Proxibarbital
Also called Hydroxydial, Ipronal, Axeen
Overview
Proxibarbital (Ipronal) is a barbiturate derivative synthesized in 1956 in Poland by Bogusław Bobrański. It has anti-anxiety and sedative properties and is, in contrast to most barbiturates, almost without hypnotic action. It was used as a sedative and anti-anxiety drug. It was also used in the treatment of migraine headaches in a similar manner to butalbital. It was a prescription drug available in Poland from the 1950s to the 1990s under trade name Ipronal.[1]
Chemistry
- Formula
- C10H14N2O4 PC
- CAS number
- 2537-29-3 PC
- Molar mass (g/mol)
- 226.23 PC
- IUPAC name (computed by PubChem)
- 5-
(2- PChydroxypropyl) - 5- prop- 2- enyl- 1, 3- diazinane- 2, 4, 6- trione - SMILES
- CC(CC1(C(=O)
NC(=O) PCNC1=O) CC=C) O - InChIKey
- VNLMRPAWAMPLNZ-
UHFFFAOYSA- PCN - PubChem CID
- 17336
- IUPAC name
- (RS)
- WP5- allyl- 5- (2- hydroxypropyl) pyrimidine- 2, 4, 6(1H, 3H, 5H) - trione
Harm reduction information
No harm reduction data is on file for this compound yet. That means no dose, timing or combination data from PsychonautWiki or TripSit. Please don't guess a dose from similar compounds. If you have taken it and feel unwell, contact emergency services or a poison control center.
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Sources
- Other Zajdel P, Kulig K, Zejc A. Chemia leków, podręcznik dla studentów farmacji i farmaceutów. 2008
- Journal / agency Sulman FG, Pfeifer Y, Tal E. Migraine therapy by enzyme induction with proxibarbital. Therapie der Gegenwart. December 1976. PMID 14412
- Journal / agency Lambrey B, Compagnon PL, Jacquot C. Pharmacokinetics of 14C-2-allophanyl-2-allyl -gamma-valero-lactone: a prodrug of proxibarbal in rats. European Journal of Drug Metabolism and Pharmacokinetics. 1981. doi:10.1007/BF03189485 · PMID 6118275
Text and values on this page are quoted from Wikipedia (CC BY-SA 4.0), PubChem (public domain). Each value links to the exact revision it came from.