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  2. Racemic acid - Wikipedia

    en.wikipedia.org/wiki/Racemic_acid

    Tartaric acid in pen sketch Computer-rendered image of right-handed molecule Racemic acid crystals drawn as if seen through an optical microscope. Racemic acid is an old name for an optically inactive or racemic form of tartaric acid. It is an equal mixture of two mirror-image isomers (enantiomers), optically active in opposing directions ...

  3. Succinic acid - Wikipedia

    en.wikipedia.org/wiki/Succinic_acid

    Succinic acid (/ s ə k ˈ s ɪ n ɪ k /) is a dicarboxylic acid with the chemical formula (CH 2) 2 (CO 2 H) 2. [5] In living organisms, succinic acid takes the form of an anion, succinate, which has multiple biological roles as a metabolic intermediate being converted into fumarate by the enzyme succinate dehydrogenase in complex 2 of the electron transport chain which is involved in making ...

  4. Racemic mixture - Wikipedia

    en.wikipedia.org/wiki/Racemic_mixture

    In chemistry, a racemic mixture or racemate (/ r eɪ ˈ s iː m eɪ t, r ə-, ˈ r æ s ɪ m eɪ t / [1]) is one that has equal amounts of left- and right-handed enantiomers of a chiral molecule or salt. Racemic mixtures are rare in nature, but many compounds are produced industrially as racemates.

  5. Carbohydrate conformation - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_conformation

    The chair conformation of six-membered rings have a dihedral angle of 60° between adjacent substituents thus usually making it the most stable conformer. Since there are two possible chair conformation steric and stereoelectronic effects such as the anomeric effect, 1,3-diaxial interactions, dipoles and intramolecular hydrogen bonding must be taken into consideration when looking at relative ...

  6. Glucose - Wikipedia

    en.wikipedia.org/wiki/Glucose

    Dextrose monohydrate is the hydrated form of D-glucose, meaning that it is a glucose molecule with an additional water molecule attached. [38] Its chemical formula is C 6 H 12 O 6 · H 2 O. [38] [39] Dextrose monohydrate is also called hydrated D-glucose, and commonly manufactured from plant starches.

  7. Biomolecule - Wikipedia

    en.wikipedia.org/wiki/Biomolecule

    Disaccharides are formed when two monosaccharides, or two single simple sugars, form a bond with removal of water. They can be hydrolyzed to yield their saccharin building blocks by boiling with dilute acid or reacting them with appropriate enzymes. [6] Examples of disaccharides include sucrose, maltose, and lactose.

  8. Glucose uptake - Wikipedia

    en.wikipedia.org/wiki/Glucose_uptake

    Glucose transporters are classified into three groups based on sequence similarity, with a total of 14 members.All GLUT proteins share a common structure: 12 transmembrane segments, a single N-linked glycosylation site, a large central cytoplasmic linker, and both N- and C-termini located in the cytoplasm. [3]

  9. Glycolysis - Wikipedia

    en.wikipedia.org/wiki/Glycolysis

    d -Glucose + 2 [NAD] + + 2 [ADP] + 2 [P] i 2 × Pyruvate 2 × + 2 [NADH] + 2 H + + 2 [ATP] + 2 H 2 O Glycolysis pathway overview The use of symbols in this equation makes it appear unbalanced with respect to oxygen atoms, hydrogen atoms, and charges. Atom balance is maintained by the two phosphate (P i) groups: Each exists in the form of a hydrogen phosphate anion, dissociating to contribute ...