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Products
Pharmacology
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- Technical support
- Resources
Staurosporine
Cat. No. KS-320
Structure:
Other Names:
Activity:
Omura (1977) A new alkaloid AM-2282 OF Streptomyces origin. Taxonomy, fermentation, isolation and preliminary characterization. J Antibiot (Tokyo) 30(4) 275 PMID: 863788
Rüegg and Burgess (1989) Staurosporine, K-252 and UCN-01: potent but nonspecific inhibitors of protein kinases. Trends Pharmacol Sci. 10(6) 218 PMID: 2672462
Lewis et al (2018) Staurosporine Increases Lentiviral Vector Transduction Efficiency of Human Hematopoietic Stem and Progenitor Cells. Mol Ther Methods Clin Dev. 9 313 PMID: 30038935
Malsy et al (2019) Staurosporine induces apoptosis in pancreatic carcinoma cells PaTu 8988t and Panc-1 via the intrinsic signaling pathway. Eur J Med Res. 24(1) 5 PMID: 30686270
Ye et al (2020) Nuclear MYH9-induced CTNNB1 transcription, targeted by staurosporin, promotes gastric cancer cell anoikis resistance and metastasis. Theranostics 10(17) 7545 PMID: 32685004
Related areas
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Technical Data
Structure | [9S-(9α,10β,11β,13α)]-2,3,10,11,12,13-Hexahydro-10-methoxy-9-methyl-11-(methylamino)-9,13-epoxy-1H,9H-diindolo[1,2,3-gh:3',2',1'-lm]pyrrolo[3,4-j][1,7]benzodiazonin-1-one |
CAS Number | 62996-74-1 |
Molecular Weight | 466.53 |
Formula | C28H26N4O3 |
Solubility and Storage
Solubility | Soluble in DMSO to 25 mg/ml |
Appearance | Off white to pale yellow solid |
Storage | Store dry, frozen and in the dark |
Batch Specific Data
Purity | >98% by tlc |
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Recent citations
A new publication from the University of Ljubljana uses MCA-AVLQSGFR-Lys(Dnp)-Lys-NH2, the FRET substrate for the severe acute respiratory syndrome coronavirus main protease (SARS-CoV Mpro), to determine the inhibitory potential of plant polyphenols
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