Ji XD - Search Results

1

Novel N6-(substituted-phenylcarbamoyl)adenosine-5'-uronamides as potent agonists for A3 adenosine receptors.

Baraldi PG, Cacciari B, Spalluto G, Ji XD, Olah ME, Stiles G, Dionisotti S, Zocchi C, Ongini E, Jacobson KA. Baraldi PG, et al. Among authors: ji xd. J Med Chem. 1996 Feb 2;39(3):802-6. doi: 10.1021/jm950518r. J Med Chem. 1996. PMID: 8576924

2

Search for new purine- and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptors.

Siddiqi SM, Jacobson KA, Esker JL, Olah ME, Ji XD, Melman N, Tiwari KN, Secrist JA 3rd, Schneller SW, Cristalli G, et al. Siddiqi SM, et al. Among authors: ji xd. J Med Chem. 1995 Mar 31;38(7):1174-88. doi: 10.1021/jm00007a014. J Med Chem. 1995. PMID: 7707320 Free PMC article.

3

Structure-activity relationships of 9-alkyladenine and ribose-modified adenosine derivatives at rat A3 adenosine receptors.

Jacobson KA, Siddiqi SM, Olah ME, Ji XD, Melman N, Bellamkonda K, Meshulam Y, Stiles GL, Kim HO. Jacobson KA, et al. Among authors: ji xd. J Med Chem. 1995 May 12;38(10):1720-35. doi: 10.1021/jm00010a017. J Med Chem. 1995. PMID: 7752196 Free PMC article.

4

Structure-activity relationships of 1,3-dialkylxanthine derivatives at rat A3 adenosine receptors.

Kim HO, Ji XD, Melman N, Olah ME, Stiles GL, Jacobson KA. Kim HO, et al. Among authors: ji xd. J Med Chem. 1994 Sep 30;37(20):3373-82. doi: 10.1021/jm00046a022. J Med Chem. 1994. PMID: 7932565 Free PMC article.

5

2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors.

Kim HO, Ji XD, Siddiqi SM, Olah ME, Stiles GL, Jacobson KA. Kim HO, et al. Among authors: ji xd. J Med Chem. 1994 Oct 14;37(21):3614-21. doi: 10.1021/jm00047a018. J Med Chem. 1994. PMID: 7932588 Free PMC article.

6

Selective ligands for rat A3 adenosine receptors: structure-activity relationships of 1,3-dialkylxanthine 7-riboside derivatives.

Kim HO, Ji XD, Melman N, Olah ME, Stiles GL, Jacobson KA. Kim HO, et al. Among authors: ji xd. J Med Chem. 1994 Nov 11;37(23):4020-30. doi: 10.1021/jm00049a021. J Med Chem. 1994. PMID: 7966162 Free PMC article.

7

Structure-activity relationships of N6-benzyladenosine-5'-uronamides as A3-selective adenosine agonists.

Gallo-Rodriguez C, Ji XD, Melman N, Siegman BD, Sanders LH, Orlina J, Fischer B, Pu Q, Olah ME, van Galen PJ, et al. Gallo-Rodriguez C, et al. Among authors: ji xd. J Med Chem. 1994 Mar 4;37(5):636-46. doi: 10.1021/jm00031a014. J Med Chem. 1994. PMID: 8126704 Free PMC article.

8

Interactions of flavonoids and other phytochemicals with adenosine receptors.

Ji XD, Melman N, Jacobson KA. Ji XD, et al. J Med Chem. 1996 Feb 2;39(3):781-8. doi: 10.1021/jm950661k. J Med Chem. 1996. PMID: 8576921 Free PMC article.

9

Synthesis and biological activities of flavonoid derivatives as A3 adenosine receptor antagonists.

Karton Y, Jiang JL, Ji XD, Melman N, Olah ME, Stiles GL, Jacobson KA. Karton Y, et al. Among authors: ji xd. J Med Chem. 1996 Jun 7;39(12):2293-301. doi: 10.1021/jm950923i. J Med Chem. 1996. PMID: 8691424 Free PMC article.

10

Derivatives of the triazoloquinazoline adenosine antagonist (CGS15943) are selective for the human A3 receptor subtype.

Kim YC, Ji XD, Jacobson KA. Kim YC, et al. Among authors: ji xd. J Med Chem. 1996 Oct 11;39(21):4142-8. doi: 10.1021/jm960482i. J Med Chem. 1996. PMID: 8863790 Free PMC article.

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