>>Signaling Pathways>> PI3K/Akt/mTOR Signaling>> GSK-3>>BRD3731

BRD3731

Catalog No.GC62875

BRD3731은 GSK3β 및 GSK3α에 대해 IC50이 각각 15nM 및 215nM인 선택적 GSK3β 억제제입니다.

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BRD3731 Chemical Structure

Cas No.: 2056262-07-6

Size 가격 재고 수량
10mM (in 1mL DMSO)
US$415.80
재고 있음
5 mg
US$378.00
재고 있음
10 mg
US$630.00
재고 있음
50 mg
US$1,755.00
재고 있음
100 mg
US$2,655.00
재고 있음

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고객 리뷰

Based on customer reviews.

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

BRD3731 is a selective GSK3β inhibitor, with IC50s of 15 nM and 215 nM for GSK3β and GSK3α, respectively. BRD3731 is potentail for the research of post-traumatic stress disorder (PTSD), psychiatric disorder, diabetes, and neurodegenerative disorders[1].

BRD3731 is a GSK3β- selective inhibitor extracted from patent US20160375006A1, compound example 272[1].BRD3731 (1-10 μM; 24 hours) inhibits the phosphorylation of CRMP2 in SH-SY5Y cells[1].BRD3731 (20 μM; 24 hours) decreases β-catenin S33/37/T41 phosphorylation and induces β-catenin S675 phosphorylation in HL-60 cells[2].BRD3731 (10-20 μM; 7-10 days) impairs colony formation in TF-1 and increases colony forming ability in the MV4-11 cell line[2]

[1]. Edward Scolnick, et al. Uses of paralog-selective inhibitors of gsk3 kinases. US20160375006A1.
[2]. Wagner FF, et, al. Exploiting an Asp-Glu "switch" in glycogen synthase kinase 3 to design paralog-selective inhibitors for use in acute myeloid leukemia. Sci Transl Med. 2018 Mar 7;10(431):eaam8460.

리뷰

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Average Rating: 5 ★★★★★ (Based on Reviews and 37 reference(s) in Google Scholar.)

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