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Chiral resolution and stereospecificity of 6-phenyl-4-phenylethynyl-1,4-dihydropyridines as selective A3 adenosine receptor antagonistsJIANG, J.-L; LI, A.-H; JANG, S.-Y et al.Journal of medicinal chemistry (Print). 1999, Vol 42, Num 16, pp 3055-3065, issn 0022-2623Article

Structure-activity relationships of 4-(phenylethynyl)-6-phenyl-1,4-dihydropyridines as highly selective A3 adenosine receptor antagonistsJIANG, J.-L; VAN RHEE, A. M; CHANG, L et al.Journal of medicinal chemistry (Print). 1997, Vol 40, Num 16, pp 2596-2608, issn 0022-2623Article

A diagonal recurrent neural network-based hybrid direct adaptive SPSA control systemJI, X. D; FAMILONI, B. O.IEEE transactions on automatic control. 1999, Vol 44, Num 7, pp 1469-1473, issn 0018-9286Article

Use of the triazolotriazine [3H]ZM 241385 as a radioligand at recombinant human A2B adenosine receptorsJI, X.-D; JACOBSON, K. A.Drug design and discovery (Print). 1999, Vol 16, Num 3, pp 217-226, issn 1055-9612Article

Acyl-hydrazide derivatives of a xanthine carboxylic congener (XCC) as selective antagonists at human A2B adenosine receptorsKIM, Y.-C; KARTON, Y; JI, X.-D et al.Drug development research. 1999, Vol 47, Num 4, pp 178-188, issn 0272-4391Article

Structure-activity relationships and molecular modeling of 3,5-diacyl-2,4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonistsLI, A.-H; MORO, S; MELMAN, N et al.Journal of medicinal chemistry (Print). 1998, Vol 41, Num 17, pp 3186-3201, issn 0022-2623Article

Activation of A3, adrenosine receptors on human eosinophils elevates intracellular calciumKOHNO, Y; JI, X.-D; MAWHORTER, S. D et al.Blood. 1996, Vol 88, Num 9, pp 3569-3574, issn 0006-4971Article

[3H]XAC (xanthine amine congener) is a radioligand for A2-adenosine receptors in rabbit striatumJI, X.-D; STILES, G. L; JACOBSON, K. A et al.Neurochemistry international. 1991, Vol 18, Num 2, pp 207-213, issn 0197-0186, 7 p.Article

Synthesis and biological activity of a new series of N6-arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-carboxamido derivatives of adenosine-5'-N-ethyluronamide as A1 and A3 adenosine receptor agonistsBARALDI, P. G; CACCIARI, B; PARK, K.-S et al.Journal of medicinal chemistry (Print). 1998, Vol 41, Num 17, pp 3174-3185, issn 0022-2623Article

Adenosine A3 receptor agonist-induced neurotoxicity in rat cerebellar granule neuronsSEI, Y; VON LUBITZ, D. K. J. E; ABBRACCHIO, M. P et al.Drug development research. 1997, Vol 40, Num 3, pp 267-273, issn 0272-4391Article

Riboflavin : Inhibitory effects on receptors, G-proteins, and adenylate cyclaseDALY, J. W; DAN SHI; PADGETT, W. L et al.Drug development research. 1997, Vol 42, Num 2, pp 98-108, issn 0272-4391Article

Pharmacological characterization of novel A3 adenosine receptor-selective antagonistsJACOBSON, K. A; PARK, K.-S; JIANG, J.-L et al.Neuropharmacology. 1997, Vol 36, Num 9, pp 1157-1165, issn 0028-3908Conference Paper

Anilide derivatives of an 8-phenylxanthine carboxylic congener are highly potent and selective antagonists at human A2B adenosine receptorsKIM, Y.-C; JI, X.-D; MELMAN, N et al.Journal of medicinal chemistry (Print). 2000, Vol 43, Num 6, pp 1165-1172, issn 0022-2623Article

Pyran template approach to the design of novel A3 adenosine receptor antagonistsLI, A.-H; JI, X.-D; HAK SUNG KIM et al.Drug development research. 1999, Vol 48, Num 4, pp 171-177, issn 0272-4391Article

Synthesis, CoMFA analysis, and receptor docking of 3,5-diacyl-2,4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonistsLI, A.-H; MORO, S; FORSYTH, N et al.Journal of medicinal chemistry (Print). 1999, Vol 42, Num 4, pp 706-721, issn 0022-2623Article

Synthesis and biological activities of flavonoid derivatives as A3 adenosine receptor antagonistsKARTON, Y; JIANG, J.-L; JI, X.-D et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 12, pp 2293-2301, issn 0022-2623Article

The utilization of a unified pharmacophore query in the discovery of new antagonists of the adenosine receptor familyWEBB, T. R; MELMAN, N; LVOVSKIY, D et al.Bioorganic & medicinal chemistry letters (Print). 2000, Vol 10, Num 1, pp 31-34, issn 0960-894XArticle

Methanocarba analogues of purine nucleosides as potent and selective adenosine receptor agonistsJACOBSON, K. A; JI, X.-D; LI, A.-H et al.Journal of medicinal chemistry (Print). 2000, Vol 43, Num 11, pp 2196-2203, issn 0022-2623Article

Selective as adenosine receptor antagonists : Water-soluble 3,5-diacyl-1,2,4-trialkylpyridinium salts and their oxidative generation from dihydropyridine precursorsRONGYUAN XIE; LI, A.-H; JI, X.-D et al.Journal of medicinal chemistry (Print). 1999, Vol 42, Num 20, pp 4232-4238, issn 0022-2623Article

Synthesis and structure-activity relationships of pyridoxal-6-arylazo-5'-phosphate and phosphonate derivatives as P2 receptor antagonistsKIM, Y.-C; CAMAIONI, E; HARDEN, T. K et al.Drug development research. 1998, Vol 45, Num 2, pp 52-66, issn 0272-4391Article

Derivatives of the triazoloquinazoline adenosine antagonist (CGS15943) are selective for the human A3 receptor subtypeKIM, Y.-C; JI, X.-D; JACOBSON, K. A et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 21, pp 4142-4148, issn 0022-2623Article

6-Phenyl-1,4-dihydropyridine derivatives as potent and selective A3 adenosine receptor antagonistsJIANG, J-I; VAN RHEE, A. M; MELMAN, N et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 23, pp 4667-4675, issn 0022-2623Article

Simultaneous immobilization of ammonium and phosphate from aqueous solution using zeolites synthesized from fly ashesJI, X. D; ZHANG, M. L; KE, Y. Y et al.Water science and technology. 2013, Vol 67, Num 6, pp 1324-1331, issn 0273-1223, 8 p.Article

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