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NU6027

CAT: 0804-HY-13816-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-13816-01Size:5 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
NU6027 is a potent and ATP-competitive inhibitor of both CDK1 and CDK2, with Kis of 2.5 μM and 1.3 μM, respectively. NU6027 is also a potent inhibitor of ATR and enhances hydroxyurea and cisplatin cytotoxicity in an ATR-dependent manner[1][2].
CAS Number
220036-08-8
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
ATM/ATR; CDK
Type
Reference compound
Related Pathways
Cell Cycle/DNA Damage; PI3K/Akt/mTOR
Applications
Cancer-Kinase/protease
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/nu6027.html
Concentration
10mM
Purity
99.04
Solubility
DMSO : 12.5 mg/mL (ultrasonic; warming; heat to 60°C)
Smiles
NC1=NC(OCC2CCCCC2)=C(N=O)C(N)=N1
Molecular Formula
C11H17N5O2
Molecular Weight
251.28
Precautions
H302, H315, H319, H335
References & Citations
[1]Arris CE, et, al. Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles. J Med Chem. 2000 Jul 27; 43 (15) : 2797-804.|[2]Peasland A, et, al. Identification and evaluation of a potent novel ATR inhibitor, NU6027, in breast and ovarian cancer cell lines. Br J Cancer. 2011 Jul 26;105 (3) :372-81.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, protect from light)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
ATR; CDK1; CDK2

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