CORN GLUTEN AMINO ACIDS

Base Information

• Chemical Name: CORN GLUTEN AMINO ACIDS
• CAS No.: 65072-01-7
• Molecular Formula: RCHNH2COOH
• Molecular Weight: 0
• Mol file: 65072-01-7.mol

Synonyms:Corn gluten amino acids;Travasol;AMI-U-II;Albumaid X;Alkyl amino acid;Aminess 5.2% essential amino acids w/ histadine;Amino Acid Blend;Amino acids solution, Moripron-F;Aminocarboxylic acids;Aminogen G;Aminomix;Aminosyn;Aminosyn 10%;Aminosyn 10% (ph6);Aminosyn 3.5%;Aminosyn 3.5% in plastic container;Aminosyn 5%;Aminosyn 7%;Aminosyn 7% (ph6);Aminosyn 8.5%;Aminosyn 8.5% (ph6);Aminosyn II 10%;Aminosyn II 10% in plastic container;Aminosyn II 15% in plastic container;Aminosyn II 3.5%;Aminosyn II 3.5% in plastic container;Aminosyn II 5%;Aminosyn II 7%;Aminosyn II 8.5%;Aminosyn II in dextrose;Aminosyn-HBC 7%;Aminosyn-HBC 7% in plastic container;Aminosyn-HF 8%;Aminosyn-PF 10%;Aminosyn-PF 7%;Aminosyn-RF 5.2%;Branchamin 4%;Branchamin 4% in plastic container;Chargex;Clinisol 15% sulfite free in plastic container;Clinomel;Clinomix;Complexamine;Diatrofen;ES Polytamin;Freamine;Freamine 8.5%;Freamine HBC 6.9%;Freamine II 8.5%;Freamine III 10%;Freamine III 8.5%;Glavamin;Hepatamine;Hepatamine 8%;Hepatasol 8%;Hepatosan;Isopuramin Plus;Ispol;Klinitamin;L-Amino acids;Moripron-F (amino acids solution);Neopham 6.4%;Nephramine;Nephramine 5.4%;Novamine 11.4%;Novamine 15%;Novamine 15% sulfite free in plastic container;Novamine 8.5%;Premasol 10% in plastic container;Premasol 6% in plastic container;Prosol 20% sulfite free in plastic container;Renamin w/o electrolytes;Travasol;Travasol 10% in plastic container;Travasol 10% w/o electrolytes;Travasol 5.5% in plastic container;Travasol 5.5% w/o electrolytes;Travasol 8.5% in plastic container;Travasol 8.5% w/o electrolytes;TrophAmine;Trophamine 10%;Amino acids;Amino acids solution, MPR-F;

Chemical Property of CORN GLUTEN AMINO ACIDS

Chemical Property:

• PSA: 0.00000
• LogP: 0.00000

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Refernces

Synthesis of new compounds derived from metronidazole and amino acids and their esters as antiparasitic agents

10.1007/s00044-011-9689-y

The research focuses on the synthesis and evaluation of new compounds derived from metronidazole and amino acids and their esters as potential antiparasitic agents. The synthesis involved a reaction between 2-(2-methyl-5-nitro-1H-imidazol-1-yl)acetic acid and various amino acid esters in the presence of N,N'-carbonyldiimidazole (CDI) and triethylamine (TEA), followed by hydrolysis with sodium hydroxide and acidification with hydrochloric acid to obtain the corresponding acids. The synthesized compounds were characterized using elemental analysis and spectroscopic techniques such as 1H-NMR, 13C-NMR, and mass spectrometry. The biological activity of these compounds was assessed through in vitro antiamoebic and antigiardial activity assays, as well as cytotoxicity tests on Hep-2 and Vero cell lines, with metronidazole serving as a standard drug for comparison. The study aimed to identify new derivatives with enhanced antiparasitic activity and lower cytotoxicity, which could contribute to overcoming drug resistance in pathogens.

On the activity and specificity of leucine aminopeptidase in eye lenses. Amino acid and dipeptide anilides as substrates.

10.1515/bchm2.1960.322.1.101

The research investigates the activity and specificity of leucine aminopeptidase (LAP) in bovine lenses using amino acid and dipeptide anilides as substrates. The study confirms that bovine lenses contain a significant amount of LAP, which is highly stable and active under optimal conditions (pH 8.5 and 56°C). The enzyme effectively hydrolyzes various amino acid anilides, with leucine anilide showing the highest activity. However, alanine anilide is hydrolyzed by a different enzyme with an optimum pH of 7.5 and temperature of 38°C. The study also demonstrates that the hydrolysis of peptide bonds in dipeptide anilides is significantly higher than that of the amino acid-anilide bond, with leucinamide being hydrolyzed about 30 times faster than its corresponding anilide. Comparative analysis across different species reveals considerable variation in LAP activity, while no significant differences were observed between normal and cataract human lenses.

Catalytic three-component Ugi reaction

10.1002/anie.200800494

The study presents a novel catalytic three-component Ugi reaction, which is a significant advancement in the field of multicomponent reactions (MCRs) for diversity-oriented synthesis. This reaction involves combining an aldehyde, a primary amine, and an isocyanide to produce α-amino amides, which are valuable for the synthesis of α-amino acids and their derivatives. The researchers identified phenyl phosphinic acid as the most effective catalyst for this atom-economic reaction, which proceeds via a nitrilium ion intermediate and results in water as the sole by-product. The study explored the reaction's scope by testing various aldehydes, amines, and isocyanides, demonstrating good yields for a broad range of substrates. This new reaction offers a practical and efficient method for generating α-amino amides and may have applications in the synthesis of pharmaceutical and agrochemical substance libraries.