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NU 6102

Katalog-Nr.GC18278

NU 6102 ist ein potenter CDK1- und CDK2-Inhibitor mit IC50-Werten von 9,5 nM bzw. 5,4 nM für CDK1/CyclinB und CDK2/CyclinA3. NU 6102 zeigt Selektivität für CDK1/CDK2 gegenüber CDK4 (IC50 von 1,6 μM), DYRK1A (IC50 von 0,9 μM), PDK1 (IC50 von 0,8 μM) und ROCKII (IC50 von 0,6 μM).

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NU 6102 Chemische Struktur

Cas No.: 444722-95-6

Größe Preis Lagerbestand Menge
10mM (in 1mL DMSO)
157,00 $
Auf Lager
5mg
144,00 $
Auf Lager
10mg
228,00 $
Auf Lager
25mg
455,00 $
Auf Lager
50mg
733,00 $
Auf Lager
100mg
1.168,00 $
Auf Lager

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Sample solution is provided at 25 µL, 10mM.

Description of NU 6102

Cyclin-dependent kinases (CDKs) play a key role in regulating cell division by phosphorylating distinct substrates in different phases of the cell cycle. Cell cycle deregulation in many cancers often results from altered CDK activity. Thus, CDKs are potential pharmacological targets for anticancer agents. NU 6102 is a potent inhibitor of Cdk1 and Cdk2 with Ki values of 9 and 6 nM and IC50 values of 9.5 and 5.4 nM, respectively. NU 6102 inhibits Cdk4 activity with an IC50 value of 1.6 μM, suggesting it is most selective for Cdk2. Time-lapse videomicroscopy reveals that 20 μM NU 6102 delays cell entry into mitosis where most cells appear to eventually complete mitotic division but cannot correctly undergo cytokinesis, and hence become binucleated with an abnormal number of centrosomes. In SKUT-1B cancer cells a 24 h exposure to NU 6102 induced G2 arrest, inhibition of target protein phosphorylation, and cytotoxicity with an LC50 value of 2.6 μM.

Chemical Properties of NU 6102

Cas No. 444722-95-6 SDF
Chemical Name 4-[[6-(cyclohexylmethoxy)-9H-purin-2-yl]amino]-benzenesulfonamide
Canonical SMILES NS(C(C=C1)=CC=C1NC2=NC(NC=N3)=C3C(OCC4CCCCC4)=N2)(=O)=O
Formula C18H22N6O3S M.Wt 402.5
Löslichkeit DMSO: >1 mg/ml,Ethanol: >1 mg/ml Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of NU 6102

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.4845 mL 12.4224 mL 24.8447 mL
5 mM 0.4969 mL 2.4845 mL 4.9689 mL
10 mM 0.2484 mL 1.2422 mL 2.4845 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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3. All of the above co-solvents are available for purchase on the GlpBio website.

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Average Rating: 5 ★★★★★ (Based on Reviews and 17 reference(s) in Google Scholar.)

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