主页 / 药理学 / Enzymes / Kinases / Broad Spectrum Protein Kinase Inhibitors / Broad Spectrum Protein Kinase Inhibitor Inhibitors / Staurosporine

Staurosporine

Cat. No. 1285 20 篇引用文献 1 条评论 提交评论 说明书 / 分析证书（CoA） / 化学品安全技术说明书（SDS）
Pricing Availability   Qty
说明： Non-selective protein kinase inhibitor
别名： AM-2282
化学名： [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
纯度： ≥98% (HPLC)
说明书
引用文献 (20)
评论 (1)
生物活性 Scientific Data 技术数据 溶解性 计算器 说明书 参考文献

生物活性 for Staurosporine

Staurosporine is a broad spectrum protein kinase inhibitor. Enzymes inhibited include protein kinase C, p60v-src tyrosine protein kinase, protein kinase A, and CaM kinase II (IC50 values are 3nM, 6 nM, 7 nM and 20 nM, respectively). Staurosporine reduces nuclear myosin heavy chain 9 phosphorylation which inhibits gastric cancer cell progression in transgenic mouse models. Staurosporine inhibits cell viability and promotes apoptosis in oral and pancreatic cancer cells. Staurosporine also enhances efficiency of lentiviral transduction of human hematopoietic stem and progenitor cells by 2-fold, induces dopaminergic axonal outgrowth in vitro and triggers mitophagy. Staurosporine has high affinity (Kd = 100 nM) for the yjdF aptamer. The riboswitch function of yjdF motif RNAs is activated by Staurosporine and leads to robust reporter gene expressions in B. subtilis.

Staurosporine synthesized to Ancillary Material Grade is also available.

Scientific Data

Cell Viability View Larger

Reduced viability of differentiated cardiomyocytes exposed to cardiotoxic small molecules. The viability of differentiated cardiomyocytes was assessed using a Resazurin metabolism assay. A) Untreated cells metabolize Resazurin (Catalog # AR002) to produce resorufin, a fluorescent molecule that can be measured using a fluorometric plate reader. Resorufin fluorescence accumulated in untreated cardiomyocytes. Cells treated with the cardiotoxic small molecules Staurosporine (blue; Catalog # 1285), a non-selective protein kinase inhibitor, or Doxazosin (tan; Catalog # 2964), an alpha 1 antagonist, did not metabolize Resazurin, as shown by lack of fluorescence accumulation, indicating a loss of viability upon treatment. B) Cell morphology of untreated, Staurosporine-treated, and Doxazosin-treated cardiomyocytes was assessed by brightfield microscopy.

技术数据 for Staurosporine

分子量 466.54
公式 C28H26N4O3
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 62996-74-1
PubChem ID 44259
InChI Key HKSZLNNOFSGOKW-FYTWVXJKSA-N
Smiles O=C(NC6)C1=C6C4=C3C2=C1C8=C(C=CC=C8)N2[C@](C[C@@H](NC)[C@H]7OC)([H])O[C@]7(C)N3C5=CC=CC=C45

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for Staurosporine

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 23.33 50

制备储备液 for Staurosporine

以下数据基于产品分子量 466.54。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
0.5 mM 4.29 mL 21.43 mL 42.87 mL
2.5 mM 0.86 mL 4.29 mL 8.57 mL
5 mM 0.43 mL 2.14 mL 4.29 mL
25 mM 0.09 mL 0.43 mL 0.86 mL

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.
=
x
x
g/mol

*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and CoA (available online).

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

=
÷

Dilution Calculator

Calculate the dilution required to prepare a stock solution.
x
=
x

产品说明书 for Staurosporine

分析证书/产品说明书
选择另一批次：
化学品安全技术说明书

参考文献 for Staurosporine

参考文献是支持产品生物活性的出版物。

Ruegg and Burgess (1989) Staurosporine, K-252 and UCN-01: potent but nonspecific inhibitors of protein kinases. TiPS 10 218 PMID: 2672462

Tamaoki et al (1986) Staurosporine, a potent inhibitor of phospholipid/Ca2+ dependent protein kinase. Biochem.Biophys.Res.Commun. 135 397 PMID: 3457562

Yanagihara et al (1991) Staurosporine: an effective inhibitor for Ca2+/calmodulin-dependent protein kinase II. J.Neurochem. 56 294 PMID: 1846174

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

Ye et al (2020) Nuclear MYH9-induced CTNNB1 transcription, targeted by staurosporin, promotes gastric cancer cell anoikis resistance and metastasis. Theranostics 10 7545 PMID: 32685004

Zhang et al (2005) Effect of protein kinase C alpha, caspase-3, and survivin on apoptosis of oral cancer cells induced by staurosporine. Acta Pharmacol.Sinica 26 1365 PMID: 16225760

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 5 PMID: 30686270

Wakita et al (2014) Staurosporine induces dopaminergic neurite outgrowth through AMP-activated protein kinase/mammalian target of rapamycin signaling pathway. Neuropharmacology 77 39 PMID: 24067927

Li et al (2016) The yjdF riboswitch candidate regulates gene expression by binding diverse azaaromatic compounds. RNA 22 530 PMID: 26843526

If you know of a relevant reference for Staurosporine, please let us know.

