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  2. Amino acid - Wikipedia

    en.wikipedia.org/wiki/Amino_acid

    Structure of a typical L-alpha-amino acid in the "neutral" form. Amino acids are organic compounds that contain both amino and carboxylic acid functional groups. [1] Although over 500 amino acids exist in nature, by far the most important are the 22 α-amino acids incorporated into proteins. [2]

  3. Aminopolycarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Aminopolycarboxylic_acid

    The parent of this family of ligands is the amino acid glycine, H 2 NCH 2 COOH, in which the amino group, NH 2, is separated from the carboxyl group, COOH by a single methylene group, CH 2. When the carboxyl group is deprotonated the glycinate ion can function as a bidentate ligand , binding the metal centre through the nitrogen and one of two ...

  4. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    Carboxylic acids are typically weak acids, meaning that they only partially dissociate into [H 3 O] + cations and R−CO − 2 anions in neutral aqueous solution. For example, at room temperature, in a 1- molar solution of acetic acid , only 0.001% of the acid are dissociated (i.e. 10 −5 moles out of 1 mol).

  5. Imino acid - Wikipedia

    en.wikipedia.org/wiki/Imino_acid

    proline. Secondary amino acids, amino acids containing a secondary amine group are sometimes named imino acids, [2] [3] though this usage is obsolescent. [1] The only proteinogenic amino acid of this type is proline, although the related non-proteinogenic amino acids hydroxyproline [4] [5] [6] and pipecolic acid [7] have often been included in studies of this class of compounds.

  6. Amino acid N-carboxyanhydride - Wikipedia

    en.wikipedia.org/wiki/Amino_acid_N-carboxyanhydride

    Glycine N-carboxyanhydride is the parent member of the amino acid N-carboxyanhydrides. NCAs are typically prepared by phosgenation of amino acids : [ 4 ] They were first synthesized by Hermann Leuchs by heating an N -ethoxycarbonyl or N -methoxycarbonyl amino acid chloride in a vacuum at 50-70 °C: [ 5 ] [ 6 ]

  7. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    Coupling of two amino acids in solution. The unprotected amine of one reacts with the unprotected carboxylic acid group of the other to form a peptide bond.In this example, the second reactive group (amine/acid) in each of the starting materials bears a protecting group.

  8. Here's What 30 Grams Of Protein Actually Looks Like For Every ...

    www.aol.com/30-grams-protein-looks-110000107.html

    In case you didn’t know: aiming for 20 to 30 grams of protein at each meal is ideal for keeping you full and energized. (And, FYI, experts recommend spacing out your protein intake across ...

  9. Aromatic acid - Wikipedia

    en.wikipedia.org/wiki/Aromatic_acid

    Aromatic acids are a type of aromatic compound. Included in that class are substances containing an aromatic ring and an organic acid functional group. There are several categories of aromatic acids including: Phenolic acids: substances containing an aromatic ring and an organic carboxylic acid function (C6-C1 skeleton). Aromatic amino acids [1]