|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
250 mg 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|
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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