Amino Acids (AA)

<p>Applications L-Citrulline-d7, is the labeled analogue of L-Citrulline (C535700), which is an amino acid, first isolated from the juice of watermelon, Citrullus vulgaris Schrad., Cucurbitaceae. It is also used in the treatment of asthenia.<br>References Kurtz, et al.: J. Biol. Chem., 122, 477 (1938), Rajantie, J., et al.: J. Pediatr., 97, 927 (1980), Carpenter, T.O., et al.: N. Engl. J. Med., 312, 290 (1985),<br></p>

<p>Applications DL-Methionine methylsulfonium chloride (cas# 3493-12-07) is a useful research chemical.<br></p>

<p>2-Amino-3-methylpyridine is a colorless crystalline compound. It has the molecular formula of CHN and a molecular weight of 115.2 g/mol. 2-Amino-3-methylpyridine has an asymmetric carbon atom, so it is chiral and can be found in two different forms, enantiomers. The intermolecular hydrogen bond between nitrogen atoms is responsible for the high melting point of -40°C. The coordination geometry of group P2 is pyramidal with the nitrogen atom at the apex and two hydrogen atoms bonded to each other on either side of the nitrogen atom at 120° angles. X ray crystal structures have shown that 2-amino-3-methylpyridine exists as a molecule with an acylation reaction mechanism and intramolecular hydrogen bonding. Methanol solvent was used in this study to dissolve 2 amino 3 methyl pyridine because it does not react with copper chloride</p>

<p>5-Methylindole-3-acetic acid (5MI3A) is a molecule that has been shown to have antiproliferative properties in bladder cancer cells. 5MI3A binds to the receptor for GABA, which is an inhibitory neurotransmitter. It also inhibits the production of proinflammatory mediators and reactive oxygen species in cancer cells. 5MI3A has anticancer activity in prostate cancer cells and may act by inducing apoptosis and inhibiting cell proliferation. Consumption of 5MI3A may reduce the risk of cancer development by preventing DNA damage from carcinogens, suppressing inflammation, and regulating cell growth through its antagonistic properties.</p>

<p>N,N'-Di-boc-(L)-cystine-dimethyl ester is a fine chemical that can be used as a versatile building block. It is a complex compound with CAS No. 77826-55-2 and can be used as a reagent or speciality chemical in research. This chemical is also useful for the synthesis of various compounds and has been proven to be an excellent scaffold for chemical reactions.</p>

<p>1-(3,4-Methylenedioxyphenyl) 2-nitropropene (1-MPNP) is a phosphatase inhibitor that is active against gram-negative bacteria by inhibiting enterotoxins and chlamydia. 1-MPNP inhibits the activity of tyrosine phosphatases, which are enzymes that play a major role in bacterial virulence. 1-MPNP competitively inhibits the activity of tyrosine phosphatases and prevents them from catalyzing the hydrolysis of polyphosphate substrates. This inhibition leads to an accumulation of polyphosphates in the bacterial cell membrane, which disrupts its permeability and leads to cell death.</p>

<p>1-[4-Methyl-6-(trifluoromethyl)pyrimidin-2-yl]piperidine-3-carboxylic acid is a reagent that is used as a complex compound, as a useful intermediate, and as a fine chemical. It has been used in the manufacture of pharmaceuticals, agrochemicals, dyes, and pigments. It also has many applications in research such as its use as a building block for organic synthesis or to synthesize other compounds with potential uses in medicine.</p>

<p>3,4-Methylenedioxy propiophenone is a synthetic compound with a fatty acid chain. It has been shown to have potent activity against leishmania and has been used as an intermediate in the synthesis of other drugs. 3,4-Methylenedioxy propiophenone can be synthesized by acylation reactions with chloride and acetylcholinesterase inhibition. This product also has molecular docking properties, which have been analyzed using computational methods, such as profiling and profile analysis.</p>

<p>DL-Proline is a biological molecule that has been shown to bind to the DNA binding domains of proteins. This binding can be seen with the crystal structures of DL-proline and protein. The reaction mechanism for DL-proline is as follows:<br><br>DL-Proline + Protein → Proline + Protein<br><br>The equilibrium constant for this reaction is 1.0 at 298 K. The pKa value for the amide group in DL-proline is 4.8, which means that it will react with water and form an amine group at physiological pH levels. DL-Proline has been shown to have metabolic disorders.</p>