|Related Categories||Bioactive Small Molecules, Building Blocks, Carbazoles, Cell Biology, Chemical Synthesis,|
|Gene Information||human ... CDC2(983), CYP2D6(1565)|
Central nervous system stimulant.
1 g in glass bottle
Bottomless glass bottle. Contents are inside inserted fused cone.
Certificate of Analysis
|Precautionary statements||P280-P305 + P351 + P338|
|Personal Protective Equipment||dust mask type N95 (US), Eyeshields, Gloves|
|Hazard Codes (Europe)||Xn|
|Risk Statements (Europe)||20/21/22-36|
|Safety Statements (Europe)||26-36/37|
Metabolic pathways of the psychotropic-carboline alkaloids, harmaline and harmine, by liquid chromatography/mass spectrometry and NMR spectroscopy. Zhao T, Zheng SS, Zhang BF, et al. Food Chem. 134(2), 1096-105, (2012)
Photosensitized electron transfer within a self-assembled norharmane-2'-deoxyadenosine 5'-monophosphate (dAMP) complex. Gonzalez MM, Rasse-Suriani FA, Franca CA, et al. Org. Biomol. Chem. 10(47), 9359-72, (2012)
In vivo comparison of harmine efficacy against psychostimulants: preferential inhibition of the cocaine response through a glutamatergic mechanism. Owaisat S, Raffa RB, and Rawls SM Neurosci. Lett. 525(1), 12-6, (2012)
Intracerebral injection of low amounts of norharman induces moderate Parkinsonism-like behavioral symptoms in rat. Esmaeili MH, Movahedi M, Faraji A, et al. Neurotoxicol. Teratol. 34(5), 489-94, (2012)
Blood harmane (1-methyl-9H-pyrido[3,4-b]indole) concentrations in essential tremor: repeat observation in cases and controls in New York. Louis ED, Jiang W, Gerbin M, et al. J. Toxicol. Environ. Health A 75(12), 673-83, (2012)
The alkaloid compound harmane increases the lifespan of Caenorhabditis elegans during bacterial infection, by modulating the nematode's innate immune response. Jakobsen H, Bojer MS, Marinus MG, et al. PLoS ONE 8(3), e60519, (2013)
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)
Leucettines, a class of potent inhibitors of cdc2-like kinases and dual specificity, tyrosine phosphorylation regulated kinases derived from the marine sponge leucettamine B: modulation of alternative pre-RNA splicing. Mansour Debdab et al J. Med. Chem. 54, 4172-86, (2011)
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)
Catalysis by molecular iodine: A rapid synthesis of 1,8-dioxo-octahydroxanthenes and their evaluation as potential anticancer agents. Naveen Mulakayala et al Bioorg. Med. Chem. Lett. 22, 2186-91, (2012)
Ultrasound mediated catalyst free synthesis of 6H-1-benzopyrano[4,3-b]quinolin-6-ones leading to novel quinoline derivatives: their evaluation as potential anti-cancer agents. Naveen Mulakayala et al Bioorg. Med. Chem. 20, 759-68, (2012)
Corp MSDS 1 (1), 1810:C / FT-IR 2 (3), 3616:B / FT-NMR 1 (3), 166:B / RegBook 1 (2), 2427:I / Sax 6, 1781 / Sigma FT-IR 1 (2), 600:B / Structure Index 1, 385:C:2
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