enantiomer|enantiomers in English

noun

each of the pair of crystals or molecules that are mirror images of each othe

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1. Both enantiomers may be separated by chiral resolution of the racemic mixture, and the (S)- enantiomer may be specifically obtained by fermentation of fumaric acid.

2. The yield of desired enantiomers can be increased by transformed racemic resolution, the diastereomeric salt being precipitated when the undesired enantiomer is racemised in the presence of (hetero)aromatic aldehydes.

3. The (−) enantiomers of pindolol and isoprenaline showed pronounced higher affinities for the receptor sites than the respective (+) enantiomers.

4. L-Alanine is the L-enantiomer of Alanine

5. Androsterone is a major metabolite of testosterone and androstenedione along with the enantiomer etiocholanolone

6. Two mirror images of a Chiral molecule are called enantiomers or optical isomers

7. According to some research, the (+)-enantiomer is more effective in treating malaria, and the (–)-enantiomer specifically binds to adenosine receptors in the central nervous system, which may explain some of its psychotropic effects.

8. The naturally occurring optically pure enantiomer (+)ABA was a more potent germination inhibitor than synthetic (−)-ABA.

9. The enantiomers were equal to the racemate in analgesic potency, but inferior by far to morphine.

10. Enantiomer-enriched alpha-,omega amino alcohol derivatives, their production and use as insect- and mite-repelling agents

11. Claimed are compound srepresented by Formula II, its enantiomers, diastereoisomers, tautomers, or a pharmaceutically acceptable salt thereof.

12. Malic acid has two stereoisomeric forms (L- and D-enantiomers), though only the L-isomer exists naturally.

13. The enantiomers of the monosulfides could be separated quite well, while those of the Bisulfides could not at all.

14. The enantiomers of the monosulfides could be separated quite well, while those of the Bisulfides could not at all.

15. Enantiomers are separated based on the number and type of each interaction that occurs during their exposure to the Chiral stationary phase.

16. Optically active 1-aminoindan derivatives are prepared by reacting a N-benzyl analog of the desired compound with an enantiomer of mandelic acid.

17. Chiral chromatography refers to the separation of enantiomers using a Chiral HPLC column, an HPLC column that is packed with a Chiral stationary phase (CSP)

18. Clearly, Chiral molecules have two forms which are mirror-symmetric; these two molecules are called enantiomers, and are chemically similar, but structurally distinct, molecules

19. When Chiral compounds are created from aChiral compounds, the products are racemic unless a single enantiomer of a Chiral co-reactant or catalyst is involved in the reaction

20. Several Acylamido boronic acids and difluoroborane analogs of amino acids, some as single enantiomers, have been synthesized and evaluated as "transition state" inhibitors of the serine proteases (alpha)-chymotrypsin and elastase

21. Six new pairs of bibenzyl-based meroterpenoid enantiomers, (±)-rasumatranin A-D (1-4) and (±)-radulanin M and N (5 and 6), and six known compounds were isolated from the Adnascent Chinese liverwort, Radula sumatrana

22. L-Ascorbate is the L-enantiomer of Ascorbate and conjugate base of L-ascorbic acid, arising from selective deprotonation of the 3-hydroxy group.Required for a range of essential metabolic reactions in all animals and plants

23. Abscisic acid (ABA) is a single 15-C sequiterpenoid hormone that was originally isolated from Abscising cotton fruits and maple dormant buds; the (+)-cis ABA enantiomer is the naturally active form found in plants

24. The invention relates to the use of 2-amino-4,5,6,7-tetrahydro-6-propylamino-benzothiazole (Pramipexol), its (+) or (-) enantiomers or one of their pharmacologically compatible salts in combination with another antidepressant, for the improved treatment of depressions and depressive states.

25. ‘The resulting Chiral nematic giant liquid crystals had wide temperature ranges for their liquid crystal phases, from room temperature to about 80° Celsius.’ ‘The most common examples of Chiral molecules are enantiomers.’ ‘The second type is the cholesteric liquid crystal phase, also called the Chiral nematic liquid crystal phase.’