الصفحة الرئيسية>>Signaling Pathways>> Chromatin/Epigenetics>> Epigenetic Reader Domain>>SGC-SMARCA-BRDVIII

SGC-SMARCA-BRDVIII

رقم الكتالوجGC63887

SGC-SMARCA-BRDVIII هو مثبط قوي وانتقائي لـ SMARCA2 / 4 و PB1 (5) ، مع Kds من 35 نانومتر ، 36 نانومتر ، و 13 نانومتر ، على التوالي

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

SGC-SMARCA-BRDVIII التركيب الكيميائي

Cas No.: 1997319-84-2

الحجم السعر المخزون الكميّة
5 mg
72٫00
متوفر
10 mg
122٫00
متوفر
25 mg
270٫00
متوفر
50 mg
432٫00
متوفر
100 mg
691٫00
متوفر

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

مراجعات العميل

بناء على آراء العملاء.

  • GlpBio Citations

    GlpBio Citations
  • Bioactive Compounds Premium Provider

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

SGC-SMARCA-BRDVIII is a potent and selective inhibitor of SMARCA2/4 and PB1(5), with Kds of 35 nM, 36 nM, and 13 nM, respectively. SGC-SMARCA-BRDVIII also inhibits PB1(2) and PB1(3), with Kds of 3.7 and 2.0 μM, respectively. SGC-SMARCA-BRDVIII can block adipogenesis of 3T3-L1 murine fibroblasts[1][2].

SGC-SMARCA-BRDVIII (compound 22) (1 μM; 14 days) blocks adipocyte differentiation in 3T3-L1 murine fibroblasts[1].

[1]. Wanior M, et, al. Pan-SMARCA/PB1 Bromodomain Inhibitors and Their Role in Regulating Adipogenesis. J Med Chem. 2020 Dec 10;63(23):14680-14699.
[2]. MÉlin L, et, al. Design and Synthesis of LM146, a Potent Inhibitor of PB1 with an Improved Selectivity Profile over SMARCA2. ACS Omega. 2021 Aug 9;6(33):21327-21338.

مراجعات

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