Brimonidine drug data and news

Brimonidine 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 Brimonidine
Brand Names/Synonyms Alphagan; Alphagan P; Brimonidine; Brimonidine Tartrate; Bromoxidine; CHEMBANK1623
Indication For the lowering of intraocular pressure in patients with open-angle glaucoma or ocular hypertension.
Sponsored links
Description Not Available
Pharmacology Brimonidine significantly lowers intraocular pressure with minimal effects on cardiovascular and pulmonary parameters. It lowers intraocular pressure by reducing aqueous humor production and increasing uveoscleral outflow.
Mechanism Of Action Brimonidine is an alpha adrenergic receptor agonist. It has a peak ocular hypotensive effect occurring at two hours post-dosing. Fluorophotometric studies in animals and humans suggest that Brimonidine has a dual mechanism of action by reducing aqueous humor production and increasing uveoscleral outflow.
Brimonidine News
(When available)
[an error occurred while processing this directive]
Dosage Forms 0.2% solution
Drug_Category Antihypertensive Agents; EENT Drugs; ATC:S01EA05
Absorption Minimal systemic absorption occurs after ocular insertion.
Interactions -->Interactions for Brimonidine:

Although specific drug interaction studies have not been conducted with ALPHAGAN® P, the possibility of an additive or potentiating effect with CNS depressants (alcohol, barbiturates, opiates, sedatives, or anesthetics) should be considered. Alpha-agonists, as a class, may reduce pulse and blood pressure. Caution in using concomitant drugs such as beta-blockers (ophthalmic and systemic), anti-hypertensives and/or cardiac glycosides is advised.

Tricyclic antidepressants have been reported to blunt the hypotensive effect of systemic clonidine.It is not known whether the concurrent use of these agents with ALPHAGAN® P in humans can lead to resulting interference with the IOP lowering effect. No data on the level of circulating catecholamines after ALPHAGAN® P administration are available. Caution, however, is advised in patients taking tricyclic antidepressants which can affect the metabolism and uptake of circulating amines.

Toxicity Oral LD50 is 50 mg/kg in mice and 100 mg/kg in rats.
Organisms Affected Humans and other mammals
Chemical IUPAC Name 5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)quinoxalin-6-amine
Chemical Formula C11H10BrN5
Molecular Weight 292.135 g/mol
Smiles String C1CN=C(N1)NC2=C(C3=NC=CN=C3C=C2)Br
Melting Point 207.5 °C
Water Solubility Soluble (1.5 mg/mL)
State Yellow crystals from ethanol
LogP/Hphobicity 0.782
Isoelectric Point Not Available
Biotransformation Metabolized primarily by the liver.
Half Life 2 hours
Protein Binding [%] Not Available
RxList Link RXlist
Sponsored links
Drug Reference http://www.drugs.com/cons/Brimonidine.html
http://www.rxlist.com/cgi/generic3/alphagan-p.htm
Drug Type Approved Drug
Accession No APRD00034
CAS Registry Number 59803-98-4
KEGG Compound ID C07886
PubChem ID SID:213378
PharmGKB ID Not Available
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 2243026

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