Methaqualone

Template:Short description Template:Cs1 config Template:Main other {{#invoke:Infobox|infobox}}Template:Template other{{#invoke:TemplatePar |check |template=Template:Infobox_drug |all= |opt= pronounce= pronounce_ref= pronounce_comment= ATC_prefix= ATC_suffix= ATC_supplemental= ATCvet= biosimilars= CAS_number_Ref= CAS_number= CAS_supplemental= ChEBI= ChEBI_Ref= ChEMBL_Ref= ChEMBL= ChemSpiderID= ChemSpiderID_Ref= chirality= class= container_only= DailyMedID= data_page= DrugBank_Ref= DrugBank= Drugs.com= duration_of_action= INN= INN_EMA= IUPAC_name= IUPHAR_ligand= KEGG_Ref= KEGG= MedlinePlus= NIAID_ChemDB= PDB_ligand= PubChemSubstance= PubChem= StdInChIKey_Ref= StdInChIKey= StdInChI_Ref= StdInChI_comment= StdInChI= UNII_Ref= UNII= DTXSID= Verifiedfields= Watchedfields= addiction_liability= alt2= altL= altR= alt= bioavailability= boiling_high= boiling_notes= boiling_point= captionLR= caption= caption2= charge= chemical_formula= chemical_formula_ref= chemical_formula_comment= class1= class2= class3= class4= class5= class6= component1= component2= component3= component4= component5= component6= density= density_notes= dependency_liability= drug_name= elimination_half-life= engvar= excretion= image2= imageL= imageR= image= image_class= image_class2= image_classL= image_classR= Jmol= legal_AU= legal_BR= legal_CA= legal_DE= legal_EU= legal_NZ= legal_UK= legal_UN= legal_US= legal_AU_comment= legal_BR_comment= legal_CA_comment= legal_DE_comment= legal_UK_comment= legal_NZ_comment= legal_US_comment= legal_UN_comment= legal_EU_comment= legal_status= licence_CA= licence_EU= licence_US= license_CA= license_EU= license_US= mab_type= melting_high= melting_notes= melting_point= metabolism= metabolites= molecular_weight= molecular_weight_round= molecular_weight_unit= molecular_weight_ref= molecular_weight_comment= onset= pregnancy_AU= pregnancy_AU_comment= pregnancy_category= protein_bound= routes_of_administration= SMILES= smiles= solubility= sol_units= source= specific_rotation= synonyms= target= tradename= type= vaccine_type= verifiedrevid= width2= widthL= widthR= width= AAN= BAN= JAN= USAN= source_tissues= target_tissues= receptors= agonists= antagonists= precursor= biosynthesis= gt_target_gene= gt_vector= gt_nucleic_acid_type= gt_editing_method= gt_delivery_method= sec_combustion= Ac=Ag=Al=Am=Ar=As=At=Au=B=Ba=Be=Bh=Bi=Bk=Br=C=Ca=Cd=Ce=Cf=Cl=Cm=Cn=Co=Cr=Cs=Cu= D=Db=Ds=Dy=Er=Es=Eu=F=Fe=Fl=Fm=Fr=Ga=Gd=Ge=H=He=Hf=Hg=Ho=Hs=I=In=Ir=K=Kr=La=Li=Lr=Lu=Lv= Mc=Md=Mg=Mn=Mo=Mt=N=Na=Nb=Nd=Ne=Nh=Ni=No=Np=O=Og=Os=P=Pa=Pb=Pd=Pm=Po=Pr=Pt=Pu=Ra=Rb=Re=Rf=Rg=Rh=Rn=Ru=S=Sb=Sc=Se=Sg=Si=Sm=Sn=Sr=Ta=Tb=Tc=Te=Th=Ti=Tl=Tm=Ts=U=V=W=Xe=Y=Yb=Zn=Zr= index_label= index2_label= index_comment= index2_comment= CAS_number2= CAS_supplemental2= ATC_prefix2= ATC_suffix2= ATC_supplemental2= PubChem2= PubChemSubstance2= IUPHAR_ligand2= DrugBank2= ChemSpiderID2= UNII2= KEGG2= ChEBI2= ChEMBL2= PDB_ligand2= NIAID_ChemDB2= SMILES2= smiles2= StdInChI2= StdInChIKey2= CAS_number2_Ref= ChEBI2_Ref= ChEMBL2_Ref= ChemSpiderID2_Ref= DrugBank2_Ref= KEGG2_Ref= StdInChI2_Ref= StdInChIKey2_Ref= UNII2_Ref= DTXSID2= QID= QID2=PLLR= pregnancy_US= pregnancy_US_comment= |cat=Pages using infobox drug with unknown parameters |format=0|errNS=0

