A.J. Jennings
Tri-Institutional Therapeutics Discovery Institute(US)
Publications by Year
Research Areas
Magnetic and transport properties of perovskites and related materials, Receptor Mechanisms and Signaling, Pharmacological Receptor Mechanisms and Effects, Chemical Synthesis and Analysis, Asymmetric Synthesis and Catalysis
Most-Cited Works
- → A Novel, Potent, and Selective 5-HT7Antagonist: (R)-3-(2-(2-(4-Methylpiperidin-1-yl)ethyl)pyrrolidine-1-sulfonyl)phenol (SB-269970)(2000)249 cited
- → (R)-3,N-Dimethyl-N-[1-methyl-3-(4-methylpiperidin-1-yl)propyl]benzenesulfonamide: The First Selective 5-HT7Receptor Antagonist(1998)102 cited
- → The Selective 5-HT1BReceptor Inverse Agonist 1‘-Methyl-5-[[2‘-methyl-4‘- (5-methyl-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]carbonyl]-2,3,6,7-tetrahydro- spiro[furo[2,3-f]indole-3,4‘-piperidine] (SB-224289) Potently Blocks Terminal 5-HT Autoreceptor Function Both in Vitro and in Vivo(1998)81 cited
- → Phenyl benzenesulfonamides are novel and selective 5-HT6 antagonists: identification of N-(2,5-dibromo-3-fluorophenyl)-4-methoxy-3-piperazin-1-ylbenzenesulfonamide (SB-357134)(2001)56 cited
- → (1-Butyl-4-piperidinyl)methyl 8-amino-7-chloro-1,4-benzodioxane-5-carboxylate hydrochloride: a highly potent and selective 5-HT4 receptor antagonist derived from metoclopramide(1993)39 cited
- → Thermal stability and conduction properties of the LaxSr2−xFeO4+δ system(2002)34 cited
- → Structural properties of La Sr2−FeO4± at high temperature and under reducing conditions(2003)30 cited
- → Discovery Strategies in a BioPharmaceutical Startup: Maximising your Chances of Success Using Computational Filters(2005)9 cited
- → Synthesis of (endo) 3,9-disubstituted diazabicyclo[3.3.1]nonan-7-amines(1995)7 cited
- → External fertilization is orchestrated by a pH-regulated soluble adenylyl cyclase controlling sperm motility and chemotaxis(2021)6 cited