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  2. Glycerol phosphate shuttle - Wikipedia

    en.wikipedia.org/wiki/Glycerol_phosphate_shuttle

    The glycerol phosphate shuttle was first characterized as a major route of mitochondrial hydride transport in the flight muscles of blow flies. [5] [6] It was initially believed that the system would be inactive in mammals due to the predominance of lactate dehydrogenase activity over glycerol-3-phosphate dehydrogenase 1 (GPD1) [5] [7] until high GPD1 and GPD2 activity were demonstrated in ...

  3. Phosphoranes - Wikipedia

    en.wikipedia.org/wiki/Phosphoranes

    Phosphoranes are also considered to be one of the resonance structures of ylides, these compounds feature a tetrahedral phosphorus center including a phosphorus–carbon double bond. These compounds are used as reagents in the Wittig reaction , for instance methylenetriphenylphosphorane or Ph 3 P=CH 2 .

  4. Phosphates in detergent - Wikipedia

    en.wikipedia.org/wiki/Phosphates_in_detergent

    [25] [26] [4] [27] [28] Similarly, testing found that phosphate bans in laundry detergent led to newer products which did not clean clothes as well but still could compete with the older products containing phosphate. [29] [30] A 1973 paper in psychology predicted a consumer response from the perspective of removing a behavioral freedom. [31]

  5. Phosphoryl group - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_group

    [2] [3] "Phosphoryl" groups are covalently bonded by a single bond to an organic molecule, phosphate group(s) or another "phosphoryl" group(s), and those groups are sp 3 hybridized at the phosphorus atom. [4] The term "phosphoryl" in the mentioned branches is usually used in the description of catalytic mechanisms in living organisms.

  6. Phosphodiester bond - Wikipedia

    en.wikipedia.org/wiki/Phosphodiester_bond

    The 5' end has a 5' carbon attached to a phosphate, and the other end, the 3' end, has a 3' carbon attached to a hydroxyl group. In chemistry, a phosphodiester bond occurs when exactly two of the hydroxyl groups (−OH) in phosphoric acid react with hydroxyl groups on other molecules to form two ester bonds.

  7. Adenosine diphosphate - Wikipedia

    en.wikipedia.org/wiki/Adenosine_diphosphate

    Steps 1 and 3 require the input of energy derived from the hydrolysis of ATP to ADP and P i (inorganic phosphate), whereas steps 7 and 10 require the input of ADP, each yielding ATP. [7] The enzymes necessary to break down glucose are found in the cytoplasm , the viscous fluid that fills living cells, where the glycolytic reactions take place.

  8. Phosphagen - Wikipedia

    en.wikipedia.org/wiki/Phosphagen

    Phosphagens, also known as macroergic compounds, are high energy storage compounds, also known as high-energy phosphate compounds, chiefly found in muscular tissue in animals. They allow a high-energy phosphate pool to be maintained in a concentration range, which, if it all were adenosine triphosphate (ATP), would create problems due to the ...

  9. Diphosphorus - Wikipedia

    en.wikipedia.org/wiki/Diphosphorus

    2. Unlike nitrogen, its lighter pnictogen neighbor which forms a stable N 2 molecule with a nitrogen to nitrogen triple bond, phosphorus prefers a tetrahedral form P 4 because P-P pi-bonds are high in energy. Diphosphorus is, therefore, very reactive with a bond-dissociation energy (117 kcal/mol or 490 kJ/mol) half that of dinitrogen. The bond ...

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