>>Signaling Pathways>> Cell Cycle/Checkpoint>> G2/S>>CD532

CD532

Catalog No.GC48982

CD532는 IC50이 45nM인 강력한 Aurora A 키나제 억제제입니다. CD532는 Aurora A 키나제 활성을 차단하고 MYCN의 분해를 유도하는 이중 효과가 있습니다. CD532는 또한 AURKA와 직접 상호 작용할 수 있으며 전체적인 형태 변화를 유도합니다. CD532는 암 연구에 사용될 수 있습니다.

Products are for research use only. Not for human use. We do not sell to patients.

CD532 Chemical Structure

Cas No.: 1639009-81-6

Size 가격 재고 수량
5 mg
US$170.00
재고 있음
10 mg
US$271.00
재고 있음
25 mg
US$636.00
재고 있음
50 mg
US$1,188.00
재고 있음

Tel:(909) 407-4943 Email: sales@glpbio.com

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

CD532 is an inhibitor of Aurora A kinase activity (IC50 = 48 nM) and the protein-protein interaction between N-Myc and Aurora A kinase.1 It also inhibits several cyclin-dependent kinases (CDKs), FGFRs, MEKs, and PDGFRs, as well as FLT3, KIT, and RET at 10 µM.2 CD532 induces degradation of N-Myc in SK-N-BE(2) neuroblastoma cells (EC50 = 223 nM).1 It prevents S-phase entry in SK-N-BE(2) cells when used at a concentration of 1 µM.1 CD532 (25 mg/kg) reduces tumor growth and increases survival in a MYCN-amplified SMS-KCN neuroblastoma mouse xenograft model.

1.Gustafson, W.C., Meyerowitz, J.G., Nekritz, E.A., et al.Drugging MYCN through an allosteric transition in Aurora kinase ACancer Cell26(3)414-427(2014) 2.Lee, J.K., Phillips, J.W., Smith, B.A., et al.N-Myc drives neuroendocrine prostate cancer initiated from human prostate epithelial cellsCancer Cell29(4)536-547(2016)

리뷰

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Average Rating: 5 ★★★★★ (Based on Reviews and 35 reference(s) in Google Scholar.)

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