enantiomer การใช้
- Enantiomer members often have different chemical reactions with other enantiomer substances.
- Enantiomer members often have different chemical reactions with other enantiomer substances.
- The molecule is chiral and the separate enantiomers have been isolated.
- The absorption and siposition of both enantiomers were studied in 1988.
- Both appear to refer to a mixture of the two enantiomers.
- The two enantiomers of HA-966 have differing pharmacological activity.
- However, the two enantiomers have been shown to exhibit different kinetics.
- Naproxen has always been marketed as the single active enantiomer.
- They can be sold as one enantiomer or as a racemic mixture.
- This means that preparing a pure enantiomer for medication is largely pointless.
- Very few studies compare individual enantiomers with racemic lipoic acid.
- The molecule has two possible enantiomers as shown in the structural diagrams.
- It is the racemic mixture of two enantiomers, dexfenfluramine and levofenfluramine.
- Individual enantiomers are often designated as either " organic and inorganic chemistry.
- Tocotrienols extracted from natural sources always consist of the dextrorotatory enantiomers only.
- The figure below shows how the D enantiomer is favored.
- It is a stereoisomer and pseudo-enantiomer of cinchonine.
- It is a stereoisomer and pseudo-enantiomer of cinchonidine.
- Styrene oxide has a chiral center and thus two enantiomers.
- Levopropylhexedrine is the " S "-enantiomer of propylhexedrine.
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