Names | |
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IUPAC name
4-[2-[5-ethyl-5-[5-[6-hydroxy-6-
(hydroxymethyl)-3,5-dimethyl-oxan-2-yl]- 3-methyl-oxolan-2-yl]oxolan-2-yl]- 9-hydroxy-2,8-dimethyl-1,6-dioxasp iro[4.5]dec-7-yl]-3-methoxy-2-methyl- pentanoic acid |
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Other names
monensic acid
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Identifiers | |
17090-79-8 | |
3D model (Jmol) | Interactive image |
ChEBI | CHEBI:27617 |
ChEMBL | ChEMBL256105 |
ChemSpider | 389937 |
ECHA InfoCard | 100.037.398 |
E number | E714 (antibiotics) |
KEGG | D08228 |
PubChem | 441145 |
UNII | 906O0YJ6ZP |
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Properties | |
C36H62O11 | |
Molar mass | 670.871 g/mol |
Appearance | solid state, white crystals |
Melting point | 104 °C (219 °F; 377 K) |
3x10−6 g/dm3 (20 °C) | |
Solubility | ethanol, acetone, diethyl ether, benzene |
Pharmacology | |
QA16QA06 (WHO) QP51AH03 (WHO) | |
Related compounds | |
Related
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antibiotics, ionophores |
Related compounds
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Monensin A methyl ester, |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|
Infobox references | |
(hydroxymethyl)-3,5-dimethyl-oxan-2-yl]- 3-methyl-oxolan-2-yl]oxolan-2-yl]- 9-hydroxy-2,8-dimethyl-1,6-dioxasp iro[4.5]dec-7-yl]-3-methoxy-2-methyl-
Monensin is a polyether antibiotic isolated from Streptomyces cinnamonensis. It is widely used in ruminant animal feeds.
The structure of monensin was first described by Agtarap et al. in 1967, and was the first polyether antibiotic to have its structure elucidated in this way. The first total synthesis of monensin was reported in 1979 by Kishi et al.
Monensin A is an ionophore related to the crown ethers with a preference to form complexes with monovalent cations such as: Li+, Na+, K+, Rb+, Ag+, and Ti+. Monensin A is able to transport these cations across lipid membranes of cells in an electroneutral (i.e. non-depolarizing) exchange, playing an important role as an Na+/H+antiporter. Recent studies have shown that monensin may transport sodium ion through the membrane in both electrogenic and electroneutral manner. This approach explains ionophoric ability and in consequence antibacterial properties of not only parental monensin, but also its derivatives that do not possess carboxylic groups. It blocks intracellular protein transport, and exhibits antibiotic, antimalarial, and other biological activities. The antibacterial properties of monensin and its derivatives are a result of their ability to transport metal cations through cellular and subcellular membranes.
Monensin is used extensively in the beef and dairy industries to prevent coccidiosis, increase the production of propionic acid and prevent bloat. Furthermore, monensin, but also its derivatives monensin methyl ester (MME), and particularly monensin decyl ester (MDE) are widely used in ion-selective electrodes.