Orphenadrine drug data and news

Orphenadrine 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 Orphenadrine
Brand Names/Synonyms Antiflex; BS-5930; Banflex; Biorphen; Brocadisipal; Brocasipal; Disipal; Flexoject; Mephenamine; Mio-Rel; Myolin; Myotrol; Norflex; O-Methyldiphenhydramine; Orfro; Orphenadine; Orphenadrin; Orphenadrine; Orphenadrine Citrate; Orphenate; Orphenedrine; WS 2434
Indication Indicated for the treatment of Parkinson's disease.
Sponsored links
Description Not Available
Pharmacology Orphenadrine is indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute painful musculoskeletal conditions. Orphenadrine is an anticholinergic with a predominantly central effect and only a weak peripheral effect. In addition, it has mild antihistaminic and local anaesthetic properties. Parkinson's syndrome is the consequence of a disturbed balance between cholinergic and dopaminergic neurotransmission in the basal ganglia caused by a decrease in dopamine. Orphenadrine restores the physiological equilibrium and has a favourable effect on the rigidity and tremor of Parkinson's disease and Parkinsonian syndromes. The effect is somewhat less on bradykinesia.
Mechanism Of Action Orphenadrine binds to both histamine H1 receptors and NMDA receptors. It restores the motor disturbances induced by neuroleptics, in particular the hyperkinesia. The dopamine deficiency in the striatum increases the stimulating effects of the cholinergic system. This stimulation is counteracted by the anticholinergic effect of orphenadrine. It may have a relaxing effect on skeletal muscle spasms and it has a mood elevating effect.
Orphenadrine News
(When available)
[an error occurred while processing this directive]
Dosage Forms TABLET (EXTENDED-RELEASE)
Drug_Category Muscle Relaxants; Antiparkinson Agents; Antidyskinetics; Skeletal Muscle Relaxants; ATC:M03BC01; ATC:N04AB02
Absorption Orphenadrine is almost completely absorbed in the gastrointestinal tract.
Interactions Interactions for Orphenadrine:

No information provided.

Toxicity Oral, mouse LD50 = 100mg/kg. Oral, rat LD50 = 255 mg/kg
Organisms Affected Humans and other mammals
Chemical IUPAC Name N,N-dimethyl-2-[(2-methylphenyl)-phenyl-methoxy]-ethanamine
Chemical Formula C18H23NO
Molecular Weight 269.381 g/mol
Smiles String CC1=CC=CC=C1C(C2=CC=CC=C2)OCCN(C)C
Melting Point 156-157 °C
Water Solubility Sparingly soluble in water
State Solid
LogP/Hphobicity 4.034
Isoelectric Point Not Available
Biotransformation Biotransformation occurs mainly in the liver. Pharmacologically active metabolites are N-demethyl orphenadrine and N,N-didemethyl orphenadrine.
Half Life 13-20 hours
Protein Binding [%] 95%
RxList Link RXlist
Sponsored links
Drug Reference http://www.drugs.com/cons/Orphenadrine.html
http://www.rxlist.com/cgi/generic/orphen.htm
Drug Type Approved Drug
Accession No APRD00097
CAS Registry Number 83-98-7
KEGG Compound ID C07935
PubChem ID SID:10137
PharmGKB ID PA450715
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 2243559

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