| Weight | 692.863 g/mol |
|---|---|
| Formula | C36H61NaO11 |
| Hydrogen Acceptors | 11 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 10 |
Coban (22373-78-0)
Monensin · Rumensin · Monensin Sodium
Score:
#2604 in Biochemistry
,
#5030 in Biology
,
#6488 in Chemistry
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- Perturbation of vesicular traffic with the carboxylic ionophore monensin (Cell, 1983)
- Alteration of intracellular traffic by monensin; mechanism, specificity and relationship to toxicity. (Biochimica et Biophysica Acta, 1990)
- Monensin Interrupts the Recycling of Low Density Lipoprotein Receptors in Human Fibroblasts (Cell, 1981)
- Influence of Monensin on the Performance of Cattle1 (Journal of Animal Science, 1984)
- Dissection of the Golgi complex. I. Monensin inhibits the transport of viral membrane proteins from medial to trans Golgi cisternae in baby hamster kidney cells infected with Semliki Forest virus. (Journal of Cell Biology, 1983)
- Methane emissions from beef cattle: Effects of monensin, sunflower oil, enzymes, yeast, and fumaric acid. (Journal of Animal Science, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H300: Fatal if swallowed
Danger Acute toxicity, oral - Category 1, 2 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - Monensin
- Rumensin
- Monensin Sodium
- Monensin-A-Sodium Complex
- Monensin A Sodium Complex
- Monensin Monosodium Salt
-
SMILESCCC1(CCC(O1)C2(CCC3(O2)CC(C(C(O3)C(C)C(C(C)C(=O)[O-])OC)C)O)C)C4C(CC(O4)C5C(CC(C(O5)(CO)O)C)C)C.[Na+]
-
InChIKeyXOIQMTLWECTKJL-UHFFFAOYSA-M
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