Ephedrine

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Ephedrine
Ephedrine v2.svg
(1R,2S)-Ephedrine molecule from xtal ball.png
(−)-(1R,2S)-ephedrine chemical structure (top) and ball-and-stick model (bottom)
Clinical data
Pronunciation /ɪˈfɛdrɪn/ ⓘ or /ˈɛfɪdriːn/
Trade names Akovaz, Corphedra, Emerphed, others
Other names(−)-Ephedrine; (1R,2S)-Ephedrine; (1R,2S)-β-Hydroxy-N-methylamphetamine; (1R,2S)-β-Hydroxy-N-methyl-α-methyl-β-phenethylamine
AHFS/Drugs.com Ephedrine: Monograph
HCl: Monograph
Sulfate: Monograph
Pregnancy
category
  • AU:A
Routes of
administration 		By mouth, intravenous (IV), intramuscular (IM), subcutaneous (SC)
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability 88% [6]
Protein binding ~24–29% (5–10% to albumin) [7] [8] [9]
Metabolism Largely unmetabolized [6] [10]
Metabolites • Norephedrine [6] [10]
Onset of action Oral: 15–60 minutes [11]
IM Tooltip Intramuscular injection: 10–20 minutes [11]
IV Tooltip Intravenous administration: Rapid [11]
Elimination half-life 6 hours [6]
Duration of action Oral: 2–4 hours
IV/IM: 60 minutes
Excretion Mainly urine (60% unchanged) [6]
Identifiers
  • (1R,2S)-2-(methylamino)-1-phenylpropan-1-ol
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.005.528 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C10H15NO
Molar mass 165.236 g·mol−1
3D model (JSmol)
  • C[C@@H]([C@@H](C1=CC=CC=C1)O)NC
  • InChI=1S/C10H15NO/c1-8(11-2)10(12)9-6-4-3-5-7-9/h3-8,10-12H,1-2H3/t8-,10-/m0/s1 Yes check.svgY
  • Key:KWGRBVOPPLSCSI-WPRPVWTQSA-N Yes check.svgY
   (verify)

Ephedrine is a central nervous system (CNS) stimulant and sympathomimetic agent that is often used to prevent low blood pressure during anesthesia. [11] It has also been used for asthma, narcolepsy, and obesity but is not the preferred treatment. [11] It is of unclear benefit in nasal congestion. [11] It can be taken by mouth or by injection into a muscle, vein, or just under the skin. [11] Onset with intravenous use is fast, while injection into a muscle can take 20 minutes, and by mouth can take an hour for effect. [11] When given by injection, it lasts about an hour, and when taken by mouth, it can last up to four hours. [11]

Contents

Common side effects include trouble sleeping, anxiety, headache, hallucinations, high blood pressure, fast heart rate, loss of appetite, and urinary retention. [11] Serious side effects include stroke and heart attack. [11] While likely safe in pregnancy, its use in this population is poorly studied. [12] [13] Use during breastfeeding is not recommended. [13] Ephedrine works by inducing the release of norepinephrine and hence indirectly activating the α- and β-adrenergic receptors. [11] Chemically, ephedrine is a substituted amphetamine and is the (1R,2S)-enantiomer of β-hydroxy-N-methylamphetamine. [14]

Ephedrine was first isolated in 1885 and came into commercial use in 1926. [15] [16] It is on the World Health Organization's List of Essential Medicines. [17] It is available as a generic medication. [11] It can normally be found in plants of the Ephedra genus. [11] [18] Over-the-counter dietary supplements containing ephedrine are illegal in the United States, [11] with the exception of those used in traditional Chinese medicine, where its presence is noted by má huáng. [11] [18]

Medical uses

Ephedrine Sulphate (1932), Ephedrine Compound (1932), and Swan-Myers Ephedrine Inhalant No. 66 (circa 1940). EphedrineInBottles.jpg
Ephedrine Sulphate (1932), Ephedrine Compound (1932), and Swan-Myers Ephedrine Inhalant No. 66 (circa 1940).

Ephedrine is a non-catecholamine sympathomimetic with cardiovascular effects similar to those of adrenaline/epinephrine: increased blood pressure, heart rate, and contractility. Like pseudoephedrine it is a bronchodilator, with pseudoephedrine having considerably less effect. [19] [20]

Ephedrine may decrease motion sickness, but it has mainly been used to decrease the sedating effects of other medications used for motion sickness. [21] [22]

Ephedrine is also found to have quick and long-lasting responsiveness in congenital myasthenic syndrome in early childhood and also even in adults with a novel COLQ mutation. [23]

Ephedrine is administered by intravenous boluses. Redosing usually requires increased doses to offset the development of tachyphylaxis, which is attributed to the depletion of catecholamine stores. [19]

Weight loss

Ephedrine promotes modest short-term weight loss, [24] specifically fat loss, but its long-term effects are unknown. [25] In mice, ephedrine is known to stimulate thermogenesis in the brown adipose tissue, but because adult humans have only small amounts of brown fat, thermogenesis is assumed to take place mostly in the skeletal muscle. Ephedrine also decreases gastric emptying. Methylxanthines such as caffeine and theophylline have a synergistic effect with ephedrine for weight loss. This led to the creation and marketing of compound products. [26] One of them, known as the ECA stack, contains ephedrine with caffeine and aspirin. It is a popular supplement taken by bodybuilders seeking to cut body fat before a competition. [27] A 2021 systematic review found that ephedrine led to a 2 kilograms (4.4 lb) weight loss greater than placebo, raised heart rate, and reduced LDL and raised HDL, with no statistically significant difference in blood pressure. [28]

Available forms

Ephedrine is available as a prescription-only pharmaceutical drug in the form of an intravenous solution, under brand names including Akovaz, Corphedra, Emerphed, and Rezipres as well as in generic forms, in the United States. [29] [30] It is also available over-the-counter in the form of 12.5 and 25 mg oral tablets for use as a bronchodilator and as a 0.5% concentration nasal spray for use as a decongestant. [30] The drug is additionally available in combination with guaifenesin in the form of oral tablets and liquids. [30] Ephedrine is provided as the hydrochloride or sulfate salt in pharmaceutical formulations. [29] [30]

Contraindications

Ephedrine should not be used in conjunction with certain antidepressants, namely norepinephrine-dopamine reuptake inhibitors (NDRIs), as this increases the risk of symptoms due to excessive serum levels of norepinephrine.

Bupropion is an example of an antidepressant with an amphetamine-like structure similar to ephedrine, and it is an NDRI. Its action bears more resemblance to amphetamine than to fluoxetine in that its primary mode of therapeutic action involves norepinephrine and to a lesser degree dopamine, but it also releases some serotonin from presynaptic clefts. It should not be used with ephedrine, as it may increase the likelihood of side effects.

