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Substituted β-hydroxyamphetamine

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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

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]

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] With regard to medical and other uses, they 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.[11][12] For comparison, the predicted log P (XLogP3) of amphetamine is 1.8,[13] of β-hydroxyamphetamine is 0.8,[14] and of cathinone is 1.1.[15] 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.[11][12][16][17] This makes the β-hydroxyamphetamines less applicable for use as centrally-acting agents but more applicable for peripherally-specific uses such as sympathomimetic stimulation.[11][12][16][17] Besides different physicochemical properties, there is also a large drop in the potency of β-hydroxyamphetamines as monoamine releasing agents relative to amphetamines and cathinones.[6][8][18][19]

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
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
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
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 [19][20]
  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 [19][21]
  Levomethamphetamine (R(–)-methamphetamine) 28.5 416 4640 Amphetamine [19]
Cathinone ND ND ND Cathinone ND
  S(–)-Cathinone (L-cathinone) 12.4 18.5 2366 Cathinone [18]
Methcathinone ND ND ND Cathinone ND
  L-Methcathinone 13.1 14.8 1772 Cathinone [18]
Phenylpropanolamine (norephedrine) ND ND ND β-Hydroxyamphetamine ND
  (+)-Phenylpropanolamine ((+)-norephedrine) 42.1 302 >10000 β-Hydroxyamphetamine [18]
  (–)-Phenylpropanolamine ((–)-norephedrine) 137 1371 >10000 β-Hydroxyamphetamine [18]
Norpseudoephedrine ND ND ND β-Hydroxyamphetamine ND
  Cathine ((+)-norpseudoephedrine) 15.0 68.3 >10000 β-Hydroxyamphetamine [18]
  (–)-Norpseudoephedrine 30.1 294 >10000 β-Hydroxyamphetamine [18]
Racephedrine (racemic ephedrine) ND ND ND β-Hydroxyamphetamine ND
  Ephedrine ((–)-ephedrine) 43.1–72.4 236–1350 >10000 β-Hydroxyamphetamine [19]
  (+)-Ephedrine 218 2104 >10000 β-Hydroxyamphetamine [19][18]
Racemic pseudoephedrine ND ND ND β-Hydroxyamphetamine ND
  (–)-Pseudoephedrine 4092 9125 >10000 β-Hydroxyamphetamine [18]
  Pseudoephedrine ((+)-pseudoephedrine) 224 1988 >10000 β-Hydroxyamphetamine [18]
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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  5. ^ Nadal-Gratacós N, Pazos MD, Pubill D, Camarasa J, Escubedo E, Berzosa X, et al. (6 August 2024). "Structure–Activity Relationship of Synthetic Cathinones: An Updated Review". ACS Pharmacology & Translational Science. doi:10.1021/acsptsci.4c00299. ISSN 2575-9108. In 1975, cathinone [(β-ketoamphetamine)] was identified as the active stimulant component in the Catha edulis shrub. Prior to this discovery, it was believed that the psychostimulant effect of the plant was mainly attributed to cathine (β-hydroxyamphetamine), first isolated from the khat plant in 1930,127 and later described as a central stimulant.128
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  12. ^ a b c Bouchard R, Weber AR, Geiger JD (July 2002). "Informed decision-making on sympathomimetic use in sport and health". Clinical Journal of Sport Medicine. 12 (4): 209–224. doi:10.1097/00042752-200207000-00003. PMID 12131054.
  13. ^ "Amphetamine". PubChem. U.S. National Library of Medicine. Retrieved 2 September 2024.
  14. ^ "2-Amino-1-phenyl-1-propanol". PubChem. U.S. National Library of Medicine. Retrieved 2 September 2024.
  15. ^ "Cathinone". PubChem. U.S. National Library of Medicine. Retrieved 2 September 2024.
  16. ^ a b Bharate SS, Mignani S, Vishwakarma RA (December 2018). "Why Are the Majority of Active Compounds in the CNS Domain Natural Products? A Critical Analysis". Journal of Medicinal Chemistry. 61 (23): 10345–10374. doi:10.1021/acs.jmedchem.7b01922. PMID 29989814.
  17. ^ a b 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 partitioned into the lipid interior of membranes and will be retained there. However, ClogP correlates nicely with LogBBB with increasing lipophilicity 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 the 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
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