stereoisomer|stereoisomers in English

noun

one of two or more isomers whose molecular structures are identical but whose atomic arrangements differ (Chemistry)

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1. Characteristic representatives of Catechins are the stereoisomers catechin and epicatechin

2. Each of these allethrins consists of the eight possible stereoisomers.

3. Question: Supplemental Question: Isotactic/syndiotactic/Atactic Match The Description Of Each Stereoisomer With The Name Of Its Configuration Classification

4. (a) Draw the product(s) of Bromination of this compound, including all expected stereoisomers (if any)

5. Cresols is an aromatic organic compound and obtained from coal tar or petroleum as a mixture of three stereoisomers i.e

6. In stereoisomers the bond structure is the same, but the geometrical positioning of atoms and functional groups in space differs.

7. Threonine can exist in four possible stereoisomers with the following configurations: (2S,3R), (2R,3S), (2S,3S) and (2R,3R).

8. Benzene hexachloride (Bhc), any of several stereoisomers of 1,2,3,4,5,6-hexachlorocyclohexane formed by the light-induced addition of chlorine to benzene

9. A partly enantiopure variant of allethrin I, consisting of only two stereoisomers in an approximate ratio of 1:1, is called bioallethrin.

10. The Cresols are obtained from coal tar or petroleum, usually as a mixture of the three stereoisomers (molecules with the same

11. The number of open chain stereoisomers for an aldose monosaccharide is larger by one than that of a ketose monosaccharide of the same length.

12. ( B ) MIXTURES OF TWO OR MORE ISOMERS OF THE SAME ORGANIC COMPOUND ( WHETHER OR NOT CONTAINING IMPURITIES ) , EXCEPT MIXTURES OF ACYCLIC HYDROCARBON ISOMERS ( OTHER THAN STEREOISOMERS ) , WHETHER OR NOT SATURATED ( CHAPTER 27 ) ;

13. (b) mixtures of two or more isomers of the same organic compound (whether or not containing impurities), except mixtures of acyclic hydrocarbon isomers (other than stereoisomers), whether or not saturated (chapter 27).’

14. (b) mixtures of two or more isomers of the same organic compound (whether or not containing impurities), except mixtures of acyclic hydrocarbon isomers (other than stereoisomers), whether or not saturated (Chapter 27);

15. The present invention concerns the use of a 3-mercaptoheptyl carboxylate, in the form of any one of its stereoisomers or mixture thereof, as flavoring ingredient, in particular to impart fruity, teas and citrus aftertaste.

16. Without including E/Z stereoisomers, how many different structural isomers could be formed when the following Bromize undergoes E2 elimination upon treatment with NaOH? NOTE: some structural isomers may be formed in small amounts! a) 2

17. Purine compounds of Formula I, and including stereoisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting lipid kinases including p110 alpha and other isoforms of PI3K, and for treating disorders such as cancer mediated by lipid kinases.

18. Compounds of Formula I, and including stereoisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting lipid kinases including p110 alpha and other isoforms of PI3K, and for treating disorders such as cancer mediated by lipid kinases.

19. Compounds of Formula (I), and including stereoisomers, geometric isomers, tautomers, solvates, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting lipid kinases including p110 alpha and other isoforms of PI3K, and for treating disorders such as cancer or inflammation mediated by lipid kinases.

20. ChEBI Name Ambiguine I: ChEBI ID CHEBI:65401: Definition An Ambiguine that consists of a 5,5,7,10,10-pentamethyl-4,5,5a,6a,6b,7,8,9,9a,10-decahydro-10dH-6-oxa-4-azacyclopropa[6,7]cyclohepta[1,2,3,4-mno]aceanthrylen-10d-ol skeleton with an ethenyl substituent at position 7 and an isocyano group at position 6b (the 5aS,6aR,6bR,7R,9aR,10dR stereoisomer).

21. Con·for·ma·tion (kon'fōr-mā'shŭn), The spatial arrangement of a molecule achieved by rotation of groups about single covalent bonds, without breaking any covalent bonds; the latter restriction differentiates Conformation from configuration (as in anomers and related stereoisomers) where a bond or bonds must be broken in going from one form

22. Con·for·ma·tion (kon'fōr-mā'shŭn), The spatial arrangement of a molecule achieved by rotation of groups about single covalent bonds, without breaking any covalent bonds; the latter restriction differentiates Conformation from configuration (as in anomers and related stereoisomers) where a bond or bonds must be broken in going from one form

23. The present invention relates to a compound of formula (I), wherein A represents an optionally substituted phenyl or a 5- or 6-membered heteroaromatic ring system containing up to 4 heteroatoms selected from O, S and N, B represents a single bond, O, S or NR1, wherein R1 is selected from hydrogen or a C1-C6-alkyl group; L represents a linker; C represents an amino moiety; n represents 0 or 1; m represents 0, 1, 2, 3, 4, 5 or 6; X represents O or S; and Y represents hydrogen or an optionally substituted carbon moiety; and to stereoisomers, pharmaceutically acceptable salts or esters, or prodrugs thereof.