Paullone CAS: 142273-18-5
MF: C16H12N2O
MW: 248.28
A potent inhibitor of Cdk.

Paullone (CAS 142273-18-5)

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应用; Paullone is a potent inhibitor of Cdk
CAS号码: 142273-18-5
分子量: 248.28
分子式: C16H12N2O
仅供科研使用。不可用于诊断或治疗。
* 参考分析证明 大量特定数据 (包括水 含量).

Paullone is a potent inhibitor of Cdk (cyclin-dependent kinases), which are involved in the regulation of the cell cycle.


参考文献

1. Kamb, A., et al., 1998. Cyclin-dependent kinase inhibitors and human cancer. Current topics in microbiology and immunology. 227(): 139-48. PMID: 9479829
2. Schultz, C., et al., 1999. Paullones, a series of cyclin-dependent kinase inhibitors: synthesis, evaluation of CDK1/cyclin B inhibition, and in vitro antitumor activity. Journal of medicinal chemistry. 42(15): 2909-19. PMID: 10425100
3. Lahusen, Tyler., et al., 2003. Alsterpaullone, a novel cyclin-dependent kinase inhibitor, induces apoptosis by activation of caspase-9 due to perturbation in mitochondrial membrane potential. Molecular carcinogenesis. 36(4): 183-94. PMID: 12669310
4. Kunick, Conrad., et al., 2005. Structure-aided optimization of kinase inhibitors derived from alsterpaullone. Chembiochem : a European journal of chemical biology. 6(3): 541-9. PMID: 15696597

物理状态 :
Solid
溶解度 :
Soluble in methanol, DMSO, and DMF.
保存 :
Store at room temperature
熔点 :
212.71°C (Predicted; Mean or Weighted)
沸点 :
571.19° C at 760 mmHg (Predicted)
密度 :
1.32 g/cm3
折射率 :
n20D 1.72
IC50 :
Cyclin-dependent kinase 9: IC50 = 810 nM (human); Glycogen synthase kinase-3 beta: IC50 = 620 nM (human); Cyclin T1: IC50 = 810 nM (human); Glycogen synthase kinase-3 beta: IC50 = 100 nM (human); Glutamate NMDA receptor: IC50 = >1000 nM (Rattus norvegicus); Serotonin 1d (5-HT1d) receptor: IC50 = >1000 nM (Rattus norvegicus); Beta-2 adrenergic receptor: IC50 = >1000 nM (Canis lupus familiaris Multiple homologous proteins); Alpha-1a adrenergic receptor: IC50 = >1000 nM (Rattus norvegicus)
pK值 :
pKb: 1.47
仅供科研使用。不可用于诊断或治疗。
PubChem CID :
369401
MDL 号码 :
MFCD18252383
SMILES :
C1C2=C(C3=CC=CC=C3NC1=O)NC4=CC=CC=C24

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