Ephedrine should be used with caution in patients with inadequate fluid replacement, impaired adrenal function, hypoxia, hypercapnia, acidosis, hypertension, hyperthyroidism, prostatic hypertrophy, diabetes mellitus, cardiovascular disease, during delivery if maternal blood pressure is >130/80 mmHg, and during lactation. [31]

Contraindications for the use of ephedrine include: closed-angle glaucoma, phaeochromocytoma, asymmetric septal hypertrophy (idiopathic hypertrophic subaortic stenosis), concomitant or recent (previous 14 days) monoamine oxidase inhibitor (MAOI) therapy, general anaesthesia with halogenated hydrocarbons (particularly halothane), tachyarrhythmias or ventricular fibrillation, or hypersensitivity to ephedrine or other stimulants.[ citation needed ]

Ephedrine should not be used at any time during pregnancy unless specifically indicated by a qualified physician and only when other options are unavailable. [31]

Side effects

Ephedrine is a potentially dangerous natural compound; as of 2004 the US Food and Drug Administration had received over 18,000 reports of adverse effects in people using it. [32]

Adverse drug reactions (ADRs) are more common with systemic administration (e.g. injection or oral administration) compared to topical administration (e.g. nasal instillations). ADRs associated with ephedrine therapy include [33]

Overdose

Overdose of ephedrine may result in sympathomimetic symptoms like tachycardia and hypertension.[ citation needed ]

Interactions

Ephedrine with monoamine oxidase inhibitors (MAOIs) like phenelzine and tranylcypromine can result in hypertensive crisis.[ citation needed ]

Pharmacology

Pharmacodynamics

Monoamine release by ephedrine and related agents (EC50 Tooltip half maximal effective concentration, nM) [34] [35]
Compound NE Tooltip Norepinephrine DA Tooltip Dopamine 5-HT Tooltip SerotoninRef
Dextroamphetamine (S(+)-amphetamine)6.6–7.25.8–24.8698–1765 [36] [37]
S(–)-Cathinone 12.418.52366 [38]
Ephedrine ((–)-ephedrine)43.1–72.4236–1350>10000 [36]
(+)-Ephedrine2182104>10000 [36] [38]
Dextromethamphetamine (S(+)-methamphetamine)12.3–13.88.5–24.5736–1291.7 [36] [39]
Levomethamphetamine (R(–)-methamphetamine)28.54164640 [36]
(+)-Phenylpropanolamine ((+)-norephedrine)42.1302>10000 [38]
(–)-Phenylpropanolamine ((–)-norephedrine)1371371>10000 [38]
Cathine ((+)-norpseudoephedrine)15.068.3>10000 [38]
(–)-Norpseudoephedrine 30.1294>10000 [38]
(–)-Pseudoephedrine40929125>10000 [38]
Pseudoephedrine ((+)-pseudoephedrine)2241988>10000 [38]
Notes: The smaller the value, the more strongly the substance releases the neurotransmitter. See also Monoamine releasing agent § Activity profiles for a larger table with more compounds.

Ephedrine, a sympathomimetic amine, acts on part of the sympathetic nervous system (SNS). The principal mechanism of action relies on its indirect stimulation of the adrenergic receptor system by increasing activation of α- and β-adrenergic receptors via induction of norepinephrine release. [40] The presence of direct interactions with α-adrenergic receptors is unlikely but still controversial. [41] [20] [42] [43] L-ephedrine, and particularly its stereoisomer norpseudoephedrine (which is also present in Catha edulis ) has indirect sympathomimetic effects and due to its ability to cross the blood–brain barrier, it is a CNS stimulant similar to amphetamines, but less pronounced, as it releases norepinephrine and dopamine in the brain. [44]

Pharmacokinetics

Absorption

The oral bioavailability of ephedrine is 88%. [6] The onset of action of ephedrine orally is 15 to 60 minutes, via intramuscular injection is 10 to 20 minutes, and via intravenous infusion is within seconds. [11]

Distribution

Its plasma protein binding is approximately 24 to 29%, with 5 to 10% bound to albumin. [7] [8] [9]

Metabolism

Ephedrine is largely not metabolized. [6] Norephedrine (phenylpropanolamine) is an active metabolite of ephedrine formed via N-demethylation. [6] [10] About 8 to 20% of an oral dose of ephedrine is demethylated into norephedrine, about 4 to 13% is oxidatively deaminated into benzoic acid, and a small fraction is converted into 1,2-dihydroxy-1-phenylpropane. [10]

Elimination

Ephedrine is eliminated mainly in urine, with 60% (range 53–79%) excreted unchanged. [6] [10]

The elimination half-life of ephedrine is 6 hours. [6] Its duration of action orally is 2 to 4 hours and via intravenous or intramuscular injection is 60 minutes.[ citation needed ]

The elimination of ephedrine is dependent on urinary pH. [10]

Chemistry

Ephedrine, or (−)-(1R,2S)-ephedrine, also known as (1R,2S)-β-hydroxy-N-methyl-α-methyl-β-phenethylamine or as (1R,2S)-β-hydroxy-N-methylamphetamine, is a substituted phenethylamine and amphetamine derivative. It is similar in chemical structure to phenylpropanolamine, methamphetamine, and epinephrine (adrenaline). It differs from methamphetamine only by the presence of a hydroxyl group (–OH). Chemically, ephedrine is an alkaloid with a phenethylamine skeleton found in various plants in the genus Ephedra (family Ephedraceae). It is most usually marketed as the hydrochloride or sulfate salt. [45]

It has an experimental log P of 1.13, while its predicted log P values range from 0.9 to 1.32. [14] [6] [46] The lipophilicity of amphetamines is closely related to their brain permeability. [47] For comparison to ephedrine, the experimental log P of methamphetamine is 2.1, [48] of amphetamine is 1.8, [49] [48] of pseudoephedrine is 0.89, [50] of phenylpropanolamine is 0.7, [51] of phenylephrine is -0.3, [52] and of norepinephrine is -1.2. [53] Methamphetamine has high brain permeability, [48] whereas phenylephrine and norepinephrine are peripherally selective drugs. [54] [55] The optimal log P for brain permeation and central activity is about 2.1 (range 1.5–2.7). [56]

Ephedrine hydrochloride has a melting point of 187−188 °C. [57]

The racemic form of ephedrine is racephedrine ((±)-ephedrine; dl-ephedrine; (1RS,2SR)-ephedrine). [58] A stereoisomer of ephedrine is pseudoephedrine. [58] Derivatives of ephedrine include methylephedrine (N-methylephedrine), etafedrine (N-ethylephedrine), cinnamedrine (N-cinnamylephedrine), and oxilofrine (4-hydroxyephedrine). [58] Analogues of ephedrine include phenylpropanolamine (norephedrine) and metaraminol (3-hydroxynorephedrine). [58]

The presence of an N-methyl group decreases binding affinities at α-adrenergic receptors, compared with norephedrine. Ephedrine, though, binds better than N-methylephedrine, which has an additional methyl group at the nitrogen atom. Also, the steric orientation of the hydroxyl group is important for receptor binding and functional activity. [42]

Nomenclature

The four stereoisomers of ephedrine. Ephedrine and pseudoephedrine isomers.svg
The four stereoisomers of ephedrine.

