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TG693

  Cat. No.:  DC21748   Featured
Chemical Structure
885272-55-9
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More than 5000 active chemicals with high quality for research!
Field of application
TG693 is an orally available, selective, ATP-competitive CLK1 inhibitor with IC50 of 112.6 nM.
Cas No.: 885272-55-9
Chemical Name: 5-(pyridin-4-yl)-1H-indazole
Synonyms: TG-693;TG 693
SMILES: N1C=CC(C2=CC=C3C(C=NN3)=C2)=CC=1
Formula: C12H9N3
M.Wt: 195.225
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: TG693 is an orally available, selective, ATP-competitive CLK1 inhibitor with IC50 of 112.6 nM.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
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DC37321 AI3-15902 AI3-15902 is a biochemical.
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DC36443 DC-Chol DC-Chol is a cationic cholesterol derivative. DC-Chol, as a component of lipoplexes with DOPE, has been used for transfection of mRNA into A549 cells without affecting cell viability. Incubation of DC-chol/DOPE liposomes or lipoplexes with human whole blood has no effect on neutrophil elastase or β-thromboglobulin levels or the number of platelets and red and white blood cells, indicating hemocompatibility. DC-Chol has also been widely used in the synthesis of liposomes for the delivery of siRNA, DNA, and chemotherapeutic agents into cells and mice.
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