Chemistry:Desglymidodrine
From HandWiki
Desglymidodrine (developmental code name ST-1059) is the active metabolite of the prodrug antihypotensive agent midodrine.[1][2][3] It acts as a selective α1-adrenergic receptor agonist.[1][2][3] Desglymidodrine is formed from midodrine via deglycination.[1][2][3]
Pharmacology
Pharmacokinetics
The elimination half-life of desglymidodrine is 2 to 4 hours.[4]
Chemistry
Desglymidodrine, also known as 3,6-dimethoxy-β-hydroxy-2-phenylethylamine, is a substituted phenethylamine derivative.[5][6]
Midodrine's experimental log P is -0.5 and its predicted log P ranges from -0.49 to -0.95.[7][8] The predicted log P of desglymidodrine ranges from -0.01 to 0.15.[5][6]
An analogue of desglymidodrine is dimetofrine (3,5-dimethoxy-4,β-dihydroxy-N-methylphenethylamine).
See also
- List of investigational orthostatic intolerance drugs
References
- ↑ 1.0 1.1 1.2 "Midodrine. A review of its therapeutic use in the management of orthostatic hypotension". Drugs & Aging 12 (1): 76–86. January 1998. doi:10.2165/00002512-199812010-00007. PMID 9467688.
- ↑ 2.0 2.1 2.2 "Midodrine: a selective alpha-adrenergic agonist for orthostatic hypotension and dialysis hypotension". Expert Opinion on Pharmacotherapy 1 (4): 835–840. May 2000. doi:10.1517/14656566.1.4.835. PMID 11249519.
- ↑ 3.0 3.1 3.2 "The Role of Midodrine for Hypotension Outside of the Intensive Care Unit". Journal of Population Therapeutics and Clinical Pharmacology = Journal de la Therapeutique des Populations et de la Pharmacologie Clinique 24 (3): e45–e50. August 2017. doi:10.22374/1710-6222.24.3.4. PMID 28873293.
- ↑ Cite error: Invalid
<ref>tag; no text was provided for refs namedGilden2004 - ↑ 5.0 5.1 "Desglymidodrine". PubChem. U.S. National Library of Medicine. https://pubchem.ncbi.nlm.nih.gov/compound/43260.
- ↑ 6.0 6.1 "Metabolite desglymidodrine". https://go.drugbank.com/metabolites/DBMET00829.
- ↑ "Midodrine". PubChem. U.S. National Library of Medicine. https://pubchem.ncbi.nlm.nih.gov/compound/4195.
- ↑ "Midodrine: Uses, Interactions, Mechanism of Action". 31 December 1992. https://go.drugbank.com/drugs/DB00211.
