Substituted β-hydroxyamphetamine

Substituted β-hydroxyamphetamines, also known as substituted phenylisopropanolamines, substituted phenylpropanolamines, substituted norephedrines, or substituted cathinols, are derivatives of β-hydroxyamphetamine with one or more chemical substituents.[1][2][3][4] They are substituted phenethylamines, phenylethanolamines (β-hydroxyphenethylamines), and amphetamines (α-methylphenethylamines), and are closely related to but distinct from the substituted cathinones (β-ketoamphetamines).[1][2][3][5] 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.[1][2]

Substituted β-hydroxyamphetamines
Drug class
Racemic β-hydroxyamphetamine skeleton
Racemic β-hydroxyamphetamine skeleton
Class identifiers
SynonymsSubstituted phenylisopropanolamines; Substituted phenylpropanolamines; Substituted norephedrines; Substituted amphetanolamines; Substituted cathinols; Substituted cathines
Chemical classSubstituted derivatives of β-hydroxyamphetamine
Legal status
In Wikidata

In terms of pharmacological activity, the β-hydroxyamphetamines include indirectly acting norepinephrine and dopamine releasing agents and directly acting α- and β-adrenergic receptor agonists, among other actions.[6][7][8][9][10][1][2] In contrast to their amphetamine counterparts, ephedrine and 4-fluoroephedrine are not agonists of the human trace amine-associated receptor 1 (TAAR1).[11] With regard to medical and other uses, β-hydroxyamphetamines are employed as sympathomimetics, decongestants, bronchodilators, vasoconstrictors, vasodilators, tocolytics, antitussives, cardiac stimulants, antihypotensive agents, appetite suppressants, psychostimulants, wakefulness-promoting agents, antidepressants, euphoriants or recreational drugs, and performance-enhancing drugs (in exercise and sports), among others.[1][2][9][3][10]

β-Hydroxyamphetamines have increased hydrophilicity and lower lipophilicity relative to their amphetamine counterparts owing to their β-hydroxyl group.[12][13] For comparison, the predicted log P (XLogP3) of amphetamine is 1.8,[14] of β-hydroxyamphetamine is 0.8,[15] and of cathinone is 1.1.[16] As a result of their reduced lipophilicity, they are generally less able to cross the blood–brain barrier and show greater peripheral selectivity in comparison to the corresponding amphetamine analogues.[12][13][17][18] This makes the β-hydroxyamphetamines less applicable for use as centrally-acting agents but more applicable for peripherally-specific uses such as sympathomimetic stimulation.[12][13][17][18] Besides different physicochemical properties, there is also a large drop in the potency of β-hydroxyamphetamines as monoamine releasing agents in vitro relative to amphetamines and cathinones.[6][8][19][20]

List of substituted β-hydroxyamphetamines[1][2]

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Generic or Trivial Name Chemical Name # of Subs
β-Hydroxyamphetamine (phenylisopropanolamine) β-Hydroxy-α-methylphenethylamine 0
  Phenylpropanolamine (PPA; norephedrine) β-Hydroxyamphetamine, (1RS,2SR)- 0
    (1R,2S)-Phenylpropanolamine β-Hydroxyamphetamine, (1R,2S)- 0
    (1S,2R)-Phenylpropanolamine β-Hydroxyamphetamine, (1S,2R)- 0
  Norpseudoephedrine β-Hydroxyamphetamine, (1SR,2RS)- 0
    Cathine (D-norpseudoephedrine) β-Hydroxyamphetamine, (1S,2S)- 0
    L-Norpseudoephedrine β-Hydroxyamphetamine, (1R,2R)- 0
β-Hydroxy-N-methylamphetamine β-Hydroxy-N-methylamphetamine 1
  Racephedrine (racemic ephedrine) β-Hydroxy-N-methylamphetamine, (1RS,2SR)- 1
    Ephedrine β-Hydroxy-N-methylamphetamine, (1R,2S)- 1
    (1S,2R)-Ephedrine β-Hydroxy-N-methylamphetamine, (1S,2R)- 1
  Racemic pseudoephedrine β-Hydroxy-N-methylamphetamine, (1RS,2RS)- 1
    Pseudoephedrine β-Hydroxy-N-methylamphetamine, (1S,2S)- 1
    (1R,2R)-Pseudoephedrine β-Hydroxy-N-methylamphetamine, (1R,2R)- 1
meta-Hydroxynorephedrine 3,β-Dihydroxyamphetamine 1
  Metaraminol (metaradrine) 3,β-Dihydroxyamphetamine, (1R,2S)- 1
para-Hydroxynorephedrine 4,β-Dihydroxyamphetamine 1
Oxyfedrine β-Hydroxy-N-(...)-amphetamine, (1R,2S)- 1
Alifedrine β-Hydroxy-N-(...)-amphetamine, (1R,2S)- 1
Tinofedrine β-Hydroxy-N-(3,3-di-3-thienyl)-2-propenyl)amphetamine, (1R,2S)- 1
Cafedrine (ethyltheophyllinylnorephedrine) β-Hydroxy-N-(ethyltheophyllinyl)amphetamine 1
Methylephedrine (N-methylephedrine) β-Hydroxy-N,N-dimethylamphetamine, (1R,2S)- 2
N-Methylpseudoephedrine β-Hydroxy-N,N-dimethylamphetamine, (1S,2S)- 2
Cinnamedrine (cinnamylephedrine) β-Hydroxy-N-methyl-N-cinnamylamphetamine 2
Etafedrine (ethylephedrine) β-Hydroxy-N-methyl-N-ethylamphetamine, (1R,2S)- 2
4-Fluoroephedrine 4-Fluoro-β-hydroxy-N-methylamphetamine 2
Oxilofrine (4-hydroxyephedrine) 4,β-Dihydroxy-N-methylamphetamine 2
Corbadrine (levonordefrin; α-methylnorepinephrine) 3,4,β-Trihydroxyamphetamine 2
Methoxamine (methoxamedrine) 2,6-Dimethoxy-β-hydroxyamphetamine 2
Hexapradol α-Desmethyl-α-hexyl-β-hydroxy-β-phenylamphetamine 2
Erythrohydrobupropion 3-Chloro-β-hydroxy-N-tert-butylamphetamine, erythro- 2
Threohydrobupropion 3-Chloro-β-hydroxy-N-tert-butylamphetamine, threo- 2
Ritodrine 4,β-Dihydroxy-N-(4-hydroxyphenylethyl)amphetamine 2
Isoxsuprine 4,β-Dihydroxy-N-(...)-amphetamine 2
Suloctidil 4-Isopropylthio-β-hydroxy-N-octylamphetamine 2
Buphenine 4,β-Dihydroxy-N-(...)-amphetamine 2
Trecadrine β-Hydroxy-N-methyl-N-(...)-amphetamine 2
Ethylnorepinephrine (butanefrine) β,3,4-Trihydroxy-α-desmethyl-α-ethylamphetamine 3
Dioxifedrine (α-methylepinephrine; 3,4-dihydroxyephedrine) 3,4,β-Trihydroxy-N-methylamphetamine 3
Dioxethedrin (α-methyl-N-ethylnorepinephrine) 3,4,β-Trihydroxy-N-ethylamphetamine 3
Butaxamine 3,6-Dimethoxy-β-hydroxy-N-tert-butylamphetamine, (1S,2S)- 3
Isoetarine 3,4,β-Trihydroxy-α-desmethyl-α-ethyl-N-isopropylamphetamine 4
Procaterol 2,3-(...)-4,β-dihydroxy-N-isopropyl-α-desmethyl-α-ethyl-
amphetamine, (1R,2S)-
5

