Literature DB >> 1120990

Correlation of psychotomimetic activity of phenethylamines and amphetamines with 1-octanol-water partition coefficients.

C F Barfknecht, D E Nichols.   

Abstract

In an attempt to relate the hallucinogenic potencies in man of some biologically important amphetamines and phenethylamines, the 1-octanol-water partition coefficients for 11 amphetamines were determined. Using these values and published Hansch pi constants, the log P for 17 additional amines was estimated. It was found that lipophilicity, as measured by the log of the partition coefficient, may be a significant determinant of the level of hallucinogenic potency. The study also suggests that an ideal log P value for psychotomimetric activity in man may be from 2.89 to 3.72.

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Year:  1975        PMID: 1120990     DOI: 10.1021/jm00236a023

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  8 in total

1.  QSAR of benzene derivatives: comparison of classical descriptors, quantum theoretic parameters and flip regression, exemplified by phenylalkylamine hallucinogens.

Authors:  Brian W Clare
Journal:  J Comput Aided Mol Des       Date:  2002 Aug-Sep       Impact factor: 3.686

Review 2.  Interpretation of oral fluid tests for drugs of abuse.

Authors:  Edward J Cone; Marilyn A Huestis
Journal:  Ann N Y Acad Sci       Date:  2007-03-01       Impact factor: 5.691

3.  The role of lipophilicity in determining binding affinity and functional activity for 5-HT2A receptor ligands.

Authors:  Matthew A Parker; Deborah M Kurrasch; David E Nichols
Journal:  Bioorg Med Chem       Date:  2008-02-14       Impact factor: 3.641

4.  Comparison of the behavioral effects of mescaline analogs using the head twitch response in mice.

Authors:  Adam L Halberstadt; Muhammad Chatha; Stephen J Chapman; Simon D Brandt
Journal:  J Psychopharmacol       Date:  2019-02-21       Impact factor: 4.153

5.  Oral fluid and plasma 3,4-methylenedioxymethamphetamine (MDMA) and metabolite correlation after controlled oral MDMA administration.

Authors:  Nathalie A Desrosiers; Allan J Barnes; Rebecca L Hartman; Karl B Scheidweiler; Erin A Kolbrich-Spargo; David A Gorelick; Robert S Goodwin; Marilyn A Huestis
Journal:  Anal Bioanal Chem       Date:  2013-03-08       Impact factor: 4.142

6.  Receptor Interaction Profiles of 4-Alkoxy-Substituted 2,5-Dimethoxyphenethylamines and Related Amphetamines.

Authors:  Karolina E Kolaczynska; Dino Luethi; Daniel Trachsel; Marius C Hoener; Matthias E Liechti
Journal:  Front Pharmacol       Date:  2019-11-28       Impact factor: 5.810

7.  Receptor Interaction Profiles of 4-Alkoxy-3,5-Dimethoxy-Phenethylamines (Mescaline Derivatives) and Related Amphetamines.

Authors:  Karolina E Kolaczynska; Dino Luethi; Daniel Trachsel; Marius C Hoener; Matthias E Liechti
Journal:  Front Pharmacol       Date:  2022-02-09       Impact factor: 5.810

8.  Structural requirements for the antifungal activities of natural drimane sesquiterpenes and analogues, supported by conformational and electronic studies.

Authors:  Marcos Derita; Iván Montenegro; Francisco Garibotto; Ricardo D Enriz; Mauricio Cuellar Fritis; Susana A Zacchino
Journal:  Molecules       Date:  2013-02-05       Impact factor: 4.411

  8 in total

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