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557364

Roscovitine

InSolution, ≥95%, inhibitor of cyclin-dependent kinases (CDKs)

Synonim(y):

InSolution Roscovitine

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Rozmiar/SKUDostępnośćCena netto
5 mg

Przewidywany termin wysyłki02 listopada 2026zKuehne + Nagel Sp. z o.o.

943,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C19H26N6O
Masa cząsteczkowa:
354.45
NACRES:
NA.77
UNSPSC Code:
12352200
eCl@ss:
32039090
Assay:
≥95% (HPLC)
Form:
liquid
Storage condition:
OK to freeze, desiccated (hygroscopic), protect from light

943,00 zł


Przewidywany termin wysyłki02 listopada 2026Szczegóły


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Quality Segment

assay

≥95% (HPLC)

form

liquid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, desiccated (hygroscopic), protect from light

shipped in

wet ice

storage temp.

2-8°C

General description

A potent and selective inhibitor of cyclin-dependent kinases (Cdks). Exhibits greater inhibitory potency compared to olomoucine (Cat. No. 495620). Inhibits p34 Cdc2/cyclin B (IC50 = 650 nM), p33 Cdk2/cyclin A (IC50 = 700 nM), p33 Cdk2/cyclin E (IC50 = 700 nM), and p33 Cdk2/p35 (IC50 = 200 nM) by competing for the ATP binding domain of these kinases. Exhibits very low sensitivity towards related kinases, such as Erk1 and Erk2 (IC50 = 34 µM and 14 µM, respectively). Roscovitine does not significantly affect the activity of other protein kinases even at 100 µM and compared to olomoucine, roscovitine displays increased anti-mitotic activity at the G1/S and G2/M phases of the cell cycle.

Biochem/physiol Actions

Cell permeable: no
Primary Target
p34cdk1/cyclin B
Product competes with ATP.
Reversible: yes
Target IC50: 650 nM, 700 nM, 700 nM, and 200 nM against p34cdk1/cyclin B, p33cdk2/cyclin A, p33cdk2/cyclin E, and p33cdk5/p35, respectively

Packaging

Packaged under inert gas

Physical form

A 50 mM (5 mg/282 µl) solution of Roscovitine (Cat. No. 557360) in DMSO.

Preparation Note

Following initial use, aliquot and freeze (-20°C). Once opened, the DMSO aliquots are stable for up to 6 months at -20°C.

Other Notes

Meijer, L. 1996. Trends Cell Biol.6, 393.
Rudolph, B., et al. 1996. EMBO J.15, 3053.

Legal Information

Sold under license of U.S. Patent 6,316,456.
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Irritant (B)
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Ta pozycja
557360R7772218708
description

InSolution, ≥95%, inhibitor of cyclin-dependent kinases (CDKs)

description

A potent, reversible, and selective inhibitor of Cdks that exhibits about 10-fold greater efficacy towards p34-cdk1 and p33-cdk2 and 20-fold greater efficacy towards p33-cdk5 relative to Olomoucine.

description

≥98% (TLC)

description

InSolution

assay

≥95% (HPLC)

assay

≥95% (HPLC)

assay

≥98% (TLC)

assay

-

form

liquid

form

solid

form

powder

form

liquid

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

Calbiochem®

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

storage condition

desiccated (hygroscopic), OK to freeze, protect from light

storage condition

OK to freeze

storage condition

-

storage condition

OK to freeze, protect from light, desiccated (hygroscopic)


Klasa składowania

10 - Combustible liquids

WGK

WGK 2

Temperatura zapłonu (°F)

188.6 °F - closed cup - (Dimethylsulfoxide)

Temperatura zapłonu (°C)

87 °C - closed cup - (Dimethylsulfoxide)



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