Methaqualone

Methaqualone
Clinical data
Pronunciation /mɛθəˈkweɪloʊn/
Trade names Bon-Sonnil, Dormogen, Dormutil, Mequin, Mozambin, Pro Dorm, Somnotropon, Torinal, Tuazolona. Methaqualone hydrochloride: Cateudyl, Dormir, Hyptor, Melsed, Melsedin, Mequelon, Methasedil, Nobadorm, Normorest, Noxybel, Optimil, Optinoxan, Parest, Parmilene, Pexaqualone, Revonal, Riporest, Sedalone, Somberol, Somnafac, Somnium, Sovelin, Soverin, Sovinal, Toraflon, Tualone, Tuazol.
Pregnancy
category
  • US: D (Evidence of risk)
    ATC code
    Legal status
    Legal status
    Pharmacokinetic data
    Protein binding 70-80%
    Elimination half-life Biphasic (10-40; 20-60 hours)
    Identifiers
    CAS Number
    PubChem CID
    DrugBank
    ChemSpider
    UNII
    KEGG
    ChEMBL
    ECHA InfoCard 100.000.710 Edit this at Wikidata
    Chemical and physical data
    Formula C16H14N2O
    Molar mass 250.30 g/mol
    3D model (JSmol)
    Melting point 113 °C (235 °F)
      (verify)

    Methaqualone, sold under the brand name Quaalude (pronounced KWAY-lood) and sometimes stylized "Quāālude"[1] in the United States and Mandrax in the United Kingdom and South Africa, is a sedative and hypnotic medication. It is a member of the quinazolinone class.

    The sedative–hypnotic activity of methaqualone was first noted by researchers in the 1950s. In 1962, methaqualone was patented in the US by Wallace and Tiernan.[2] Its use peaked in the early 1970s as a hypnotic, for the treatment of insomnia, and as a sedative and muscle relaxant.

    Methaqualone became increasingly popular as a recreational drug and club drug in the late 1960s and 1970s, known variously as "ludes" or "sopers" (also "soaps") in the U.S. and "mandrakes" and "mandies" in the UK, Australia and New Zealand. The substance is sold both as a free base and as salt (hydrochloride).

    Uses

    Medical

    Methaqualone is a sedative that increases the activity of the GABA receptors in the brain and nervous system. When GABA activity is increased, blood pressure drops and the breathing and pulse rates slow, leading to a state of deep relaxation. These properties explain why methaqualone was originally mainly prescribed for insomnia.[3] Methaqualone peaks in the bloodstream within several hours, with a half-life of 20–60 hours. Regular users build up a physical tolerance, requiring larger doses for the same effect. Overdose can lead to nervous system shutdown, coma and death.[4]

    Methaqualone is not recommended for use while pregnant and is in pregnancy category D.[5]

    Overdose

    An overdose can cause delirium, convulsions, hypertonia, hyperreflexia, vomiting, kidney failure, coma, and death through cardiac or respiratory arrest. It resembles barbiturate poisoning, but with increased motor difficulties and a lower incidence of cardiac or respiratory depression. The standard one tablet adult dose of Quaalude was 300 mg when made by Lemmon. A dose of 8000 mg is lethal and a dose as little as 2000 mg could induce a coma if taken with an alcoholic beverage.[6]

    History

    Methaqualone was first synthesized in India in 1951 by Indra Kishore Kacker and Syed Husain Zaheer, for use as an antimalarial drug.[6][7][8] By 1965, it was the most commonly prescribed sedative in Britain, where it has been sold legally under the names Malsed, Malsedin, and Renoval. In 1965, a methaqualone/antihistamine combination was sold as the sedative drug Mandrax, by Roussel Laboratories (now part of Sanofi S.A.). In 1972, it was the sixth-bestselling sedative in the US,[9] where it was legal under the brand name Quaalude. Quaalude in the United States was originally manufactured in 1965 by the Fort Washington, Pennsylvania, based pharmaceutical firm William H. Rorer Inc. The drug name "Quaalude" combined the words "quiet interlude" and shared a stylistic reference to another drug marketed by the firm, Maalox.[10]

    In 1978, Rorer sold the rights to manufacture Quaalude to the Lemmon Company of Sellersville, Pennsylvania. At that time, Rorer chairman John Eckman commented on Quaalude's bad reputation stemming from illegal manufacture and use of methaqualone, and illegal sale and use of legally prescribed Quaalude: "Quaalude accounted for less than 2% of our sales but created 98% of our headaches."[6] Both companies still regarded Quaalude as an excellent sleeping drug. Lemmon, well aware of Quaalude's public image problems, used advertisements in medical journals to urge physicians "not to permit the abuses of illegal users to deprive a legitimate patient of the drug". Lemmon also marketed a small quantity under another name, Mequin, so doctors could prescribe the drug without the negative connotations.[6] The rights to Quaalude were held by the JB Roerig & Company division of Pfizer, before the drug was discontinued in the United States in 1985, mainly due to its psychological addictiveness and recreational use.[11]

    Society and culture

    Regulation

    Methaqualone was initially placed in Schedule I as defined by the UN Convention of Psychotropic Substances, but was moved to Schedule II in 1979. [12]

    In Canada, methaqualone is listed in Schedule III of the Controlled Drugs and Substances Act and requires a prescription but is Schedule I according to NAPRA.[13] Methaqualone is banned in India.[14]

    Recreational

    A variety of Quaalude pills and capsules.

