Orphenadrine-d3 hydrochloride

Modify Date: 2024-04-09 19:19:15

Orphenadrine-d3 hydrochloride Structure
Orphenadrine-d3 hydrochloride structure
Common Name Orphenadrine-d3 hydrochloride
CAS Number 1309283-23-5 Molecular Weight 308.86100
Density N/A Boiling Point N/A
Molecular Formula C18H21ClD3NO Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Orphenadrine-d3 hydrochloride


Orphenadrine-d3 (hydrochloride) is the deuterium labeled Orphenadrine hydrochloride[1]. Orphenadrine hydrochloride is an orally active and non-competitive NMDA receptor antagonist (crosses the blood-brain barrier) with a Ki of 6.0 μM. Orphenadrine hydrochloride relieves stiffness, pain and discomfort due to muscle strains, sprains or other injuries. Orphenadrine hydrochloride is also used to relieve tremors associated with parkinson's disease. Orphenadrine citrate has good neuroprotective properties, can be used in studies of neurodegenerative diseases[2][3].

 Names

Name N-Methyl-N-(2H3)methyl-2-[(2-methylphenyl)(phenyl)methoxy]ethanamine hydrochloride (1:1)

 Orphenadrine-d3 hydrochloride Biological Activity

Description Orphenadrine-d3 (hydrochloride) is the deuterium labeled Orphenadrine hydrochloride[1]. Orphenadrine hydrochloride is an orally active and non-competitive NMDA receptor antagonist (crosses the blood-brain barrier) with a Ki of 6.0 μM. Orphenadrine hydrochloride relieves stiffness, pain and discomfort due to muscle strains, sprains or other injuries. Orphenadrine hydrochloride is also used to relieve tremors associated with parkinson's disease. Orphenadrine citrate has good neuroprotective properties, can be used in studies of neurodegenerative diseases[2][3].
Related Catalog
In Vitro Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.  

[2]. Pubill D, et al. Orphenadrine prevents 3-nitropropionic acid-induced neurotoxicity in vitro and in vivo. Br J Pharmacol. 2001 Feb;132(3):693-702.  

[3]. Kornhuber J, et al. Orphenadrine is an uncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist: binding and patch clamp studies. J Neural Transm Gen Sect. 1995102(3):237-46.  

 Chemical & Physical Properties

Molecular Formula C18H21ClD3NO
Molecular Weight 308.86100
Exact Mass 308.17300
PSA 12.47000
LogP 4.46460