Search results
Results from the WOW.Com Content Network
A meso compound or meso isomer is an optically inactive isomer in a set of stereoisomers, at least two of which are optically active. [1] [2] This means that despite containing two or more stereocenters, the molecule is not chiral. A meso compound is superposable on its mirror image (not to be confused with superimposable, as any two objects ...
However, since all other isomers are meso (non-chiral) compounds, the name myo-inositol is now preferred (myo- being a medical prefix for "muscle"). Inositol was once considered a member of the vitamin B complex, namely vitamin B 8 before the discovery that it is made naturally in the human body, and therefore cannot be a vitamin or essential ...
These include meso compounds, cis–trans isomers, E-Z isomers, and non-enantiomeric optical isomers. Diastereomers seldom have the same physical properties. In the example shown below, the meso form of tartaric acid forms a diastereomeric pair with both levo- and dextro-tartaric acids, which form an enantiomeric pair.
The meso-form is the second most abundant in nature, after 3R,3′R-zeaxanthin, which is produced by plants and algae. [1] Meso-zeaxanthin has been identified in specific tissues of marine organisms [2] and in the macula lutea, also known as the "yellow spot" of the human retina. [3] [4]
Of the three stereoisomers, two are enantiomers (levo- and dextro-2,3-butanediol) and one is a meso compound. [ 1 ] [ 2 ] The enantiomeric pair have (2 R , 3 R ) and (2 S , 3 S ) configurations at carbons 2 and 3, while the meso compound has configuration (2 R , 3 S ) or, equivalently, (2 S , 3 R ).
Diaminopimelic acid (DAP) is an amino acid, representing an epsilon-carboxy derivative of lysine. meso-α,ε-Diaminopimelic acid is the last intermediate in the biosynthesis of lysine and undergoes decarboxylation by diaminopimelate decarboxylase to give the final product.
The compound exists as three stereoisomers, a pair of enantiomers and the meso isomer. All are colorless liquids. Preparation and reactions 2,3 ...
It occurs in two diastereomers, meso and the chiral dl forms. The 2,3-dimercaptosuccinic acid molecule has two stereocentres (two asymmetric carbon atoms), and can exist as three different stereoisomers. The 2S,3S and 2R,3R isomers are a pair of enantiomers, whereas the 2R,3S isomer (succimer) is a meso compound and thus optically inactive.