© 2008 Alexis Corporation
ALX-380-014
Revised 15-May-08
Staurosporine
SYNONYMS
Antibiotic AM-2282
PRODUCT LINE
Natural Products / Antibiotics
PRODUCT CATEGORY
Antibiotics - Apoptosis Inducers & Inhibitors
Ordering Information
Product Numbers:
Format:
Size:
Unit Price:
Quantity:
Add To Cart
ALX-380-014-C100
100 µg
47.00 USD
ALX-380-014-C250
250 µg
112.00 USD
ALX-380-014-M001
1 mg
270.00 USD
ALX-380-014-M005
5 mg
790.00 USD
Product Specification
FORMULA:
C
28
H
26
N
4
O
3
MW:
466.5
CAS NUMBER:
62996-74-1
MERCK INDEX:
14:
8802
RTECS:
KC655000
SOURCE/HOST:
Isolated from
Streptomyces staurosporeus.
PURITY:
≥98%
APPEARANCE:
Off-white to green powder.
SOLUBILITY:
Soluble in ethyl acetate, DMSO or dimethyl formamide; only slightly soluble in chloroform and methanol. Insoluble in water.
SHIPPING:
AMBIENT
LONG TERM STORAGE:
+4°C
USE/STABILITY:
Stable for at least 2 years after receipt when stored +4°C.
HANDLING:
Protect from light and moisture.
HAZARD:
HARMFUL. MAY BE CARCINOGENIC.
Product Description
Model apoptosis inducer. Potent cell-permeable inhibitor of a variety of protein kinases, e.g. protein kinase C (PKC), CDK1/cyclin B (IC
50
~5nM), CDK2/cyclin A (IC
50
=7nM), CDK4/cyclin D (IC
50
=3-10µM), CDK5/p25 (IC
50
=4nM) and GSK-3β (IC
50
=15nM).
Product Specific Literature References
A new alkaloid AM-2282 of Streptomyces origin. Taxonomy, fermentation, isolation and preliminary characterization:
S. Omura, et al.; J. Antibiot. (Tokyo)
30
, 275 (1977)
Abstract
A. Furusaki, et al.; J. C. S. Chem. Commun. 800 (1978)
Staurosporine, a potent inhibitor of phospholipid/Ca++dependent protein kinase:
T. Tamaoki, et al.; BBRC
135
, 397 (1986)
Abstract
Staurosporine, a potent platelet aggregation inhibitor from a
Streptomyces
species:
S. Oka, et al.; Agric. Biol. Chem.
50
, 2723 (1986)
Staurosporine inhibits tyrosine-specific protein kinase activity of Rous sarcoma virus transforming protein p60:
N. Nakano, et al.; J. Antibiot. (Tokyo)
40
, 706 (1987)
Abstract
Contrasting actions of staurosporine, a protein kinase C inhibitor, on human neutrophils and primary mouse epidermal cells:
T. Sako, et al.; Cancer Res.
48
, 4646 (1988)
Abstract
Staurosporine, a protein kinase C inhibitor interferes with proliferation of arterial smooth muscle cells:
H. Matsumoto & Y. Sasaki; Biochem. Biophys. Res. Commun.
158
, 105 (1989)
Abstract
Staurosporine, K-252 and UCN-01: potent but nonspecific inhibitors of protein kinases:
U.T. Ruegg & G.M. Burgess; TIPS
10
, 218 (1989), (Review)
Abstract
Staurosporine: an effective inhibitor for Ca2+/calmodulin-dependent protein kinase II:
N. Yanagihara, et al.; J. Neurochem.
56
, 294 (1991)
Abstract
Is staurosporine a specific inhibitor of protein kinase C in intact porcine coronary arteries?:
M. Kageyama, et al.; J. Pharmacol. Exp. Ther.
259
, 1019 (1991)
Abstract
Induction of a common pathway of apoptosis by staurosporine:
R. Bertrand, et al.; Exp. Cell Res.
211
, 314 (1994)
Abstract
First total synthesis of Staurosporine and ent-Staurosporine:
J.T. Link et al.; J. Am. Chem. Soc.
117
, 552 (1995)
Staurosporine induces programmed cell death in embryonic neurons and activation of the ceramide pathway:
D.A. Wiesner & G. Dawson; J. Neurochem
66
, 1418 (1996)
Abstract
Staurosporine and ent-staurosporine: the first total synthesis, prospects for a regioselective approach, and activity profile:
J.T. Link et al.; J. Am. Chem. Soc.
118
, 2825 (1996)
K252a and staurosporine microbial alkaloid toxins as prototype of neurotropic drugs:
P. Lazarovici, et al.; Adv. Exp. Med. Biol.
391
, 367 (1996), Review
Abstract
Characterization of the cell death process induced by staurosporine in human neuroblastoma cell lines:
J. Boix, et al.; Neuropharmacology
36
, 811 (1997)
Abstract
Caspase-3-dependent cleavage of Bcl-2 promotes release of cytochrome c
:
D.G. Kirsch, et al.; J. Biol. Chem.
274
, 21155 (1999)
Abstract
;
Full Text
Molecular mechanism of staurosporine-induced apoptosis in osteoblasts:
H.J. Chae, et al.; Pharmacol. Res.
42
, 373 (2000)
Abstract
Glycogen synthase kinase-3beta facilitates staurosporine- and heat shock-induced apoptosis. Protection by lithium:
G.N. Bijur, et al.; J. Biol. Chem.
275
, 7583 (2000)
Abstract
;
Full Text
Dissociation of staurosporine-induced apoptosis from G2-M arrest in SW620 human colonic carcinoma cells: initiation of the apoptotic cascade is associated with elevation of the mitochondrial membrane potential (deltapsim):
B.G. Heerdt, et al.; Cancer Res.
60
, 6704 (2000)
Abstract
Changes in mitochondrial membrane potential during staurosporine- induced apoptosis in Jurkat cells:
J.L. Scarlett, et al.; FEBS Lett.
475
, 267 (2000)
Abstract
Equivalent death of P-glycoprotein expressing and nonexpressing cells induced by the protein kinase C inhibitor staurosporine:
K.M. Tainton, et al.; BBRC
276
, 231 (2000)
Abstract
Caspase-8 activation and bid cleavage contribute to MCF7 cellular execution in a caspase-3-dependent manner during staurosporine-mediated apoptosis:
D. Tang, et al.; J. Biol. Chem.
275
, 9303 (2000)
Abstract
;
Full Text
Insulin-stimulated protein kinase B phosphorylation on Ser-473 is independent of its activity and occurs through a staurosporine-insensitive kinase
:
M.M. Hill, et al.; J. Biol. Chem.
276
, 25643 (2001)
Abstract
;
Full Text
Single-cell fluorescence resonance energy transfer analysis demonstrates that caspase activation during apoptosis is a rapid process. Role of caspase-3
:
M. Rehm, et al.; J. Biol. Chem.
277
, 24506 (2002)
Abstract
;
Full Text
Related Products
ALX-380-281
PKC412
Further Categories Containing This Product:
CDK & Cyclin Inhibitors
•
Myosin Light Chain Kinase Inhibitors
•
PKC Inhibitors
•
Staurosporine / Related Products
•
Antibiotics - Protein Kinase Inhibitors
•
Alkaloids
•
Antibiotics for Cell Cycle Research
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