Rev-erbα agonist GS4112

产品编号: DC8648
Rev-erbα agonist GS4112
结构式
1216744-19-2
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应用领域
GSK4112 is a Rev-erbα agonist with EC50 of 0.4 μM, also is a small molecule chemical probe for the cell biology of the nuclear heme receptor Rev-erbα.
Cas No.: 1216744-19-2
名称:
别名: SR6452; SR-6452; SR 6452
SMILES: ClC1C=CC(CN(CC2=CC=C([N+]([O-])=O)S2)CC(OC(C)(C)C)=O)=CC=1
分子式: C18H21ClN2O4S
分子量: 396.89
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: GSK4112 is a Rev-erbα agonist with EC50 of 0.4 μM, also is a small molecule chemical probe for the cell biology of the nuclear heme receptor Rev-erbα.in vitro: GSK4112 profiled as a Rev-erb agonist in cells to inhibit expression of the circadian target gene bmal1. In addition, GSK4112 repressed the expression of gluconeogenic genes in liver cells and reduced glucose output in primary hepatocytes. Therefore, GSK4112 is useful as a chemical tool to probe the function of Rev-erb in transcriptional repression, regulation of circadian biology, and metabolic pathways. Additionally, GSK4112 may serve as a starting point for design of Rev-erb chemical probes with in vivo pharmacologicalm activity.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
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MSDS_3496_DC8648_1216744-19-2
COA
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产品编号 产品名称 应用领域
DC8648 Rev-erbα agonist GS4112 GSK4112 is a Rev-erbα agonist with EC50 of 0.4 μM, also is a small molecule chemical probe for the cell biology of the nuclear heme receptor Rev-erbα.
DC7404 DMXAA DMXAA (Vadimezan) is a vascular disrupting agents (VDA) and competitive inhibitor of DT-diaphorase with Ki of 20 μM and IC50 of 62.5 μM, respectively. Phase 3.