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Relevant bibliographies by topics / Pipradrol

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Academic literature on the topic 'Pipradrol'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Pipradrol"

1

White, Norman M., and Noboru Hiroi. "Pipradrol conditioned place preference is blocked by SCH23390." Pharmacology Biochemistry and Behavior 43, no. 2 (October 1992): 377–80. http://dx.doi.org/10.1016/0091-3057(92)90165-c.

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2

Simmler, Linda D., Anna Rickli, York Schramm, Marius C. Hoener, and Matthias E. Liechti. "Pharmacological profiles of aminoindanes, piperazines, and pipradrol derivatives." Biochemical Pharmacology 88, no. 2 (March 2014): 237–44. http://dx.doi.org/10.1016/j.bcp.2014.01.024.

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3

Coppola, M., and R. Mondola. "Research chemicals marketed as legal highs: The case of pipradrol derivatives." Toxicology Letters 212, no. 1 (July 2012): 57–60. http://dx.doi.org/10.1016/j.toxlet.2012.04.019.

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4

Kotteswari, M., M. R. K. Rao, Siva Kumar, K. Prabhu, R. Lakshmi Sundaram, and Shruthi Dinakar. "GC MS Analysis of One Ayurvedic Preparation ‘Aswagandharishtam." Biomedical and Pharmacology Journal 11, no. 2 (June 27, 2018): 1061–72. http://dx.doi.org/10.13005/bpj/1467.

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Aswagandharishtam is classical medicine for diseases pertaining to nervous system and digestive system prepared by a number of plants and plant parts. The present work is to know the types of biomolecules present in it by GC MS analysis. Aswagandharishtam was procured from standard Ayurvedic outlet and was subjected to Gas Chromatography Mass Spectrometry after due processing. The GC MS analysis of Aswagandharishtam has shown some promising molecules like Prostaglandin A2, Cholesterol, Piperine, Gentamicin a, d-Mannose, Eugenol, Pipradrol among others, which have activities similar to that of Aswagadharistham. This is a preliminary report where some clue about the various types of biomolecules present in Aswagandharishtam was obtained. Further work is on to prove the efficacy of this medicine by other parameters.

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5

Al-Imam, Ahmed, and Ban A. AbdulMajeed. "The Most Popular Chemical Categories of NPS in Four Leading Countries of the Developed World: An Integrative Analysis of Trends Databases, Surface Web, and the Deep Web." Global Journal of Health Science 9, no. 11 (September 18, 2017): 27. http://dx.doi.org/10.5539/gjhs.v9n11p27.

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BACKGROUND: New psychoactive substances are very diverse; hundreds exist today. Several schemes exist to categorise them; NPS can be classified into Cannabinoids and Cannabimimetics (1), Phenethylamines (2), Cathinones (3), Tryptamines (4), Piperazines (5), Pipradrol derivatives (6), and miscellaneous substances (7)MATERIALS & METHODS: Observational analyses via multiple internet snapshots will be carried out on the surface web and the deep web. The analyses will be hierarchical and integrative to infer the most popular categories of NPS based on the attentiveness (interest) of web users.RESULTS: Analysis of Google Trends from 2012 to the end of 2016, shows that interest in cannabinoids was the highest (98%), while all other chemical categories of NPS summed up to a tiny fragment (2%). The trends were highly oscillating over the years and shooting up during holiday seasons. Geo-mapping and localisation of the Middle East were not possible (not allowed) via Google Trends, while trends were attributed to four major leading countries of the developed world; US (35%), UK (17%), Canada (26%), and Australia (22%). Cannabinoids and stimulants were also found to be the most popular on the darknet.CONCLUSION: A novel method is proposed in this study; it has been carried out to provide an updated extrapolation on the most favoured chemical categories of NPS. This method is based on a combinatory examination at multiple levels of the surface web and the deep web. Furthermore, this method when potentially combined with data mining tools should provide unprecedented real-time analyses of high quality.

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Ramudu, B. Sri, D. Ramachandran, S. Venkat Rao, Ch Murali Krishna, B. Satya Narayana, and Kallam Naveen Reddy. "Design and Synthesis of Antimicrobial Active New Molecular Entities of N-Substituted Pipradol Derivatives." Asian Journal of Chemistry 29, no. 10 (2017): 2113–15. http://dx.doi.org/10.14233/ajchem.2017.20588.

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7

Liechti, Matthias, Linda Simmler, Anna Rickli, and Marius Hoener. "In vitro pharmacology of pipradrol derivatives, 3,4‐methylenedioxypyrovalerone, and naphyrone (1145.3)." FASEB Journal 28, S1 (April 2014). http://dx.doi.org/10.1096/fasebj.28.1_supplement.1145.3.

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Book chapters on the topic "Pipradrol"

1

Beyer, Karl-Heinz. "Pipradrol." In Biotransformation der Arzneimittel, 451. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74386-3_258.

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2

White, Michael W., and John R. H. Archer. "Pipradrol and Pipradrol Derivatives." In Novel Psychoactive Substances, 233–59. Elsevier, 2013. http://dx.doi.org/10.1016/b978-0-12-415816-0.00010-9.

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