Ablordeppey SY - Search Results

1

Benzothieno[3,2-b]quinolinium and 3-(phenylthio)quinolinium compounds: Synthesis and evaluation against opportunistic fungal pathogens.

Boateng CA, Eyunni SV, Zhu XY, Etukala JR, Bricker BA, Ashfaq MK, Jacob MR, Khan SI, Walker LA, Ablordeppey SY. Boateng CA, et al. Among authors: ablordeppey sy. Bioorg Med Chem. 2011 Jan 1;19(1):458-70. doi: 10.1016/j.bmc.2010.11.008. Epub 2010 Nov 10. Bioorg Med Chem. 2011. PMID: 21134759 Free PMC article.

2

Probing the N-5 region of the indoloquinoline alkaloid, cryptolepine for anticryptococcal activity.

Ablordeppey SY, Fan P, Clark AM, Nimrod A. Ablordeppey SY, et al. Bioorg Med Chem. 1999 Feb;7(2):343-9. doi: 10.1016/s0968-0896(98)00244-2. Bioorg Med Chem. 1999. PMID: 10218827

3

Systemic antifungal agents against AIDS-related opportunistic infections: current status and emerging drugs in development.

Ablordeppey SY, Fan P, Ablordeppey JH, Mardenborough L. Ablordeppey SY, et al. Among authors: ablordeppey jh. Curr Med Chem. 1999 Dec;6(12):1151-95. Curr Med Chem. 1999. PMID: 10519919 Review.

4

Is a nitrogen atom an important pharmacophoric element in sigma ligand binding?

Ablordeppey SY, Fischer JB, Glennon RA. Ablordeppey SY, et al. Bioorg Med Chem. 2000 Aug;8(8):2105-11. doi: 10.1016/s0968-0896(00)00148-6. Bioorg Med Chem. 2000. PMID: 11003156

5

Substituted indoloquinolines as new antifungal agents.

Ablordeppey SY, Fan P, Li S, Clark AM, Hufford CD. Ablordeppey SY, et al. Bioorg Med Chem. 2002 May;10(5):1337-46. doi: 10.1016/s0968-0896(01)00401-1. Bioorg Med Chem. 2002. PMID: 11886797

6

Probing the proposed phenyl-A region of the sigma-1 receptor.

Ablordeppey SY, Fischer JB, Law H, Glennon RA. Ablordeppey SY, et al. Bioorg Med Chem. 2002 Aug;10(8):2759-65. doi: 10.1016/s0968-0896(02)00096-2. Bioorg Med Chem. 2002. PMID: 12057665

7

The acute EPS of haloperidol may be unrelated to its metabolic transformation to BCPP+.

Sikazwe DM, Li S, Lyles-Eggleston M, Ablordeppey SY. Sikazwe DM, et al. Among authors: ablordeppey sy. Bioorg Med Chem Lett. 2003 Nov 3;13(21):3779-82. doi: 10.1016/j.bmcl.2003.07.015. Bioorg Med Chem Lett. 2003. PMID: 14552778

8

Design, synthesis, and evaluation of metabolism-based analogues of haloperidol incapable of forming MPP+-like species.

Lyles-Eggleston M, Altundas R, Xia J, Sikazwe DM, Fan P, Yang Q, Li S, Zhang W, Zhu X, Schmidt AW, Vanase-Frawley M, Shrihkande A, Villalobos A, Borne RF, Ablordeppey SY. Lyles-Eggleston M, et al. Among authors: ablordeppey sy. J Med Chem. 2004 Jan 29;47(3):497-508. doi: 10.1021/jm0301033. J Med Chem. 2004. PMID: 14736232

9

Identification of bis-quindolines as new antiinfective agents.

Mardenborough LG, Zhu XY, Fan P, Jacob MR, Khan SI, Walker LA, Ablordeppey SY. Mardenborough LG, et al. Among authors: ablordeppey sy. Bioorg Med Chem. 2005 Jun 2;13(12):3955-63. doi: 10.1016/j.bmc.2005.04.008. Bioorg Med Chem. 2005. PMID: 15911310

10

Evaluation of the eutomer of 4-{3-(4-chlorophenyl)-3-hydroxypyrrolidin-1-yl}-1-(4-fluorophenyl)butan-1-one, {(+)-SYA 09}, a pyrrolidine analog of haloperidol.

Ablordeppey SY, Lyles-Eggleston M, Bricker B, Zhang W, Zhu X, Goodman C, Roth BL. Ablordeppey SY, et al. Bioorg Med Chem Lett. 2006 Jun 15;16(12):3219-23. doi: 10.1016/j.bmcl.2006.03.057. Epub 2006 Apr 18. Bioorg Med Chem Lett. 2006. PMID: 16621538

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