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  2. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    In quasi-enantiomers majority of the molecule is reflected; however, an atom or group within the molecule is changed to a similar atom or group. [34] Quasi-enantiomers can also be defined as molecules that have the potential to become enantiomers if an atom or group in the molecule is replaced. [35]

  3. Deoxyribose - Wikipedia

    en.wikipedia.org/wiki/Deoxyribose

    The term "2-deoxyribose" may refer to either of two enantiomers: the biologically important d-2-deoxyribose and to the rarely encountered mirror image l-2-deoxyribose. [3] d-2-deoxyribose is a precursor to the nucleic acid DNA. 2-deoxyribose is an aldopentose, that is, a monosaccharide with five carbon atoms and having an aldehyde functional group.

  4. Glycerol 3-phosphate - Wikipedia

    en.wikipedia.org/wiki/Glycerol_3-phosphate

    Glycerol 1-phosphate, sometimes called as D-glycerol 3-phosphate, is the enantiomer of glycerol 3-phosphate. Eukaryotes use the 3-phosphate, or L -configuration, for glycerolipid backbone. The 1-phosphate is specifically found in archeal lipids.

  5. Organic synthesis - Wikipedia

    en.wikipedia.org/wiki/Organic_synthesis

    Organic compounds are molecules consisting of combinations of covalently-linked hydrogen, carbon, oxygen, and nitrogen atoms. Within the general subject of organic synthesis, there are many different types of synthetic routes that can be completed including total synthesis, [1] stereoselective synthesis, [2] automated synthesis, [3] and many ...

  6. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    The two enantiomers can be distinguished, for example, by the right-hand rule. This type of isomerism is called axial isomerism. Enantiomers behave identically in chemical reactions, except when reacted with chiral compounds or in the presence of chiral catalysts, such as most enzymes. For this latter reason, the two enantiomers of most chiral ...

  7. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    A homogeneous mixture of the two enantiomers in equal parts is said to be racemic, and it usually differs chemically and physically from the pure enantiomers. Chiral molecules will usually have a stereogenic element from which chirality arises. The most common type of stereogenic element is a stereogenic center, or stereocenter.

  8. What Happens to Your Body on a Strictly Vegan Diet - AOL

    www.aol.com/happens-body-strictly-vegan-diet...

    “A healthy vegan diet is packed with antioxidants, fiber and anti-inflammatory compounds that help protect cells from damage and lower the risk of some types of cancer like colorectal and breast ...

  9. Cell (biology) - Wikipedia

    en.wikipedia.org/wiki/Cell_(biology)

    Embedded within this membrane is a macromolecular structure called the porosome the universal secretory portal in cells and a variety of protein molecules that act as channels and pumps that move different molecules into and out of the cell. [2]