SGC-SMARCA-BRDVIII |
| Catalog No.GC63887 |
SGC-SMARCA-BRDVIII est un inhibiteur puissant et sélectif de SMARCA2/4 et PB1(5), avec des Kd de 35 nM, 36 nM et 13 nM, respectivement.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1997319-84-2
Sample solution is provided at 25 µL, 10mM.
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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.
Average Rating: 5 (Based on Reviews and 3 reference(s) in Google Scholar.)
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