Na+ ionophore
Antibiotic that functions as Na+ ionophore. Blocks glycoprotein secretion. Inhibits proliferation of several lymphoma cell lines through cell cycle arrest and apoptosis. Blocks ceramide transport through the Golgi apparatus.
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Product Details
| Appearance |
White to light yellow powder. |
|---|---|
| CAS |
22373-78-0 |
| Formula |
C36H61O11 . Na |
| MI |
14: 6246 |
| MW |
669.9 . 23.0 |
| Purity |
≥90% |
| Solubility |
Soluble in 100% ethanol (25mg/ml), methanol (50mg/ml), chloroform or DMSO (25mg/ml). Slightly soluble in water. |
Handling & Storage
| Use/Stability |
As indicated on product label or CoA when stored as recommended. |
|---|---|
| Handling |
Store tightly sealed in the dark. |
| Long Term Storage |
-20°C |
| Shipping |
Ambient Temperature |
| Regulatory Status |
RUO – Research Use Only |
|---|
- A purinergic mechanism underlying metformin regulation of hyperglycemia: Senfeld, J., Peng, Q., et al.; iScience 26, 106898 (2023), Abstract
- Increased Th9 cells and IL-9 levels accelerate disease progression in experimental atherosclerosis: Q. Li, et al.; Am. J. Transl. Res. 9, 1335 (2017), Abstract — Full Text
- Image-based drug screen identifies HDAC inhibitors as novel Golgi disruptors synergizing with JQ1: M. Gendarme, et al.; Mol. Biol. Cell. 28, 3756 (2017), Abstract — Full Text
- Elevated Th22 cells and related cytokines in patients with epithelial ovarian cancer: T. Wang, et al.; Medicine (Baltimore) 96, e8359 (2017), Application(s): Flow Cytometry, Abstract — Full Text
- Interleukin-37 and Dendritic Cells Treated With Interleukin-37 Plus Troponin I Ameliorate Cardiac Remodeling After Myocardial Infarction: R. Zhu, et al.; J. Am. Heart Assoc. 5, e004406 (2016), Abstract — Full Text
- Olfactory ecto-mesenchymal stem cells possess immunoregulatory function and suppress autoimmune arthritis: K. Rui, et al.; Cell. Mol. Immunol. 13, 401 (2015), Application(s): Flow cytometric analysis in mouse cells, Abstract
- The Profile of T Helper Subsets in Bone Marrow Microenvironment Is Distinct for Different Stages of Acute Myeloid Leukemia Patients and Chemotherapy Partly Ameliorates These Variations: T. Tian, et al.; PLoS One 10, e0131761 (2015), Application(s): Cell Culture, Abstract — Full Text
- Inactivation of Notch signaling reverses the Th17/Treg imbalance in cells from patients with immune thrombocytopenia: Yu, S., Liu, C., et al.; Lab. Invest. 95, 157 (2015), Abstract
- Monensin-mediated growth inhibition in human lymphoma cells through cell cycle arrest and apoptosis: W. H. Park, et al.; Br. J. Haematol. 119, 400 (2002), Abstract
- Sphingomyelin transport to the cell surface occurs independently of protein secretion in rat hepatocytes: Y.J. Shiao & J.E. Vance; J. Biol. Chem. 268, 26085 (1993), Abstract
- Monensin inhibits synthesis of plasma membrane sphingomyelin by blocking transport of ceramide through the Golgi: evidence for two sites of sphingomyelin synthesis in BHK cells: K.J. Kallen et al.; Biochim. Biophys. Acta 1166, 305 (1993), Abstract
- Alteration of intracellular traffic by monensin; mechanism, specificity and relationship to toxicity: H. H. Mollenhauer, et al.; Biochim. Biophys. Acta 1031, 225 (1990), Review, Abstract
- Expression of membrane IGM by a human B lymphoblastoid cell line in the presence of monensin: R.T. Kubo and M.L. Pigeon; Mol. Immunol. 20, 345 (1983), Abstract
- Undersulfated proteoglycans are secreted by cultured chondrocytes in the presence of the ionophore monensin: K. Tajiri, et al.; J. Biol. Chem. 255, 6036 (1980), Abstract — Full Text
- Solution chemistry of monensin and its alkali metal ion complexes. Potentiometric and spectroscopic studies: P.G. Gertenbach & A.I. Popov; JACS 97, 4738 (1975), Abstract
- Monensin, a new biologically active compound. I. Discovery and isolation: M. E. Haney, Jr. & M. M. Hoehn; Antimicrobial Agents Chemother. (Bethesda) 7, 349 (1967), Abstract
Related Products
| CAS | 38966-21-1 |
|---|---|
| Couple Type | Inhibitor |
| Purity | ≥98% (TLC) |
| Alternative Name | 6-(6-Methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-6,8-dihydrofuro[3,4-E][1,3]benzodioxol-8-ol, (+)-Decumbensine |
|---|---|
| CAS | 6883-44-9 |
| Purity | ≥98% (HPLC) |
| Alternative Name | (3S,3aR,4R,4aS,8aR,9aS)-4-[(1E)-2-[(2R,6S)-1,6-Dimethyl-2-piperdinyl]ethenyl]decahydro-3-methyl-naphtho[2,3-c]furan-1(3H)-one |
|---|---|
| CAS | 6879-74-9 |
| Couple Type | Inhibitor |
| Purity | ≥98% |
Last modified: May 29, 2024
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