569 results on '"Leander J"'
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102. Ethnopharmacology of ska Maria Pastora (Salvia divinorum, Epling AND Jativa-M.)
103. Introduction to the Report and Recommendations of the Florida Supreme Court Racial and Ethnic Bias Study Commission.
104. ChemInform Abstract: Preparation and Anticonvulsant Activity of a Series of Functionalized . alpha.-Heteroatom-Substituted Amino Acids.
105. ChemInform Abstract: Anticonvulsant Properties of N-Substituted α,α-Diamino Acid Derivatives.
106. ChemInform Abstract: (3SR,4aRS,6SR,8aRS)-6-(1H-Tetrazol-5-yl)decahydroisoquinoline-3- carboxylic Acid, a Novel, Competitive, Systemically Active NMDA, and AMPA Receptor Antagonist.
107. ChemInform Abstract: Structure-Activity Studies of 6-(Tetrazolylalkyl)-Substituted Decahydroisoquinoline-3-carboxylic Acid AMPA Receptor Antagonists. Part 1. Effects of Stereochemistry, Chain Length, and Chain Substitution.
108. ChemInform Abstract: Salvinorin C, a New Neoclerodane Diterpene from a Bioactive Fraction of the Hallucinogenic Mexican Mint Salvia divinorum.
109. Art. XXII.—Report of the Trial, “The People v. Dr. Horatio N. Loomis for Libel.” Tried at the Erie County Oyer and Terminer June 24th, 1850, &c. &c. Justice Mullett presiding.
110. Combined effects of ethanol and diazepam on performance and acquisition of serial position sequences by pigeons
111. SKF-525A on schedule-controlled responding: Not antagonized by naloxone
112. Interactions of clozapine, thioridazine, and mezilamine with oxotremorine on schedule-controlled responding
113. Comparison of Ensemble Techniques for Incremental Learning of New Concept Classes under Hostile Non-stationary Environments.
114. Salvinorin C, a New Neoclerodane Diterpene from a Bioactive Fraction of the Hallucinogenic Mexican Mint Salvia divinorum
115. ChemInform Abstract: Synthesis and Anticonvulsant Activity of 3‐Aryl‐5H‐2,3‐benzodiazepine AMPA Antagonists.
116. Disinhibitory effects of LY354740, a new mGluR2 agonist, on behaviors suppressed by electric shock in rats and pigeons
117. ChemInform Abstract: Heteroatom‐Substitution as a Strategy for Increasing the Potency of Competitive NMDA Antagonists.
118. The Quick-Flip Precision Locator for Micro Machining
119. Increased food consumption by clozapine, but not by olanzapine, in satiated rats
120. Pharmacological profile of LY301317, a potent and selective 5-HT1A agonist
121. Structure−Activity Studies of 6-(Tetrazolylalkyl)-Substituted Decahydroisoquinoline-3-carboxylic Acid AMPA Receptor Antagonists. 1. Effects of Stereochemistry, Chain Length, and Chain Substitution
122. Structure−Activity Studies of 6-Substituted Decahydroisoquinoline-3-carboxylic Acid AMPA Receptor Antagonists. 2. Effects of Distal Acid Bioisosteric Substitution, Absolute Stereochemical Preferences, and in Vivo Activity
123. (3SR,4aRS,6SR,8aRS)-6-(1H-Tetrazol-5-yl)decahydroisoquinoline-3-carboxylic Acid, a Novel, Competitive, Systemically Active NMDA and AMPA Receptor Antagonist
124. Machining Sub-Millimeter Beryllium and Aluminum Components of Laser Targets
125. Pharmacological characterization of enantiomers of 8-thiomethyl-2-(di-n-propylamino)tetralin, potent and selective 5-HT1A receptor agonists
126. ChemInform Abstract: Discovery of a Potent, Peripherally Selective trans‐3,4‐Dimethyl‐4‐(3‐ hydroxyphenyl)piperidine Opioid Antagonist for the Treatment of Gastrointestinal Motility Disorders.
127. Salvia divinorumand the Unique Diterpene Hallucinogen, Salvinorin (Divinorin) A
128. Discovery of a Potent, Peripherally Selective trans-3,4-Dimethyl-4-(3-hydroxyphenyl)piperidine Opioid Antagonist for the Treatment of Gastrointestinal Motility Disorders
129. Anticonvulsant Properties ofN‐Substituted α,α‐Diamino Acid Derivatives
130. Structure-activity relationships of trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine antagonists for .mu.- and .kappa.-opioid receptors
131. Synthesis and anticonvulsant activities of .alpha.-heterocyclic .alpha.-acetamido-N-benzylacetamide derivatives
132. 3,4-Dimethyl-4-(3-hydroxyphenyl)piperidines: opioid antagonists with potent anorectant activity
133. (3SR,4aRS,6RS,8aRS)-6-[2-(1H-Tetrazol-5-yl)ethyl]decahydroisoquinoline-3-carboxylic acid: a structurally novel, systemically active, competitive AMPA receptor antagonist
134. NMDA antagonist activity of (.+-.)-(2SR,4RS)-4-(1H-tetrazol-5-ylmethyl)piperidine-2-carboxylic acid residues with the (-)-2R,4S-isomer
135. Relation of Plasma and Brain Concentrations of the Anticonvulsant Ameltolide to Its Pharmacologic Effects
136. Intraction of the Anticonvulsant Ameltolide with standard Anticonvulsants
137. Fluoxetine, a Selective Serotonin-Uptake Inhibitor, Enhances the Anticonvulsant Effects of Phenytoin, Carbamazepine, and Ameltolide (LY 201116)
138. PRECLINICAL BEHAVIORAL DIFFERENCES BETWEEN COMPETITIVE AND PHENCYCLIDINE-LIKE NMDA ANTAGONISTS THAT MIGHT PREDICT DIFFERENCES IN CLINICAL EFFECTS
139. Subchronic Toxicity, Metabolism, and Pharmacokinetics of the Aminobenzamide Anticonvulsant Ameltolide (LY2O1 116) in Rhesus Monkeys
140. Preparation and anticonvulsant activity of a series of functionalized .alpha.-heteroatom-substituted amino acids
141. ChemInform Abstract: 4‐(Tetrazolylalkyl)piperidine‐2‐carboxylic Acids. Potent and Selective N‐Methyl‐D‐aspartic Acid Receptor Antagonists with a Short Duration of Action.
142. Synthesis and pharmacological evaluation of a major metabolite of ameltolide, a potent anticonvulsant
143. 4-(Tetrazolylalkyl)piperidine-2-carboxylic acids. Potent and selective N-methyl-D-aspartic acid receptor antagonists with a short duration of action
144. Synthesis of the 6-benzoyl derivative of 1-deoxy-1-oxo-7-desacetylforskolin and an unambiguous assignment of the absolute stereochemistry of forskolin
145. The Absolute Stereochemistry of Salvinorins
146. ChemInform Abstract: Selective Opioid Receptor Agonists and Antagonists: Research Tools and Potential Therapeutic Agents
147. Preparation and anticonvulsant activity of a series of functionalized .alpha.-aromatic and .alpha.-heteroaromatic amino acids
148. Selective opioid receptor agonists and antagonists: research tools and potential therapeutic agents
149. Opioid Antagonists: Structure Activity Relationships
150. SR141716A, a cannabinoid CB1 receptor antagonist, improves memory in a delayed radial maze task
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