Side-chain-cyclized substituted β-hydroxyamphetamines

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Some β-hydroxyamphetamines have had their side chain extended and cyclized. Examples include certain substituted phenylmorpholines like phenmetrazine and phendimetrazine and their analogues; substituted phenylmorpholines related to bupropion like radafaxine (cyclized (2S,3S)-hydroxybupropion) and manifaxine; certain substituted aminorexes like 4-methylaminorex and 4,4'-dimethylaminorex; and other compounds including cilobamine, diphenylprolinol, ifenprodil, levophacetoperane, pipradrol, rimiterol, traxoprodil, vibegron, and zilpaterol.

Activity profiles

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Monoamine release by β-hydroxyamphetamines and related agents (EC50Tooltip half maximal effective concentration, nM)[6][8]
Compound NETooltip Norepinephrine DATooltip Dopamine 5-HTTooltip Serotonin Class Ref
Amphetamine ND ND ND Amphetamine ND
  Dextroamphetamine (S(+)-amphetamine) 6.6–7.2 5.8–24.8 698–1765 Amphetamine [20][21]
  Levoamphetamine (R(–)-amphetamine) ND ND ND Amphetamine ND
Methamphetamine ND ND ND Amphetamine ND
  Dextromethamphetamine (S(+)-methamphetamine) 12.3–13.8 8.5–24.5 736–1291.7 Amphetamine [20][22]
  Levomethamphetamine (R(–)-methamphetamine) 28.5 416 4640 Amphetamine [20]
Cathinone ND ND ND Cathinone ND
  S(–)-Cathinone (L-cathinone) 12.4 18.5 2366 Cathinone [19]
Methcathinone ND ND ND Cathinone ND
  L-Methcathinone 13.1 14.8 1772 Cathinone [19]
Phenylpropanolamine (norephedrine) ND ND ND β-Hydroxyamphetamine ND
  (+)-Phenylpropanolamine ((+)-norephedrine) 42.1 302 >10000 β-Hydroxyamphetamine [19]
  (–)-Phenylpropanolamine ((–)-norephedrine) 137 1371 >10000 β-Hydroxyamphetamine [19]
Norpseudoephedrine ND ND ND β-Hydroxyamphetamine ND
  Cathine ((+)-norpseudoephedrine) 15.0 68.3 >10000 β-Hydroxyamphetamine [19]
  (–)-Norpseudoephedrine 30.1 294 >10000 β-Hydroxyamphetamine [19]
Racephedrine (racemic ephedrine) ND ND ND β-Hydroxyamphetamine ND
  Ephedrine ((–)-ephedrine) 43.1–72.4 236–1350 >10000 β-Hydroxyamphetamine [20]
  (+)-Ephedrine 218 2104 >10000 β-Hydroxyamphetamine [20][19]
Racemic pseudoephedrine ND ND ND β-Hydroxyamphetamine ND
  (–)-Pseudoephedrine 4092 9125 >10000 β-Hydroxyamphetamine [19]
  Pseudoephedrine ((+)-pseudoephedrine) 224 1988 >10000 β-Hydroxyamphetamine [19]
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.

See also

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References

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