    Methaqualone became increasingly popular as a recreational drug in the late 1960s and 1970s, known variously as "ludes" or "sopers" (also "soaps") in the U.S. and "mandrakes" and "mandies" in the UK, Australia and New Zealand.

    The drug was more tightly regulated in Britain under the Misuse of Drugs Act 1971 and in the U.S. from 1973. It was withdrawn from many developed markets in the early 1980s. In the United States it was withdrawn in 1982 and made a Schedule I drug in 1984. It has a DEA ACSCN of 2565 and in 2013 the aggregate annual manufacturing quota for the US was 10 grams. Mention of its possible use in some types of cancer and AIDS has periodically appeared in the literature since the late 1980s; research does not appear to have reached an advanced stage. The DEA has also added the methaqualone analogue mecloqualone (also a result of some incomplete clandestine syntheses) to Schedule I as ACSCN 2572, with zero manufacturing quota.

    Gene Haislip, the former head of the Chemical Control Division of the Drug Enforcement Administration (DEA), told the PBS documentary program Frontline: "We beat 'em." By working with governments and manufacturers around the world, the DEA was able to halt production and, Haislip said, "eliminated the problem".[15][16][17] Methaqualone was manufactured in the United States under the name Quaalude by the pharmaceutical firms Rorer and Lemmon with the numbers 714 stamped on the tablet, so people often referred to Quaalude as 714's, "Lemmons", or "Lemmon 7's". Methaqualone was also manufactured in the US under the trade names Sopor and Parest. After the legal manufacture of the drug ended in the United States in 1982, underground laboratories in Mexico continued the illegal manufacture of methaqualone throughout the 1980s, continuing the use of the "714" stamp, until their popularity waned in the early 1990s. Drugs purported to be methaqualone are in a significant majority of cases found to be inert, or contain diphenhydramine or benzodiazepines.

    Methaqualone is one of the most commonly used recreational drugs in South Africa.[18][19] It is also popular elsewhere in Africa and in India.[19]

    See also

    References

    1. ↑ Rile, Karen (1983). Winter Music (First ed.). Boston and Toronto: Little, Brown and Company. pp. 41, 59. ISBN 0-316-74657-6.
    2. ↑ U.S. Patent 3,135,659 – Hydroxy and Alkoxy Aryl Quinazolones
    3. ↑ "methaqualone reference". Enotes. Archived from the original on February 23, 2012.
    4. ↑ "recreational drugs tranquilizers". drug library eu. Archived from the original on 2013-03-02.
    5. ↑ Drug Safety. "Methaqualone in Pregnancy and Breastfeeding". Retrieved 15 August 2012.
    6. 1 2 3 4 Linder, Lee (28 May 1981). "Quaalude manufacturer: Image hurt by street use". Lawrence Journal-World. Associated Press. p. 6. Retrieved 16 August 2013. Eckman/Fisher
    7. ↑ van Zyl, Etienne F. (2001). "A survey of reported synthesis of methaqualone and some positional and structural isomers". Forensic Science International. 122 (2–3): 142–149. doi:10.1016/S0379-0738(01)00484-4.
    8. ↑ Potential Analgesics. Part I. Synthesis of substituted 4-quinazolones, I. K. Kacker and S. H. Zaheer, J. Ind. Chem. Soc. 28 (1951), pp. 344–346.
    9. ↑ GC/MS Assays for Abused Drugs in Body fluids, p. 39
    10. ↑ "Dividends: Dropping the Last 'Lude". Time. 28 November 1983. Retrieved 16 August 2013.
    11. ↑ Silverstein, Shel. "Quaaludes Again". Captain Wayne's Mad Music.com.
    12. ↑ lilian.sandouk. "green-lists". www.incb.org. Archived from the original on 2017-09-18. Retrieved 2017-09-06.
    13. ↑ "Search National Drug Schedule". Archived from the original on 2014-02-01. Retrieved 2014-01-07.
    14. ↑ "Drugs banned in India". Central Drugs Standard Control Organization, Dte.GHS, Ministry of Health and Family Welfare, Government of India. Archived from the original on 2015-02-21. Retrieved 2013-09-17.
    15. ↑ "The Meth Epidemic – Haislip discusses parallels to current Methamphetamine epidemic".
    16. ↑ Ferns, Sean, "Lecture: Gene Haislip : The Chemical Connection: A Historical Perspective on Chemical Control" Archived 2014-03-31 at the Wayback Machine., Drug Enforcement Administration Museum Lecture Series, Arlington, Virginia, October 25, 2007
    17. ↑ Piccini, Sara, "DRUG WARRIOR: THE DEA’S GENE HAISLIP ’60, B.C.L. ’63 BATTLED WORLDWIDE AGAINST THE ILLEGAL DRUG TRADE – AND SCORED A RARE VICTORY", William & Mary Alumni Magazine, The College of William & Mary, Spring 2010
    18. ↑ "Mandrax". DrugAware. Reality Media. 2003. Retrieved 2009-08-13.
    19. 1 2 McCarthy, G; Myers, B; Siegfried, N (2005). "Treatment for methaqualone dependence in adults". Reviews (2): CD004146. doi:10.1002/14651858.CD004146.pub2. PMID 15846700.
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