按标靶查看相关产品

按产品操作查看相关产品

查看全部 Broad Spectrum Protein Kinase Inhibitor Inhibitors

关键词: Staurosporine, Staurosporine supplier, Non-Selective, protein, kinases, inhibitors, inhibits, Broad, Spectrum, viral, transduction, enhancers, enhances, antibiotic, AM-2282, STS, parkin, PINK, parkinsons, mitochondria, mitochondrial, apoptosis, high, affinity, to, yjdF, aptamer, activates, riboswitch, RNA, Protein, Kinase, Inhibitors, Viral, Transduction, Enhancers, DNA,, and, Synthesis, Organoids, 1285, Tocris Bioscience

20 篇 Staurosporine 的引用文献

引用文献是使用了 Tocris 产品的出版物。 Staurosporine 的部分引用包括：

Valentine et al (2014) Small molecule screen yields inhibitors of Pseudomonas homoserine lactone-induced host responses. Cell Microbiol 16 1 PMID: 23910799

Jackson et al (2013) Pharmacological inhibition of pleckstrin homology domain leucine-rich repeat protein phosphatase is neuroprotective: differential effects on astrocytes. J Pharmacol Exp Ther 347 516 PMID: 24023368

Hayes et al (2016) Integrative genomic and functional analysis of human oral squamous cell carcinoma cell lines reveals synergistic effects of FAT1 and CASP8 inactivation. Cancer Lett 383 106 PMID: 27693639

Dobson et al (2015) Caffeine Modulates Vesicle Release and Recovery at Cerebellar Parallel Fibre Terminals, Independently of Calcium and Cyclic AMP Signalling. Eur J Neurosci 10 e0125974 PMID: 25933382

Sonamoto et al (2015) Identification of a DYRK1A Inhibitor that Induces Degradation of the Target Kinase using Co-chaperone CDC37 fused with Luciferase nanoKAZ. Eneuro 5 12728 PMID: 26234946

Faulkner et al (2015) FMRP regulates neurogenesis in vivo in Xenopus laevis tadpoles. PLoS One 2 e0055 PMID: 25844398

Kawamoto et al (2012) Effect of activation of canonical Wnt signaling by the Wnt-3a protein on the susceptibility of PC12 cells to oxidative and apoptotic insults. PLoS One 45 58 PMID: 22124704

Kondo et al (2010) Poly(ADP-ribose) polymerase (PARP)-1-independent apoptosis-inducing factor (AIF) release and cell death are induced by eleostearic acid and blocked by α-tocopherol and MEK inhibition. Braz J Med Biol Res 285 13079 PMID: 20177052

Chen et al (2016) Androgen-Sensitized Apoptosis of HPr-1AR Human Prostate Epithelial Cells. Mol Pharmacol 11 e0156145 PMID: 27203692

Piccart et al (2015) Neurotensin Induces Presynaptic Depression of D2 DA Autoreceptor-Mediated Neurotransmission in Midbrain DArgic Neurons. J Neurosci 35 11144 PMID: 26245975

Barcomb et al (2013) Enzymatic activity of CaMKII is not required for its interaction with the glutamate receptor subunit GluN2B. J Biol Chem 84 834 PMID: 24056996

Mayer et al (2017) The microanatomic segregation of selection by apoptosis in the germinal center. Science 358 PMID: 28935768

Valvezan et al (2017) mTORC1 Couples Nucleotide Synthesis to Nucleotide Demand Resulting in a Targetable Metabolic Vulnerability. Cancer Cell 32 624 PMID: 29056426

Hejna et al (2017) High accuracy label-free classification of single-cell kinetic states from holographic cytometry of human melanoma cells. Sci Rep 7 11943 PMID: 28931937

Schönbrunn et al (2013) Development of highly potent and selective diaminothiazole inhibitors of cyclin-dependent kinases. J Med Chem 56 3768 PMID: 23600925

Valero et al (2011) Contractile effect of tachykinins on rabbit small intestine. Acta Pharmacol Sin 32 487 PMID: 21441943

O'Donnell et al (2015) IF. gamma induces protective non-canonical signaling pathways in primary neurons. J Neurochem 135 309 PMID: 26190522

Xu et al (2017) Matrine induces RIP3-dependent necroptosis in cholangiocarcinoma cells. Cell Death Discov 3 16096 PMID: 28179994

Park et al (2016) Pyrin inflammasome activation and RhoA signaling in the autoinflammatory diseases FMF and HIDS. Nat Immunol 17 914 PMID: 27270401

Chen et al (2006) N-myc down-regulated gene 1 modulates the response of term human trophoblasts to hypoxic injury. J Biol Chem 281 2764 PMID: 16314423

您是否知道使用了 Tocris Staurosporine 的优秀论文？ 请告知我们.

Staurosporine 的评论

平均评分: 4 (Based on 1 Review.)

5 星
0%
4 星
100%
3 星
0%
2 星
0%
1 星
0%

Have you used Staurosporine?

Submit a review and receive an Amazon gift card.

$50/€35/£30/$50CAN/¥300 Yuan/¥5000 Yen for first to review with an image

$25/€18/£15/$25CAN/¥75 Yuan/¥2500 Yen for a review with an image

$10/€7/£6/$10 CAD/¥70 Yuan/¥1110 Yen for a review without an image

Submit a Review

Filter by:


Staurosporine (Cat. No. 1285).
By Danny Johnson on 03/01/2024
分析类型： In Vitro
种属： Human

Used in cytotox control, 7CC. No issues at all, vial could be smaller to spin down easier