目录:MedChemExpress LLC>>生化试剂>> SR1001 | MCE
CAS | 1335106-03-0 | 纯度 | 99.84% |
---|---|---|---|
分子量 | 477.4 | 分子式 | C₁₅H₁₃F₆N₃O₄S₂ |
供货周期 | 现货 | 规格 | 5 mg |
货号 | HY-13421 | 应用领域 | 医疗卫生,化工,生物产业,制药/生物制药 |
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CAS No. : 1335106-03-0
产品活性:SR1001 is a selective RORα and RORγt inverse agonist with Kis 172 and 111 nM, respectively.
研究领域:Metabolic Enzyme/Protease | Vitamin D Related/Nuclear Receptor
作用靶点:ROR
In Vitro: SR1001 inhibits the development of murine TH17 cells by inhibition of IL-17A gene expression and protein production. SR1001 reduces the interaction of a coactivator TRAP220 NR box 2 peptide with RORγ in a dose dependent manner (IC50 value≈117 nM). Additionally, SR1001 inhibits the expression of cytokines when added to differentiated murine or human TH17 cells.
In Vivo: SR1001 effectively suppresses the clinical severity of autoimmune disease in mice. Administration of SR1001 to C57BL/6 mice suppresses the expression of hepatic ROR target genes, Cyp7b1, Rev-erbα, and Serpine 1. SR1001 a RORα inverse agonist eliminats the circadian pattern of expression of citrate synthase mRNA in mice.
相关产品:Bioactive Compound Library Plus | Immunology/Inflammation Compound Library | Metabolism/Protease Compound Library | Small Molecule Immuno-Oncology Compound Library | Transcription Factor-Targeted Library | Targeted Diversity Library | Human Metabolite Library | Nuclear Receptor Compound Library | Heterocyclic Compound Library | SR3335 | Methyl-3β-hydroxycholenate | Bevurogant | PF-06747711 | Zilovertamab | XY101 | RORγt inhibitor 2 | RORγt Inverse agonist 8 | RORγt agonist 3 | RORγt modulator 2 | SR0987 | AZD-0284 | RORγt Inverse agonist 6 | ARN-6039 | RORγ agonist 1 | RORγt/DHODH-IN-2 | 3-Oxo-5β-cholanoic acid | GNE-6468 | RORγt inverse agonist 29 | 7ß,27-Dihydroxycholesterol | Nobiletin | CD12681 | BMS-986251 | TAK-828F | RORγt inverse agonist 13 | RORγt Inverse agonist 3 | SHR168442 | GSK805 | SR1555
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