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  J97238    AKSci Bulk Reagent
Monensin sodium salt, ≥800 ug/mg
 
Coban
2-[5-Ethyltetrahydro-5-[tetrahydro-3-methyl-5-[tetrahydro-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyl-2H-pyran-2-yl]-2-furyl]-2-furyl]-9-hydroxy-|A-methoxy-|A,|A,2,8-tetramethyl-1,6-dioxaspiro[4.5]decane-7-butyric acid sodium




IDENTITY
CAS Number:22373-78-0
MDL Number:MFCD00077826
MF:C36H61O11.Na
MW:692.86
EINECS:244-941-7
BRN:4122200
SPECIFICATIONS & PROPERTIES
Physical Form (at 20°C):Solid
Melting Point:278-284°C
Long-Term Storage:Store long-term at 2-8°C
DOT/IATA TRANSPORT INFORMATION
UN #:UN3462
Hazard Class:6.1; Poison
Packing Group:II
A hazmat fee may apply to certain package sizes and shipment methods. Please check pricing table for an indicator of applicable hazmat fees.

BIOLOGICAL INFO
Solubility:50mg/ml in MeOH: clear colorless to light yellow solution
Form:Sodium salt
Research Area:infection

REVIEW

 Monensin is a polyether antibiotic isolated from Streptomyces cinnamonensis. It is widely used in ruminant animal feeds. When fed to beef cows, monensin reduced amounts of feed required to maintain cow weight. The structure of monensin was first described by in 1967, and was the first polyether antibiotic to have its structure elucidated in this way. 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 Tl+. Monensin A is able to transport these cations across lipid membranes of cells, playing an important role as an Na+/H+ antiporter.. The outer surface of the ionophore-ion complex is composed largely of nonpolar hydrocarbon, which imparts a high solubility to the complexes in nonpolar solvents. In biological systems, these complexes are freely soluble in the lipid components of membranes and, presumably, diffuse or shuttle through the membranes from one aqueous membrane interface to the other. The net effect for monensin is a trans-membrane exchange of sodium ions for protons. Monensin therefore 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.

REFERENCES
[1]Daniel Lowicki and Adam Huczynski. BioMed Research International 2013: 1-14.
[2] Patrick Butaye, Luc A. Devriese, Freddy Haesebrouck Antimicrobial Growth Promoters Used in Animal Feed: Effects of Less Well Known Antibiotics on Gram-Positive Bacteria Clinical Microbiology Reviews, 2003, p. 175-188, Vol. 16.
[3] Goodrich RD, Garrett JE, Gast DR, Kirick MA, Larson DA, Meiske JC Influence of monensin on the performance of cattle. J Anim Sci. 1984 Jun;58(6):1484-98.
[4] Potter EL, VanDuyn RL, Cooley CO. Monensin toxicity in cattle. J Anim Sci. 1984 Jun;58(6):1499-511.

GLOBALLY HARMONIZED SYSTEM (GHS)

Pictograms

Signal Word
Danger

Hazard Statements
H300

Precautionary Statements
P264; P270; P301+P310; P321; P330; P405; P501


Current as of December 29, 2024


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All batches backed with full quality assurance.
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All products are for research and development use only, not for any other uses, and must be handled by technically-qualified persons.

These products are explicitly not intended to be used in foods and/or cosmetics and/or drugs (human and veterinary) and/or consumer products and/or biocides and/or pesticides of any kind unless explicitly stated otherwise.

Products are not sold to individuals. We do not ship to residential addresses. Consumer orders will be cancelled without notice.

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CATEGORIES

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PubChem
  @PubMed
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