric Point | 9.5 | ||
| Biotransformation | Hepatic | ||
| Half Life | 21-25 hours | ||
| Protein Binding [%] | 95% | ||
| RxList Link | RXlist | ||
| Sponsored links | |||
| Drug Reference |
http://www.drugs.com/cons/Thioridazine.html http://www.rxlist.com/cgi/generic3/thioridazine.htm | ||
| Drug Type | Approved Drug | ||
| Accession No | APRD00596 | ||
| CAS Registry Number | 50-52-2 | ||
| KEGG Compound ID | C07133 | ||
| PubChem ID | SID:148555 | ||
| PharmGKB ID | PA451666 | ||
| SwissProt ID | Not Available | ||
| GenBank ID | Not Available | ||
| Drug ID Number [DIN] | 360244 |
|
Home | About | Cancers | Treatment | Medications Copyright onconews.org 2005. All Rights Reserved. |