Monensin methyl ester

Names

[ CAS No. ]:
28636-21-7

[ Name ]:
Monensin methyl ester

Biological Activity

[Description]:

Monensin methyl ester, a neutral analog of monensin, is an ion active component for Na+ selective disk electrodes[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[References]

[1]. J G Schindler, et al. [Monensin, an electrically charged carboxyl ionophor, and its neutral methylester as ion active components for Na+ selective disk electrodes]. Biomed Tech (Berl). Jan-Feb 1987;32(1-2):22-4.

Chemical & Physical Properties

[ Molecular Formula ]:
C₃₇H₆₄O₁₁

[ Molecular Weight ]:
684.89700

[ Exact Mass ]:
684.44500

[ PSA ]:
142.37000

[ LogP ]:
4.36130

[ Vapour Pressure ]:
4.17E-26mmHg at 25°C

[ Storage condition ]:
2-8°C

Safety Information

[ Symbol ]:

GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H310

[ Precautionary Statements ]:
P280-P301 + P310-P302 + P350-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges

[ Hazard Codes ]:
T

[ Risk Phrases ]:
24/25

[ Safety Phrases ]:
36/37-45

[ RIDADR ]:
UN 2811 6.1 / PGIII

Articles

Monensin A methyl ester complexes with Li+, Na+, and K+ cations studied by ESI-MS, 1H- and 13C-NMR, FTIR, as well as PM5 semiempirical method.

J. Mol. Struct. 788 , 176-183, (2006)

Monensin A methyl ester (MON1) was synthesized by a new method and its ability to form complexes with Li+, Na+, and K+ cations was studied by electrospray ionization-mass spectroscopy (ESI-MS), 1H and...

[Monensin, an electrically charged carboxyl ionophor, and its neutral methylester as ion active components for Na+ selective disk electrodes].

Biomed. Tech. (Berl.) 32(1-2) , 22-4, (1987)

Spectroscopic and semiempirical studies of a proton channel formed by the methyl ester of monensin A.

J. Phys. Chem. B 110(31) , 15615-23, (2006)

Monensin A is an ionophore able to carry protons and cations through the cell membrane. Its methyl ester (MON1) and its hydrates have been studied in acetonitrile, and its deuterated analogue by Fouri...

Related Compounds

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