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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4-METHYL-3-(3-(4-METHYLPIPERAZIN-1-YL)PROPOXY)PHENYLBORONIC ACID
CAS:Purity:97%Molecular weight:292.19000243-((4-(Piperidin-4-yl)phenyl)amino)piperidine-2,6-dione hydrochloride
CAS:Purity:98%Molecular weight:323.82tert-Butyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate
CAS:Purity:97%Molecular weight:226.324-Piperidineacetic acid, α-amino-1-[(1,1-dimethylethoxy)carbonyl]-
CAS:Purity:98%Molecular weight:258.318N-Methylpiperidin-4-amine dihydrochloride
CAS:Formula:C6H16Cl2N2Purity:97%Color and Shape:LiquidMolecular weight:187.11tert-Butyl 4-(3-amino-4-nitrophenyl)piperazine-1-carboxylate
CAS:Purity:98%Molecular weight:322.3649902Nordalbergin
CAS:<p>Nordalbergin, a coumarin isolated from the bark of Dalbergia sissoo, can significantly induce the differentiation of HL-60 cells.</p>Formula:C15H10O4Purity:99.84% - 99.86%Color and Shape:SolidMolecular weight:254.24Sulfo-Cy3 diacid NHS ester
CAS:<p>Cy 3 (Non-Sulfonated) is a CY3-derived dye. CY3 is an amine-reactive cyanine orange dye for fluorescent labelling of proteins and nucleic acids.</p>Formula:C43H50N4O14S2Purity:98%Color and Shape:SolidMolecular weight:911.01(S)-(-)-Carbidopa
CAS:Controlled Product<p>Stability Unstable in Solution<br>Applications (S)-(-)-Carbidopa is a peripheral decarboxylase inhibitor that is commonly used in combination with L-DOPA (D533751) for treatment of Parkinsonism. S(-)-Carbidopa ( has also been shown to prolong the elimination half-life of L-DOPA from blood plasma and skeletal muscle.<br>References Henry, G.M. et al.: Psychosom. Med., 38, 95 (1976); Leguire, L.E. et al.: Invest. Ophthalmol. Vis. Sci. 34, 3090 (1993); Deleu, D. et al.: Naun. Schmied. Arch. Pharmacol. 348: 576 (1993);<br></p>Formula:C10H14N2O4Color and Shape:NeatMolecular weight:226.235-Hydroxy Tryptophol-d4
CAS:Controlled Product<p>Applications A labelled metabolite of Tryptophan (T947200).<br>References da Prada, M., et al.: Biochem. Pharmacol., 14, 1721 (1965), Curzon, G., et al.: Br. J. Pharmacol., 63, 627 (1978), Fukumori, R., et al.: J. Pharm. Pharmacol., 33, 586 (1981), Aasmoe, L., et al.: Biochem. Pharmacol., 57, 1067 (1999), Karamanakos, P., et al.: Pharmacol. Toxicol., 88, 106 (2001),<br></p>Formula:C102H4H7NO2Color and Shape:Light Orange Colour To Light RedMolecular weight:181.22Indole-3-acetyl-L-aspartic Acid
CAS:<p>Stability Hygroscopic<br>Applications Indole-3-acetyl-L-aspartic Acid is an indole-3-acetyl-amino acid conjugate involved in regulatory mechanisms for the control of auxin activity during physiological and pathophysiological responses.<br>References Ostrowski, M., et al.: J Plant Physiol, 191, 63-72 (2016)<br></p>Formula:C14H14N2O5Color and Shape:NeatMolecular weight:290.27L-Histidine Monohydrochloride Monohydrate
CAS:Controlled Product<p>Applications L-Histidine Monohydrochloride Monohydrate is a histamine precursor via histidine decarboxylase. Also, they are grown as crystals which possesses anti-bacterial activity.<br>References Chandra, J. S., et al.: World J. Pharm. Res., 4, 1408-1429 (2015)<br></p>Formula:C6H9N3O2·ClH·H2OColor and Shape:NeatMolecular weight:209.63Betaine-15N
CAS:Controlled Product<p>Applications Betaine-15N is an isotopically labelled analog of Betaine (B325005), which is an endogenous zwitterioin present in many biological systems and referred to as Glycine Betaine. It can be used as an organic osmolyte, a methyl donor and it can also be used for the treatment of homocystinuria, an inherited disorder of the metabolism of amino acid methionine.<br>References Ashraf, M. & Foolad, M.: Environ. Exp. Bot., 59, 206 (2006);Yancey, P.: J. Exp. Biol., 208, 2819 (2005);Rees, W., et. al.: Biochem., 32, 137 (1993)<br></p>Formula:C5H1115NO2Color and Shape:NeatMolecular weight:118.14DL-threo-β-(3,4-Methylenedioxyphenyl)serine-13C2,15N Acetate Salt
CAS:Controlled ProductFormula:C1013C2H1515NO7Color and Shape:NeatMolecular weight:288.233S-Hydroxy-N6,N6,N6-trimethyl-L-lysine Inner Salt (~90%)
CAS:Controlled ProductFormula:C9H20N2O3Purity:~90%Color and Shape:NeatMolecular weight:204.27
![tert-Butyl (4aS,7aS)-octahydro-1H-pyrrolo[3,4-b]pyridine-1-carboxylate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF792012.webp&w=3840&q=75)
![4-Piperidineacetic acid, α-amino-1-[(1,1-dimethylethoxy)carbonyl]-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb-webp%2FF980082.webp&w=3840&q=75)
