Haider N - Search Results

1

Semicarbazide-sensitive amine oxidase: current status and perspectives.

Mátyus P, Dajka-Halász B, Földi A, Haider N, Barlocco D, Magyar K. Mátyus P, et al. Among authors: haider n. Curr Med Chem. 2004 May;11(10):1285-98. doi: 10.2174/0929867043365305. Curr Med Chem. 2004. PMID: 15134520 Review.

2

Semicarbazide-sensitive amine oxidase/vascular adhesion protein 1: recent developments concerning substrates and inhibitors of a promising therapeutic target.

Dunkel P, Gelain A, Barlocco D, Haider N, Gyires K, Sperlágh B, Magyar K, Maccioni E, Fadda A, Mátyus P. Dunkel P, et al. Among authors: haider n. Curr Med Chem. 2008;15(18):1827-39. doi: 10.2174/092986708785133022. Curr Med Chem. 2008. PMID: 18691041 Review.

3

Synthesis of ortho-functionalized 4-aminomethylpyridazines as substrate-like semicarbazide-sensitive amine oxidase inhibitors.

Haider N, Hochholdinger I, Mátyus P, Wobus A. Haider N, et al. Chem Pharm Bull (Tokyo). 2010 Jul;58(7):964-70. doi: 10.1248/cpb.58.964. Chem Pharm Bull (Tokyo). 2010. PMID: 20606348 Free article.

4

Unexpected hydrazinolysis behaviour of 1-chloro-4-methyl-5H-pyridazino[4,5-b]indole and a convenient synthesis of new [1,2,4]-triazolo[4',3':1,6]pyridazino[4,5-b]indoles.

El-Kashef H, Farghaly AA, Haider N, Wobus A. El-Kashef H, et al. Among authors: haider n. Molecules. 2004 Sep 30;9(10):849-59. doi: 10.3390/91000849. Molecules. 2004. PMID: 18007485 Free PMC article.

5

1,5-dimethyl-6H-pyridazino[4,5-b]carbazole, a 3-aza bioisoster of the antitumor alkaloid olivacine.

Haider N, Sotelo E. Haider N, et al. Chem Pharm Bull (Tokyo). 2002 Nov;50(11):1479-83. doi: 10.1248/cpb.50.1479. Chem Pharm Bull (Tokyo). 2002. PMID: 12419913 Free article.

6

Synthesis and in-vitro antitumor activity of 1-[3-(indol-1-yl)prop-1-yn-1-yl]phthalazines and related compounds.

Haider N, Kabicher T, Käferböck J, Plenk A. Haider N, et al. Molecules. 2007 Aug 17;12(8):1900-9. doi: 10.3390/12081900. Molecules. 2007. PMID: 17960095 Free PMC article.

7

Weinreb amidation as the cornerstone of an improved synthetic route to A-ring-modified derivatives of luotonin A.

Haider N, Nuß S. Haider N, et al. Molecules. 2012 Sep 25;17(10):11363-78. doi: 10.3390/molecules171011363. Molecules. 2012. PMID: 23011278 Free PMC article.

8

Position-Selective Synthesis and Biological Evaluation of Four Isomeric A-Ring Amino Derivatives of the Alkaloid Luotonin A.

Ibric A, Eckerstorfer S, Eder M, Louko I, Tunjic L, Heffeter P, Schueffl HH, Marian B, Haider N. Ibric A, et al. Among authors: haider n. Molecules. 2019 Feb 16;24(4):716. doi: 10.3390/molecules24040716. Molecules. 2019. PMID: 30781470 Free PMC article.

9

Fingerprint-based in silico models for the prediction of P-glycoprotein substrates and inhibitors.

Poongavanam V, Haider N, Ecker GF. Poongavanam V, et al. Among authors: haider n. Bioorg Med Chem. 2012 Sep 15;20(18):5388-95. doi: 10.1016/j.bmc.2012.03.045. Epub 2012 Mar 29. Bioorg Med Chem. 2012. PMID: 22595422 Free PMC article.

10

A-ring and E-ring modifications of the cytotoxic alkaloid Luotonin A: Synthesis, computational and biological studies.

Ibric A, Battisti V, Deckardt S, Haller AV, Lee C, Prötsch C, Langer T, Heffeter P, Schueffl HH, Marian B, Haider N. Ibric A, et al. Among authors: haider n. Bioorg Med Chem. 2020 May 1;28(9):115443. doi: 10.1016/j.bmc.2020.115443. Epub 2020 Mar 16. Bioorg Med Chem. 2020. PMID: 32201190 Free article.

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