AG-CN2-0510-M01010 mgCHF 25.00
AG-CN2-0510-M05050 mgCHF 75.00
AG-CN2-0510-M250250 mgCHF 190.00
|Synonyms||7-Methoxy-1-methyl-9H-pyrido[3,4-b]indole; Banisterine; Leucoharmine; Telepathine; Yageine; BRN0178813|
|Source/Host Chemicals||Synthetic. Originally isolated from the seeds of Peganum harmala (Syrian rue).|
|Appearance||White ot off-white solid.|
|Solubility||Soluble in DMSO. Slightly soluble in ethanol. Insoluble in water.|
|Other Product Data||
Stock Solution: Prior to performing biological experiments the stock solution should be further diluted into water or other aqueous buffers to ensure that the residual amount of DMSO/ethanol is insignificant, since DMSO and ethanol may have physiological effects at high concentrations.
We do not recommend to store the stock solution for more than one day.
|Shipping and Handling|
|Short Term Storage||+4°C|
|Long Term Storage||-20°C|
Keep cool and dry.
Protect from light.
Protect from moisture and oxygen.
|Use/Stability||Stable for at least 2 years after receipt when stored at -20°C.|
|Product Specification Sheet|
- Fluorescent β-carboline alkaloid.
- Potent ATP-competitive and selective inhibitor of DYRK1A, DYRK2 and DYRK3 with IC50 values of 0.08, 0.9 and 0.8µM. Shown to inhibit CLK2, PIM3 (at 4.3µM) and CK1 at 1.5µM as well. Inhibits DYRK1A-mediated tau phosphorylation.
- Competitive and reversible monoamine oxidase inhibitor (MAOI) that reversibly inhibits MAO-A (monoamine oxidase A) but has no effect on MAO-B.
- Acetylcholinesterase inhibitor (AChEI). Could potentially ameliorate impaired memory.
- Useful fluorescent pH indicator. Shows a color change from pH 7.2 (blue fluorescence) to pH 8.9 (yellow fluorescence). With the radioisotope carbon-11, used in positron emission tomography neuroimaging to examine its binding to MAO-A.
- Antiviral and antileishmanial compound.
- Antiangiogenic and antitumor agent. Inhibits cellular proliferation, migration, invasion and induced apoptosis in vitro, as well as inhibited tumor growth in vivo.
- Antidiabetic. Unique regulator of PPARγ expression that acts by inhibiting the Wnt signaling pathway in a cell-specific manner. Induces pancreatic β-cell proliferation. Reduced blood glucose, free fatty acids and triglyceride levels, delayed hyperglycemia and improved insulin sensitivity.
- Shown to induce adipocyte thermogenesis through the RAC1-MEK-ERK-CHD4 axis. CHD4 directly binds the proximal promoter region of UCP1, serving as a negative modulator of UCP1 and inducing browning in brown (BAT) and white adipose tissue (WAT).
- Inhibits DNA topoisomerases and interferes with DNA synthesis. Interacts with DNA via both groove binding and intercalative modes and cause major DNA structural changes.
- Shown to promote differentiation of osteoblasts (bone-forming cells) and chondrocytes (cells in the cartilage) and to inhibit osteoclastogenesis (the formation of bone resorbing cells).
- Antimalarial by inhibiting the Plasmodium falciparum heat shock protein 90 (PfHSP90) ATP-binding domain.