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| vaccine_type= | mab_type= | _number_of_combo_chemicals={{#invoke:ParameterCount |main |component1 |component2 |component3 |component4|component5|component6 }} | _vaccine_data= | _mab_data= | _mab_vaccine_data= | _mab_other_data=161421Cc1ccccc1-n1c(C)nc2ccccc2c1=O1S/C16H14N2O/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19/h3-10H,1-2H3JEYCTXHKTXCGPB-UHFFFAOYSA-NTemplate:StdinchiciteTemplate:Stdinchicite113 | _combo_data= | _physiological_data= | _clinical_data= Bon-Sonnil, Dormogen, Dormutil, Mequin, Mozambin, Pro Dorm, Quaalude, Somnotropon, Torinal, Tuazolona
Methaqualone hydrochloride:
Cateudyl, Dormir, Hyptor, Melsed, Melsedin, Mequelon, Methasedil, Nobadorm, Normorest, Noxybel, Optimil, Optinoxan, Pallidan, Parest, Parmilene, Pexaqualone, Renoval, Riporest, Sedalone, Somberol, Somnifac, Somnium, Sopor, Sovelin, Soverin, Sovinal, Toquilone, Toraflon, Tualone, TuazolN05 | _legal_data=S9<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>F2Schedule IIIAnlage IIClass BP IISchedule I

| _other_data=2-Methyl-3-o-tolyl-4(3H)-quinazolinone;
3,4-Dihydro-2-methyl-4-oxo-3-o-tolylquinazoline;
2-Methyl-3-(2-methylphenyl)-4-(3H)-quinazolinone

| _image_0_or_2 = Methaqualone2.svg | _image_LR =

| _datapage = Methaqualone (data page) | _vaccine_target={{#ifeq: | vaccine | | _type_not_vaccine }} | _legal_all=S9F2Schedule IIIClass BSchedule IP II | _ATC_prefix_supplemental=N05 | _has_EMA_link = | CAS_number=72-44-6 | PubChem=6292 | ChemSpiderID=6055 | ChEBI=6821 | ChEMBL=282052 | DrugBank=DB04833 | KEGG=D00557 | _hasInChI_or_Key={{#if:1S/C16H14N2O/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19/h3-10H,1-2H3JEYCTXHKTXCGPB-UHFFFAOYSA-N |yes}} | UNII=7ZKH8MQW6T | _hasJmol02 = |_hasMultipleCASnumbers = |_hasMultiplePubChemCIDs = |_hasMultipleChEBIs =

| _countSecondIDs={{#invoke:ParameterCount |main |CAS_number2 |ATC_prefix2 |PubChem2 |PubChemStructure2 |IUPHAR_ligand2 |DrugBank2 |ChemSpiderID2 |UNII2 |KEGG2 |ChEBI2 |ChEMBL2 |PDB_ligand2 |NIAID_ChemDB2 |SMILES2 |smiles2 |StdInChI2 |StdInChIKey2 |DTXCID2}} | _countIndexlabels={{#invoke:ParameterCount |main |index_label |index2_label}} | _trackListSortletter= |QID = |QID2 = |Verifiedfields= |Watchedfields=changed |verifiedrevid=418472840}} Methaqualone is a hypnotic sedative. It was sold under the brand names Quaalude (Template:IPAc-en Template:Respell) and Sopor among others, which contained 300 mg of methaqualone, and sold as a combination drug under the brand name Mandrax, which contained 250 mg methaqualone and 25 mg diphenhydramine within the same tablet, mostly in Europe. Commercial production of methaqualone was halted in the mid-1980s due to widespread abuse and addictiveness. It is a member of the quinazolinone class.

Medical use

The sedative–hypnotic activity of methaqualone was recognized in 1955. Its use peaked in the early 1970s for the treatment of insomnia, and as a sedative and muscle relaxant.

