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  2. Cysteine - Wikipedia

    en.wikipedia.org/wiki/Cysteine

    Cysteine (/ ˈ s ɪ s t ɪ iː n /; [5] symbol Cys or C [6]) is a semiessential [7] proteinogenic amino acid with the formula HOOC−CH(−NH 2)−CH 2 −SH. The thiol side chain in cysteine enables the formation of disulfide bonds, and often participates in enzymatic reactions as a nucleophile. Cysteine is chiral, but both D and L-cysteine ...

  3. Cystamine - Wikipedia

    en.wikipedia.org/wiki/Cystamine

    Cystamine (2,2'-dithiobisethanamine) is an organic disulfide.It is formed when cystine is heated, the result of decarboxylation.Cystamine is an unstable liquid and is generally handled as the dihydrochloride salt, C 4 H 12 N 2 S 2 ·2HCl, which is stable to 203-214 °C at which point it decomposes.

  4. Cysteine (data page) - Wikipedia

    en.wikipedia.org/wiki/Cysteine_(data_page)

    The complete data for Cysteine. General information. ... 2-amino-3-sulfanylpropanoic acid 3-mercaptoalanine AIDS{-}160777 CHEBI:15356 CHEMBANK2703 NSC 63864 NSC647530

  5. Cysteine metabolism - Wikipedia

    en.wikipedia.org/wiki/Cysteine_metabolism

    L-Cysteine consumption pathways; Enzyme → Products Cofactor/Additional Reactant cysteine dioxygenase [1] →: cysteine sulfinic acid: iron serine racemase [2] →: D-cysteine pyridoxal phosphate cysteine lyase [3] →: L-cysteate/hydrogen sulfide pyridoxal phosphate/sulfite cystathionine γ-lyase [4] →: pyruvate/NH 3 /H 2 S pyridoxal ...

  6. Cystine - Wikipedia

    en.wikipedia.org/wiki/Cystine

    Cystine is the oxidized derivative of the amino acid cysteine and has the formula (SCH 2 CH(NH 2)CO 2 H) 2.It is a white solid that is poorly soluble in water. As a residue in proteins, cystine serves two functions: a site of redox reactions and a mechanical linkage that allows proteins to retain their three-dimensional structure.

  7. Cysteamine - Wikipedia

    en.wikipedia.org/wiki/Cysteamine

    Cysteamine is an organosulfur compound with the formula HSCH 2 CH 2 NH 2.A white, water-soluble solid, it contains both an amine and a thiol functional groups. It is often used as salts of the ammonium derivative [HSCH 2 CH 2 NH 3] + [12] including the hydrochloride, phosphocysteamine, and the bitartrate. [13]

  8. Buffered charcoal yeast extract agar - Wikipedia

    en.wikipedia.org/wiki/Buffered_charcoal_yeast...

    Do not mix iron and cysteine before adding to medium as the L-cysteine is a chelating agent. Adjust the pH of the medium to 6.9 at room temperature. Since reagents may vary, each laboratory must determine the amount of KOH required. Hold the completed medium at 50 °C, pour a 10 mL sample, and check the pH at room temperature. When necessary ...

  9. Hydrochloride - Wikipedia

    en.wikipedia.org/wiki/Hydrochloride

    In chemistry, a hydrochloride is an acid salt resulting, or regarded as resulting, from the reaction of hydrochloric acid with an organic base (e.g. an amine). An alternative name is chlorhydrate, which comes from French. An archaic alternative name is muriate, derived from hydrochloric acid's ancient name: muriatic acid.

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