Cridanimod NEW
Price | $30 | $61 | $101 |
Package | 1mg | 5mg | 10mg |
Min. Order: | |
Supply Ability: | 10g |
Update Time: | 2024-11-01 |
Product Details
Product Name: Cridanimod | CAS No.: 38609-97-1 |
Purity: 99.96% | Supply Ability: 10g |
Release date: 2024/11/01 |
Product Introduction
Bioactivity
名稱 | Cridanimod |
描述 | Cridanimod (10-carboxymethyl-9-acridanone, CMA) is a potent STING agonist that directly binds to STING and triggers a strong antiviral response through the TBK1/IRF3 route. |
細(xì)胞實(shí)驗(yàn) | For transfection experiments, primary macrophages were seeded with a density of 1 × 10^5?per?ml. Cells were transfected with poly(I:C) (2?μg/ml), pppRNA (1.33?μg/ml), ISD (2?μg/ml) and c-diGMP (8.66?μg/ml) using Lipofectamine 2000, according to the manufacturer's instructions. LPS (200?ng/ml) and CMA were directly added to the medium. Human PBMCs were transfected as described above, at a density of 4 × 10^6?per?ml, human fibroblasts at a density of 1.5 × 105?per?ml. For western blot experiments, cells were lysed after 2?h, if not indicated otherwise. For cytokine assays, supernatants were collected after 18–20?h. For RNA isolation, cells were lysed after 4?h [1]. |
體外活性 | CMA induced robust IRF3 phosphorylation that was followed by strong Ifnb mRNA induction and translation. CMA-mediated IFNβ production reached peak levels already 4?h after stimulation, even exceeding LPS in its readiness to trigger IFNβ synthesis [1]. rSTING and hSTING do not respond or only respond weakly to CMA, whereas it strongly activated mSTING. Endogenous mRNA level of Ifnb, Cxcl10, and Il6 were robustly increased when treated with CMA in murine macrophages, but not in rat macrophages and human THP-1 cells [2]. |
存儲(chǔ)條件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
溶解度 | DMSO : 50 mg/mL (197.43 mM), Sonication is recommended. |
關(guān)鍵字 | XBIO101 | inhibit | Interferon-α/β receptor | Progesterone Receptor | Cridanimod | XBIO 101 | NR3C3 | IFNAR | Interferon-alpha/beta receptor | Inhibitor |
相關(guān)產(chǎn)品 | Mifepristone | Progesterone |
相關(guān)庫 | 經(jīng)典已知活性庫 | 抗癌臨床化合物庫 | 藥物功能重定位化合物庫 | 抗病毒庫 | 已知活性化合物庫 | 抗癌活性化合物庫 | 抗癌藥物庫 |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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