Methaqualone was not recommended for use while pregnant and is in pregnancy category D.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Similar to other GABAergic agents, methaqualone will produce tolerance and physical dependence with extended periods of use.<ref>Template:Cite journal</ref>

Overdose

An overdose of methaqualone can lead to coma and death.<ref> {{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Additional effects are delirium, convulsions, hypertonia, hyperreflexia, vomiting, kidney failure, and death through cardiac or respiratory arrest. Methaqualone overdose resembles barbiturate poisoning, but with increased motor difficulties and a lower incidence of cardiac or respiratory depression. The standard single tablet adult dose of Quaalude brand of methaqualone 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.<ref name=Linder>Template:Cite news</ref>

Pharmacology

Pharmacodynamics

Methaqualone primarily acts as a sedative, relieving anxiety and promoting sleep. Methaqualone binds to GABA_A receptors, and it shows negligible affinity for a wide array of other potential targets, including other receptors and neurotransmitter transporters.<ref name="Hammer-2015">Template:Cite journal</ref> Methaqualone is a positive allosteric modulator at many subtypes of GABA_A receptor, similar to classical benzodiazepines such as diazepam. GABA_A receptors are inhibitory, so methaqualone tends to inhibit action potentials, similar to GABA itself or other GABA_A receptor agonists. Unlike most benzodiazepines, methaqualone acts as a negative allosteric modulator at a few GABA_A receptor subtypes, which tends to cause an excitatory response in neurons expressing those receptors. Because methaqualone can be either excitatory or inhibitory depending on the subunit composition of the GABA_A receptor, it can be characterized as a mixed GABA_A receptor modulator.<ref name="Hammer-2015" /> The methaqualone binding site is distinct from the benzodiazepine, barbiturate, and neurosteroid binding sites on the GABA_A receptor complex, and it may partially overlap with the etomidate binding site.<ref name="Hammer-2015" />

Pharmacokinetics

Methaqualone peaks in the bloodstream within several hours, with a half-life of 20–60 hours.

History

Methaqualone was first synthesized in India in 1951 by Indra Kishore Kacker and Syed Husain Zaheer, who were conducting research on finding new antimalarial medications.<ref name=Linder /><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> In 1962, methaqualone was patented in the United States by Wallace and Tiernan.<ref>Template:US Patent</ref> 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 in Europe, by Roussel Laboratories (now part of Sanofi S.A.). In 1972, it was the sixth-bestselling sedative in the US,<ref name="pmid6261132">Template:Cite journal</ref> where it was legal under the brand name Quaalude.

Quaalude in the United States was originally manufactured in 1965 by the pharmaceutical firm William H. Rorer, Inc., based in Fort Washington, Pennsylvania. The drug name "Quaalude" is a portmanteau, combining the words "quiet interlude" and shared a stylistic reference to another drug marketed by the firm, Maalox.<ref name="Time">Template:Cite magazine</ref>

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."<ref name=Linder />

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.<ref name=Linder />

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, widespread abuse, and illegal recreational use.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

A 2024 Hungarian investigative documentary reported on large-scale production and sales of the drug by the Hungarian People's Republic to the United States in the 1970s and 1980s. It asserts that a Hungarian state-owned company utilized connections to Colombian drug cartels to facilitate the sale of extraordinary amounts to the United States.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>Template:Citation</ref>

Society and culture

Methaqualone became increasingly popular as a recreational drug and club drug in the late 1960s and 1970s, known variously as "ludes" or "disco biscuits"<ref name="newsweek">Template:Cite news</ref> due to its widespread use during the popularity of disco in the 1970s, or "sopers" (also "soaps") in the United States and Canada, and "mandrakes" and "mandies" in the United Kingdom, Australia and New Zealand. The substance was sold both as a free base and as a salt (hydrochloride).

Brand names

It was sold under the brand name Quaalude (sometimes stylized "Quāālude" in the United States and Canada),<ref>Template:Cite book</ref> and Mandrax in the UK, South Africa, and Australia.

