Mycophenolic acid sodium NEW
| Price | $2140 | $2785 | $3520 |
| Package | 25mg | 50mg | 100mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2025-04-27 |
Product Details
| Product Name: Mycophenolic acid sodium | CAS No.: 37415-62-6 |
| Supply Ability: 10g | Release date: 2025/04/27 |
Product Introduction
Bioactivity
| Name | Mycophenolic acid sodium |
| Description | Mycophenolic acid sodium is a potent uncompetitive inhibitor of inosine monophosphate dehydrogenase (IMPDH) with an EC50 of 0.24 μM, exhibiting broad antiviral activity against RNA viruses, including influenza, along with immunosuppressive properties and antiangiogenic and antitumor effects [1][2]. |
| In vitro | Mycophenolic acid sodium has been demonstrated to possess antiviral properties against an array of RNA viruses, including influenza, dengue virus, Zika virus, rotavirus, CCHFV, and hantavirus [1]. It targets IMPDH, a crucial enzyme in guanosine nucleotides' de novo synthesis [2]. When tested at concentrations ranging from 0.01 to 1 μM over 72 hours, mycophenolic acid sodium displayed a selective inhibitory effect on the proliferation of endothelial cells and fibroblasts, with endothelial cells being more susceptible (IC 50 <500 nM) to its antimitotic effects [2]. In contrast, fibroblasts showed a higher tolerance (IC 50 <1 μM). Among human tumor cell lines tested, A549 non-small cell lung cancer and PC3 prostate cancer cells manifested moderate sensitivity (IC 50 >1 μM), whereas U87 glioblastoma cells were resistant to up to 1 μM of mycophenolic acid sodium treatment [2]. Furthermore, a dose-dependent modulation of HDAC2 and MYC (down-regulation) and NDRG1 (up-regulation) was observed with mycophenolic acid sodium treatment (0.05-2 μM; 18 hours) [2]. In cell proliferation assays, primary isolated human dermal microvascular endothelial cells and fibroblasts were preferentially inhibited by the treatment, contrasting with U87 glioblastoma cells' resistance and the intermediate sensitivity of A549 and PC3 cancer cells [2]. Western Blot analysis further confirmed the dose-dependent regulatory effect of mycophenolic acid sodium on HDAC2, MYC, and NDRG1 in human dermal microvascular endothelial cells, providing a detailed understanding of its mechanism [2]. |
| In vivo | Mycophenolic acid (120 mg/kg; oral gavage; b.i.d.) exhibits potent anti-tumor activity by altering the tumor microenvironment and significantly inhibiting U87 tumor growth in BALB/c nude mice [2]. Using an athymic 8-week-old, 20 g BALB/c nu/nu mouse model with a Mycophenolic acid-resistant U87 tumor, 120 mg/kg of MMF (the morpholinoethyl ester prodrug of Mycophenolic acid) was administered orally twice daily. After 14 days post-tumor implantation, the MMF-treated group showed a 70% reduction in tumor growth compared to controls. Furthermore, MMF treatment significantly decreased microvessel density (by 44%) and pericyte coverage (by 78%), as indicated by CD31 and α-smooth muscle actin staining, respectively, suggesting impaired tumor vascularization and underscoring its efficacy against tumor proliferation [2]. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
Company Profile Introduction
TargetMol Chemicals Inc. is headquartered in Boston, MA, and specializes in products and services that serve the research needs of chemical and biological scientists worldwide. With a client base in 40+ countries, TargetMol has evolved into one of the biggest global research suppliers for compound libraries and small molecule compounds.
170+ Compound Libraries， 10000+ Noval Small Molecucles，16000+ Nature Compounds
TargetMol diligently updates and offers over 170 types of compound libraries and a wide range of high-quality research chemicals, including inhibitors, activators, natural products, peptides, antibodies , and novel life-science kits for laboratory and scientific use. In addition, our lab allows us to conduct CADD (computer-aided drug design) and chemical synthesis to meet the customization needs of our clients.
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