Examples of 'lanosterol' in a sentence
Meaning of "lanosterol"
Lanosterol (noun): Lanosterol is a tetracyclic triterpenoid compound involved in the biosynthesis of steroids. It is a precursor to cholesterol and is found in high concentrations in the lens of the eye. Research has shown potential therapeutic applications of lanosterol in the treatment of cataracts
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- A triterpenoid sterol found in lanolin
How to use "lanosterol" in a sentence
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lanosterol
Examples of triterpenoids include squalene and lanosterol.
Modifications of lanosterol into other steroids are classified as steroidogenesis transformations.
Oxidosqualene cyclase then cyclizes squalene to form lanosterol.
Lanosterol is then converted to cholesterol through a number of enzymatic steps.
The sitosterol peak must be adequately resolved from lanosterol.
Lanosterol is converted through a number of subsequent enzymatic steps to cholesterol.
Examples of zoosterols which may be mentioned are cholesterol and lanosterol.
Lanosterol can then be converted into other steroids such as and.
These siblings shared a mutation that stopped the production of lanosterol.
Lanosterol and cycloartenol derive from cyclization of the triterpenoid squalene.
These siblings shared a change that stopped the production of lanosterol.
Results repeatedly showed that lanosterol was able to significantly shrink cataract size.
Zoosterols which may be mentioned by way of example are cholesterol and lanosterol.
Lanosterol can then be converted into other steroids such as cholesterol and ergosterol.
Many coding sequences and protein sequences are known for lanosterol synthase.
See also
FXRB is a lanosterol sensor and its physiological function remains unclear.
Inhibition of oxidosqualene cyclase decreases the amount of lanosterol available for conversion to cholesterol.
Finally, lanosterol is then converted to cholesterol.
Zhang said he hopes to begin human testing with lanosterol within two years.
Lanosterol is a tetracyclic triterpenoid, which is the compound from which all steroids are derived.
This enzyme participates in the sterol biosynthesis pathway that leads from lanosterol to ergosterol.
This interrupts the conversion of lanosterol to ergosterol, a component of the fungal cell membrane.
What was discovered is that these children had a mutation which prevented their lanosterol production.
Through a complicated series of reactions, lanosterol leads to the formation of zymosterol.
In yeast, squalene is converted to squalene epoxide, which is then cyclized to form lanosterol.
Benefits of Lanosterol.
Lanosterol has the following chemical formula, -.
This is followed by 19 additional steps to convert the resulting lanosterol into cholesterol.
Furthermore, lanosterol was detected in these azole-treated cells.
All steroids are manufactured in cells from the sterols lanosterol ( opisthokonts ) or cycloartenol plants.
Through a series of 19 additional reactions, cholesterol is synthesized from lanosterol.
After drying, radioactive MOS and lanosterol were observed on the silica gel plate.
The column must be capable of resolving trimethyl-silyl derivatives of lanosterol and sitosterol.
For example, for lanosterol, the triterpene synthase is a lanosterol synthase.
These occur after ring formation from squalene, in the transformation of lanosterol to other sterols.
Lanosterol also cleared up cataracts in lenses dissected from 13 lab rabbits.
In some aspects, the triterpenoid can be, without limitation, squalene or lanosterol.
Lanosterol and cycloartenol are derived from the cyclization of the triterpene squalene . [ 5 ].
The inhibition of 14α-demethylase results in inhibition of lanosterol to ergosterol conversion.
For the lanosterol ethoxylate, the best performance was obtained with product D containing 75 radicals.
Examples of the sterols include cholesterol, sitosterol, phytosterol, and lanosterol.
Demethylation of lanosterol by CYP51 eventually yields cholesterol.
The strain shows supersensitivity to ketoconazole and other lanosterol 14-a-demethylase inhibitors.
Finally, lanosterol is converted to cholesterol through a 19-step process.
Thus, triterpenoids suitable for use in the adjuvant compositions include saponins, squalene, and lanosterol.
A lanosterol ethoxylate ( lanoline ethoxylated containing 75 ethylene oxide radical ).
The conversion of 2,3-oxido-squalene to lanosterol is a key step in the biosynthesis of cholesterol.
Triterpenes comprise six isoprene units and comprise, e.g., squalene, lanosterol and cycloartenol.
Small amounts of lanosterol are also detectable ( only in the analyses of total sterols ) . EXAMPLE 11.
Adding to a corresponding culture a positive control comprising a known lanosterol 14-a-demethylase inhibitor ;.
