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NU6140

Cat. No. M8497
NU6140 Structure
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5mg USD 350  USD350 4-7 Days
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Quality Control & Documentation
Biological Activity

NU6140 is a CDK2 inhibitor with 10-36-fold selectivity over other CDK family members. NU6140 induces apoptosis and cell cycle arrest in cancer cells in the G2-M phase, and potentiates the cytotoxic effects of paclitaxel.

Chemical Information
Molecular Weight 422.52
Formula C23H30N6O2
CAS Number 444723-13-1
Form Solid
Solubility (25°C) DMSO: 20 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Sumalatha Rani Talapati, et al. Structural and binding studies of cyclin-dependent kinase 2 with NU6140 inhibitor

[2] Radek Jorda, et al. How Selective Are Pharmacological Inhibitors of Cell-Cycle-Regulating Cyclin-Dependent Kinases?

[3] Ade Kallas, et al. Assessment of the Potential of CDK2 Inhibitor NU6140 to Influence the Expression of Pluripotency Markers NANOG, OCT4, and SOX2 in 2102Ep and H9 Cells

[4] Sujoy Bhattacharya, et al. Cyclin-dependent kinases regulate apoptosis of intestinal epithelial cells

[5] Marzia Pennati, et al. Potentiation of paclitaxel-induced apoptosis by the novel cyclin-dependent kinase inhibitor NU6140: a possible role for survivin down-regulation

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  Catalog
Abmole Inhibitor Catalog




Keywords: NU6140 supplier, CDK, inhibitors, activators


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