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  2. Phenylpiperazine - Wikipedia

    en.wikipedia.org/wiki/Phenylpiperazine

    1-Phenylpiperazine (1-PP or PP) is a simple chemical compound and drug featuring a phenyl group bound to a piperazine ring. [1] The suffix ‘-piprazole’ is sometimes used in the names of drugs to indicate they belong to this class. [2] It is a rigid analogue of amphetamine.

  3. Osazone - Wikipedia

    en.wikipedia.org/wiki/Osazone

    Osazone formation was developed by Emil Fischer, [3] who used the reaction as a test to identify monosaccharides. The formation of a pair of hydrazone functionalities involves both oxidation and condensation reactions. [4] Since the reaction requires a free carbonyl group, only "reducing sugars" participate.

  4. 2,3-Dichlorophenylpiperazine - Wikipedia

    en.wikipedia.org/wiki/2,3-Dichlorophenylpiperazine

    It is both a precursor in the synthesis of aripiprazole and one of its metabolites. [1] [2] It is unclear whether 2,3-DCPP is pharmacologically active as a serotonin receptor agonist similar to its close analogue 3-chlorophenylpiperazine (mCPP), though it has been shown to act as a partial agonist of the dopamine D 2 and D 3 receptors. [3]

  5. Piperazine - Wikipedia

    en.wikipedia.org/wiki/Piperazine

    Two common salts in the form of which piperazine is usually prepared for pharmaceutical or veterinary purposes are the citrate, 3C 4 H 10 N 2 ·2C 6 H 8 O 7 (i.e. containing 3 molecules of piperazine to 2 molecules of citric acid), and the adipate, C 4 H 10 N 2 ·C 6 H 10 O 4 (containing 1 molecule each of piperazine and adipic acid). [6]

  6. Phenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/Phenylhydrazine

    Phenylhydrazine is used to prepare indoles by the Fischer indole synthesis, which are intermediates in the synthesis of various dyes and pharmaceuticals. Phenylhydrazine is used to form phenylhydrazones of natural mixtures of simple sugars in order to render the differing sugars easily separable from each other. [9]

  7. 2,5-Diketopiperazine - Wikipedia

    en.wikipedia.org/wiki/2,5-Diketopiperazine

    It is the parent of a large class of 2,5-Diketopiperazines (2,5-DKPs) with the formula (NHCH 2 (R)C(O)) 2 (R = H, CH 3, etc.). They are ubiquitous peptide in nature. They are often found in fermentation broths and yeast cultures as well as embedded in larger more complex architectures in a variety of natural products as well as several drugs. [ 2 ]

  8. George Pickens injury update: Latest on Steelers WR's ... - AOL

    www.aol.com/george-pickens-injury-latest...

    He's averaging 4.8 catches and 81.2 yards per game, scoring all three of his touchdowns with Wilson under center. This article originally appeared on USA TODAY: George Pickens injury update ...

  9. Uridine diphosphate - Wikipedia

    en.wikipedia.org/wiki/Uridine_diphosphate

    Before glucose can be stored as glycogen in the liver and muscles, the enzyme UDP-glucose pyrophosphorylase forms a UDP-glucose unit by combining glucose 1-phosphate with uridine triphosphate, cleaving a pyrophosphate ion in the process. Then, the enzyme glycogen synthase combines UDP-glucose units to form a glycogen chain. The UDP molecule is ...