- The pH-dependence of the absorption and fluorescence spectra of harmine and harmol: drastic differences in the tautomeric equilibria of ground and first excited singlet state: O.S. Wolfbeis & E. Furlinger; Z. Physik. Chem. 129, 171 (1982)
- Antiviral effect of harmine, a photoactive beta-carboline alkaloid: J.B. Hudson, et al.; Photochem. Photobiol. 43, 21 (1986)
- Harmine as a substitute for 33258 Hoechst in the FPG technique: M.G. Gutierrez-Gonzalvez, et al.; Histochemistry 89, 199 (1988)
- Effect of moclobemide on rat brain monoamine oxidase A and B: comparison with harmaline and clorgyline: J. Gerardy; Prog. Neuropsychopharmacol. Biol. Psychiatry 18, 793 (1994)
- 11C-harmine as a tracer for monoamine oxidase A (MAO-A): in vitro and in vivo studies: M. Bergstrom, et al.; Nucl. Med. Biol. 24, 287 (1997)
- Antitumor agents 201. Cytotoxicity of harmine and beta-carboline analogs: J. Ishida, et al.; Bioorg. Med. Chem. Lett. 9, 3319 (1999)
- Harmine: evaluation of its antileishmanial properties in various vesicular delivery systems: S. Lala, et al.; J. Drug Target 12, 165 (2004)
- The small molecule harmine is an antidiabetic cell-type-specific regulator of PPARgamma expression: H. Waki, et al.; Cell Metab. 5, 357 (2007)
- The selectivity of protein kinase inhibitors: a further update: J. Bain, et al.; Biochem. J. 408, 297 (2007)
- DYRK1A phosphorylates caspase 9 at an inhibitory site and is potently inhibited in human cells by harmine: A. Seifert, et al.; FEBS J. 275, 6268 (2008)
- Harmine specifically inhibits protein kinase DYRK1A and interferes with neurite formation: N. Gockler, et al.; FEBS J. 276, 6324 (2009)
- β-Carboline alkaloids bind DNA: S. Nafisi, et al.; J. Photochem. Photobiol. B: Biol. 100, 84 (2010)
- Harmine, a β-carboline alkaloid, inhibits osteoclast differentiation and bone resorption in vitro and in vivo: T. Yonezawa, et al.; Eur. J. Pharmacol. 650, 511 (2011)
- Harmine is an ATP-competitive inhibitor for dual-specificity tyrosine phosphorylation-regulated kinase 1A (Dyrk1A): T. Adayev, et al.; Arch. Biochem. Biophys. 507, 212 (2011)
- The small molecule harmine regulates NFATc1 and Id2 expression in osteoclast progenitor cells: H. Egusa, et al.; Bone 49, 264 (2011)
- β-carboline compounds, including harmine, inhibit DYRK1A and tau phosphorylation at multiple Alzheimer's disease-related sites: D. Frost, et al.; PLoS One 6, e19264 (2011)
- Harmine is a potent antimalarial targeting Hsp90 and synergizes with chloroquine and artemisinin: D. Shahinas, et al.; Antimicrob. Agents Chemother. 56, 4207 (2012)
- Harmine induces apoptosis and inhibits tumor cell proliferation, migration and invasion through down-regulation of cyclooxygenase-2 expression in gastric cancer: H. Zhang, et al.; Phytomedicine 21, 348 (2014)
- A high-throughput chemical screen reveals that harmine-mediated inhibition of DYRK1A increases human pancreatic beta cell replication: P. Wang, et al.; Nat. Med. 21, 383 (2015)
- Effects of harmine, an acetylcholinesterase inhibitor, on spatial learning and memory of APP/PS1 transgenic mice and scopolamine-induced memory impairment mice: D. He, et al.; Eur. J. Pharmacol. 768, 96 (2015)
- Selectivity profiling and biological activity of novel β-carbolines as potent and selective DYRK1 kinase inhibitors: K. Ruben, et al.; PLos One 10, e0132453 (2015)
- Harmine induces cell cycle arrest and mitochondrial pathway-mediated cellular apoptosis in SW620 cells via inhibition of the Akt and ERK signaling pathways: J. Liu, et al.; Oncol. Rep. 35, 3363 (2016)
- Harmine Induces Adipocyte Thermogenesis through RAC1-MEK-ERK-CHD4 Axis: T. Nie,et al.; Sci. Rep. 6, 36382 (2016)