Ephedrine exhibits optical isomerism and has two chiral centres, giving rise to four stereoisomers. By convention, the pair of enantiomers with the stereochemistry (1R,2S) and (1S,2R) is designated ephedrine, while the pair of enantiomers with the stereochemistry (1R,2R) and (1S,2S) is called pseudoephedrine.

The isomer which is marketed is (−)-(1R,2S)-ephedrine. [59]

In the outdated D/L system (+)-ephedrine is also referred to as D-ephedrine and (−)-ephedrine as L-ephedrine (in which case, in the Fisher projection, the phenyl ring is drawn at the bottom). [59] [60]

Often, the D/L system (with small caps) and the d/l system (with lower-case) are confused. The result is that the levorotary l-ephedrine is wrongly named L-ephedrine and the dextrorotary d-pseudoephedrine (the diastereomer) wrongly D-pseudoephedrine.

The IUPAC names of the two enantiomers are (1R,2S)- respectively (1S,2R)-2-methylamino-1-phenylpropan-1-ol. A synonym is erythro-ephedrine.

Detection in body fluids

Ephedrine may be quantified in blood, plasma, or urine to monitor possible abuse by athletes, confirm a diagnosis of poisoning, or assist in a medicolegal death investigation. Many commercial immunoassay screening tests directed at the amphetamines cross-react appreciably with ephedrine, but chromatographic techniques can easily distinguish ephedrine from other phenethylamine derivatives. Blood or plasma ephedrine concentrations are typically in the 20–200 μg/L range in persons taking the drug therapeutically, 300–3000 μg/L in abusers or poisoned patients, and 3–20 mg/L in cases of acute fatal overdosage. The current World Anti-Doping Agency (WADA) limit for ephedrine in an athlete's urine is 10 μg/mL. [61] [62] [63] [64]

History

Asia

Ephedrine in its natural form, known as máhuáng (麻黄) in traditional Chinese medicine, has been documented in China since the Han dynasty (206 BC – 220 AD) as an antiasthmatic and stimulant. [65] In traditional Chinese medicine, máhuáng has been used as a treatment for asthma and bronchitis for centuries. [66]

In 1885, the chemical synthesis of ephedrine was first accomplished by Japanese organic chemist Nagai Nagayoshi based on his research on traditional Japanese and Chinese herbal medicines.

The industrial manufacture of ephedrine in China began in the 1920s, when Merck began marketing and selling the drug as ephetonin. Ephedrine exports from China to the West grew from 4 to 216 tonnes between 1926 and 1928. [67]

Western medicine

Ephedrine was first introduced for medical use in the United States in 1926. [32]

It was introduced in 1948 in Vicks Vatronol nose drops (now discontinued) which contained ephedrine sulfate as the active ingredient for rapid nasal decongestion.

Society and culture

Names

Ephedrine is the generic name of the drug and its BAN Tooltip British Approved Name. [58] [45] [68] Its DCF Tooltip Dénomination Commune Française is ephédrine while its DCIT Tooltip Denominazione Comune Italiana is efedrina. [45] [68] In the case of the hydrochloride salt, its generic name is ephedrine hydrochloride and this is its USAN Tooltip United States Adopted Name, BANM Tooltip British Approved Name, and JAN Tooltip Japanese Accepted Name. [58] [45] [68] In the case of the sulfate salt, its generic name is ephedrine sulfate or ephedrine sulphate and the former is its USAN Tooltip United States Adopted Name while the latter is its BANM Tooltip British Approved Name. [58] [45] [68] A synonym of ephedrine sulfate is isofedrol. [58] These names all refer to the (1R,2R)-enantiomer of ephedrine. [58] [45] The racemic form of ephedrine is known as racephedrine and this is its INN Tooltip International Nonproprietary Name and BAN Tooltip British Approved Name, while the hydrochloride salt of the racemic form is racephedrine hydrochloride and this is its USAN Tooltip United States Adopted Name. [69]

Recreational use

Ephedrine tablets. Ephedrine - 10 x 30mg.jpg
Ephedrine tablets.

As a phenethylamine, ephedrine has a similar chemical structure to amphetamines and is a methamphetamine analog having the methamphetamine structure with a hydroxyl group at the β position. Because of ephedrine's structural similarity to methamphetamine, it can be used to create methamphetamine using chemical reduction in which ephedrine's hydroxyl group is removed; this has made ephedrine a highly sought-after chemical precursor in the illicit manufacture of methamphetamine.

The most popular method for reducing ephedrine to methamphetamine is similar to the Birch reduction, in that it uses anhydrous ammonia and lithium metal in the reaction. The second-most popular method uses red phosphorus and iodine in the reaction with ephedrine. Moreover, ephedrine can be synthesized into methcathinone via simple oxidation. As such, ephedrine is listed as a table-I precursor under the United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances . [70]

Use in exercise and sports

Ephedrine has been used as a performance-enhancing drug in exercise and sports. [41] [71] [72] [73] It can increase heart rate, blood pressure, and cardiac contractility as well as act as a psychostimulant. [41] Ephedrine is often used in combination with caffeine for performance-enhancing purposes. [72] [73]

Other uses

In chemical synthesis, ephedrine is used in bulk quantities as a chiral auxiliary group. [74]

EphedrineChiralAuxiliary.svg

In saquinavir synthesis, the half-acid is resolved as its salt with l-ephedrine.