Regulation

Methaqualone was initially placed in Schedule I as defined by the UN Convention on Psychotropic Substances, but was moved to Schedule II in 1979.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

In Canada, methaqualone is listed in Schedule III of the Controlled Drugs and Substances Act and requires a prescription, but it is no longer manufactured. Methaqualone is banned in India.<ref name=ban>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

In the United States it was withdrawn from the market in 1983 and made a Schedule I drug in 1984.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Recreational

File:Quaalude.jpg

A variety of methaqualone pills and capsules

Methaqualone became increasingly popular as a recreational drug in the late 1960s and 1970s, known variously as "ludes" or "sopers" and "soaps" (sopor is a Latin word for sleep) in the United States 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 1983 and made a Schedule I drug in 1984. It has a DEA ACSCN of 2565 and in 2022 the aggregate annual manufacturing quota for the United States was 60<ref name=":0">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> grams.

Mention of its possible use in some types of cancer and AIDS treatments 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 a manufacturing quota of 30 g.<ref name=":0" />

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".<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> 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.

Illicit methaqualone is one of the most commonly used recreational drugs in South Africa. Manufactured clandestinely, often in India, it comes in tablet form, but is smoked with marijuana. This method of ingestion is known as "white pipe".<ref name="SA">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref name="Cochrane">Template:Cite journal</ref> It is popular elsewhere in Africa and in India.<ref name="Cochrane" />

Chemical weapon – Project Coast

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}}

Illegal efforts to weaponize methaqualone have occurred. During the 1980s, the apartheid regime in South Africa ordered the covert manufacture of a large amount of methaqualone at the front company Delta G Scientific Company, as part of a secret chemical weapons program known as Project Coast.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Methaqualone was given the codename MosRefCat (Mossgas Refinery Catalyst). Details of this activity came to light during the 1998 hearings of the post-apartheid Truth and Reconciliation Commission.

Sexual assault

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} Actor Bill Cosby admitted in a 2015 civil deposition to giving methaqualone to women before allegedly sexually assaulting them.<ref>Template:Cite news</ref><ref>Template:Cite news</ref> Film director Roman Polanski was convicted in 1977 of sexually assaulting a 13-year-old girl after giving her alcohol and methaqualone.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Popular culture

Quaaludes are mentioned in the 1983 film Scarface, when Al Pacino's character Tony Montana says, "Another quaalude... she'll love me again." The little white pills, referred to as "ludes," get a cameo along with several other illicit drugs in the 1983 Baby Boomer drama, The Big Chill.<ref name=ludes>The Big Chill: When Boomers Stumble on the Truth about Their Own Failings, National Review, Kyle Smith, April 7, 2021</ref> Quaaludes are also referenced extensively in the 2013 film The Wolf of Wall Street.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> They are briefly mentioned in the movie Dinner in America as the reason behind the behavior of one of the characters.

Parody glam rocker "Quay Lewd", one of the costumed performance personae used by Tubes singer Fee Waybill, was named after the drug. Many songs also refer to quaaludes, including the following: David Bowie's "Time" ("Time, in quaaludes and red wine") and "Rebel Rebel" ("You got your cue line/And a handful of 'ludes"); "Cosmic Doo Doo" by the American country music singer-songwriter Blaze Foley ("Got some quaaludes in their purse"); "That Smell" by Lynyrd Skynyrd ("Can't speak a word when you're full of 'ludes"); "Flakes" by Frank Zappa ("(Wanna buy some mandies, Bob?)"); "Straight Edge" by Minor Threat ("Laugh at the thought of eating ludes"); "Kind of Girl" by French Montana ("That high got me feelin' like the Quaaludes from Wolf of Wall Street"); and "Nights" by Frank Ocean ("This feel like a Quaalude")

Season 18 of Law & Order: Special Victims Unit addresses Quaalude administration as a date rape drug in episode 9, "Decline and Fall", which aired January 18, 2017.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> In True Detective season 1, Rust Cohle's use of Quaaludes is briefly mentioned in several episodes.<ref>Template:Cite AV media</ref>

It is also used by Patrick Melrose in Edward St Aubyn's 1992 novel Bad News.Template:Cn

In the 2024 film Maria, Maria Callas, played by Angelina Jolie, stuffs Mandrax into the pockets of her coats and bags so that she'll be able to escape detection by her butler/guardian Ferruccio (Pierfrancesco Favino).

Further reading

• Template:Cite journal

External links

• Erowid Vault – Methaqualone (Quaaludes)

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