الصفحة الرئيسية>>Signaling Pathways>> Stem Cell>> Smoothened>>LDE225 (NVP-LDE225,Erismodegib)

LDE225 (NVP-LDE225,Erismodegib)

رقم الكتالوجGC13655

LDE225 (NVP-LDE225 ، Erismodegib) (Erismodegib) هو مضاد Smo قوي وانتقائي مع IC50 من 1.3 نانومتر و 2.5 نانومتر للفأر والبشر Smo في اختبار الربط ، على التوالي.

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LDE225 (NVP-LDE225,Erismodegib) التركيب الكيميائي

Cas No.: 956697-53-3

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
40٫00
متوفر
5mg
38٫00
متوفر
10mg
54٫00
متوفر
50mg
114٫00
متوفر
100mg
172٫00
متوفر
200mg
324٫00
متوفر

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مراجعات العميل

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

LDE225 is a potent and selective inhibitor of smoothened with IC50 values of 1.3nM in mouse and 2.5nM in human, respectively [1].

LDE225 is screened out from a high-throughput cell-based screen of in-house diversity combinatorial libraries and is developed to be an antagonist of Smo. Smo is an activator of the hedgehog(Hh) signaling pathway and aberrant activation links to tumorigenesis in several cancers. The antitumor efficacy of LDE225 has been evaluated in vivo. In the subcutaneous Ptch+/-p53-/- medulloblastoma allograft mouse model, LDE225 can significantly inhibit tumor growth at a dose of 5mg/kg/day. And in an orthotopic Ptch+/-p53-/- medulloblastoma allograft model, LDE225 is suggested to penetrate the blood-brain barrier in tumor-bearing animals and cause the tumor growth inhibition after 4 days of treatment. Additionally, the preclinical safety assays show that LDE225 has no genotoxicity and has good selectivity [1].

References:
[1] Shifeng Pan, Xu Wu, Jiqing Jiang, et al. Discovery of NVP-LDE225, a potent and selective smoothened antagonist. ACS Med. Chem. Lett. 2010, 1: 130–134.

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