Baricitinib NEW
| Price | $43 | $67 | $92 |
| Package | 5mg | 10mg | 25mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2024-11-19 |
Product Details
| Product Name: Baricitinib | CAS No.: 1187594-09-7 |
| Purity: 99.79% | Supply Ability: 10g |
| Release date: 2024/11/19 |
Product Introduction
Bioactivity
| Name | Baricitinib |
| Description | Baricitinib (INCB028050) is a JAK1 and JAK2 inhibitor (IC50=5.9/5.7 nM) with selective and oral activity. Baricitinib has potential anti-inflammatory, immunomodulatory and anti-tumor activity. |
| Cell Research | Baricitinib(INCB 028050) is dissolved in stock solutions, and then diluted with appropriate media before use[1]. Human PBMCs are isolated by leukapheresis followed by Ficoll-Hypaque centrifugation. For the determination of IL-6-induced MCP-1 production, PBMCs are plated at 3.3×105 cells per well in RPMI 1640+10% FCS in the presence or absence of various concentrations of INCB028050 (1 nM, 10 nM, 100 nM, 1 μM, and 10 μM). Following preincubation with compound for 10 min at room temperature, cells are stimulated by adding 10 ng/mL human recombinant IL-6 to each well. Cells are incubated for 48 h at 37°C, 5% CO2. Supernatants are harvested and analyzed by ELISA for levels of human MCP-1. The ability of INCB028050 to inhibit IL-6-induced secretion of MCP-1 is reported as the concentration required for 50% inhibition (IC50). Proliferation of Ba/F3-TEL-JAK3 cells is performed over 3 d using Cell-Titer Glo[1]. |
| Kinase Assay | Enzyme assays are performed using a homogeneous time-resolved fluorescence assay with recombinant epitope tagged kinase domains (JAK1, 837-1142; JAK2, 828-1132; JAK3, 718-1124; Tyk2, 873-1187) or full-length enzyme (cMET and Chk2) and peptide substrate. Each enzyme reaction is performed with or without test compound (11-point dilution), JAK, cMET, or Chk2 enzyme, 500 nM (100 nM for Chk2) peptide, ATP (at the Km specific for each kinase or 1 mM), and 2.0% DMSO in assay buffer. The calculated IC50 value is the compound concentration required for inhibition of 50% of the fluorescent signal. Additional kinase assays are performed at Cerep using standard conditions at 200 nM. Enzymes tested included: Abl, Akt1, AurA, AurB, CDC2, CDK2, CDK4, CHK2, c-kit, EGFR, EphB4, ERK1, ERK2, FLT-1, HER2, IGF1R, IKKα, IKKβ, JNK1, Lck, MEK1, p38α, p70S6K, PKA, PKCα, Src, and ZAP70[1]. |
| In vitro | METHODS: PBMC cells were pre-incubated with Baricitinib (0-10,000 nM) for 10 min, and the cells were stimulated with IL-6 (10 ng/mL) for 48 h. Related factors were detected by ELISA assay. RESULTS: In PBMC, Baricitinib inhibited IL-6-stimulated phosphorylation of the classical substrate STAT3 and subsequent production of the chemokine MCP-1 with IC50 values of 44 nM and 40 nM, respectively.[1] METHODS: CD19+ B cells were treated with IgM antibody (1 µg/mL), sCD40L (250 ng/mL), IL-4 (100 ng/mL), and Baricitinib (0.05-5 µM) for 2-5 days, and gene expression levels were measured using real-time PCR. RESULTS: After two days of stimulation, Baricitinib was found to significantly inhibit the expression level of Aicda in a dose-dependent manner, while the expression level of Bcl6 was increased. After five days of stimulation, the expression levels of Xbp1 and Irf4 were also significantly reduced. IgG production measured from the supernatant under the same conditions was significantly reduced depending on the increase in Baricitinib dose after two and five days of stimulation, respectively. [2] |
| In vivo | METHODS: To investigate the potential therapeutic utility in autoimmune arthritis, Baricitinib (1-10 mg/kg) was administered orally to DBA/1j mice with collagen-induced arthritis (CIA) twice daily for 15 days. RESULTS: Clinical signs of disease improved as early as 4 days after administration, and at study termination, clinical scores were reduced by 19%, 67%, and 61%, respectively, in a dose-dependent manner compared to the vector control group. [1] |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| Solubility Information | H2O : < 1 mg/mL (insoluble or slightly soluble) 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 6.9 mg/mL (18.58 mM), Suspension. Please add co-solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. Ethanol : < 1 mg/mL (insoluble or slightly soluble) DMSO : 55 mg/mL (148.08 mM) |
| Keywords | Inhibitor | JAK | Janus kinase | INCB-028050 | inhibit | Baricitinib | LY 3009104 | INCB 028050 | LY-3009104 |
| Inhibitors Related | Tofacitinib Citrate | Ruxolitinib phosphate | Gefitinib |
| Related Compound Libraries | Bioactive Compound Library | Drug Repurposing Compound Library | FDA-Approved Drug Library | FDA-Approved Kinase Inhibitor Library | Anti-Aging Compound Library | Bioactive Compounds Library Max | Anti-Cancer Drug Library | Anti-Cancer Active Compound Library |
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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