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The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/(100 mL)), unless shown otherwise. The substances are listed in alphabetical order.
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
Printable version; In other projects Wikidata item; Appearance. move to sidebar hide. The complete data for Tyrosine General information. Chemical formula: C 9 H 11 N ...
Plant biosynthesis of tyrosine from prephenate. In plants and most microorganisms, tyrosine is produced via prephenate , an intermediate on the shikimate pathway . Prephenate is oxidatively decarboxylated with retention of the hydroxyl group to give p -hydroxyphenylpyruvate, which is transaminated using glutamate as the nitrogen source to give ...
In plants, the shikimate pathway first leads to the formation of chorismate, which is the precursor of phenylalanine, tyrosine, and tryptophan. These aromatic amino acids are the precursors of many secondary metabolites, all essential to a plant's biological functions, such as the hormones salicylate and auxin. This pathway contains enzymes ...
Methionyl-tyrosine is a dipeptide consisting of the amino acids methionine and tyrosine. [1] Methionyl-tyrosine has been detected, but not quantified in, a few different foods, such as birds in the anatidae family, chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). It is expected to form during digestion of protein. [2]
Chorismic acid, more commonly known as its anionic form chorismate, is an important biochemical intermediate in plants and microorganisms. It is a precursor for: The aromatic amino acids phenylalanine, tryptophan, and tyrosine; Indole, indole derivatives and tryptophan; 2,3-Dihydroxybenzoic acid (DHB) used for enterobactin biosynthesis
N-Methyltyramine (NMT), also known as 4-hydroxy-N-methylphenethylamine, is a human trace amine [1] [2] and natural phenethylamine alkaloid found in a variety of plants. [3] As the name implies, it is the N-methyl analog of tyramine, which is a well-known biogenic trace amine with which NMT shares many pharmacological properties.