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Hyoscyamine
drug data and news
Hyoscyamine 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.
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| Generic name | Hyoscyamine | ||
| Brand Names/Synonyms | ATROPINE; Anaspaz; Cystospaz; Daturine; Duboisine; Duretter; Egacene; Egazil; Gastrosed; Hyocyamine; Hyoscyamine; Hyoscyamine, L-; L-Atropine; L-Hyopscyamine; L-Hyoscamine; L-Hyoscyamine; L-Hyoscyamine Free Base; L-Tropine Tropate; Levbid; Levsin; Levsinex; OIN; Peptard; Scopolia Extract | ||
| Indication | For treatment of bladder spasms, peptic ulcer disease, diverticulitis, colic, irritable bowel syndrome, cystitis, and pancreatitis. Hyoscyamine may also be used to treat certain heart conditions, to control the symptoms of Parkinson's disease and rhinitis | ||
| Sponsored links | Description | Not Available | |
| Pharmacology | L-Hyoscyamine, the active optical isomer of atropine (dl-hyoscyamine), is a tertiary amine anticholinergic gastrointestinal agent. Hyoscyamine is used to manage peptic ulcer disease, biliary tract disorders, cystitis, severe allergic rhinitis, hypermotility disorders of the lower urinary tract, infant colic, and to control salivation and excessive secretions before an operation. | ||
| Mechanism Of Action | Hyoscyamine competes favorably with acetylcholine for binding at muscarinic receptors in the salivary, bronchial, and sweat glands as well as in the eye, heart, and gastrointestinal tract. The actions of hyoscyamine result in a reduction in salivary, bronchial, gastric and sweat gland secretions, mydriasis, cycloplegia, change in heart rate, contraction of the bladder detrusor muscle and of the gastrointestinal smooth muscle, and decreased gastrointestinal motility. | ||
| Hyoscyamine News (When available) |
From the analyst's couch: The IBS market Feb 15, 2006 Inkine Pharmaceutical Announces Approval of Merger with Salix ... Sep 30, 2005 InKine Reports Seven INKP-102 Study Data Abstracts Accepted for ... Aug 4, 2005 Italy: Lettuce uncovered as sexual stimulant Jun 29, 2005 InKine Announces Final Court Approval in Securities Class Action ... Jun 16, 2005 InKine Announces Final Court Approval in Securities Class Action ... Jun 16, 2005 Inkine's Visicol Tablets Associated with Significantly Less After ... May 19, 2005 InKine CEO To Present at the Rodman & Renshaw Techvest 2nd Annual ... 29 Apr 2005 Inappropriate medication prescribed to elderly Mar 8, 2005 Almost One In Three Seniors Given Inappropriate Meds Feb 26, 2005 InKine to Present at BIO CEO & Investor Conference Feb 17, 2005 Almost One In Three Seniors Given Inappropriate Meds Feb 25, 2005 With Positive INKP-102 Results, InKine Prepares For NDA Filing Feb 22, 2005 | ||
| Dosage Forms | Oral tablets, oral drops, elixir, injection | ||
| Drug_Category | Mydriatics; Bronchodilator Agents; Antiarrhythmic Agents; Adjuvants; Antimuscarinics; Antispasmodics; ATC:A03BA03 | ||
| Absorption | absorbed totally and completely by sublingual administration as well as oral administration | ||
| Interactions |
Interactions for Hyoscyamine: Additive adverse effects resulting from cholinergic blockade may occur when LEVSIN is administered concomitantly with other antimuscarinics, amantadine, haloperidol, phenothiazines, monoamine oxidase (MAO) inhibitors, tricyclic antidepressants or some antihistamines. Antacids may interfere with the absorption of LEVSIN. Administer LEVSIN before meals; antacids after meals. | ||
| Toxicity | headache nausea, vomiting, blurred vision, dilated pupils, hot dry skin, dizziness, dryness of the mouth, difficulty in swallowing, and CNS stimulation. LD50=mg/kg(orally in rat) | ||
| Organisms Affected | Humans and other mammals | ||
| Chemical IUPAC Name | (8-methyl-8-azabicyclo[3.2.1]oct-3-yl)3-hydroxy-2-phenyl-propanoate | ||
| Chemical Formula | C17H23NO3 | ||
| Molecular Weight | 289.369 g/mol | ||
| Smiles String | CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 | ||
| Melting Point | 141°C | ||
| Water Solubility | 1g/281mL | ||
| State | Solid | ||
| LogP/Hphobicity | 2.904 | ||
| Isoelectric Point | 11.7 | ||
| Biotransformation | Hepatic | ||
| Half Life | 2-3 1/2 hours | ||
| Protein Binding [%] | 50% | ||
| RxList Link | RXlist | ||
| Sponsored links | |||
| Drug Reference |
http://www.drugs.com/cons/Hyoscyamine.html http://www.rxlist.com/cgi/generic/hyoscy.htm | ||
| Drug Type | Approved Drug | ||
| Accession No | APRD00607 | ||
| CAS Registry Number | 101-31-5 | ||
| KEGG Compound ID | Not Available | ||
| PubChem ID | SID:206628 | ||
| PharmGKB ID | Not Available | ||
| SwissProt ID | Not Available | ||
| GenBank ID | Not Available | ||
| Drug ID Number [DIN] | 125857 |
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