Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kristjan M. Arason"'
Autor:
Stephen C. Bergmeier, Dennis B. McKay, Susan B. McKay, Crina M. Orac, Michael X. Zhu, Kristjan M. Arason, Peter W. Swaan, Tatiana F. González-Cestari, Darrell L. Bryant, Aravinda B. Pulipaka, Cheng Chang, Raed A. El-Hajj
Publikováno v:
Molecular Pharmacology. 71:1288-1297
As a novel approach to drug discovery involving neuronal nicotinic acetylcholine receptors (nAChRs), our laboratory targeted nonagonist binding sites (i.e., noncompetitive binding sites, negative allosteric binding sites) located on nAChRs. Cultured
Autor:
Susan B. McKay, Stephen C. Bergmeier, Darrell L. Bryant, Dennis B. McKay, K. A. Ismail, Kristjan M. Arason
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 14:3739-3742
The development of novel agents for the differentiation of neuronal nicotinic acetylcholine receptors (nAChRs) is important for the treatment of a variety of pathological conditions. We have prepared and evaluated a number of simpler analogues of the
Publikováno v:
Organic Preparations and Procedures International. 34:337-366
(2002). THE SYNTHESIS OF SUCCINIC ACIDS AND DERIVATIVES. A REVIEW. Organic Preparations and Procedures International: Vol. 34, No. 4, pp. 337-366.
Publikováno v:
Tetrahedron Letters. 41:5799-5802
We have discovered a simple one-pot procedure to convert trityl ethers into esters, using the corresponding acid chloride as the only reagent.
Autor:
Sara M Thomasy, K. A. Ismail, David J. Lapinsky, Dennis B. McKay, Stephen C. Bergmeier, Kristjan M. Arason, R. Benjamin Free, Darrell L. Bryant
Publikováno v:
Annals of the New York Academy of Sciences. 971:139-141
Adrenal secretion and binding studies were performed using ring E analogues of methyllycaconitine to assess structural determinants affecting activity on bovine adrenal alpha3beta4* nicotinic receptors. The most potent analogues are as potent as many
Publikováno v:
ChemInform. 33
Publikováno v:
ChemInform. 31
We have discovered a simple one-pot procedure to convert trityl ethers into esters, using the corresponding acid chloride as the only reagent.
Publikováno v:
Organic Preparations & Procedures International; Aug2002, Vol. 34 Issue 4, p337-366, 30p