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Dimethylthiambutene
go.drugbank.com/drugs/DB01444ExperimentalIllicitDimethylthiambutene (N,N-Dimethyl-1-methyl-3,3-di-2-thienylallylamine, Dimethibutin, Ohton) is an opioid analgesic drug. … It is now under international control under Schedule I of the UN Single Convention On Narcotic Drugs 1961, presumably due to high abuse potential, although little more information is available.
Synonyms: N,N-dimethyl-4,4-di(2-thienyl)-3-buten-2-amine, N,N,1-trimethyl-3,3-di(2-thienyl)-2-propenylamineBeta-hydroxyfentanyl
go.drugbank.com/drugs/DB01453ExperimentalIllicitCategories: Heterocyclic Compounds, 1-RingDimenoxadol
go.drugbank.com/drugs/DB01461ExperimentalIllicitIt is structurally similar to methadone and is a benzilic acid derivative. In the United States it is classified as a Schedule I controlled drug.
Haloxazolam
go.drugbank.com/drugs/DB01476ExperimentalIllicitCategories: Heterocyclic Compounds, 2-RingBarbital
go.drugbank.com/drugs/DB01483ExperimentalIllicitBarbital is a schedule IV controlled drug. … A long-acting barbiturate that depresses most metabolic processes at high doses. It is used as a hypnotic and sedative and may induce dependence.
Categories: Cytochrome P-450 Substrates, Cytochrome P-450 CYP3A InducersEtorphine
go.drugbank.com/drugs/DB01497ExperimentalIllicitVet approvedA narcotic analgesic morphinan used as a sedative in veterinary practice. … In the US, Etorphine is listed as a Schedule I drug, although Etorphine hydrochloride is classified as Schedule II.
Categories: Heterocyclic Compounds with 4 or More RingsAlphameprodine
go.drugbank.com/drugs/DB01499ExperimentalIllicitAlphameprodine is a structural analogue of meperidine. … Alphameprodine is an opioid analgesic classified by the United States Drug Enforcement Administration under Schedule I of illegal substances.
Synonyms: alpha-3-ethyl-1-methyl-4-phenyl-4-propionoxypiperidine, alpha-3-Ethyl-1-methyl-4-phenyl-4-propionyloxypiperidineTenamfetamine
go.drugbank.com/drugs/DB01509IllicitInvestigationalIt is a hallucinogen. It is less toxic than its methylated derivative but in sufficient doses may still destroy serotonergic neurons and has been used for that purpose experimentally. [PubChem]
Androstenediol
go.drugbank.com/drugs/DB01524ExperimentalIllicitto a 3-keto group (3-hydroxysteroid dehydrogenases). … Androstenediol, derived from dehydroepiandrosterone by the reduction of the 17-keto group (17-hydroxysteroid dehydrogenases), is converted to testosterone by the oxidation of the 3-beta hydroxyl group
Synonyms: 5-andendiol, 5-androstenediol4-Methyl-2,5-dimethoxyamphetamine
go.drugbank.com/drugs/DB01528ExperimentalIllicitA psychedelic phenyl isopropylamine derivative, commonly called DOM, whose mood-altering effects and mechanism of action may be similar to those of LSD.
Salts: 2,5-dimethoxy-4-methylamphetamine hydrochloride