Canada

In January 2002, Health Canada issued a voluntary recall of all ephedrine products containing more than 8 mg per dose, all combinations of ephedrine with other stimulants such as caffeine, and all ephedrine products marketed for weight-loss or bodybuilding indications, citing a serious risk to health. [75] Ephedrine is still sold as an oral nasal decongestant [76] in 8 mg pills as a natural health product, with a limit of 0.4 g (400 mg) per package, the limit established by the Controlled Drugs and Substances Act as it is considered as Class A Precursor. [77]

United States

In 1997, the FDA proposed a regulation on ephedra (the herb from which ephedrine is obtained), which limited an ephedra dose to 8 mg (of active ephedrine) with no more than 24 mg per day. [78] This proposed rule was withdrawn, in part, in 2000 because of "concerns regarding the agency's basis for proposing a certain dietary ingredient level and a duration of use limit for these products." [79] In 2004, the FDA created a ban on ephedrine alkaloids marketed for reasons other than asthma, colds, allergies, other disease, or traditional Asian use. [80] On April 14, 2005, the U.S. District Court for the District of Utah ruled the FDA did not have proper evidence that low dosages of ephedrine alkaloids are actually unsafe, [81] but on August 17, 2006, the U.S. Court of Appeals for the Tenth Circuit in Denver upheld the FDA's final rule declaring all dietary supplements containing ephedrine alkaloids adulterated, and therefore illegal for marketing in the United States. [82] Furthermore, ephedrine is banned by the NCAA, MLB, NFL, and PGA. [83] Ephedrine is, however, still legal in many applications outside of dietary supplements. Purchasing is currently limited and monitored, with specifics varying from state to state.

The House passed the Combat Methamphetamine Epidemic Act of 2005 as an amendment to the renewal of the USA PATRIOT Act. Signed into law by President George W. Bush on March 6, 2006, the act amended the US Code (21 USC 830) concerning the sale of products containing ephedrine and the closely related drug pseudoephedrine. Both substances are used as precursors in the illicit production of methamphetamine, and to discourage that use the federal statute included the following requirements for merchants who sell these products:

  • A retrievable record of all purchases identifying the name and address of each party to be kept for two years
  • Required verification of proof of identity of all purchasers
  • Required protection and disclosure methods in the collection of personal information
  • Reports to the Attorney General of any suspicious payments or disappearances of the regulated products
  • Non-liquid dose form of regulated product may only be sold in unit-dose blister packs
  • Regulated products are to be sold behind the counter or in a locked cabinet in such a way as to restrict access
  • Daily sales of regulated products not to exceed 3.6 g to a single purchaser, without regard to the number of transactions
  • Monthly sales to a single purchaser not to exceed 9 g of pseudoephedrine base in regulated products

The law gives similar regulations to mail-order purchases, except the monthly sales limit is 7.5 g.

As a pure herb or tea, má huáng, containing ephedrine, is still sold legally in the US. The law restricts/prohibits its being sold as a dietary supplement (pill) or as an ingredient/additive to other products, like diet pills.

Australia

Ephedrine and all Ephedra species that contain it are considered Schedule 4 substances under the Poisons Standard. A Schedule 4 drug is considered a Prescription Only Medicine, or Prescription Animal Remedy – Substances, the use or supply of which should be by or on the order of persons permitted by State or Territory legislation to prescribe and should be available from a pharmacist on prescription under the Poisons Standard.

South Africa

In South Africa, ephedrine was moved to schedule 6 on 27 May 2008, [84] which makes pure ephedrine tablets prescription only. Pills containing ephedrine up to 30mg per tablet in combination with other medications are still available OTC, schedule 1 and 2, for sinus, head colds, and influenza.

Germany

Ephedrine was freely available in pharmacies in Germany until 2001. Afterward, access was restricted since it was mostly bought for unindicated uses. Similarly, ephedra can only be bought with a prescription. Since April 2006, all products, including plant parts, that contain ephedrine are only available with a prescription. [85]

Sources

Agricultural

Ephedrine is obtained from the plant Ephedra sinica and other members of the genus Ephedra, from which the name of the substance is derived. Raw materials for the manufacture of ephedrine and traditional Chinese medicines are produced in China on a large scale. As of 2007, companies produced for export US$13 million worth of ephedrine from 30,000 tons of ephedra annually, or about ten times the amount used in traditional Chinese medicine. [86]

Synthetic

Most of the l-ephedrine produced today for official medical use is made synthetically as the extraction and isolation process from E. sinica is tedious and no longer cost-effective. [87] [ unreliable source? ]

Biosynthetic

Proposed biosynthetic pathway of ephedrine from L-phenylalanine and pyruvic acid. Ephedrine biosynthesis.svg
Proposed biosynthetic pathway of ephedrine from L-phenylalanine and pyruvic acid.

Ephedrine was long thought to come from modifying the amino acid L-phenylalanine. [90] L-Phenylalanine would be decarboxylated and subsequently attacked with ω-aminoacetophenone. Methylation of this product would then produce ephedrine. This pathway has since been disproven. [90] A new pathway proposed suggests that phenylalanine first forms cinnamoyl-CoA via the enzymes phenylalanine ammonia-lyase and acyl CoA ligase. [88] The cinnamoyl-CoA is then reacted with a hydratase to attach the alcohol functional group. The product is then reacted with a retro-aldolase, forming benzaldehyde. Benzaldehyde reacts with pyruvic acid to attach a 2-carbon unit. This product then undergoes transamination and methylation to form ephedrine and its stereoisomer, pseudoephedrine. [89]

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<span class="mw-page-title-main">Levmetamfetamine</span> Topical nasal decongestant

Levmetamfetamine, also known as l-desoxyephedrine or levomethamphetamine, and commonly sold under the brand name Vicks VapoInhaler among others, is an optical isomer of methamphetamine primarily used as a topical nasal decongestant. It is used to treat nasal congestion from allergies and the common cold. It was first used medically as decongestant beginning in 1958 and has been used for such purposes, primarily in the United States, since then.

A cardiac stimulant is a drug which acts as a stimulant of the heart – e.g., via positive chronotropic action and/or inotropic action. They increase cardiac output.

<span class="mw-page-title-main">Levoamphetamine</span> CNS stimulant and isomer of amphetamine

Levoamphetamine is a stimulant medication which is used in the treatment of certain medical conditions. It was previously marketed by itself under the brand name Cydril, but is now available only in combination with dextroamphetamine in varying ratios under brand names like Adderall and Evekeo. The drug is known to increase wakefulness and concentration in association with decreased appetite and fatigue. Pharmaceuticals that contain levoamphetamine are currently indicated and prescribed for the treatment of attention deficit hyperactivity disorder (ADHD), obesity, and narcolepsy in some countries. Levoamphetamine is taken by mouth.

<span class="mw-page-title-main">Norepinephrine releasing agent</span> Catecholaminergic type of drug

A norepinephrine releasing agent (NRA), also known as an adrenergic releasing agent, is a catecholaminergic type of drug that induces the release of norepinephrine (noradrenaline) and epinephrine (adrenaline) from the pre-synaptic neuron into the synapse. This in turn leads to increased extracellular concentrations of norepinephrine and epinephrine therefore an increase in adrenergic neurotransmission.

