Examples of 'ester bonds' in a sentence
Meaning of "ester bonds"
ester bonds: a type of chemical bond that is formed from the reaction between alcohols and carboxylic acids
How to use "ester bonds" in a sentence
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ester bonds
Ester bonds are also found in many polymers.
Ether bonds are chemically more resistant than ester bonds.
Since BBPcontains two ester bonds it is difficult to perform a chemoselective reaction.
The extension of the polyether chains is provided by ester bonds.
Such ester bonds break apart when exposed to an aqueous environment.
The lengthening of the polyether chains is ensured by ester bonds.
This polymer contains ester bonds which hydrolyze in a hydrophilic environment.
Derivatisation may require the formation of phosphate ester bonds.
Those lipids having metabolizable ester bonds are preferred for in vivo use.
Romidepsin is a depsipeptide which contains both amide and ester bonds.
Polyestercarbonates have ester bonds and carbonate bonds in their polymer chain.
Phospholipases are enzymes that hydrolyze the ester bonds of phospholipids.
Ester bonds are preferred because the biodegradability of the biodegradable material will be increased.
The polyester polyol preferably comprises at least four ester bonds.
This result suggests that the two ester bonds have similar reactivities.
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Derivatisation generally requires the formation of one or more ester bonds.
These polyester carbonates have ester bonds and carbonate bonds in the polymeric chain.
The soft segments and the rigid segments are attached by ester bonds.
The saponification method used will hydrolyse ester bonds but is unlikely to break peptide bonds.
The rigid blocks and the flexible blocks are connected by ester bonds.
Since BBP contains two ester bonds it can react in a variety of chemical pathways.
The term is often used to refer to the hydrolysis of all ester bonds.
The existence of ester bonds between cellulose and butanetetracarboxylic acid was verified by IR spectroscopy.
Enzymes present in the respiratory system later cleave the ester bonds.
Ester bonds are known to be water-labile bonds.
Lactides are cyclic compounds containing two or more ester bonds in the ring.
Ester bonds are very labile, and are easily hydrolyzed at high temperatures.
A suitable enzyme for modification is one that can hydrolyse ester bonds.
For example, most hydrogels containing ester bonds can be hydrolyzed under physiological pH.
The hard segments and the flexible segments are attached together by ester bonds.
GALC hydrolyzes the galactose ester bonds of galactocerebroside, galactosylsphingosine, lactosylceramide, and monogalactosyldiglyceride.
Crosslinking must occur under acidic conditions to prevent reversion of the ester bonds.
Example, more cleavable linkers with ester bonds instrumentation.
In one suitable copolymer, polyether blocks are linked to polyamide blocks through ester bonds.
Examples of the hydrolytically decomposable bond include ester bonds and amide bonds.
This enzyme belongs to the family of hydrolases, specifically those acting on carboxylic ester bonds.
A strategy for the synthesis of libraries containing ester bonds is shown in Scheme IV.
Proteases, lipases and esterases are often used for hydrolysis of carboxylic ester bonds.
In preferred executions, it is believed that ester bonds are formed.
Preferably, a tandem arrangement of iminodiacetic acid groups provides for both types of ester bonds.
By ring opening, the lactones provide a unit having ester bonds at both ends.
The compounds V1 preferably comprise from three to ten functional groups capable of forming ester bonds.
Examples of hydrolysable units include, for example, ester bonds and ether bonds.
Thus, the groups RA and RB are linked to the glycerol backbone vía ester bonds.
Preferably, the copolymer according to the invention comprises ester bonds between each of the blocks.
PEG-PCL and PEG-PBT block copolymers all contain fragments with ester bonds.
Phospholipases A2 are a family of esterases that hydrolyze the sn-2 ester bonds in phosphoglyceride molecules.
The covalent bonds can be, for example, peptide, amide, thioether or ester bonds.
For example, anionic hydrophilic units capable of forming two ester bonds may be used.
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