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CAS: 338-69-2 (D), 56-41-7 (L) ... ^a EINECS for L-alanine ^a CID 602 from PubChem ^a CID 5950 from PubChem This page was last edited on 12 April 2023, at 11: ...
Alanine was first synthesized in 1850 when Adolph Strecker combined acetaldehyde and ammonia with hydrogen cyanide. [8] [9] [10] The amino acid was named Alanin in German, in reference to aldehyde, with the interfix-an-for ease of pronunciation, [11] the German ending -in used in chemical compounds being analogous to English -ine.
At room temperature with 1 atmosphere of pressure, L-alanyl-L-glutamine has a solubility of about 586 g/L, which is more than 10 times glutamine's solubility (35 g/L). Also, glutamine does not withstand sterilization procedures, whereas alanyl-glutamine does. Alanyl-glutamine's high solubility makes it valuable in parenteral nutrition. [6] [7]
C 41 H 50 N 2 O 10: Neopluramycin: C 41 H 50 N 2 O 11: Hedamycin: 11048-97-8 C 44 H 55 NO 16: Milataxel: 352425-37-7 C 44 H 69 N 15 O 9 S: adrenorphin: C 48 H 56 N 10 O 12 S 6: Thiocoraline: C 52 H 48 MoN 4 P 4: Bis(dinitrogen)bis(1,2-bis(diphenylphosphino)ethane)molybdenum(0) 25145-64-6 C 55 H 74 IN 3 O 21 S 4: calicheamicin: C 58 H 84 N 12 O ...
In enzymology, an alanine-oxo-acid transaminase (EC 2.6.1.12) is an enzyme that catalyzes the chemical reaction. L-alanine + a 2-oxo acid pyruvate + an L-amino acid. Thus, the two substrates of this enzyme are L-alanine and 2-oxo acid, whereas its two products are pyruvate and L-amino acid.
Alanine dehydrogenase (EC 1.4.1.1) is an enzyme that catalyzes the chemical reaction. L-alanine + H 2 O + NAD + pyruvate + NH 3 + NADH + H +. The 2 substrates of this enzyme are L-alanine, water, and nicotinamide adenine dinucleotide + because water is 55M and does not change, whereas its 4 products are pyruvate, ammonia, NADH, and hydrogen ion.