Substituted amphetamines, or simply amphetamines, are a class of compounds based upon the amphetamine structure; it includes all derivative compounds which are formed by replacing, or substituting, one or more hydrogen atoms in the amphetamine core structure with substituents. The compounds in this class span a variety of pharmacological subclasses, including stimulants, empathogens, and hallucinogens, among others. Examples of substituted amphetamines are amphetamine (itself), methamphetamine, ephedrine, cathinone, phentermine, mephentermine, tranylcypromine, bupropion, methoxyphenamine, selegiline, amfepramone (diethylpropion), pyrovalerone, MDMA (ecstasy), and DOM (STP).

Oxilofrine, sold under the brand names Carnigen and Suprifen among others, is a sympathomimetic medication which has been used as an antihypotensive agent and cough suppressant. It is taken by mouth.

<span class="mw-page-title-main">Methylephedrine</span> Chemical compound

Methylephedrine, sold under the brand name Metheph among others, is a sympathomimetic medication described as an antiasthmatic agent and used to treat coughing and nasal congestion. It is reported to be used in various over-the-counter cough and cold preparations throughout the world, including Japan.

Amphetamine and methamphetamine are central nervous system stimulants used to treat a variety of conditions. When used recreationally, they are colloquially known as "speed" or sometimes "crank". Amphetamine was first synthesized in 1887 in Germany by Romanian chemist Lazăr Edeleanu, who named it phenylisopropylamine. Around the same time, Japanese organic chemist Nagai Nagayoshi isolated ephedrine from the Chinese ephedra plant and later developed a method for ephedrine synthesis. Methamphetamine was synthesized from ephedrine in 1893 by Nagayoshi. Neither drug had a pharmacological use until 1934, when Smith, Kline & French began selling amphetamine as an inhaler under the trade name Benzedrine for congestion.

Amphetamine type stimulants (ATS) are a group of synthetic drugs that are chemical derivatives of the parent compound alpha-methylphenethylamine, also known as amphetamine. Common ATS includes amphetamine, methamphetamine, ephedrine, pseudoephedrine, 3,4-methylenedioxymethamphetamine (MDMA), 3,4-methylenedioxyamphetamine (MDA) and 3,4-methylenedioxyethylamphetamine (MDEA). ATS when used illicitly has street names including ice, meth, crystal, crank, bennies, and speed. Within the group of amphetamine-type stimulants, there are also prescription drugs including mixed amphetamine salts, dextroamphetamine, and lisdexamfetamine.

<span class="mw-page-title-main">Substituted β-hydroxyamphetamine</span> Class of compounds based upon the β-hydroxyamphetamine structure

Substituted β-hydroxyamphetamines, or simply β-hydroxyamphetamines, also known as phenylisopropanolamines, phenylpropanolamines, norephedrines, or cathinols, are derivatives of β-hydroxyamphetamine with one or more chemical substituents. They are substituted phenethylamines, phenylethanolamines (β-hydroxyphenethylamines), and amphetamines (α-methylphenethylamines), and are closely related to but distinct from the substituted cathinones (β-ketoamphetamines). Examples of β-hydroxyamphetamines include the β-hydroxyamphetamine stereoisomers phenylpropanolamine and cathine and the stereospecific N-methylated β-hydroxyamphetamine derivatives ephedrine and pseudoephedrine, among many others.

