Methantheline drug data and news

Methantheline 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 Methantheline
Brand Names/Synonyms Asabaine; Avagal; Banthin; Banthine; Banthine Bromide; CHEMBANK4382; Dixamone Bromide; Doladene; Frenogastrico; Gastrin I; Gastrin-1 Human; Gastron; Gastrosedan; METHANTHELINE; MTB 51; Mantheline; Metantyl; Metaxan; Methanide; Methantheline; Methantheline Bromide; Methanthelinium; Methanthelinium Bromide; Methanthelinum; Methanthine Bromide; Methelina; Resobantin; SC 2910; Ulcine; Ulcudexter; Vagamin; Vagantin; Xanteline
Indication For use in the treatment of peptic ulcer disease, irritable bowel syndrome, pancreatitis, gastritis, biliary dyskinesia, pylorosplasm, and reflex neurogenic bladder in children.
Sponsored links
Description Not Available
Pharmacology Methantheline is a synthetic quarternary ammonium antimuscarinic used to relieve cramps or spasms of the stomach, intestines, and bladder. It can be used together with antacids or other medicines, such as H2-receptor antagonists, in the treatment of peptic ulcer. Methantheline inhibits muscarinic actions at postganglionic parasympathetic neuroeffector sites.
Mechanism Of Action Methantheline inhibits the muscarinic actions of acetylcholine on structures innervated by postganglionic cholinergic nerves as well as on smooth muscles that respond to acetylcholine but lack cholinergic innervation. These postganglionic receptor sites are present in the autonomic effector cells of the smooth muscle, cardiac muscle, sinoatrial and atrioventricular nodes, and exocrine glands. Depending on the dose, anticholinergics may reduce the motility and secretory activity of the gastrointestinal system, and the tone of the ureter and urinary bladder and may have a slight relaxant action on the bile ducts and gallbladder.
Methantheline News
(When available)
[an error occurred while processing this directive]
Dosage Forms TABLET (50 mg)
Drug_Category Anticholinergic Agents; Antispasmodics; ATC:A03AB07
Absorption Rapidly absorbed.
Interactions Interactions for Methantheline:
This drug may interact with the following: antacids, diarrhea medicine containing kaolin or attapulgite, ketoconazole (using these medicines with an anticholinergic may lessen the effects of the anticholinergic), central nervous system (CNS) depressants (taking scopolamine with CNS depressants may increase the effects of either medicine), other anticholinergics (medicine for abdominal or stomach spasms or cramps), tricyclic antidepressants (taking anticholinergics with tricyclic antidepressants or other anticholinergics may cause an increase in the effects of the anticholinergic), and potassium chloride (using this medicine with an anticholinergic may make gastrointestinal problems caused by potassium worse).
Toxicity Symptoms of overdose: blurred vision (continuing) or changes in near vision; clumsiness or unsteadiness; confusion; convulsions; difficulty in breathing, muscle weakness (severe), or tiredness (severe); dizziness; drowsiness (severe); dryness of mouth, nose, or throat (severe); fast heartbeat; fever; hallucinations; slurred speech; unusual excitement, nervousness, restlessness, or irritability; unusual warmth, dryness, and flushing of skin.
Organisms Affected Humans and other mammals
Chemical IUPAC Name diethyl-methyl-[2-(9H-xanthen-9-ylcarbonyloxy)ethyl]ammonium
Chemical Formula C21H26NO3
Molecular Weight 340.436 g/mol
Smiles String CC[N+](C)(CC)CCOC(=O)C1C2=CC=CC=C2OC3=CC=CC=C13
Melting Point Not Available
Water Solubility Not Available
State Solid
LogP/Hphobicity Not Available
Isoelectric Point Not Available
Biotransformation Hepatic, by enzymatic hydrolysis.
Half Life Not Available
Protein Binding [%] Not Available
RxList Link Not Available>RXlist
Sponsored links
Drug Reference http://www.drugs.com/cons/Methantheline.html
Drug Type Approved Drug
Accession No APRD00751
CAS Registry Number 5818-17-7
KEGG Compound ID C07849
PubChem ID SID:10051
PharmGKB ID PA450408
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] Not Available

Home | About | Cancers | Treatment | Medications
Copyright onconews.org 2005.
All Rights Reserved.
Google
 
Web onconews.org