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D. E. Nichols

5 papers in the library · 8 citations · publishing 1977-2014

Papers

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Chronic LSD alters gene expression profiles in the mPFC relevant to schizophrenia

Neuropharmacology April 3, 2014 David Martin, Danuta Marona‐lewicka, D. E. Nichols et al.

Chronic administration of lysergic acid diethylamide (LSD) every other day to rats results in a variety of abnormal behaviors. These build over the 90 day course of treatment and can persist at full strength for at least several months after cessation of treatment. The behaviors are consistent with those observed in animal models of schizophrenia and include hyperactivity, reduced...

ChemInform Abstract: Dihydrobenzofuran Analogues of Hallucinogens. Part 4. Mescaline Derivatives.

ChemInform January 6, 1998 Aaron Monte, Steve R. Waldman, Danuta Marona‐lewicka et al.

AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Effect of a Chiral 4-Alkyl Substituent in Hallucinogenic Amphetamines

Journal of Medicinal Chemistry September 1, 1995 Robert Oberlender, P. V. Ramachandran, Michael P. Johnson et al. 8 citations

The potency of hallucinogenic amphetamine derivatives of the 1-(2,5-dimethoxy-4-alkylphenyl)-2-aminopropane type drops dramatically when the length of the 4-alkyl substituent exceeds propyl or when the substituent is branched. This investigation was directed toward evaluating changes in behavioral and biochemical pharmacology resulting from introducing chirality into the 4-alkyl group of such...

ChemInform Abstract: Synthesis und Evaluation of 2,3‐Dihydrobenzofuran Analogues of the Hallucinogen 1‐(2,5‐Dimethoxy‐4‐methylphenyl)‐2‐aminopropane: Drug Discrimination Studies in Rats.

Chemischer Informationsdienst June 10, 1986 D. E. Nichols, Andrew J. Hoffman, Robert Oberlender et al.

AbstractDie aus den Dihydrobenzofuranen (I) zugänglichen Aldehyde (II) werden durch Kondensation mit Nitroethan und anschließende Reduktion in die Aminopropyl‐Derivate (V) übergeführt, die auf LSD‐analoge Wirkung bei Ratten geprüft werden.