References

  1. ↑ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-15.
  2. ↑ "Ephedrine Hydrochloride 15mg Tablets Summary of Product Characteristics (SmPC)". emc. Retrieved 8 October 2020.
  3. ↑ "Ephedrine Nasal Drops 1.0% Summary of Product Characteristics (SmPC)". emc. 11 March 2015. Archived from the original on 24 October 2020. Retrieved 8 October 2020.
  4. ↑ "Akovaz- ephedrine sulfate injection". DailyMed. 16 April 2020. Retrieved 8 October 2020.
  5. ↑ "Title 21: Food And Drugs Part 341—Cold, Cough, Allergy, Bronchodilator, And Antiasthmatic Drug Products For Over-The-Counter Human Use". Electronic Code of Federal Regulations. Retrieved 8 October 2020.
  6. 1 2 3 4 5 6 7 8 9 10 11 "Ephedrine: Uses, Interactions, Mechanism of Action". DrugBank Online. 29 April 2016. Retrieved 14 July 2024.
  7. 1 2 Volpp M, Holzgrabe U (January 2019). "Determination of plasma protein binding for sympathomimetic drugs by means of ultrafiltration". Eur J Pharm Sci. 127: 175–184. doi:10.1016/j.ejps.2018.10.027. PMID   30391401.
  8. 1 2 Schmidt S (2023). Lang-etablierte Arzneistoffe genauer unter die Lupe genommen: Enantioselektive Proteinbindung und Stabilitätsstudien[A closer look at long-established drugs: enantioselective protein binding and stability studies] (Thesis) (in German). Universität Würzburg. doi:10.25972/opus-34594.
  9. 1 2 Gad MZ, Azab SS, Khattab AR, Farag MA (October 2021). "Over a century since ephedrine discovery: an updated revisit to its pharmacological aspects, functionality and toxicity in comparison to its herbal extracts". Food Funct. 12 (20): 9563–9582. doi:10.1039/d1fo02093e. PMID   34533553.
  10. 1 2 3 4 5 6 Chua SS, Benrimoj SI, Triggs EJ (1989). "Pharmacokinetics of non-prescription sympathomimetic agents". Biopharm Drug Dispos. 10 (1): 1–14. doi:10.1002/bdd.2510100102. PMID   2647163.
  11. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 "Ephedrine". The American Society of Health-System Pharmacists. Archived from the original on 2017-09-09. Retrieved 8 September 2017.
  12. ↑ Briggs GG, Freeman RK, Yaffe SJ (2011). Drugs in pregnancy and lactation: a reference guide to fetal and neonatal risk (9th ed.). Philadelphia: Lippincott Williams & Wilkins. p. 495. ISBN   9781608317080. Archived from the original on 2017-09-08.
  13. 1 2 "Ephedrine Pregnancy and Breastfeeding Warnings". Archived from the original on 5 August 2017. Retrieved 8 October 2017.
  14. 1 2 "Ephedrine". PubChem. Retrieved 30 August 2024.
  15. ↑ Soni MG, Shelke K, Amin R, Talati (2013). "A Lessons from the Use of Ephedra Products as a Dietary Supplement". In Bagchi D, Preuss HG (eds.). Obesity epidemiology, pathophysiology, and prevention (2nd ed.). Boca Raton, Florida: CRC Press. p. 692. ISBN   9781439854266. Archived from the original on 2017-09-08.
  16. ↑ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 541. ISBN   9783527607495.
  17. ↑ World Health Organization (2021). World Health Organization model list of essential medicines: 22nd list (2021). Geneva: World Health Organization. hdl: 10665/345533 . WHO/MHP/HPS/EML/2021.02.
  18. 1 2 Abourashed EA, El-Alfy AT, Khan IA, Walker L (August 2003). "Ephedra in perspective—a current review". Phytotherapy Research. 17 (7): 703–712. doi:10.1002/ptr.1337. PMID   12916063. S2CID   41083359.
  19. 1 2 Butterworth IV JF, Mackey DC, Wasnick JD (2022). "Chapter 14. Adrenergic Agonists & Antagonists.". Morgan & Mikhail's Clinical Anesthesiology (7th ed.). McGraw-Hill Education. ISBN   978-1-260-47379-7.
  20. 1 2 Drew CD, Knight GT, Hughes DT, Bush M (September 1978). "Comparison of the effects of D-(-)-ephedrine and L-(+)-pseudoephedrine on the cardiovascular and respiratory systems in man". British Journal of Clinical Pharmacology. 6 (3): 221–5. doi:10.1111/j.1365-2125.1978.tb04588.x. PMC   1429447 . PMID   687500.
  21. ↑ Buckey Jr JC (2006). Space Physiology. Oxford University Press. p. 201. ISBN   978-0-1997-4790-0.
  22. ↑ Sanford CA, Jong EC (2008). The Travel and Tropical Medicine Manual E-Book. Elsevier Health Sciences. p. 139. ISBN   978-1437710694.
  23. ↑ Higashida K, Yamada M, Shimohata T (2021-04-13). "Quick and long-lasting responsiveness by ephedrine in an adult woman with congenital myasthenic syndrome associated with a novel COLQ mutation. (2928)". Neurology. 96 (15 Supplement). doi:10.1212/WNL.96.15_supplement.2928. ISSN   0028-3878. S2CID   266124150.
  24. ↑ Shekelle PG, Hardy ML, Morton SC, Maglione M, Mojica WA, Suttorp MJ, et al. (March 2003). "Efficacy and safety of ephedra and ephedrine for weight loss and athletic performance: a meta-analysis". JAMA. 289 (12): 1537–45. doi:10.1001/jama.289.12.1470. PMID   12672771.
  25. ↑ Dwyer JT, Allison DB, Coates PM (May 2005). "Dietary supplements in weight reduction". Journal of the American Dietetic Association. 105 (5 Suppl 1): S80-6. doi:10.1016/j.jada.2005.02.028. PMID   15867902.
  26. ↑ Bray GA, Bouchard C (2004). Handbook of obesity. CRC Press. pp. 494–496. ISBN   978-0-8247-4773-2. Archived from the original on 2014-06-26.
  27. ↑ Magkos F, Kavouras SA (2004). "Caffeine and ephedrine: physiological, metabolic and performance-enhancing effects". Sports Medicine. 34 (13): 871–89. doi:10.2165/00007256-200434130-00002. PMID   15487903. S2CID   1966020.
  28. ↑ Yoo HJ, Yoon HY, Yee J, Gwak HS (November 2021). "Effects of Ephedrine-Containing Products on Weight Loss and Lipid Profiles: A Systematic Review and Meta-Analysis of Randomized Controlled Trials". Pharmaceuticals. 14 (11): 1198. doi: 10.3390/ph14111198 . PMC   8618781 . PMID   34832979.
  29. 1 2 "Drugs@FDA: FDA-Approved Drugs". accessdata.fda.gov. Food and Drug Administration. Retrieved 14 July 2024.
  30. 1 2 3 4 "Search Results for ephedrine". DailyMed. Retrieved 14 July 2024.
  31. 1 2 Mayne Pharma. Ephedrine sulfate injection DBL (Approved Product Information). Melbourne: Mayne Pharma; 2004
  32. 1 2 Palamar J (January 2011). "How ephedrine escaped regulation in the United States: a historical review of misuse and associated policy". Health Policy. 99 (1): 1–9. doi:10.1016/j.healthpol.2010.07.007. PMID   20685002.
  33. ↑ Joint Formulary Committee. British National Formulary, 47th edition. London: British Medical Association and Royal Pharmaceutical Society of Great Britain; 2004. ISBN   0-85369-587-3
  34. ↑ Rothman RB, Baumann MH (2003). "Monoamine transporters and psychostimulant drugs". Eur. J. Pharmacol. 479 (1–3): 23–40. doi:10.1016/j.ejphar.2003.08.054. PMID   14612135.
