Staurosporine is a natural product isolated from the bacterium Streptomyces staurosporeus. It is a very potent and broad spectrum protein kinase inhibitor through the prevention of ATP binding to the kinase. It inhibits protein kinase C (IC50=0.7nM), CDK1/cyclin B (IC50=5nM), CDK2/cyclin A (IC50=7nM), CDK4/cyclin D (IC50=3-10nM), CDK5/p25 (IC50=4nM), GSK-3β (IC50=15nM), Pim-1 kinase (IC50=10nM). It induces apoptosis in human neuroblastoma cell lines and chick embryonic neurons. Due to its broad and potent kinase inhibition activities, staurospoine is routinely used as cytotoxic, anti-proliferative reference compound.
Technical information:
Chemical Formula: | C28H26N4O3 | |
CAS #: | 62996-74-1 | |
Molecular Weight: | 466.53 | |
Purity: | >98% | |
Appearance: | White solid | |
Chemical Name: | (5S,6R,7R,9R)-6-methoxy-5-methyl-7-(methylamino)-6,7,8,9,15,16-hexahydro-17-oxa-4b,9a,15-triaza-5,9-methanodibenzo[b,h]cyclonona[jkl]cyclopenta[e]-as-indacen-14(5H)-one | |
Solubility: | Up to 100 mM in DMSO |
Shipping Condition: The product is shipped in a glass vial at ambient temperature.
Storage: For longer shelf life, store solid powder at 4oC desiccated, or store DMSO solution at -20oC.
Reference:
1. | Tamaoki et al. Staurosporine, a potent inhibitor of phospholipid/Ca2+ dependent protein kinase. Biochem Biophys Res Commun. (1986) 135 397. |
2. | Boix, J., et al. Characterization of the cell death process induced by staurosporine in human neuroblastoma cell lines. Neuropharmacology (1997) 36: 811-821 |
3. | Karaman MW, et al. A quantitative analysis of kinase inhibitor selectivity. Nat. Biotechnol. (2008) 26 (1): 127–132 |
Other Information:
Product Specification (pdf)
MSDS (pdf)