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Items: 1 to 20 of 72

1.

Comparative structural analysis of α-glucosidase inhibitors on difference species: a computational study.

Narayana Moorthy NS, Ramos MJ, Fernandes PA.

Arch Pharm (Weinheim). 2012 Apr;345(4):265-74. doi: 10.1002/ardp.201100047. Epub 2011 Oct 18.

PMID:
22006830
2.

Structural analysis of structurally diverse α-glucosidase inhibitors for active site feature analysis.

Moorthy NS, Ramos MJ, Fernandes PA.

J Enzyme Inhib Med Chem. 2012 Oct;27(5):649-57. doi: 10.3109/14756366.2011.605359. Epub 2011 Sep 8.

PMID:
21899493
3.
4.

Chlorogenic acid derivatives with alkyl chains of different lengths and orientations: potent alpha-glucosidase inhibitors.

Ma CM, Hattori M, Daneshtalab M, Wang L.

J Med Chem. 2008 Oct 9;51(19):6188-94. doi: 10.1021/jm800621x. Epub 2008 Sep 11.

PMID:
18783210
5.

Topological, hydrophobicity, and other descriptors on α-glucosidase inhibition: a QSAR study on xanthone derivatives.

Moorthy NS, Ramos MJ, Fernandes PA.

J Enzyme Inhib Med Chem. 2011 Dec;26(6):755-66. doi: 10.3109/14756366.2010.549089. Epub 2011 Feb 1.

PMID:
21284409
6.

Prediction of the relationship between the structural features of andrographolide derivatives and α-glucosidase inhibitory activity: a quantitative structure-activity relationship (QSAR) study.

Moorthy NS, Ramos MJ, Fernandes PA.

J Enzyme Inhib Med Chem. 2011 Feb;26(1):78-87. doi: 10.3109/14756361003724760. Epub 2010 Dec 20.

PMID:
21171896
7.

In silico based structural analysis of some piperidine analogs as farnesyltransferase inhibitors.

Moorthy NS, Sousa SF, Ramos MJ, Fernandes PA.

Med Chem. 2012 Sep;8(5):853-64.

PMID:
22741784
8.

Studies on α-glucosidase inhibitors development: magic molecules for the treatment of carbohydrate mediated diseases.

Moorthy NS, Ramos MJ, Fernandes PA.

Mini Rev Med Chem. 2012 Jul;12(8):713-20. Review.

PMID:
22512574
9.

Aglycon specificity profiling of alpha-glucosidases using synthetic probes.

Hakamata W, Muroi M, Kadokura K, Nishio T, Oku T, Kimura A, Chiba S, Takatsuki A.

Bioorg Med Chem Lett. 2005 Mar 1;15(5):1489-92.

PMID:
15713413
10.

Aspergillusol A, an alpha-glucosidase inhibitor from the marine-derived fungus Aspergillus aculeatus.

Ingavat N, Dobereiner J, Wiyakrutta S, Mahidol C, Ruchirawat S, Kittakoop P.

J Nat Prod. 2009 Nov;72(11):2049-52. doi: 10.1021/np9003883.

PMID:
19824618
11.

Planar catechin analogues with alkyl side chains: a potent antioxidant and an alpha-glucosidase inhibitor.

Hakamata W, Nakanishi I, Masuda Y, Shimizu T, Higuchi H, Nakamura Y, Saito S, Urano S, Oku T, Ozawa T, Ikota N, Miyata N, Okuda H, Fukuhara K.

J Am Chem Soc. 2006 May 24;128(20):6524-5.

PMID:
16704229
12.

Synthesis, inhibitory activities, and QSAR study of xanthone derivatives as alpha-glucosidase inhibitors.

Liu Y, Ke Z, Cui J, Chen WH, Ma L, Wang B.

Bioorg Med Chem. 2008 Aug 1;16(15):7185-92. doi: 10.1016/j.bmc.2008.06.043. Epub 2008 Jun 26.

PMID:
18632275
13.

QSAR and pharmacophore analysis of a series of piperidinyl urea derivatives as HERG blockers and H3 antagonists.

Moorthy NS, Ramos MJ, Fernandes PA.

Curr Drug Discov Technol. 2013 Mar;10(1):47-58.

PMID:
22564166
14.

A novel alpha-glucosidase inhibitor from pine bark.

Kim YM, Wang MH, Rhee HI.

Carbohydr Res. 2004 Feb 25;339(3):715-7.

PMID:
15013410
15.

Virtual screening and QSAR study of some pyrrolidine derivatives as α-mannosidase inhibitors for binding feature analysis.

Moorthy NS, Brás NF, Ramos MJ, Fernandes PA.

Bioorg Med Chem. 2012 Dec 15;20(24):6945-59. doi: 10.1016/j.bmc.2012.10.011. Epub 2012 Oct 26.

PMID:
23151473
16.

Binding mode analyses and pharmacophore model development for sulfonamide chalcone derivatives, a new class of alpha-glucosidase inhibitors.

Bharatham K, Bharatham N, Park KH, Lee KW.

J Mol Graph Model. 2008 Jun;26(8):1202-12. Epub 2007 Nov 17.

PMID:
18096420
17.
18.

Structural feature study of benzofuran derivatives as farnesyltransferase inhibitors.

Moorthy NS, Sousa SF, Ramos MJ, Fernandes PA.

J Enzyme Inhib Med Chem. 2011 Dec;26(6):777-91. doi: 10.3109/14756366.2011.552885. Epub 2011 Mar 7.

PMID:
21381884
19.

In silico-based structural analysis of arylthiophene derivatives for FTase inhibitory activity, hERG, and other toxic effects.

Narayana Moorthy NS, Sousa SF, Ramos MJ, Fernandes PA.

J Biomol Screen. 2011 Oct;16(9):1037-46. doi: 10.1177/1087057111414899. Epub 2011 Aug 5.

PMID:
21821787
20.

Quantitative structure-activity relationship (QSAR) study of a series of benzimidazole derivatives as inhibitors of Saccharomyces cerevisiae.

Podunavac-Kuzmanović SO, Cvetković DD, Jevrić LR, Uzelac NJ.

Acta Chim Slov. 2013;60(1):26-33.

PMID:
23841329

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