
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 12270 products of "Aminoacids and derivatives"
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2-(4-Fluorophenyl)-2-[4-(2-methylphenyl)piperazin-1-yl]acetic acid
CAS:Molecular weight:328.3869934082031Benzylamine
CAS:Controlled Product<p>Applications Benzylamine has been used as a reactant in the preparation of diacetylated benzylamide which has shown to induce a G1/G0 arrest in tumor cells and cytotoxicity against human ovarian cancer cells.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Siewert, B., et. al.: Bioorg. Med. Chem., 22, 594 (2014)<br></p>Formula:C7H9NColor and Shape:ColourlessMolecular weight:107.15(R)-N-Benzyl-3-methoxy-2-(N-methylacetamido)propanamide
CAS:Controlled Product<p>Applications N-Methyl Lacosamide is derived from (R)-2-Amino-N-benzyl-3-methoxypropionamide (A598000), which is an impurity of Lacosamide which is a potent anticonvulsant.<br>References Letiran, A., et al.: J. Med. Chem., 45, 4762 (2002); Wadavrao, S., et al.: Synthesis, 45, 3383 (2013);<br></p>Formula:C14H20N2O3Color and Shape:NeatMolecular weight:264.321-(2-Methylsulfonyl-4-nitrophenyl)piperazine
CAS:Formula:C11H15N3O4SPurity:98%Color and Shape:SolidMolecular weight:285.324-[4-(dimethylamino)benzoyl]-8-methyl-1-oxa-4,8-diazaspiro[4.5]decane-3-carboxylic acid
CAS:Purity:95.0%Molecular weight:347.41500854492192-(2-(4-((4-Chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethoxy)ethanol
CAS:Purity:95.0%Molecular weight:374.9100036621094Nε-(1-Carboxymethyl)-L-lysine
CAS:<p>Applications CEL and CML are two stable, nonenzymatic chemical modifications of protein lysine residues resulting from glycation and oxidation reactions.<br>References Fu, M.X., et al.: J. Biol. Chem., 271, 9982 (1996), Ahmed M.U., et al.: Biochem.J., 324, 565 (1997), Schleicher, E.D., et al.: J. Clin. Invest., 99, 457 (1997), Shibayama, R., et al.: Diabetes, 48, 1842 (1999),<br></p>Formula:C8H16N2O4Color and Shape:NeatMolecular weight:204.22(R)-tert-Butyl 3-[2-(dimethylamino)acetamido]piperidine-1-carboxylate
CAS:Purity:95.0%Molecular weight:285.38800048828125Ref: 10-F801706
1gTo inquire5gTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire250mgTo inquire2,3-Bis(4-(diphenylamino)phenyl)benzo[b]thiophene 1,1-dioxide
CAS:Purity:97%Molecular weight:652.80999755859383-Nitro-4-piperidin-1-ylaniline
CAS:Formula:C11H15N3O2Purity:98%Color and Shape:SolidMolecular weight:221.261,3-Bis(4-aminophenoxy)benzene
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:292.3380126953125L-Histidine
CAS:Controlled Product<p>Applications L-Histidine is an essential amino acid for human development which the body cannot produce on its own. L-Histidine is one of the 22 proteinogenic amino acids. L-Histidine precursor to histamine (H436500) and a component of carnosine.<br>References Kopple, J.D. et al.: J. Clin. Invest., 55, 881 (1975); Sachs, D.H., et al.: J. Biol. Chem., 246, 6576 (1971); Mercer, L.P., et al.: Nutrition, 6, 273 (1990); Morgan, W.T., et al.: J. Biol. Chem., 268, 6256 (1993);<br></p>Formula:C6H9N3O2Color and Shape:NeatMolecular weight:155.15[4-(3,4-dimethylphenyl)piperazin-1-yl](3-methylphenyl)acetic acid
Molecular weight:338.45098876953125

