Harmane

Papers

Synthesis of 3,8,9-trisubstituted-1,7,9-triaza-fluorene-6-carboxylic acid derivatives as a new class of insulin secretagogues. Rajesh H Bahekar et al Bioorg. Med. Chem. 15, 5950-64, (2007)

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Chemical genetics reveals a complex functional ground state of neural stem cells Diamandis, P., et. al. Nat. Chem. Biol. 3(5), 268-273, (2007)

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The selectivity of protein kinase inhibitors: a further update Bain, J., et al. Biochem. J. 408, 297-315, (2007)

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Synthesis and cytotoxic activities of 1-benzylidine substituted beta-carboline derivatives. Rihui Cao et al Bioorg. Med. Chem. Lett. 18, 6558-61, (2008)

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The use of natural product scaffolds as leads in the search for trypanothione reductase inhibitors. Galarreta, B., C.; et al. Bioorg. Med. Chem. 16, 6689, (2008)

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Quantitative structure-activity relationship studies of a series of non-benzodiazepine structural ligands binding to benzodiazepine receptor. Binbin Xia et al Eur. J. Med. Chem. 43, 1489-98, (2008)

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3D and quantum QSAR of non-benzodiazepine compounds. F A Pasha et al Eur. J. Med. Chem. 43, 2361-72, (2008)

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Structure-activity relationship of antiparasitic and cytotoxic indoloquinoline alkaloids, and their tricyclic and bicyclic analogues. Van Baelen, G., et al. Bioorg. Med. Chem. 17, 7209-7217, (2009)

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Identification and characterization of mefloquine efficacy against JC virus in vitro. Margot Brickelmaier et al Antimicrob. Agents Chemother. 53, 1840-9, (2009)

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5-Bromo-8-methoxy-1-methyl-beta-carboline, an alkaloid from the New Zealand marine bryozoan Pterocella vesiculosa. Marisa Till et al J. Nat. Prod. 72, 796-8, (2009)

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Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum. Jing Yuan et al Nat. Chem. Biol. 5, 765-71, (2009)

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A class of 3S-2-aminoacyltetrahydro-beta-carboline-3-carboxylic acids: their facile synthesis, inhibition for platelet activation, and high in vivo anti-thrombotic potency. Jiawang Liu et al J. Med. Chem. 53, 3106-16, (2010)

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A class of novel N-(1-methyl-?-carboline-3-carbonyl)-N'-(aminoacid-acyl)-hydrazines: aromatization leaded design, synthesis, in vitro anti-platelet aggregation/in vivo anti-thrombotic evaluation and 3D QSAR analysis. Chunyu Li et al Eur. J. Med. Chem. 46, 5598-608, (2011)

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Vasorelaxant effect of harman. Shi, C.C., et al. Eur. J. Pharmacol. 390, 319-325, (2000)

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Harmane produces hypotension following microinjection into the RVLM: possible role of I(1)-imidazoline receptors. Musgrave, I.F., Badoer, E. Br. J. Pharmacol. 129, 1057, (2000)

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Merck 14,4615

Beil. 23,V,8,261

Aldrich MSDS 1, 1000:D / Corp MSDS 1 (1), 1810:B / FT-IR 2 (3), 3615:D / FT-IR 1 (2), 682:A / FT-NMR 1 (3), 165:B / IR-Spectra (3), 1264:A / IR-Spectra (2), 1099:B / NMR-Reference 2 (2), 550:C / RegBook 1 (2), 2427:F / Sax 6, 1923 / Sigma FT-IR 1 (1), 591:C / Structure Index 1, 385:A:2