Enantiomers

The stereochemistry of enantiomers can be determined using NMR spectroscopy.

Enantiomers can have different toxicological profiles, which can impact their safety as pharmaceuticals.

The study of enantiomers is important in the field of chiral separation science, which has applications in industries such as pharmaceuticals and biotechnology.

The resolution of enantiomers is important in the production of chiral drugs.

Enantiopure compounds are used to investigate the biological activity of enantiomers.

Enantiomers are used in pharmaceutical industry to make drugs.

Some flavors, such as carvone, have different smells depending on whether they are R or S enantiomers.

The two enantiomers of thalidomide have vastly different effects on developing fetuses.

The two enantiomers of limonene differ in their ability to rotate polarized light.

Enantiomers of this compound exhibit distinct odor profiles.

The enantiomers of tartaric acid can be separated by a process called chiral resolution.

The enantiomers of this drug have different side effect profiles.

Some pesticides contain enantiomers that are toxic to certain pests but harmless to others.

The enantiomers of this compound have different solubilities in water.

The chirality of the enantiomers in this reaction affects the yield of the product.

The enantiomers of aspartame have different tastes, with the L form being sweeter than the D form.

The enantiomers of adrenaline have different physiological effects on the body.

Enantiomers of this compound can have different affinities for receptors in the body.

The enantiomers of ibuprofen are mirror images of each other.

The two enantiomers of this molecule have different biological activities.

The enantiomers of warfarin have different effects on blood clotting and are used to treat and prevent thrombosis.

This medication contains both enantiomers, one rotates light clockwise and the other counterclockwise.

This substance is a mixture of enantiomers, which can have varying pharmacological effects.

The enantiomers of this amino acid have different biological functions.

The synthesis of this compound yields a racemic mixture of enantiomers.

Racemic glycidol is a mixture of both enantiomers that is used in the production of chiral epoxides.

The racemic mixture of the compound was separated into its individual enantiomers using chiral chromatography.

The physical properties of a racemic mixture, such as melting point and boiling point, can be different from those of the individual enantiomers.

A racemic mixture is a combination of equal amounts of both enantiomers.

The racemic mixture of the drug was found to have lower toxicity than its individual enantiomers.

The racemic mixture of the compound was resolved into its enantiomers using a chiral stationary phase.

The resolution of racemic mixtures into their individual enantiomers can be achieved through chiral chromatography.

The racemic form of a drug is often less potent than its pure enantiomers.

Racemic ketamine has been shown to be more effective than its individual enantiomers in treating depression.

Racemic acid is a compound that consists of both the R and S enantiomers in equal amounts.

The enantiomers of amphetamine have different effects on mood and attention.

The separation of enantiomers is important in the pharmaceutical industry to ensure the purity of drug products.

The formation of enantiomers in chemical reactions can be influenced by the use of chiral reagents or catalysts.

The study of enantiomers is important in the field of asymmetric synthesis.

Enantiomers can have different physical properties, such as melting points and boiling points.

The enantiomers of limonene have different aromas, but equal and opposite physiological effects.

The enantiomers of salbutamol have opposite effects on the airways, making it useful in the treatment of asthma.

The two enantiomers of adrenaline have opposite effects on the body.

The enantiomers of carvone are used as flavoring agents in food, with the R-form giving a spearmint-like flavor and the S-form giving a caraway-like flavor.

The enantiomers of amphetamines have opposite effects on the central nervous system.

The enantiomers of methamphetamine have different effects on the central nervous system.

The enantiomers of ephedrine have opposite effects on blood pressure and heart rate.

The enantiomers of omeprazole have opposite effects on acid secretion in the stomach.

The two enantiomers of ibuprofen have different pharmacokinetic profiles but equivalent pharmacodynamic activity.

The enantiomers of ibuprofen have opposite effects on the body's pain response.