These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
203 related items for PubMed ID: 18834105
1. 2-Phenyl-imidazo[1,2-a]pyridine compounds containing hydrophilic groups as potent and selective ligands for peripheral benzodiazepine receptors: synthesis, binding affinity and electrophysiological studies. Denora N, Laquintana V, Pisu MG, Dore R, Murru L, Latrofa A, Trapani G, Sanna E. J Med Chem; 2008 Nov 13; 51(21):6876-88. PubMed ID: 18834105 [Abstract] [Full Text] [Related]
2. Exploring selectivity requirements for peripheral versus central benzodiazepine receptor binding affinity: QSAR modeling of 2-phenylimidazo[1,2-a]pyridine acetamides using topological and physicochemical descriptors. Dalai MK, Leonard JT, Roy K. Indian J Biochem Biophys; 2006 Apr 13; 43(2):105-18. PubMed ID: 16955759 [Abstract] [Full Text] [Related]
3. Structure-activity relationships and effects on neuroactive steroid synthesis in a series of 2-phenylimidazo[1,2-a]pyridineacetamide peripheral benzodiazepine receptors ligands. Trapani G, Laquintana V, Denora N, Trapani A, Lopedota A, Latrofa A, Franco M, Serra M, Pisu MG, Floris I, Sanna E, Biggio G, Liso G. J Med Chem; 2005 Jan 13; 48(1):292-305. PubMed ID: 15634024 [Abstract] [Full Text] [Related]
4. Synthesis and binding affinity of 2-phenylimidazo[1,2-alpha]pyridine derivatives for both central and peripheral benzodiazepine receptors. A new series of high-affinity and selective ligands for the peripheral type. Trapani G, Franco M, Ricciardi L, Latrofa A, Genchi G, Sanna E, Tuveri F, Cagetti E, Biggio G, Liso G. J Med Chem; 1997 Sep 12; 40(19):3109-18. PubMed ID: 9301675 [Abstract] [Full Text] [Related]
5. Synthesis and biological evaluation of substituted [18F]imidazo[1,2-a]pyridines and [18F]pyrazolo[1,5-a]pyrimidines for the study of the peripheral benzodiazepine receptor using positron emission tomography. Fookes CJ, Pham TQ, Mattner F, Greguric I, Loc'h C, Liu X, Berghofer P, Shepherd R, Gregoire MC, Katsifis A. J Med Chem; 2008 Jul 10; 51(13):3700-12. PubMed ID: 18557607 [Abstract] [Full Text] [Related]
6. Novel 2-phenylimidazo[1,2-a]pyridine derivatives as potent and selective ligands for peripheral benzodiazepine receptors: synthesis, binding affinity, and in vivo studies. Trapani G, Franco M, Latrofa A, Ricciardi L, Carotti A, Serra M, Sanna E, Biggio G, Liso G. J Med Chem; 1999 Sep 23; 42(19):3934-41. PubMed ID: 10508441 [Abstract] [Full Text] [Related]
8. Potent 4-aryl- or 4-arylalkyl-substituted 3-isoxazolol GABA(A) antagonists: synthesis, pharmacology, and molecular modeling. Frølund B, Jensen LS, Guandalini L, Canillo C, Vestergaard HT, Kristiansen U, Nielsen B, Stensbøl TB, Madsen C, Krogsgaard-Larsen P, Liljefors T. J Med Chem; 2005 Jan 27; 48(2):427-39. PubMed ID: 15658856 [Abstract] [Full Text] [Related]
9. Synthesis and structure--activity relationships of fused imidazopyridines: a new series of benzodiazepine receptor ligands. Takada S, Sasatani T, Chomei N, Adachi M, Fujishita T, Eigyo M, Murata S, Kawasaki K, Matsushita A. J Med Chem; 1996 Jul 05; 39(14):2844-51. PubMed ID: 8709114 [Abstract] [Full Text] [Related]
10. Synthesis, in vitro affinity, and efficacy of a bis 8-ethynyl-4H-imidazo[1,5a]- [1,4]benzodiazepine analogue, the first bivalent alpha5 subtype selective BzR/GABA(A) antagonist. Li X, Cao H, Zhang C, Furtmueller R, Fuchs K, Huck S, Sieghart W, Deschamps J, Cook JM. J Med Chem; 2003 Dec 18; 46(26):5567-70. PubMed ID: 14667209 [Abstract] [Full Text] [Related]
15. 8-Fluoroimidazo[1,2-a]pyridine: synthesis, physicochemical properties and evaluation as a bioisosteric replacement for imidazo[1,2-a]pyrimidine in an allosteric modulator ligand of the GABA A receptor. Humphries AC, Gancia E, Gilligan MT, Goodacre S, Hallett D, Merchant KJ, Thomas SR. Bioorg Med Chem Lett; 2006 Mar 15; 16(6):1518-22. PubMed ID: 16386901 [Abstract] [Full Text] [Related]
16. Neurosteroid analogues. 9. Conformationally constrained pregnanes: structure-activity studies of 13,24-cyclo-18,21-dinorcholane analogues of the GABA modulatory and anesthetic steroids (3alpha,5alpha)- and (3alpha,5beta)-3-hydroxypregnan-20-one. Jiang X, Manion BD, Benz A, Rath NP, Evers AS, Zorumski CF, Mennerick S, Covey DF. J Med Chem; 2003 Dec 04; 46(25):5334-48. PubMed ID: 14640542 [Abstract] [Full Text] [Related]