Basic information Safety Supplier Related

monazomycin

Basic information Safety Supplier Related

monazomycin Basic information

Product Name:
monazomycin
Synonyms:
  • monazomycin
  • Oxacyclooctatetraconta-13,17,21,29-tetraen-2-one, 48-(7-amino-1-methylheptyl)-8,10,16,20,24,26,28,32,36,38,40,42,44,46-tetradecahydroxy-23-(α-D-mannopyranosyloxy)-9,15,17,19,21,25,31,33,39,41,47-undecamethyl-
  • Monazomycin DISCONTINUED
CAS:
11006-31-8
MF:
C72H133NO22
MW:
1364.82
Mol File:
11006-31-8.mol
More
Less

monazomycin Chemical Properties

Melting point:
127°C
Boiling point:
866.56°C (rough estimate)
Density 
0.9708 (rough estimate)
refractive index 
1.5280 (estimate)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
form 
solid
pka
12.89±0.70(Predicted)
More
Less

monazomycin Usage And Synthesis

Uses

Monazomycin is a macrocylic polyol lactone isolated from several species of Streptoverticillium, first reported in 1963. Monazomycin is active against Gram positive bacteria with weak Gram negative activity. In solution, monazomycin exists as hydrophilic clusters which, when adsorbed onto a lipid bilayer, can induce channel formation. Monazomycin is an important bioprobe for understanding membrane channels.

Uses

Monazomycin is a macrocyclic polyol lactone antibiotic isolated from Streptoverticilium.

Biological Activity

monazomycin is a positively charged and polyenelike antibiotic produced by streptomyces [1].monazomycin is able to induce a voltage-dependent conductance in lipid bilayer membranes. monazomycin is selective for monovalent cations and can alter the membrane conductance when applied to one or both sides of the membrane [1]. application of micromolar amounts of monazomycin on one side of phospholipid bilayer membranes induced dramatic voltage-dependent conductance effects. the steady-state conductance was proportional to the 5th power of the monazomycin concentration and increased exponentially with positive voltage (monazomycin side positive); there was an e-fold change in conductance per 4–6 mv. the major current-carrying ions were univalent cations. monazomycin monomers cooperated to form a multimolecular conductance channel. the voltage control of conductance arose from the electric field driving monazomycin molecules at the membrane surface into the membrane and thus affecting the number of channels that were formed [2].

References

[1] bamberg e, janko k. single channel conductance at lipid bilayer membranes in presence of monazomycin[j]. biochimica et biophysica acta (bba)-biomembranes, 1976, 426(3): 447-450.
[2] muller r u, finkelstein a. voltage-dependent conductance induced in thin lipid membranes by monazomycin[j]. the journal of general physiology, 1972, 60(3): 263-284.

monazomycinSupplier

Lynnchem
Tel
86-(0)29-85992781 17792393971
Email
info@lynnchem.com
Novachemistry
Tel
44-20819178-90 02081917890
Email
info@novachemistry.com
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com
BOC Sciences
Tel
16314854226; +16314854226
Email
inquiry@bocsci.com
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Email
sales@chemegen.com