Aminoacids and derivatives
Amino acids are compounds with a structure based on an amino group (-NH₂) and a carboxyl group (-COOH), both attached to a central carbon atom. This structure makes them essential for the synthesis of proteins and other biomolecules. Their derivatives can have regulatory properties over metabolic processes and biological systems, with applications in nutrition, health, and regenerative medicine.
At CymitQuimica, we offer a wide range of amino acids and their derivatives, ideal for research and the formulation of bioactive products.
Found 12278 products of "Aminoacids and derivatives"
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(S)-(1-Methylazetidin-2-yl)methanamine dihydrochloride
CAS:Purity:97.0%Molecular weight:173.0800018310547O-Acetyl Lacosamide
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications O-Acetyl Lacosamide is an impurity of Lacosamide (L098500) which is a potent anticonvulsant.<br>References Lees, G., et al.: Brain Res., 612, 190 (1993), Kuo, C., et al.: Mol. Pharmacol., 51, 1077 (1997), Barton, M., et al.: Epilepsy Res., 47, 217 (2001), Beyreuther, B., et al.: Eur. J. Pharmacol., 539, 64 (2006), Beyreuther, B., et al.: CNS Drug Rev., 13, 21 (2007),<br></p>Formula:C14H18N2O4Color and Shape:NeatMolecular weight:278.3037Tert-Butyl 2,3-dihydro-1H-spiro[isoquinoline-4,4'-piperidine]-1'-carboxylate
CAS:Purity:95.0%Molecular weight:302.41799926757811-(Phenoxypropyl)piperazine
CAS:Formula:C13H20N2OPurity:98.0%Color and Shape:SolidMolecular weight:220.316Glycine-15N,d2
CAS:Controlled Product<p>Applications Glycine-15N,d2, is the labeled analogue of Glycine (G615990), a non-essential amino acid for human development. Glycine is an inhibitory neurotransmitter in spinal cord, allosteric regulator of NMDA receptors.<br>References Scott, D. et al.: J. Neurosci., 21, 3063 (2001); Laube, B. et al.: Neuropharmacology, 47, 994 (2004); Papadakis, M. et al.: J. Biol. Chem., 279, 14703 (2004); Chen, P. et al.: Mol. Pharmacol., 67, 1470 (2005); Wolosker, H. et al.: Mol. Neurobiol., 36, 152 (2007);<br></p>Formula:C2D2H315NO2Color and Shape:NeatMolecular weight:78.0726-Aminocaproic Acid Dimer
CAS:<p>Applications 6-Aminocaproic Acid Dimer is a reactant with citric acid in the formation of 3-hydroxy-3,4-dicarboxy-butanamide-N-hexanoic acid.<br>References Schou-Pedersen, A. V., et al.: J. Pharm. Biomed. Anal., 107, 333-340 (2015)<br></p>Formula:C12H24N2O3Color and Shape:White To Off-WhiteMolecular weight:244.333',4'-Dihydroxyphenylacetone
CAS:<p>Applications A metabolite of 3,4-methylenedioxyethylamphetamine (M303975).<br>References Nichols, D., et al.: J. Med. Chem., 29, 2009 (1986), Ricaurte, G., et al.: Brain Res., 446, 165 (1988), Colado, M., et al.: Br. J. Pharmacol., 111, 131 (1994), Helmlin, H., et al.: J. Anal. Toxicol., 20, 432 (1996), Maurer, H., et al.: Ther. Drug Monit., 18, 465 (1996),<br></p>Formula:C9H10O3Color and Shape:NeatMolecular weight:166.176-Amino-4-{[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]amino}-7-ethoxyquinoline-3-carbonitrile
CAS:Purity:98%Molecular weight:445.9100036621094cis-9-Hexadecenoylcarnitine Inner
CAS:Controlled Product<p>Applications cis-9-Hexadecenoylcarnitine Inner Salt is an L-carnitine metobolite which are often used to diagnose specific inherited metabolic diseases.<br>References Yang, S. et l.: J. Chrom. B., Anal. Tech. Biomed. Life Sci., 857, 251 (2007); Minkler, P. et al.: J. Chrom. B., Anal. Tech. Biomed. Life Sci. 1061, 128 (2017);<br></p>Formula:C23H43NO4Color and Shape:NeatMolecular weight:397.5922-(1-Methylpyrrolidin-3-yl)ethylamine
CAS:Formula:C7H16N2Purity:95.0%Color and Shape:LiquidMolecular weight:128.2195-Morpholin-4-yl-1,3,4-oxadiazol-2-ylamine
CAS:Formula:C6H10N4O2Purity:95.0%Color and Shape:SolidMolecular weight:170.1723-(Carboxymethyl-methyl-amino)-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS:Purity:95.0%Molecular weight:258.31799316406252-(furan-2-yl)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine
CAS:Purity:95.0%Molecular weight:214.26800537109375Tert-butyl (2-oxo-2-(piperidin-4-ylamino)ethyl)carbamate
CAS:Purity:98%Molecular weight:257.33401489257816-Aminohexanoic Acid
CAS:Controlled Product<p>Applications 6-Aminohexanoic Acid is a reagent commonly used for the extraction of aldehydes from reaction mixtures. 6-Aminohexanoic Acid has also been shown to improve solubilization of membrane proteins in electrophoresis. Studies suggest that 6-Aminohexanoic Acid inhibits the activation of the first component of the complement system.<br>References Ohta ,S. et al.: Chem. Pharm. Bull., 28, 1917 (1980); Shagger, H. et al.: Anal. Biochem., 199, 223 (1991); Soter, N.A. et al.: J. Immunol., 114, 928 (1975);<br></p>Formula:C6H13NO2Color and Shape:WhiteMolecular weight:131.17
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