  35. ↑ Rothman RB, Baumann MH (2006). "Therapeutic potential of monoamine transporter substrates". Curr Top Med Chem. 6 (17): 1845–1859. doi:10.2174/156802606778249766. PMID   17017961.
  36. 1 2 3 4 5 Rothman RB, Baumann MH, Dersch CM, Romero DV, Rice KC, Carroll FI, Partilla JS (January 2001). "Amphetamine-type central nervous system stimulants release norepinephrine more potently than they release dopamine and serotonin". Synapse. 39 (1): 32–41. doi:10.1002/1098-2396(20010101)39:1<32::AID-SYN5>3.0.CO;2-3. PMID   11071707.
  37. ↑ Baumann MH, Partilla JS, Lehner KR, Thorndike EB, Hoffman AF, Holy M, Rothman RB, Goldberg SR, Lupica CR, Sitte HH, Brandt SD, Tella SR, Cozzi NV, Schindler CW (2013). "Powerful cocaine-like actions of 3,4-methylenedioxypyrovalerone (MDPV), a principal constituent of psychoactive 'bath salts' products". Neuropsychopharmacology. 38 (4): 552–562. doi:10.1038/npp.2012.204. PMC   3572453 . PMID   23072836.
  38. 1 2 3 4 5 6 7 8 Rothman RB, Vu N, Partilla JS, Roth BL, Hufeisen SJ, Compton-Toth BA, Birkes J, Young R, Glennon RA (October 2003). "In vitro characterization of ephedrine-related stereoisomers at biogenic amine transporters and the receptorome reveals selective actions as norepinephrine transporter substrates". J Pharmacol Exp Ther. 307 (1): 138–145. doi:10.1124/jpet.103.053975. PMID   12954796.
  39. ↑ Baumann MH, Ayestas MA, Partilla JS, Sink JR, Shulgin AT, Daley PF, Brandt SD, Rothman RB, Ruoho AE, Cozzi NV (April 2012). "The designer methcathinone analogs, mephedrone and methylone, are substrates for monoamine transporters in brain tissue". Neuropsychopharmacology. 37 (5): 1192–203. doi:10.1038/npp.2011.304. PMC   3306880 . PMID   22169943.
  40. ↑ "EPHEDrine". Merck Manuals. January 2010. Archived from the original on 24 March 2011.
  41. 1 2 3 Docherty JR (June 2008). "Pharmacology of stimulants prohibited by the World Anti-Doping Agency (WADA)". Br J Pharmacol. 154 (3): 606–622. doi:10.1038/bjp.2008.124. PMC   2439527 . PMID   18500382.
  42. 1 2 Ma G, Bavadekar SA, Davis YM, Lalchandani SG, Nagmani R, Schaneberg BT, et al. (July 2007). "Pharmacological effects of ephedrine alkaloids on human alpha(1)- and alpha(2)-adrenergic receptor subtypes". The Journal of Pharmacology and Experimental Therapeutics. 322 (1): 214–221. doi:10.1124/jpet.107.120709. PMID   17405867. S2CID   86429875.
  43. ↑ Kobayashi S, Endou M, Sakuraya F, Matsuda N, Zhang XH, Azuma M, et al. (November 2003). "The sympathomimetic actions of l-ephedrine and d-pseudoephedrine: direct receptor activation or norepinephrine release?". Anesthesia and Analgesia. 97 (5): 1239–1245. doi: 10.1213/01.ANE.0000092917.96558.3C . PMID   14570629.
  44. ↑ Munhall AC, Johnson SW (January 2006). "Dopamine-mediated actions of ephedrine in the rat substantia nigra". Brain Research. 1069 (1): 96–103. doi:10.1016/j.brainres.2005.11.044. PMID   16386715. S2CID   40626692.
  45. 1 2 3 4 5 6 Schweizerischer Apotheker-Verein (2004). Index Nominum: International Drug Directory. Medpharm Scientific Publishers. p. 450. ISBN   978-3-88763-101-7 . Retrieved 30 August 2024.
  46. ↑ "L-(−)-Ephedrine". ChemSpider. 30 August 2024. Retrieved 30 August 2024.
  47. ↑ Bharate SS, Mignani S, Vishwakarma RA (December 2018). "Why Are the Majority of Active Compounds in the CNS Domain Natural Products? A Critical Analysis". J Med Chem. 61 (23): 10345–10374. doi:10.1021/acs.jmedchem.7b01922. PMID   29989814.
  48. 1 2 3 Schep LJ, Slaughter RJ, Beasley DM (August 2010). "The clinical toxicology of metamfetamine". Clin Toxicol (Phila). 48 (7): 675–694. doi:10.3109/15563650.2010.516752. PMID   20849327. Metamfetamine acts in a manner similar to amfetamine, but with the addition of the methyl group to the chemical structure. It is more lipophilic (Log p value 2.07, compared with 1.76 for amfetamine),4 thereby enabling rapid and extensive transport across the blood–brain barrier.19
  49. ↑ "Amphetamine". PubChem. Retrieved 26 July 2024.
  50. ↑ "Pseudoephedrine". PubChem. Retrieved 25 July 2024.
  51. ↑ "Norephedrine". PubChem. Retrieved 26 July 2024.
  52. ↑ "Phenylephrine". PubChem. Retrieved 21 July 2024.
  53. ↑ "Norepinephrine". PubChem. Retrieved 26 July 2024.
  54. ↑ Eccles R (January 2007). "Substitution of phenylephrine for pseudoephedrine as a nasal decongeststant. An illogical way to control methamphetamine abuse". British Journal of Clinical Pharmacology. 63 (1): 10–14. doi:10.1111/j.1365-2125.2006.02833.x. PMC   2000711 . PMID   17116124.
  55. ↑ Froese L, Dian J, Gomez A, Unger B, Zeiler FA (October 2020). "The cerebrovascular response to norepinephrine: A scoping systematic review of the animal and human literature". Pharmacol Res Perspect. 8 (5): e00655. doi:10.1002/prp2.655. PMC   7510331 . PMID   32965778.
  56. ↑ Pajouhesh H, Lenz GR (October 2005). "Medicinal chemical properties of successful central nervous system drugs". NeuroRx. 2 (4): 541–553. doi:10.1602/neurorx.2.4.541. PMC   1201314 . PMID   16489364. Lipophilicity was the first of the descriptors to be identified as important for CNS penetration. Hansch and Leo54 reasoned that highly lipophilic molecules will be partitioned into the lipid interior of membranes and will be retained there. However, ClogP correlates nicely with LogBBB with increasing lipophilicity and increasing brain penetration. For several classes of CNS active substances, Hansch and Leo54 found that blood-brain barrier penetration is optimal when the LogP values are in the range of 1.5-2.7, with a mean value of 2.1. An analysis of small drug-like molecules suggested that for better brain permeation46 and for good intestinal permeability55 the LogD values need to be greater than 0 and less than 3. In comparison, the mean value for ClogP for the marketed CNS drugs is 2.5, which is in good agreement with the range found by Hansch et al.22
  57. ↑ Budavari S (ed.). The Merck Index: An encyclopedia of chemicals, drugs, and biologicals (12th ed.). Whitehouse Station: Merck.
  58. 1 2 3 4 5 6 7 8 9 Elks J (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 793. ISBN   978-1-4757-2085-3 . Retrieved 30 August 2024.
  59. 1 2 Reynolds J (1989). Reynolds JEF (ed.). Martindale: The complete drug reference (29th ed.). London: Pharmaceutical Press. ISBN   978-0-85369-210-2.
  60. ↑ Patil PN, Tye A, Lapidus JB (May 1965). "A Pharmacological Study of the Ephedrine Isomers" (PDF). The Journal of Pharmacology and Experimental Therapeutics. 148 (2): 158–68. PMID   14301006.
  61. ↑ "S6. Stimulants | List of Prohibited Substances and Methods". Archived from the original on 2015-10-23. Retrieved 2015-10-19.
  62. ↑ Schier JG, Traub SJ, Hoffman RS, Nelson LS (2003). "Ephedrine-induced cardiac ischemia: exposure confirmed with a serum level". Journal of Toxicology. Clinical Toxicology. 41 (6): 849–53. doi:10.1081/clt-120025350. PMID   14677795. S2CID   23359388.
  63. ↑ WADA. The World Anti-Doping Code, World Anti-Doping Agency, Montreal, Canada, 2010. url Archived 2013-09-11 at the Wayback Machine
  64. ↑ Baselt R (2008). Disposition of Toxic Drugs and Chemicals in Man (8th ed.). Foster City, CA: Biomedical Publications. pp. 542–544.
  65. ↑ Levy WO, Kalidas K (26 February 2010). Miller NS (ed.). Principles of Addictions and the Law: Applications in Forensic, Mental Health, and Medical Practice. Academic Press. pp. 307–308. ISBN   978-0-12-496736-6.
  66. ↑ Ford MD, Delaney KA, Ling LJ, Erickson T, eds. (2001). Clinical Toxicology. Philadelphia: WB Saunders. ISBN   0-7216-5485-1.
  67. ↑ Dikotter F, Laamann LP (16 April 2004). Narcotic Culture: A History of Drugs in China. University of Chicago Press. p. 199. ISBN   978-0-226-14905-9.
  68. 1 2 3 4 "Ephedrine (International database)". Drugs.com. 5 August 2024. Retrieved 30 August 2024.
  69. ↑ Schweizerischer Apotheker-Verein (2000). Index Nominum 2000: International Drug Directory. Medpharm Scientific Publishers. p. 390. ISBN   978-3-88763-075-1 . Retrieved 30 August 2024.
  70. ↑ Microsoft Word – RedListE2007.doc Archived February 27, 2008, at the Wayback Machine
  71. ↑ Lieberman HR (April 2001). "The effects of ginseng, ephedrine, and caffeine on cognitive performance, mood and energy". Nutr Rev. 59 (4): 91–102. doi:10.1111/j.1753-4887.2001.tb06995.x. PMID   11368507.
  72. 1 2 Magkos F, Kavouras SA (2004). "Caffeine and ephedrine: physiological, metabolic and performance-enhancing effects". Sports Med. 34 (13): 871–889. doi:10.2165/00007256-200434130-00002. PMID   15487903.
  73. 1 2 Graham TE (2001). "Caffeine, coffee and ephedrine: impact on exercise performance and metabolism". Can J Appl Physiol. 26 Suppl: S103–S119. PMID   11897887.
  74. ↑ Borsato G, Linden A, Lucchi OD, Lucchini V, Wolstenholme D, Zambon A (May 2007). "Chiral polycyclic ketones via desymmetrization of dihaloolefins". The Journal of Organic Chemistry. 72 (11): 4272–5. doi:10.1021/jo070222g. hdl:11380/1138891. PMID   17474779.
  75. ↑ "Health Canada requests recall of certain products containing Ephedra/ephedrine". Health Canada. January 9, 2002. Archived from the original on February 6, 2007. Retrieved July 7, 2009.
  76. ↑ Laccourreye O, Werner A, Giroud JP, Couloigner V, Bonfils P, Bondon-Guitton E (February 2015). "Benefits, limits and danger of ephedrine and pseudoephedrine as nasal decongestants". European Annals of Otorhinolaryngology, Head and Neck Diseases. 132 (1): 31–4. doi: 10.1016/j.anorl.2014.11.001 . PMID   25532441.
  77. ↑ Legislative Services Branch (2021-03-18). "Consolidated federal laws of canada, Controlled Drugs and Substances Act". laws-lois.justice.gc.ca. Archived from the original on 2021-07-30. Retrieved 2021-07-30.
  78. ↑ Federal Register: June 4, 1997 (Volume 62, Number 107): Dietary Supplements Containing Ephedrine Alkaloids; Proposed Rule
  79. ↑ Federal Register: April 3, 2000 (Volume 65, Number 64): Dietary Supplements Containing Ephedrine Alkaloids; Withdrawal in Part
  80. ↑ Federal Register: February 11, 2004 (Volume 69, Number 28): Final Rule Declaring Dietary Supplements Containing Ephedrine Alkaloids Adulterated Because They Present an Unreasonable Risk; Final Rule
  81. ↑ "Nutraceutical Corporation; Solaray, Inc., Plaintiffs-appellees, v. Andrew Von Eschenbach, Acting Commissioner, U.S. Food and Drug Administration; United States Food and Drug Administration; Michael O. Leavitt, Secretary of the Department of Health and Human Services; Department of Health and Human Services; United States of America" (PDF). Archived from the original (PDF) on 2011-07-10. Retrieved 2010-07-01. Defendants-appellants, 459 F.3d 1033 (10th Cir. 2006)
  82. ↑ Nutraceutical Corporation; Solaray, Inc. Plaintiffs-Appellees vs. Andrew Von Eschenbach, Acting Commissioner, US.. Food and Drug Administration; United States Food and Drug Administration; Michael O. Leavitt, Secretary of the Department of Health and Human Services; Department of Health and Human Services; United States of America, We find that the FDA correctly followed the congressional directive to analyze the risks and benefits of EDS in determining that there is no dosage level of EDS acceptable for the market. (United States Court of Appeals Tenth CircuitAugust 17, 2006),archived from the original .
  83. ↑ "Sport Drug Testing – Drug Programs & Policy – Athletics". Archived from the original on 2011-02-10. Retrieved 2011-03-21.
  84. ↑ "Rescheduling of Medicines that Contain Ephedrine". Archived from the original on 2009-06-28. Retrieved 2009-04-18.
  85. ↑ Verordnung zur Neuordnung der Verschreibungspflicht von Arzneimitteln (AMVVNV). Archived 2014-05-17 at the Wayback Machine V. v. 21. Dezember 2005 BGBl. I S. 3632; Geltung ab 1. Januar 2006.
  86. ↑ Long C (15 January 2007). "Chinese medicine's great waste of resources". Archived from the original on 30 May 2016. Retrieved 9 May 2016.
  87. ↑ "Chemically Synthesized Ephedrine Put into Mass Production in China". November 5, 2001. Archived from the original on June 29, 2011.
  88. 1 2 Hertweck C, Jarvis AP, Xiang L, Moore BS, Oldham NJ (October 2001). "A mechanism of benzoic acid biosynthesis in plants and bacteria that mirrors fatty acid beta-oxidation". ChemBioChem. 2 (10): 784–6. doi:10.1002/1439-7633(20011001)2:10<784::AID-CBIC784>3.0.CO;2-K. PMID   11948863. S2CID   28159196.
  89. 1 2 Grue-Sorensen G, Spenser ID (May 1, 1988). "Biosynthesis of ephedrine". Journal of the American Chemical Society. 110 (11): 3714–3715. doi:10.1021/ja00219a086. ISSN   0002-7863.
  90. 1 2 Yamasaki K, Tamaki T, Uzawa S, Sankawa U, Shibata S (1973). "Participation of C6-C1 unit in the biosynthesis of ephedrine in Ephedra". Phytochemistry. 12 (12): 2877–2882. Bibcode:1973PChem..12.2877Y. doi:10.1016/0031-9422(73)80499-6.
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